| Year |
Citation |
Score |
| 2023 |
Wongchaisuwat N, Amato A, Lamborn AE, Yang P, Everett L, Pennesi ME. Retinitis pigmentosa GTPase regulator-related retinopathy and gene therapy. Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society. 37: 276-286. PMID 38155670 DOI: 10.4103/sjopt.sjopt_168_23 |
0.305 |
|
| 2023 |
Duncan JL, Cheng P, Maguire MG, Ayala AA, Birch DG, Cheetham JK, Durham TA, Fahim AT, Hoyng CB, Ishikawa H, Michaelides M, Pennesi ME, Alain-Sahel J, Stingl K, Weng CY. Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment through Two Years. American Journal of Ophthalmology. PMID 36764426 DOI: 10.1016/j.ajo.2023.02.002 |
0.351 |
|
| 2022 |
Birch DG, Samarakoon L, Melia M, Duncan JL, Ayala AR, Audo I, Cheetham JK, Durham TA, Iannaccone A, Pennesi ME, Stingl K. The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene. Investigative Ophthalmology & Visual Science. 63: 17. PMID 35293952 DOI: 10.1167/iovs.63.3.17 |
0.307 |
|
| 2021 |
Georgiou M, Fujinami K, Vincent A, Nasser F, Khateb S, Vargas ME, Thiadens AAHJ, de Carvalho ER, Nguyen XT, De Guimarães TAC, Robson AG, Mahroo OA, Pontikos N, Arno G, Fujinami-Yokokawa Y, ... ... Pennesi ME, et al. KCNV2-associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints - KCNV2 Study Group Report 2. American Journal of Ophthalmology. PMID 33737031 DOI: 10.1016/j.ajo.2021.03.004 |
0.344 |
|
| 2020 |
Ryals RC, Huang SJ, Wafai D, Bernert C, Steele W, Six M, Bonthala S, Titus H, Yang P, Gillingham M, Pennesi ME. A Ketogenic & Low-Protein Diet Slows Retinal Degeneration in rd10 Mice. Translational Vision Science & Technology. 9: 18. PMID 33117609 DOI: 10.1167/tvst.9.11.18 |
0.317 |
|
| 2020 |
Yang P, Lockard R, Titus H, Hiblar J, Weller K, Wafai D, Weleber RG, Duvoisin RM, Morgans CW, Pennesi ME. Suppression of cGMP-Dependent Photoreceptor Cytotoxicity With Mycophenolate Is Neuroprotective in Murine Models of Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 61: 25. PMID 32785677 DOI: 10.1167/Iovs.61.10.25 |
0.405 |
|
| 2020 |
Hormel TT, Jia Y, Jian Y, Hwang TS, Bailey ST, Pennesi ME, Wilson DJ, Morrison JC, Huang D. Plexus-specific retinal vascular anatomy and pathologies as seen by projection-resolved optical coherence tomographic angiography. Progress in Retinal and Eye Research. 100878. PMID 32712135 DOI: 10.1016/J.Preteyeres.2020.100878 |
0.317 |
|
| 2019 |
Pennesi ME, Birch DG, Duncan JL, Bennett J, Girach A. CHOROIDEREMIA: Retinal Degeneration With an Unmet Need. Retina (Philadelphia, Pa.). PMID 31021898 DOI: 10.1097/Iae.0000000000002553 |
0.357 |
|
| 2019 |
Fahim AT, Bouzia Z, Branham KH, Kumaran N, Vargas ME, Feathers KL, Perera ND, Young K, Khan NW, Heckenlively JR, Webster AR, Pennesi ME, Ali RR, Thompson DA, Michaelides M. Detailed clinical characterisation, unique features and natural history of autosomal recessive -associated retinal degeneration. The British Journal of Ophthalmology. PMID 30979730 DOI: 10.1136/bjophthalmol-2018-313580 |
0.321 |
|
| 2019 |
Jiang D, Ryals RC, Huang SJ, Weller KK, Titus HE, Robb BM, Saad FW, Salam RA, Hammad H, Yang P, Marks DL, Pennesi ME. Monomethyl Fumarate Protects the Retina From Light-Induced Retinopathy. Investigative Ophthalmology & Visual Science. 60: 1275-1285. PMID 30924852 DOI: 10.1167/Iovs.18-24398 |
0.304 |
|
| 2019 |
Hagag AM, Wang J, Lu K, Harman G, Weleber RG, David Huang, Yang P, Pennesi ME, Jia Y. Projection-Resolved Optical Coherence Tomographic Angiography of Retinal Plexuses in Retinitis Pigmentosa. American Journal of Ophthalmology. PMID 30849344 DOI: 10.1016/J.Ajo.2019.02.034 |
0.322 |
|
| 2019 |
Alabduljalil T, Patel RC, Alqahtani AA, Gao SS, Gale MJ, Zhang M, Jia Y, Huang D, Chiang PW, Chen R, Wang J, Weleber RG, Pennesi ME, Yang P. Correlation of Outer Retinal Degeneration and Choriocapillaris Loss in Stargardt disease using en face OCT and OCT Angiography. American Journal of Ophthalmology. PMID 30771335 DOI: 10.1016/J.Ajo.2019.02.007 |
0.312 |
|
| 2019 |
Ong T, Pennesi ME, Birch DG, Lam BL, Tsang SH. Adeno-Associated Viral Gene Therapy for Inherited Retinal Disease. Pharmaceutical Research. 36: 34. PMID 30617669 DOI: 10.1007/S11095-018-2564-5 |
0.369 |
|
| 2017 |
Ku CA, Hull S, Arno G, Vincent A, Carss K, Kayton R, Weeks D, Anderson GW, Geraets R, Parker C, Pearce DA, Michaelides M, MacLaren RE, Robson AG, Holder GE, ... ... Pennesi ME, et al. Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration. Jama Ophthalmology. PMID 28542676 DOI: 10.1001/Jamaophthalmol.2017.1401 |
0.347 |
|
| 2016 |
Sun LW, Johnson RD, Langlo CS, Cooper RF, Razeen MM, Russillo MC, Dubra A, Connor TB, Han DP, Pennesi ME, Kay CN, Weinberg DV, Stepien KE, Carroll J. Assessing Photoreceptor Structure in Retinitis Pigmentosa and Usher Syndrome. Investigative Ophthalmology & Visual Science. 57: 2428-2442. PMID 27145477 DOI: 10.1167/Iovs.15-18246 |
0.335 |
|
| 2016 |
Weleber RG, Pennesi ME, Wilson DJ, Kaushal S, Erker LR, Jensen L, McBride MT, Flotte TR, Humphries M, Calcedo R, Hauswirth WW, Chulay JD, Stout JT. Results at 2 Years after Gene Therapy for RPE65-Deficient Leber Congenital Amaurosis and Severe Early-Childhood-Onset Retinal Dystrophy. Ophthalmology. PMID 27102010 DOI: 10.1016/J.Ophtha.2016.03.003 |
0.306 |
|
| 2015 |
Xiong WH, Pang JJ, Pennesi ME, Duvoisin RM, Wu SM, Morgans CW. The Effect of PKCα on the Light Response of Rod Bipolar Cells in the Mouse Retina. Investigative Ophthalmology & Visual Science. 56: 4961-74. PMID 26230760 DOI: 10.1167/Iovs.15-16622 |
0.578 |
|
| 2015 |
Jia Y, Bailey ST, Hwang TS, McClintic SM, Gao SS, Pennesi ME, Flaxel CJ, Lauer AK, Wilson DJ, Hornegger J, Fujimoto JG, Huang D. Quantitative optical coherence tomography angiography of vascular abnormalities in the living human eye. Proceedings of the National Academy of Sciences of the United States of America. 112: E2395-402. PMID 25897021 DOI: 10.1073/Pnas.1500185112 |
0.32 |
|
| 2015 |
Ji J, Chang P, Pennesi ME, Yang Z, Zhang J, Li D, Wu SM, Gross RL. Corrigendum to "Effects of elevated intraocular pressure on mouse retinal ganglion cells" [Vision Res. 45 (2004) 169-179] DOI: 10.1016/j.visres.2004.08.008 Vision Research. 117: 136. DOI: 10.1016/j.visres.2015.10.005 |
0.571 |
|
| 2014 |
Messenger WB, Yang P, Pennesi ME. Ophthalmic findings in an infant with phosphomannomutase deficiency. Documenta Ophthalmologica. Advances in Ophthalmology. 128: 149-53. PMID 24493206 DOI: 10.1007/s10633-014-9427-0 |
0.321 |
|
| 2013 |
Pennesi ME. A little algae a day keeps the retinal degeneration specialist away? Jama Ophthalmology. 131: 983-4. PMID 23700100 DOI: 10.1001/jamaophthalmol.2013.4468 |
0.323 |
|
| 2012 |
Pennesi ME, Michaels KV, Magee SS, Maricle A, Davin SP, Garg AK, Gale MJ, Tu DC, Wen Y, Erker LR, Francis PJ. Long-term characterization of retinal degeneration in rd1 and rd10 mice using spectral domain optical coherence tomography. Investigative Ophthalmology & Visual Science. 53: 4644-56. PMID 22562504 DOI: 10.1167/Iovs.12-9611 |
0.345 |
|
| 2012 |
Courtney RJ, Pennesi ME. Inherited retinal degenerations with systemic manifestations. International Ophthalmology Clinics. 52: 119-47. PMID 22124242 DOI: 10.1097/IIO.0b013e31823bbe56 |
0.318 |
|
| 2011 |
Courtney RJ, Pennesi ME. Retinal dystrophy in 2 brothers with α-Mannosidosis. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 799-802. PMID 21670350 DOI: 10.1001/archophthalmol.2011.134 |
0.39 |
|
| 2009 |
Abd-El-Barr MM, Pennesi ME, Saszik SM, Barrow AJ, Lem J, Bramblett DE, Paul DL, Frishman LJ, Wu SM. Genetic dissection of rod and cone pathways in the dark-adapted mouse retina. Journal of Neurophysiology. 102: 1945-55. PMID 19587322 DOI: 10.1152/Jn.00142.2009 |
0.576 |
|
| 2009 |
Hayashi A, Naseri A, Pennesi ME, de Juan E. Subretinal delivery of immunoglobulin G with gold nanoparticles in the rabbit eye. Japanese Journal of Ophthalmology. 53: 249-56. PMID 19484444 DOI: 10.1007/s10384-009-0655-x |
0.377 |
|
| 2008 |
Pennesi ME, Nishikawa S, Matthes MT, Yasumura D, LaVail MM. The relationship of photoreceptor degeneration to retinal vascular development and loss in mutant rhodopsin transgenic and RCS rats. Experimental Eye Research. 87: 561-70. PMID 18848932 DOI: 10.1016/j.exer.2008.09.004 |
0.321 |
|
| 2007 |
Abd-El-Barr MM, Sykoudis K, Andrabi S, Eichers ER, Pennesi ME, Tan PL, Wilson JH, Katsanis N, Lupski JR, Wu SM. Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndrome. Vision Research. 47: 3394-407. PMID 18022666 DOI: 10.1016/j.visres.2007.09.016 |
0.533 |
|
| 2007 |
Albini TA, Abd-El-Barr MM, Carvounis PE, Iyer MN, Lakhanpal RR, Pennesi ME, Chevez-Barrios P, Wu SM, Holz ER. Long-term retinal toxicity of intravitreal commercially available preserved triamcinolone acetonide (Kenalog) in rabbit eyes. Investigative Ophthalmology & Visual Science. 48: 390-5. PMID 17197559 DOI: 10.1167/iovs.06-0145 |
0.57 |
|
| 2006 |
Pennesi ME, Bramblett DE, Cho JH, Tsai MJ, Wu SM. A role for bHLH transcription factors in retinal degeneration and dysfunction. Advances in Experimental Medicine and Biology. 572: 155-61. PMID 17249569 DOI: 10.1007/0-387-32442-9_23 |
0.552 |
|
| 2006 |
Gao H, Pennesi ME, Qiao X, Iyer MN, Wu SM, Holz ER, Mieler WF. Intravitreal moxifloxacin: retinal safety study with electroretinography and histopathology in animal models. Investigative Ophthalmology & Visual Science. 47: 1606-11. PMID 16565399 DOI: 10.1167/iovs.05-0702 |
0.549 |
|
| 2005 |
Ji J, Chang P, Pennesi ME, Yang Z, Zhang J, Li D, Wu SM, Gross RL. Effects of elevated intraocular pressure on mouse retinal ganglion cells. Vision Research. 45: 169-79. PMID 15581918 DOI: 10.1016/j.visres.2004.08.008 |
0.566 |
|
| 2004 |
Gao H, Pennesi ME, Shah K, Qiao X, Hariprasad SM, Mieler WF, Wu SM, Holz ER. Intravitreal voriconazole: an electroretinographic and histopathologic study. Archives of Ophthalmology (Chicago, Ill. : 1960). 122: 1687-92. PMID 15534131 DOI: 10.1001/archopht.122.11.1687 |
0.564 |
|
| 2004 |
Bramblett DE, Pennesi ME, Wu SM, Tsai MJ. The transcription factor Bhlhb4 is required for rod bipolar cell maturation. Neuron. 43: 779-93. PMID 15363390 DOI: 10.1016/j.neuron.2004.08.032 |
0.564 |
|
| 2003 |
Gao H, Pennesi M, Shah K, Qiao X, Hariprasad SM, Mieler WF, Wu SM, Holz ER. Safety of intravitreal voriconazole: electroretinographic and histopathologic studies. Transactions of the American Ophthalmological Society. 101: 183-9; discussion 18. PMID 14971576 |
0.571 |
|
| 2003 |
Gross RL, Ji J, Chang P, Pennesi ME, Yang Z, Zhang J, Wu SM. A mouse model of elevated intraocular pressure: retina and optic nerve findings. Transactions of the American Ophthalmological Society. 101: 163-9; discussion 16. PMID 14971574 |
0.561 |
|
| 2003 |
Pennesi ME, Howes KA, Baehr W, Wu SM. Guanylate cyclase-activating protein (GCAP) 1 rescues cone recovery kinetics in GCAP1/GCAP2 knockout mice. Proceedings of the National Academy of Sciences of the United States of America. 100: 6783-8. PMID 12732716 DOI: 10.1073/Pnas.1130102100 |
0.542 |
|
| 2003 |
Qiao X, Pennesi M, Seong E, Gao H, Burmeister M, Wu SM. Photoreceptor degeneration and rd1 mutation in the grizzled/mocha mouse strain. Vision Research. 43: 859-65. PMID 12668055 DOI: 10.1016/S0042-6989(02)00393-0 |
0.582 |
|
| 2003 |
Yoo SY, Pennesi ME, Weeber EJ, Xu B, Atkinson R, Chen S, Armstrong DL, Wu SM, Sweatt JD, Zoghbi HY. SCA7 knockin mice model human SCA7 and reveal gradual accumulation of mutant ataxin-7 in neurons and abnormalities in short-term plasticity. Neuron. 37: 383-401. PMID 12575948 DOI: 10.1016/S0896-6273(02)01190-X |
0.581 |
|
| 2003 |
Pennesi ME, Cho JH, Yang Z, Wu SH, Zhang J, Wu SM, Tsai MJ. BETA2/NeuroD1 null mice: a new model for transcription factor-dependent photoreceptor degeneration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 453-61. PMID 12533605 DOI: 10.1523/Jneurosci.23-02-00453.2003 |
0.552 |
|
| 2003 |
Pennesi ME, Cho J, Yang Z, Wu SH, Zhang J, Wu SM, Tsai M. BETA2/NeuroD1 Null Mice: A New Model for Transcription Factor-Dependent Photoreceptor Degeneration The Journal of Neuroscience. 23: 453-461. DOI: 10.1523/JNEUROSCI.23-02-00453.2003 |
0.49 |
|
| 2002 |
Howes KA, Pennesi ME, Sokal I, Church-Kopish J, Schmidt B, Margolis D, Frederick JM, Rieke F, Palczewski K, Wu SM, Detwiler PB, Baehr W. GCAP1 rescues rod photoreceptor response in GCAP1/GCAP2 knockout mice. The Embo Journal. 21: 1545-54. PMID 11927539 DOI: 10.1093/Emboj/21.7.1545 |
0.543 |
|
| 1998 |
Pennesi ME, Lyubarsky AL, Pugh EN. Extreme responsiveness of the pupil of the dark-adapted mouse to steady retinal illumination. Investigative Ophthalmology & Visual Science. 39: 2148-56. PMID 9761294 |
0.394 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2020 |
Ryals RC, Patel S, Acosta C, McKinney M, Pennesi ME, Sahay G. The effects of PEGylation on LNP based mRNA delivery to the eye. Plos One. 15: e0241006. PMID 33119640 DOI: 10.1371/journal.pone.0241006 |
0.3 |
|
| 2017 |
Ryals RC, Andrews MD, Datta S, Coyner AS, Fischer CM, Wen Y, Pennesi ME, McGill TJ. Long-term Characterization of Retinal Degeneration in Royal College of Surgeons Rats Using Spectral-Domain Optical Coherence Tomography. Investigative Ophthalmology & Visual Science. 58: 1378-1386. PMID 28253400 DOI: 10.1167/Iovs.16-20363 |
0.297 |
|
| 2024 |
Han JH, Rodenburg K, Hayman T, Calzetti G, Kaminska K, Quinodoz M, Marra M, Wallerich S, Allon G, Nagy ZZ, Knézy K, Li Y, Chen R, Barboni MTS, Yang P, ... Pennesi ME, et al. Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 101106. PMID 38420906 DOI: 10.1016/j.gim.2024.101106 |
0.294 |
|
| 2021 |
Patterson EJ, Langlo CS, Georgiou M, Kalitzeos A, Pennesi ME, Neitz J, Hardcastle AJ, Neitz M, Michaelides M, Carroll J. Comparing Retinal Structure in Patients with Achromatopsia and Blue Cone Monochromacy Using OCT. Ophthalmology Science. 1. PMID 36186895 DOI: 10.1016/j.xops.2021.100047 |
0.293 |
|
| 2019 |
Patel S, Ryals RC, Weller KK, Pennesi ME, Sahay G. Lipid nanoparticles for delivery of messenger RNA to the back of the eye. Journal of Controlled Release : Official Journal of the Controlled Release Society. PMID 30986436 DOI: 10.1016/J.Jconrel.2019.04.015 |
0.292 |
|
| 2024 |
Lam BL, Pennesi ME, Kay CN, Panda S, Gow JA, Zhao G, MacLaren RE. Assessment of Visual Function With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa in the Randomized XIRIUS Phase 2/3 Study. Ophthalmology. PMID 38423215 DOI: 10.1016/j.ophtha.2024.02.023 |
0.29 |
|
| 2018 |
Pennesi ME, Weleber RG, Yang P, Whitebirch C, Thean B, Flotte TR, Humphries M, Chegarnov E, Beasley KN, Stout JT, Chulay JD. Results at 5 Years after Gene Therapy for RPE65-deficient Retinal Dystrophy. Human Gene Therapy. PMID 29869534 DOI: 10.1089/hum.2018.014 |
0.289 |
|
| 2015 |
Thompson DA, Ali RR, Banin E, Branham KE, Flannery JG, Gamm DM, Hauswirth WW, Heckenlively JR, Iannaccone A, Jayasundera KT, Khan NW, Molday RS, Pennesi ME, Reh TA, Weleber RG, et al. Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium. Investigative Ophthalmology & Visual Science. 56: 918-31. PMID 25667399 DOI: 10.1167/Iovs.14-16049 |
0.289 |
|
| 2018 |
Wang Z, Camino A, Hagag AM, Wang J, Weleber RG, Yang P, Pennesi ME, Huang D, Li D, Jia Y. Automated detection of preserved photoreceptor on optical coherence tomography in choroideremia based on machine learning. Journal of Biophotonics. PMID 29341445 DOI: 10.1002/Jbio.201700313 |
0.286 |
|
| 2012 |
Gregory-Evans K, Pennesi ME, Weleber RG. Retinitis Pigmentosa and Allied Disorders Retina Fifth Edition. 2: 761-835. DOI: 10.1016/B978-1-4557-0737-9.00040-0 |
0.286 |
|
| 2021 |
Igelman AD, Ku C, da Palma MM, Georgiou M, Schiff ER, Lam BL, Sankila EM, Ahn J, Pyers L, Vincent A, Ferraz Sallum JM, Zein WM, Oh JK, Maldonado RS, Ryu J, ... ... Pennesi ME, et al. Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome. Ophthalmic Genetics. 1-10. PMID 34223797 DOI: 10.1080/13816810.2021.1946704 |
0.285 |
|
| 2016 |
Patel RC, Gao SS, Zhang M, Alabduljalil T, Al-Qahtani A, Weleber RG, Yang P, Jia Y, Huang D, Pennesi ME. OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY OF CHOROIDAL NEOVASCULARIZATION IN FOUR INHERITED RETINAL DYSTROPHIES. Retina (Philadelphia, Pa.). PMID 27336230 DOI: 10.1097/Iae.0000000000001159 |
0.28 |
|
| 2018 |
Camino A, Wang Z, Wang J, Pennesi ME, Yang P, Huang D, Li D, Jia Y. Deep learning for the segmentation of preserved photoreceptors on optical coherence tomography in two inherited retinal diseases. Biomedical Optics Express. 9: 3092-3105. PMID 29984085 DOI: 10.1364/Boe.9.003092 |
0.279 |
|
| 1999 |
Lyubarsky AL, Falsini B, Pennesi ME, Valentini P, Pugh EN. UV- and midwave-sensitive cone-driven retinal responses of the mouse: a possible phenotype for coexpression of cone photopigments. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 19: 442-55. PMID 9870972 DOI: 10.1523/Jneurosci.19-01-00442.1999 |
0.278 |
|
| 2020 |
Huckfeldt RM, Grigorian F, Place E, Comander JI, Vavvas D, Young LH, Yang P, Shurygina M, Pierce EA, Pennesi ME. Biallelic -associated retinal dystrophies: Expanding the mutational and clinical spectrum. Molecular Vision. 26: 423-433. PMID 32565670 |
0.275 |
|
| 2021 |
Scruggs BA, Vasconcelos HM, Matioli da Palma M, Kogachi K, Pennesi ME, Yang P, Bailey ST, Lauer AK. Injection pressure levels for creating blebs during subretinal gene therapy. Gene Therapy. PMID 34580433 DOI: 10.1038/s41434-021-00294-2 |
0.272 |
|
| 2022 |
Patterson EJ, Kalitzeos A, Kane TM, Singh N, Kreis J, Pennesi ME, Hardcastle AJ, Neitz J, Neitz M, Michaelides M, Carroll J. Foveal Cone Structure in Patients With Blue Cone Monochromacy. Investigative Ophthalmology & Visual Science. 63: 23. PMID 36301530 DOI: 10.1167/iovs.63.11.23 |
0.262 |
|
| 2016 |
Birch DG, Bennett LD, Duncan JL, Weleber RG, Pennesi ME. Long-term follow-up of patients with retinitis pigmentosa (RP) receiving intraocular ciliary neurotrophic factor implants. American Journal of Ophthalmology. PMID 27457255 DOI: 10.1016/J.Ajo.2016.07.013 |
0.262 |
|
| 2018 |
Birch DG, Bernstein PS, Iannacone A, Pennesi ME, Lam BL, Heckenlively J, Csaky K, Hartnett ME, Winthrop KL, Jayasundera T, Hughbanks-Wheaton DK, Warner J, Yang P, Fish GE, Teske MP, et al. Effect of Oral Valproic Acid vs Placebo for Vision Loss in Patients With Autosomal Dominant Retinitis Pigmentosa: A Randomized Phase 2 Multicenter Placebo-Controlled Clinical Trial. Jama Ophthalmology. PMID 29879277 DOI: 10.1001/Jamaophthalmol.2018.1171 |
0.261 |
|
| 2016 |
Gale MJ, Feng S, Titus HE, Smith TB, Pennesi ME. Interpretation of Flood-Illuminated Adaptive Optics Images in Subjects with Retinitis Pigmentosa. Advances in Experimental Medicine and Biology. 854: 291-7. PMID 26427424 DOI: 10.1007/978-3-319-17121-0_39 |
0.26 |
|
| 2023 |
Gaston G, Babcock S, Ryals R, Elizondo G, DeVine T, Wafai D, Packwood W, Holden S, Raber J, Lindner JR, Pennesi ME, Harding CO, Gillingham MB. A G1528C Hadha knock-in mouse model recapitulates aspects of human clinical phenotypes for long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Communications Biology. 6: 890. PMID 37644104 DOI: 10.1038/s42003-023-05268-1 |
0.256 |
|
| 2018 |
Ku CA, Ryals RC, Jiang D, Coyner AS, Weller KK, Sinha W, Robb BM, Yang P, Pennesi ME. The Role of ERK1/2 Activation in Sarpogrelate-Mediated Neuroprotection. Investigative Ophthalmology & Visual Science. 59: 462-471. PMID 29368005 DOI: 10.1167/iovs.17-23159 |
0.252 |
|
| 2018 |
Chung DC, Bertelsen M, Lorenz B, Pennesi ME, Leroy BP, Hamel CP, Pierce E, Sallum J, Larsen M, Stieger K, Preising M, Weleber R, Yang P, Place E, Liu E, et al. The Natural History of Inherited Retinal Dystrophy due to Biallelic Mutations in the RPE65 Gene. American Journal of Ophthalmology. PMID 30268864 DOI: 10.1016/J.Ajo.2018.09.024 |
0.251 |
|
| 2015 |
Ku CA, Pennesi ME. Retinal Gene Therapy: Current Progress and Future Prospects. Expert Review of Ophthalmology. 10: 281-299. PMID 26609316 DOI: 10.1586/17469899.2015.1035711 |
0.25 |
|
| 2022 |
Lad EM, Duncan JL, Liang W, Maguire MG, Ayala AR, Audo I, Birch DG, Carroll J, Cheetham JK, Durham TA, Fahim AT, Loo J, Deng Z, Mukherjee D, Heon E, ... ... Pennesi ME, et al. Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation with Disease Severity. American Journal of Ophthalmology. PMID 36007554 DOI: 10.1016/j.ajo.2022.08.013 |
0.244 |
|
| 2018 |
Hirji N, Bradley PD, Li S, Vincent A, Pennesi ME, Thomas AS, Heon E, Bhan A, Mahroo OA, Robson A, Inglehearn CF, Moore AT, Michaelides M. Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients with Cone-Rod Dystrophy and Amelogenesis Imperfecta. American Journal of Ophthalmology. PMID 29421294 DOI: 10.1016/J.Ajo.2018.01.029 |
0.243 |
|
| 2014 |
Pennesi ME, Garg AK, Feng S, Michaels KV, Smith TB, Fay JD, Weiss AR, Renner LM, Hurst S, McGill TJ, Cornea A, Rittenhouse KD, Sperling M, Fruebis J, Neuringer M. Measuring cone density in a Japanese macaque (Macaca fuscata) model of age-related macular degeneration with commercially available adaptive optics. Advances in Experimental Medicine and Biology. 801: 309-16. PMID 24664712 DOI: 10.1007/978-1-4614-3209-8_39 |
0.241 |
|
| 2015 |
Yang P, Chiang PW, Weleber RG, Pennesi ME. Autosomal Dominant Retinal Dystrophy With Electronegative Waveform Associated With a Novel RAX2 Mutation. Jama Ophthalmology. 133: 653-61. PMID 25789692 DOI: 10.1001/jamaophthalmol.2015.0357 |
0.24 |
|
| 2016 |
Jain N, Jia Y, Gao SS, Zhang X, Weleber RG, Huang D, Pennesi ME. Optical Coherence Tomography Angiography in Choroideremia: Correlating Choriocapillaris Loss With Overlying Degeneration. Jama Ophthalmology. PMID 27149258 DOI: 10.1001/Jamaophthalmol.2016.0874 |
0.236 |
|
| 2016 |
Langlo CS, Patterson EJ, Higgins BP, Summerfelt P, Razeen MM, Erker LR, Parker M, Collison FT, Fishman GA, Kay CN, Zhang J, Weleber RG, Yang P, Wilson DJ, Pennesi ME, et al. Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia. Investigative Ophthalmology & Visual Science. 57: 3984-3995. PMID 27479814 DOI: 10.1167/Iovs.16-19313 |
0.236 |
|
| 2015 |
Pennesi ME. Update on gene therapy for the treatment of retinal diseases Retina Today. 53-56. |
0.235 |
|
| 2017 |
Al-Qahtani AA, Ba-Ali S, Alabduljalil T, Coyner AS, Patel RC, Weleber RG, Girach A, Christensen SK, Larsen M, Pennesi ME, Yang P. SCLERAL PITS IN CHOROIDEREMIA: Implications for Retinal Gene Therapy. Retina (Philadelphia, Pa.). PMID 29160785 DOI: 10.1097/IAE.0000000000001957 |
0.234 |
|
| 2018 |
Patel RC, Wang J, Hwang TS, Zhang M, Gao SS, Pennesi ME, Bailey ST, Lujan BJ, Wang X, Wilson DJ, Huang D, Jia Y. Plexus-Specific Detection of Retinal Vascular Pathologic Conditions with Projection-Resolved OCT Angiography. Ophthalmology. Retina. 2: 816-826. PMID 30148244 DOI: 10.1016/J.Oret.2017.11.010 |
0.231 |
|
| 2020 |
Duncan JL, Liang W, Maguire MG, Audo I, Ayala AR, Birch DG, Carroll J, Cheetham JK, Esposti SD, Durham TA, Erker L, Farsiu S, Ferris FL, Heon E, Hufnagel RB, ... ... Pennesi ME, et al. Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation with Other Measures of Disease Severity. American Journal of Ophthalmology. PMID 32446738 DOI: 10.1016/J.Ajo.2020.05.024 |
0.229 |
|
| 2021 |
Durham TA, Duncan JL, Ayala AR, Birch DG, Cheetham JK, Ferris FL, Hoyng CB, Pennesi ME, Sahel JA. Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium. Translational Vision Science & Technology. 10: 23. PMID 34004001 DOI: 10.1167/tvst.10.4.23 |
0.228 |
|
| 2019 |
Gale MJ, Harman GA, Chen J, Pennesi ME. Repeatability of Adaptive Optics Automated Cone Measurements in Subjects With Retinitis Pigmentosa and Novel Metrics for Assessment of Image Quality. Translational Vision Science & Technology. 8: 17. PMID 31114717 DOI: 10.1167/tvst.8.3.17 |
0.228 |
|
| 2023 |
Birch DG, Cheetham JK, Daiger SP, Hoyng C, Kay C, MacDonald IM, Pennesi ME, Sullivan LS. Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel. Translational Vision Science & Technology. 12: 5. PMID 37294701 DOI: 10.1167/tvst.12.6.5 |
0.226 |
|
| 2012 |
Fletcher AL, Pennesi ME, Harding CO, Weleber RG, Gillingham MB. Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies. Molecular Genetics and Metabolism. 106: 18-24. PMID 22459206 DOI: 10.1016/J.Ymgme.2012.02.015 |
0.225 |
|
| 2022 |
Hufnagel RB, Liang W, Duncan JL, Brewer CC, Audo I, Ayala AR, Branham K, Cheetham JK, Daiger SP, Durham TA, Guan B, Heon E, Hoyng CB, Iannaccone A, Kay CN, ... ... Pennesi ME, et al. Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A study. Human Mutation. PMID 35266249 DOI: 10.1002/humu.24365 |
0.224 |
|
| 2016 |
Thomas AS, Branham K, Van Gelder RN, Daiger SP, Sullivan LS, Bowne SJ, Heckenlively JR, Pennesi ME. Multimodal Imaging in Wagner Syndrome. Ophthalmic Surgery, Lasers & Imaging Retina. 47: 574-579. PMID 27327288 DOI: 10.3928/23258160-20160601-10 |
0.222 |
|
| 2020 |
Litts KM, Georgiou M, Langlo CS, Patterson EJ, Mastey RR, Kalitzeos A, Linderman RE, Lam BL, Fishman GA, Pennesi ME, Kay CN, Hauswirth WW, Michaelides M, Carroll J. Interocular symmetry of foveal cone topography in congenital achromatopsia. Current Eye Research. PMID 32108519 DOI: 10.1080/02713683.2020.1737138 |
0.218 |
|
| 2017 |
Khan KN, El-Asrag ME, Ku CA, Holder GE, McKibbin M, Arno G, Poulter JA, Carss K, Bommireddy T, Bagheri S, Bakall B, Scholl HP, Raymond FL, Toomes C, Inglehearn CF, ... Pennesi ME, et al. Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy. Investigative Ophthalmology & Visual Science. 58: 2906-2914. PMID 28586915 DOI: 10.1167/iovs.16-20608 |
0.218 |
|
| 2023 |
Ku CA, Igelman AD, Huang SJ, Vasconcelos H, da Palma MM, Bailey ST, Lauer AK, Weleber RG, Yang P, Pennesi ME. Improved Rod Sensitivity as Assessed by Two-Color Dark-Adapted Perimetry in Patients With RPE65-Related Retinopathy Treated With Voretigene Neparvovec-rzyl. Translational Vision Science & Technology. 12: 17. PMID 37058101 DOI: 10.1167/tvst.12.4.17 |
0.217 |
|
| 2015 |
Thomas AS, Flaxel CJ, Pennesi ME. Spectral-Domain Optical Coherence Tomography and Fundus Autofluorescence Evaluation of Torpedo Maculopathy. Journal of Pediatric Ophthalmology and Strabismus. 52: e8-e10. PMID 26484432 DOI: 10.3928/01913913-20150303-01 |
0.216 |
|
| 2015 |
Thomas AS, Flaxel CJ, Pennesi ME. Spectral-domain optical coherence tomography and fundus autofluorescence evaluation of torpedo maculopathy. Journal of Pediatric Ophthalmology and Strabismus. 52: e8-10. PMID 25751084 DOI: 10.3928/01913913-20150303-01 |
0.216 |
|
| 2010 |
Walia S, Fishman GA, Jacobson SG, Aleman TS, Koenekoop RK, Traboulsi EI, Weleber RG, Pennesi ME, Heon E, Drack A, Lam BL, Allikmets R, Stone EM. Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa. Ophthalmology. 117: 1190-8. PMID 20079931 DOI: 10.1016/J.Ophtha.2009.09.056 |
0.214 |
|
| 2021 |
Yang P, Pennesi ME, Weleber RG. Strategies for Treating Inherited Retinal Degeneration With Large Genes That Are Not Amenable to Adeno-Associated Virus-Based Gene Replacement Therapy. Jama Ophthalmology. PMID 33507212 DOI: 10.1001/jamaophthalmol.2020.6427 |
0.211 |
|
| 2014 |
Yang P, Michaels KV, Courtney RJ, Wen Y, Greninger DA, Reznick L, Karr DJ, Wilson LB, Weleber RG, Pennesi ME. Retinal morphology of patients with achromatopsia during early childhood: implications for gene therapy. Jama Ophthalmology. 132: 823-31. PMID 24676353 DOI: 10.1001/jamaophthalmol.2014.685 |
0.211 |
|
| 2021 |
Shughoury A, Ciulla TA, Bakall B, Pennesi ME, Kiss S, Cunningham ET. Genes and Gene Therapy in Inherited Retinal Disease. International Ophthalmology Clinics. 61: 3-45. PMID 34584043 DOI: 10.1097/IIO.0000000000000377 |
0.211 |
|
| 2017 |
Sullivan LS, Bowne SJ, Koboldt DC, Cadena EL, Heckenlively JR, Branham KE, Wheaton DH, Jones KD, Ruiz RS, Pennesi ME, Yang P, Davis-Boozer D, Northrup H, Gurevich VV, Chen R, et al. A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States. Investigative Ophthalmology & Visual Science. 58: 2774-2784. PMID 28549094 DOI: 10.1167/Iovs.16-21341 |
0.209 |
|
| 2020 |
Birch DG, Cheng P, Duncan JL, Ayala AR, Maguire MG, Audo I, Cheetham JK, Durham TA, Fahim AT, Ferris FL, Heon E, Huckfeldt RM, Iannaccone A, Khan NW, Lad EM, ... ... Pennesi ME, et al. The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline. Translational Vision Science & Technology. 9: 9. PMID 33133772 DOI: 10.1167/tvst.9.11.9 |
0.208 |
|
| 2023 |
da Palma MM, Marra M, Igelman AD, Ku CA, Burr A, Andersen K, Everett LA, Porto FBO, Sallum JMF, Yang P, Pennesi ME. Expanding the phenotypic and genotypic spectrum of patients with -related retinopathy. Ophthalmic Genetics. 1-8. PMID 37592806 DOI: 10.1080/13816810.2023.2245035 |
0.207 |
|
| 2019 |
Vasconcelos HM, Vargas ME, Pennesi ME. Multimodal imaging of ring 14 syndrome associated maculopathy. Ophthalmic Genetics. 1-4. PMID 31755799 DOI: 10.1080/13816810.2019.1688839 |
0.202 |
|
| 2022 |
Jimenez HJ, Procopio RA, Thuma TBT, Marra MH, Izquierdo N, Klufas MA, Nagiel A, Pennesi ME, Pulido JS. Signal Peptide Variants in Inherited Retinal Diseases: A Multi-Institutional Case Series. International Journal of Molecular Sciences. 23. PMID 36362148 DOI: 10.3390/ijms232113361 |
0.2 |
|
| 2021 |
Zou G, Zhang T, Cheng X, Igelman AD, Wang J, Qian X, Fu S, Wang K, Koenekoop RK, Fishman GA, Yang P, Li Y, Pennesi ME, Chen R. Noncoding mutation in contributes to inherited retinal degenerations. Molecular Vision. 27: 95-106. PMID 33907365 |
0.2 |
|
| 2016 |
Coyner AS, Ryals RC, Ku CA, Fischer CM, Patel RC, Datta S, Yang P, Wen Y, Hen R, Pennesi ME. Retinal Neuroprotective Effects of Flibanserin, an FDA-Approved Dual Serotonin Receptor Agonist-Antagonist. Plos One. 11: e0159776. PMID 27447833 DOI: 10.1371/journal.pone.0159776 |
0.2 |
|
| 2023 |
Amato A, Wongchaisuwat N, Lamborn A, Schmidt R, Everett L, Yang P, Pennesi ME. Gene therapy in bestrophinopathies: Insights from preclinical studies in preparation for clinical trials. Saudi Journal of Ophthalmology : Official Journal of the Saudi Ophthalmological Society. 37: 287-295. PMID 38155675 DOI: 10.4103/sjopt.sjopt_175_23 |
0.2 |
|
| 2012 |
Pennesi ME, Neuringer M, Courtney RJ. Animal models of age related macular degeneration. Molecular Aspects of Medicine. 33: 487-509. PMID 22705444 DOI: 10.1016/j.mam.2012.06.003 |
0.199 |
|
| 2015 |
Tullis BE, Ryals RC, Coyner AS, Gale MJ, Nicholson A, Ku C, Regis D, Sinha W, Datta S, Wen Y, Yang P, Pennesi ME. Sarpogrelate, a 5-HT2A Receptor Antagonist, Protects the Retina From Light-Induced Retinopathy. Investigative Ophthalmology & Visual Science. 56: 4560-9. PMID 26200496 DOI: 10.1167/iovs.15-16378 |
0.199 |
|
| 2020 |
Bellsmith KN, Dunaief JL, Yang P, Pennesi ME, Davis E, Hofkamp H, Lujan BJ. Bull's eye maculopathy associated with hereditary hemochromatosis. American Journal of Ophthalmology Case Reports. 18: 100674. PMID 32258826 DOI: 10.1016/j.ajoc.2020.100674 |
0.197 |
|
| 2016 |
Powers JM, Adachi K, Sivyer B, Taylor W, Pennesi M, Nakai H. 96. An Approach to Compare Multiple Adeno-Associated Virus (AAV) Capsids Side-by-Side in a Single Eye Following Intravitreal Injection Molecular Therapy. 24: S42. DOI: 10.1016/S1525-0016(16)32905-7 |
0.196 |
|
| 2017 |
Hariri AH, Velaga SB, Girach A, Ip MS, Le PV, Lam BL, Fischer MD, Sankila EM, Pennesi M, Holz FG, MacLaren RE, Birch DG, Hoyng CB, MacDonald IM, Black GC, et al. Measurement and Reproducibility of Preserved Ellipsoid Zone Area and Preserved RPE Area in a Cohort of Eyes with Choroideremia. American Journal of Ophthalmology. PMID 28499705 DOI: 10.1016/J.Ajo.2017.05.002 |
0.194 |
|
| 2011 |
Lalwani K, Tompkins BD, Burnes K, Krahmer MR, Pennesi ME, Weleber RG. The 'dark' side of sedation: 12 years of office-based pediatric deep sedation for electroretinography in the dark. Paediatric Anaesthesia. 21: 65-71. PMID 21155929 DOI: 10.1111/j.1460-9592.2010.03462.x |
0.19 |
|
| 2016 |
Hull S, Arno G, Ku CA, Ge Z, Waseem N, Chandra A, Webster AR, Robson AG, Michaelides M, Weleber RG, Davagnanam I, Chen R, Holder GE, Pennesi ME, Moore AT. Molecular and Clinical Findings in Patients With Knobloch Syndrome. Jama Ophthalmology. PMID 27259167 DOI: 10.1001/Jamaophthalmol.2016.1073 |
0.188 |
|
| 2015 |
Scoles D, Flatter JA, Cooper RF, Langlo CS, Robison S, Neitz M, Weinberg DV, Pennesi ME, Han DP, Dubra A, Carroll J. ASSESSING PHOTORECEPTOR STRUCTURE ASSOCIATED WITH ELLIPSOID ZONE DISRUPTIONS VISUALIZED WITH OPTICAL COHERENCE TOMOGRAPHY. Retina (Philadelphia, Pa.). PMID 26166796 DOI: 10.1097/Iae.0000000000000618 |
0.186 |
|
| 2022 |
Igelman AD, Park JC, Hyde RA, Everett L, Yang P, Pennesi ME, McAnany JJ. Two-Color Dark-Adapted Perimetry Implemented With a Commercially Available Perimeter to Characterize Rod-Pathway Sensitivity. Ophthalmic Surgery, Lasers & Imaging Retina. 53: 692-696. PMID 36547964 DOI: 10.3928/23258160-20221118-03 |
0.183 |
|
| 2017 |
Langlo CS, Erker LR, Parker M, Patterson EJ, Higgins BP, Summerfelt P, Razeen MM, Collison FT, Fishman GA, Kay CN, Zhang J, Weleber RG, Yang P, Pennesi ME, Lam BL, et al. REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA. Retina (Philadelphia, Pa.). PMID 28145975 DOI: 10.1097/Iae.0000000000001434 |
0.178 |
|
| 2016 |
Biggee K, Gale MJ, Smith TB, Suhler EB, Pennesi ME, Lin P. Parafoveal cone abnormalities and recovery on adaptive optics in posterior uveitis. American Journal of Ophthalmology Case Reports. 1: 16-22. PMID 29503883 DOI: 10.1016/j.ajoc.2016.03.001 |
0.178 |
|
| 2021 |
Ciulla T, Pennesi ME, Kiss S, Cunningham ET. Preface to DNA-based and RNA-based Gene Therapies in Ophthalmology: Inherited and Noninherited Retinal Disorders. International Ophthalmology Clinics. 61: 1-2. PMID 34584042 DOI: 10.1097/IIO.0000000000000372 |
0.178 |
|
| 2011 |
Pennesi ME, Stover NB, Stone EM, Chiang PW, Weleber RG. Residual electroretinograms in young Leber congenital amaurosis patients with mutations of AIPL1. Investigative Ophthalmology & Visual Science. 52: 8166-73. PMID 21900377 DOI: 10.1167/Iovs.11-8298 |
0.174 |
|
| 2017 |
Gerth-Kahlert C, Tiwari A, Hanson JVM, Batmanabane V, Traboulsi E, Pennesi ME, Al-Qahtani AA, Lam BL, Heckenlively J, Zweifel SA, Vincent A, Fierz F, Barthelmes D, Branham K, Khan N, et al. C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations. Investigative Ophthalmology & Visual Science. 58: 3840-3850. PMID 28763557 DOI: 10.1167/Iovs.17-21597 |
0.172 |
|
| 2016 |
Hollander DA, Pennesi ME, Alvarado JA. Management of plateau iris syndrome with cataract extraction and endoscopic cyclophotocoagulation. Experimental Eye Research. PMID 27475976 DOI: 10.1016/j.exer.2016.07.018 |
0.171 |
|
| 2022 |
Pennesi ME, Yang P, Birch DG, Weng CY, Moore AT, Iannaccone A, Comander JI, Jayasundera T, Chulay J. Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in X-linked Retinoschisis - 1 Year Clinical Results. Ophthalmology. Retina. PMID 35781068 DOI: 10.1016/j.oret.2022.06.013 |
0.165 |
|
| 2023 |
MacLaren RE, Fischer MD, Gow JA, Lam BL, Sankila EK, Girach A, Panda S, Yoon D, Zhao G, Pennesi ME. Subretinal timrepigene emparvovec in adult men with choroideremia: a randomized phase 3 trial. Nature Medicine. 29: 2464-2472. PMID 37814062 DOI: 10.1038/s41591-023-02520-3 |
0.163 |
|
| 2020 |
Pennesi ME, Schlecther CL. The Evolution of Retinal Gene Therapy: From Clinical Trials to Clinical Practice. Ophthalmology. 127: 148-150. PMID 31973830 DOI: 10.1016/j.ophtha.2019.12.003 |
0.163 |
|
| 2020 |
Ku CA, Pennesi ME. The new landscape of retinal gene therapy. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. PMID 32888388 DOI: 10.1002/ajmg.c.31842 |
0.163 |
|
| 2022 |
da Palma MM, Ku C, Igelman AD, Burr A, Shevchenko Sutherland L, Koerner C, Valle D, Pennesi ME, Yang P. A possible ocular biomarker for response to hyperornithinemia in gyrate atrophy: the effect of pyridoxine, lysine, and arginine-restricted diet in a patient with advanced disease. Ophthalmic Genetics. 1-7. PMID 35856163 DOI: 10.1080/13816810.2022.2098986 |
0.161 |
|
| 2023 |
Wen S, Wang M, Qian X, Li Y, Wang K, Choi J, Pennesi ME, Yang P, Marra M, Koenekoop RK, Lopez I, Matynia A, Gorin M, Sui R, Yao F, et al. Systematic assessment of the contribution of structural variants to inherited retinal diseases. Human Molecular Genetics. PMID 36811936 DOI: 10.1093/hmg/ddad032 |
0.161 |
|
| 2023 |
Wen S, Wang M, Qian X, Li Y, Wang K, Choi J, Pennesi ME, Yang P, Marra M, Koenekoop RK, Lopez I, Matynia A, Gorin M, Sui R, Yao F, et al. Systematic assessment of the contribution of structural variants to inherited retinal diseases. Biorxiv : the Preprint Server For Biology. PMID 36789417 DOI: 10.1101/2023.01.02.522522 |
0.16 |
|
| 2016 |
Shifera AS, Pennesi ME, Yang P, Lin P. ULTRA-WIDE-FIELD FUNDUS AUTOFLUORESCENCE FINDINGS IN PATIENTS WITH ACUTE ZONAL OCCULT OUTER RETINOPATHY. Retina (Philadelphia, Pa.). PMID 27755372 DOI: 10.1097/IAE.0000000000001311 |
0.157 |
|
| 2020 |
Wu S, Sun Z, Zhu T, Weleber RG, Yang P, Wei X, Pennesi ME, Sui R. Novel variants in PNPLA6 causing syndromic retinal dystrophy. Experimental Eye Research. 108327. PMID 33141049 DOI: 10.1016/j.exer.2020.108327 |
0.157 |
|
| 2015 |
Palejwala NV, Gale MJ, Clark RF, Schlechter C, Weleber RG, Pennesi ME. INSIGHTS INTO AUTOSOMAL DOMINANT STARGARDT-LIKE MACULAR DYSTROPHY THROUGH MULTIMODALITY DIAGNOSTIC IMAGING. Retina (Philadelphia, Pa.). PMID 26110599 DOI: 10.1097/IAE.0000000000000659 |
0.156 |
|
| 2016 |
Ku CA, Ng JK, Karr DJ, Reznick L, Harding CO, Weleber RG, Pennesi ME. Spectrum of ocular manifestations in cobalamin C and cobalamin A types of methylmalonic acidemia. Ophthalmic Genetics. 1-11. PMID 26979128 DOI: 10.3109/13816810.2015.1121500 |
0.155 |
|
| 2019 |
Shurygina MF, Parker MA, Schlechter CL, Chen R, Li Y, Weleber RG, Yang P, Pennesi ME. A case report of two siblings with Alstrom syndrome without hearing loss associated with two new ALMS1 variants. Bmc Ophthalmology. 19: 246. PMID 31810438 DOI: 10.1186/S12886-019-1259-Y |
0.154 |
|
| 2021 |
Litts KM, Woertz EN, Wynne N, Brooks BP, Chacon A, Connor TB, Costakos D, Dumitrescu A, Drack AV, Fishman GA, Hauswirth WW, Kay CN, Lam BL, Michaelides M, Pennesi ME, et al. Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure. Translational Vision Science & Technology. 10: 22. PMID 34111268 DOI: 10.1167/tvst.10.6.22 |
0.152 |
|
| 2023 |
Hussain HMJ, Wang M, Huang A, Schmidt R, Qian X, Yang P, Marra M, Li Y, Pennesi ME, Chen R. Novel Pathogenic Mutations Identified from Whole-Genome Sequencing in Unsolved Cases of Patients Affected with Inherited Retinal Diseases. Genes. 14. PMID 36833373 DOI: 10.3390/genes14020447 |
0.146 |
|
| 2024 |
Brock DC, Wang M, Hussain HMJ, Rauch DE, Marra M, Pennesi ME, Yang P, Everett L, Ajlan RS, Colbert J, Porto FBO, Matynia A, Gorin MB, Koenekoop RK, Lopez I, et al. Comparative analysis of in-silico tools in identifying pathogenic variants in dominant inherited retinal diseases. Human Molecular Genetics. PMID 38453143 DOI: 10.1093/hmg/ddae028 |
0.139 |
|
| 2020 |
Thompson DA, Iannaccone A, Ali RR, Arshavsky VY, Audo I, Bainbridge JWB, Besirli CG, Birch DG, Branham KE, Cideciyan AV, Daiger SP, Dalkara D, Duncan JL, Fahim AT, Flannery JG, ... ... Pennesi ME, et al. Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium. Translational Vision Science & Technology. 9: 2. PMID 32832209 DOI: 10.1167/Tvst.9.7.2 |
0.139 |
|
| 2021 |
Qian X, Wang J, Wang M, Igelman AD, Jones KD, Li Y, Wang K, Goetz KE, Birch DG, Yang P, Pennesi ME, Chen R. Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases. Frontiers in Genetics. 12: 647400. PMID 33737949 DOI: 10.3389/fgene.2021.647400 |
0.138 |
|
| 2014 |
Liu BS, Tarima S, Visotcky A, Pechauer A, Cooper RF, Landsem L, Wilk MA, Godara P, Makhijani V, Sulai YN, Syed N, Yasumura G, Garg AK, Pennesi ME, Lujan BJ, et al. The reliability of parafoveal cone density measurements. The British Journal of Ophthalmology. 98: 1126-31. PMID 24855115 DOI: 10.1136/Bjophthalmol-2013-304823 |
0.137 |
|
| 2023 |
Heon E, Melia M, Bocchino LE, Samarakoon L, Duncan JL, Ayala AR, Audo I, Bradley C, Cheetham JK, Dagnelie G, Durham TA, Hoyng CB, Jain N, Jayasundera KT, Pennesi ME, et al. Functional Vision in Patients with Bi-allelic USH2A Variants. American Journal of Ophthalmology. PMID 38135239 DOI: 10.1016/j.ajo.2023.12.009 |
0.137 |
|
| 2021 |
Igelman AD, Ku C, Mershon S, da Palma MM, McAnany JJ, Hyde RA, Park JC, Yang P, Pennesi ME. Effect of Pharmacological Pupil Dilation on Dark-Adapted Perimetric Sensitivity in Healthy Subjects Using an Octopus 900 Perimeter. Translational Vision Science & Technology. 10: 18. PMID 34919129 DOI: 10.1167/tvst.10.14.18 |
0.135 |
|
| 2023 |
Wongchaisuwat N, Wang J, Yang P, Everett L, Gregor A, Sahel JA, Nischal KK, Pennesi ME, Gillingham MB, Jia Y. Optical coherence tomography angiography of choroidal neovascularization in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). American Journal of Ophthalmology Case Reports. 32: 101958. PMID 38161518 DOI: 10.1016/j.ajoc.2023.101958 |
0.132 |
|
| 2024 |
Gillingham MB, Choi D, Gregor A, Wongchaisuwat N, Black D, Scanga HL, Nischal KK, Sahel JA, Arnold G, Vockley J, Harding CO, Pennesi ME. Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long-chain 3-hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy. Journal of Inherited Metabolic Disease. PMID 38623632 DOI: 10.1002/jimd.12738 |
0.12 |
|
| 2021 |
Litts KM, Woertz EN, Georgiou M, Patterson EJ, Lam BL, Fishman GA, Pennesi ME, Kay CN, Hauswirth WW, Michaelides M, Carroll J. Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in Achromatopsia. Translational Vision Science & Technology. 10: 11. PMID 33510950 DOI: 10.1167/tvst.10.1.11 |
0.113 |
|
| 2021 |
da Palma MM, Vargas ME, Burr A, Chen R, Pennesi ME, Weleber RG, Yang P. Variable expressivity of -associated autosomal dominant vitreoretinochoroidopathy (ADVIRC) in a three-generation pedigree. Bmj Open Ophthalmology. 6: e000813. PMID 34746433 DOI: 10.1136/bmjophth-2021-000813 |
0.112 |
|
| 2009 |
Marcocci E, Uliana V, Bruttini M, Artuso R, Silengo MC, Zerial M, Bergesio F, Amoroso A, Savoldi S, Pennesi M, Giachino D, Rombolà G, Fogazzi GB, Rosatelli C, Martinhago CD, et al. Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 24: 1464-71. PMID 19129241 DOI: 10.1093/ndt/gfn681 |
0.112 |
|
| 2015 |
Feng S, Gale MJ, Fay JD, Faridi A, Titus HE, Garg AK, Michaels KV, Erker LR, Peters D, Smith TB, Pennesi ME. Assessment of Different Sampling Methods for Measuring and Representing Macular Cone Density Using Flood-Illuminated Adaptive Optics. Investigative Ophthalmology & Visual Science. 56: 5751-63. PMID 26325414 DOI: 10.1167/Iovs.15-16954 |
0.11 |
|
| 2018 |
Hariri AH, Ip MS, Girach A, Lam BL, Fischer MD, Sankila EM, Pennesi ME, Holz FG, Maclaren RE, Birch DG, Hoyng CB, MacDonald IM, Black GC, Tsang SH, Bressler NM, et al. Macular spatial distribution of preserved autofluorescence in patients with choroideremia. The British Journal of Ophthalmology. PMID 30297337 DOI: 10.1136/Bjophthalmol-2018-312620 |
0.11 |
|
| 2021 |
Lambert NG, Grigorian F, Vasconcelos H, Watzke RC, Pennesi ME. Adaptive optics ophthalmoscopy, multifocal ERG and OCTA in unique case of suspected torpedo maculopathy presenting with vitelliform lesion. American Journal of Ophthalmology Case Reports. 21: 100996. PMID 33376833 DOI: 10.1016/j.ajoc.2020.100996 |
0.107 |
|
| 2018 |
Abalem MF, Musch DC, Birch DG, Pennesi ME, Heckenlively JR, Jayasundera T. Diurnal variations of foveoschisis by optical coherence tomography in patients with RS1 X-linked juvenile retinoschisis. Ophthalmic Genetics. 1-6. PMID 29902095 DOI: 10.1080/13816810.2018.1466340 |
0.107 |
|
| 2023 |
de Guimaraes TAC, Georgiou M, Robson AG, Fujinami K, Vincent A, Nasser F, Khateb S, Mahroo OA, Pontikos N, Vargas ME, Thiadens AAHJ, Carvalho ER, Nguyen XT, Arno G, Fujinami-Yokokawa Y, ... ... Pennesi ME, et al. -associated retinopathy: genotype-phenotype correlations - study group report 3. The British Journal of Ophthalmology. PMID 37852740 DOI: 10.1136/bjo-2023-323640 |
0.106 |
|
| 2020 |
Vasconcelos HM, Lujan BJ, Pennesi ME, Yang P, Lauer AK. Intraoperative optical coherence tomographic findings in patients undergoing subretinal gene therapy surgery. International Journal of Retina and Vitreous. 6: 13. PMID 32377379 DOI: 10.1186/s40942-020-00216-1 |
0.103 |
|
| 2022 |
Price KW, Pennesi ME, Lauer AK, Bailey ST. Iatrogenic choroidal neovascularization associated with subretinal gene therapy surgery. American Journal of Ophthalmology Case Reports. 27: 101677. PMID 36034763 DOI: 10.1016/j.ajoc.2022.101677 |
0.102 |
|
| 2020 |
Shurygina MF, Simonett JM, Parker MA, Mitchell A, Grigorian F, Lifton J, Nagiel A, Shpak AA, Dadali EL, Mishina IA, Weleber RG, Yang P, Pennesi ME. Genotype Phenotype Correlation and Variability in Microcephaly Associated With Chorioretinopathy or Familial Exudative Vitreoretinopathy. Investigative Ophthalmology & Visual Science. 61: 2. PMID 33137195 DOI: 10.1167/iovs.61.13.2 |
0.099 |
|
| 1995 |
Longo F, Di Leo G, Lepore L, Pennesi M. [Vascular hyperfragility in systemic lupus erythematosus treated with low doses of cortisone]. La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics. 17: 535-7. PMID 8668590 |
0.099 |
|
| 2017 |
Gao SS, Patel RC, Jain N, Zhang M, Weleber RG, Huang D, Pennesi ME, Jia Y. Choriocapillaris evaluation in choroideremia using optical coherence tomography angiography. Biomedical Optics Express. 8: 48-56. PMID 28101400 DOI: 10.1364/Boe.8.000048 |
0.097 |
|
| 2010 |
Pennesi ME, Weleber RG. High-resolution optical coherence tomography shows new aspects of Bietti crystalline retinopathy. Retina (Philadelphia, Pa.). 30: 531-2. PMID 20139800 DOI: 10.1097/IAE.0b013e3181c96a15 |
0.096 |
|
| 2004 |
Foschini MP, Gaiba A, Cocchi R, Pennesi MG, Gatto MR, Frezza GP, Pession A. Pattern of p63 expression in squamous cell carcinoma of the oral cavity. Virchows Archiv : An International Journal of Pathology. 444: 332-9. PMID 14997391 DOI: 10.1007/s00428-003-0969-x |
0.092 |
|
| 1987 |
Lepore L, Longo F, Pennesi M, Barbi E. [Immunologic function in children with recurrent respiratory infections evaluated in a state of well-being]. La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics. 9: 695-7. PMID 3502179 |
0.089 |
|
| 2021 |
da Palma MM, Igelman AD, Ku C, Burr A, You JY, Place EM, Wang NK, Oh JK, Branham KE, Zhang X, Ahn J, Gorin MB, Lam BL, Ronquillo CC, Bernstein PS, ... ... Pennesi ME, et al. Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome. Investigative Ophthalmology & Visual Science. 62: 27. PMID 34185059 DOI: 10.1167/iovs.62.7.27 |
0.088 |
|
| 2005 |
Pennesi M, Marchetti F, Crovella S, Boaretto F, Travan L, Lazzerini M, Neri E, Ventura A. A new mutation in two siblings with cystinosis presenting with Bartter syndrome. Pediatric Nephrology (Berlin, Germany). 20: 217-9. PMID 15583946 DOI: 10.1007/s00467-004-1702-y |
0.085 |
|
| 2019 |
Hanif AM, Armenti ST, Taylor SC, Shah RA, Igelman AD, Jayasundera KT, Pennesi ME, Khurana RN, Foote JE, O'Keefe GA, Yang P, Hubbard GB, Hwang TS, Flaxel CJ, Stein JD, et al. Phenotypic Spectrum of Pentosan Polysulfate Sodium-Associated Maculopathy: A Multicenter Study. Jama Ophthalmology. PMID 31486843 DOI: 10.1001/jamaophthalmol.2019.3392 |
0.085 |
|
| 2020 |
Georgiou M, Robson AG, Fujinami K, Leo SM, Vincent A, Nasser F, Cabral De Guimarães TA, Khateb S, Pontikos N, Fujinami-Yokokawa Y, Liu X, Tsunoda K, Hayashi T, Vargas ME, Thiadens AAHJ, ... ... Pennesi ME, et al. KCNV2-associated Retinopathy: Genetics, Electrophysiology and Clinical Course - KCNV2 Study Group Report 1. American Journal of Ophthalmology. PMID 33309813 DOI: 10.1016/j.ajo.2020.11.022 |
0.083 |
|
| 2013 |
Courtney RJ, Pennesi ME. Interval spectral-domain optical coherence tomography and electrophysiology findings in neonatal adrenoleukodystrophy. Jama Ophthalmology. 131: 807-10. PMID 23599131 DOI: 10.1001/jamaophthalmol.2013.2089 |
0.083 |
|
| 2022 |
da Palma MM, Marrra M, Pennesi ME. A double hyperautofluorescent ring in a 33-year-old-female patient. Retinal Cases & Brief Reports. PMID 36067420 DOI: 10.1097/ICB.0000000000001337 |
0.081 |
|
| 2022 |
Parker MA, Erker LR, Audo I, Choi D, Mohand-Said S, Sestakauskas K, Benoit P, Appelqvist T, Krahmer M, Ségaut-Prévost C, Lujan BJ, Faridi A, Chegarnov EN, Steinkamp PN, Ku C, ... ... Pennesi ME, et al. Three-year safety results of SAR422459 (EIAV-ABCA4) gene therapy in patients with ABCA4-associated Stargardt disease: An open-label dose-escalation phase I/IIa clinical trial, cohorts 1-5. American Journal of Ophthalmology. PMID 35248547 DOI: 10.1016/j.ajo.2022.02.013 |
0.081 |
|
| 2024 |
MacLaren RE, Lam BL, Fischer MD, Holz FG, Pennesi ME, Birch DG, Sankila EM, Meunier IA, Stepien KE, Sallum JMF, Li J, Yoon D, Panda S, Gow JA. A Prospective, Observational, Non-Interventional Clinical Study of Participants With Choroideremia: The NIGHT Study. American Journal of Ophthalmology. PMID 38311152 DOI: 10.1016/j.ajo.2024.01.022 |
0.08 |
|
| 2016 |
Bennett LD, Wang YZ, Klein M, Pennesi ME, Jayasundera T, Birch DG. Structure/Psychophysical Relationships in X-Linked Retinoschisis. Investigative Ophthalmology & Visual Science. 57: 332-7. PMID 26830370 DOI: 10.1167/Iovs.15-18354 |
0.078 |
|
| 2010 |
Montebugnoli L, Cervellati F, Cocchi R, Farnedi A, Pennesi MG, Flamminio F, Foschini MP. Immunohistochemical expression of p16(INK4A) protein as a helpful marker of a subset of potentially malignant oral epithelial lesions: study on a series with long-term follow-up. Histopathology. 57: 528-34. PMID 20955378 DOI: 10.1111/j.1365-2559.2010.03671.x |
0.076 |
|
| 2020 |
Shah R, Simonett JM, Lyons RJ, Rao RC, Pennesi ME, Jain N. Disease Course in Patients With Pentosan Polysulfate Sodium-Associated Maculopathy After Drug Cessation. Jama Ophthalmology. PMID 32644147 DOI: 10.1001/jamaophthalmol.2020.2349 |
0.075 |
|
| 2014 |
Ruggenenti P, Ruggiero B, Cravedi P, Vivarelli M, Massella L, Marasà M, Chianca A, Rubis N, Ene-Iordache B, Rudnicki M, Pollastro RM, Capasso G, Pisani A, Pennesi M, Emma F, et al. Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome. Journal of the American Society of Nephrology : Jasn. 25: 850-63. PMID 24480824 DOI: 10.1681/ASN.2013030251 |
0.072 |
|
| 2013 |
Bassanese G, Travan L, D'Ottavio G, Monasta L, Ventura A, Pennesi M. Prenatal anteroposterior pelvic diameter cutoffs for postnatal referral for isolated pyelectasis and hydronephrosis: more is not always better. The Journal of Urology. 190: 1858-63. PMID 23707454 DOI: 10.1016/j.juro.2013.05.038 |
0.072 |
|
| 2015 |
Martenson ME, Halawa OI, Tonsfeldt KJ, Maxwell CA, Hammack N, Mist SD, Pennesi ME, Bennett RM, Mauer KM, Jones KD, Heinricher MM. A possible neural mechanism for photosensitivity in chronic pain. Pain. PMID 26785323 DOI: 10.1097/J.Pain.0000000000000450 |
0.069 |
|
| 1995 |
Lepore L, Pizzul MG, Longo F, Pennesi M, Di Leo G. [Systemic lupus erythematosus: description of a pediatric series]. La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics. 17: 443-6. PMID 8685001 |
0.067 |
|
| 1992 |
Peratoner L, Ferrufino U, Pennesi M. Levamisole in steroid responsive nephrotic syndrome | RUOLO DEL LEVAMISOLO NEL TRATTAMENTO DELLA SINDROME NEFROSICA CORTICO-SENSIBILE Rivista Italiana Di Pediatria. 18: 57-62. |
0.067 |
|
| 2003 |
Gianviti A, Tozzi AE, De Petris L, Caprioli A, Ravà L, Edefonti A, Ardissino G, Montini G, Zacchello G, Ferretti A, Pecoraro C, De Palo T, Caringella A, Gaido M, Coppo R, ... ... Pennesi M, et al. Risk factors for poor renal prognosis in children with hemolytic uremic syndrome. Pediatric Nephrology (Berlin, Germany). 18: 1229-35. PMID 14593522 DOI: 10.1007/s00467-003-1262-6 |
0.066 |
|
| 1993 |
Longo F, Saletta S, Lepore L, Pennesi M. Localized scleroderma after infection with Epstein-Barr virus. Clinical and Experimental Rheumatology. 11: 681-3. PMID 8299265 |
0.066 |
|
| 1992 |
Lepore L, Pennesi M. [Treatment with low-dose methotrexate in intractable juvenile chronic arthritis]. La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics. 14: 509-12. PMID 1488307 |
0.065 |
|
| 2016 |
Boese EA, Jain N, Jia Y, Schlechter CL, Harding CO, Gao SS, Patel RC, Huang D, Weleber RG, Gillingham MB, Pennesi ME. Characterization of Chorioretinopathy Associated with Mitochondrial Trifunctional Protein Disorders: Long-Term Follow-up of 21 Cases. Ophthalmology. PMID 27491397 DOI: 10.1016/J.Ophtha.2016.06.048 |
0.064 |
|
| 2003 |
Pennesi M, Gagliardo A, Minisini S. Effective tacrolimus treatment in a child suffering from severe nephrotic syndrome. Pediatric Nephrology (Berlin, Germany). 18: 477-8. PMID 12687465 DOI: 10.1007/s00467-003-1098-0 |
0.061 |
|
| 2016 |
Parker MA, Choi D, Erker LR, Pennesi ME, Yang P, Chegarnov EN, Steinkamp PN, Schlechter CL, Dhaenens CM, Mohand-Said S, Audo I, Sahel J, Weleber RG, Wilson DJ. Test-Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy Trial. Translational Vision Science & Technology. 5: 10. PMID 27730010 DOI: 10.1167/tvst.5.5.10 |
0.06 |
|
| 2024 |
Wongchaisuwat N, Gillingham MB, Yang P, Everett L, Gregor A, Harding CO, Sahel JA, Nischal KK, Scanga HL, Black D, Vockley J, Arnold G, Pennesi ME. A proposal for an updated staging system for LCHADD retinopathy. Ophthalmic Genetics. 1-7. PMID 38288966 DOI: 10.1080/13816810.2024.2303682 |
0.056 |
|
| 2005 |
Foschini MP, Gaiba A, Cocchi R, Pennesi MG, Pession A. p63 expression in salivary gland tumors: role of DeltaNp73L in neoplastic transformation. International Journal of Surgical Pathology. 13: 329-35. PMID 16273188 DOI: 10.1177/106689690501300404 |
0.055 |
|
| 2014 |
Pellegrin MC, Matarazzo L, Neri E, Pennesi M, Crovella S. HLA-B35, a common genetic trait, in a familial case of Henoch-Schoenlein purpura and Berger's disease. Genetics and Molecular Research : Gmr. 13: 2669-73. PMID 24782055 DOI: 10.4238/2014.April.8.9 |
0.055 |
|
| 1988 |
Lepore L, Agosti E, Pennesi M, Barbi E, De Manzini A. [Long-term remission induced by measles infection and followed by immunosuppressive therapy in a case of refractory juvenile rheumatoid arthritis]. La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics. 10: 191-3. PMID 3174483 |
0.054 |
|
| 2017 |
Pasini A, Benetti E, Conti G, Ghio L, Lepore M, Massella L, Molino D, Peruzzi L, Emma F, Fede C, Trivelli A, Maringhini S, Materassi M, Messina G, Montini G, ... ... Pennesi M, et al. The Italian Society for Pediatric Nephrology (SINePe) consensus document on the management of nephrotic syndrome in children: Part I - Diagnosis and treatment of the first episode and the first relapse. Italian Journal of Pediatrics. 43: 41. PMID 28427453 DOI: 10.1186/s13052-017-0356-x |
0.053 |
|
| 2010 |
Abbate M, Remuzzi G, Coppo R, Pennesi M, Carraro M, Emma F, Pecoraro C, Pisani A, Capasso G. Prospective and sequential study to establish the efficacy of rituximab therapy in maintaining remission of nephritic syndrome in patients with nephropathy at minimal injury or steroid-dependent, recurrent focal segmental glomerulosclerosis (NEMO) | Studio prospettico e sequenziale per stabilire l'efficacia della terapia con rituximab nel mantenere la remissione della sindrome nefrosica in pazienti con nefropatia a lesioni minime o glomerulosclerosi focale steroido-dipendenti o recidivanti (NEMO) Ricerca E Pratica. 26: 25. |
0.049 |
|
| 1991 |
Lepore L, Pennesi M, Barbi E, Pozzi R. Treatment and prevention of osteoporosis in juvenile chronic arthritis with disodium clodronate. Clinical and Experimental Rheumatology. 9: 33-5. PMID 2060176 |
0.049 |
|
| 2008 |
Foschini MP, Cocchi R, Morandi L, Marucci G, Pennesi MG, Righi A, Tosi AL, de Biase D, Pession A, Montebugnoli L. E-cadherin loss and Delta Np73L expression in oral squamous cell carcinomas showing aggressive behavior. Head & Neck. 30: 1475-82. PMID 18704970 DOI: 10.1002/hed.20908 |
0.046 |
|
| 2023 |
Jahrig C, Ku CA, Marra M, Pennesi ME, Yang P. Vitelliform maculopathy in MELAS syndrome. American Journal of Ophthalmology Case Reports. 30: 101842. PMID 37096132 DOI: 10.1016/j.ajoc.2023.101842 |
0.046 |
|
| 2020 |
Pennesi ME. When the Disease Does Not Follow the Textbook. Jama Ophthalmology. PMID 32970121 DOI: 10.1001/jamaophthalmol.2020.3645 |
0.045 |
|
| 1994 |
Lepore L, Pennesi M, Saletta S, Perticarari S, Presani G, Prodan M. Study of IL-2, IL-6, TNF alpha, IFN gamma and beta in the serum and synovial fluid of patients with juvenile chronic arthritis. Clinical and Experimental Rheumatology. 12: 561-5. PMID 7531125 |
0.044 |
|
| 1993 |
Lepore L, Pennesi M, Ventura A, Torre G, Falcini F, Lucchesi A, Perticarari S. Anti-alpha-gliadin antibodies are not predictive of celiac disease in juvenile chronic arthritis. Acta Paediatrica (Oslo, Norway : 1992). 82: 569-73. PMID 8338992 |
0.043 |
|
| 2003 |
Tozzi AE, Caprioli A, Minelli F, Gianviti A, De Petris L, Edefonti A, Montini G, Ferretti A, De Palo T, Gaido M, Rizzoni G, Bettinelli A, Capasso G, Caringella A, Coppo R, ... ... Pennesi M, et al. Shiga toxin-producing Escherichia coli infections associated with hemolytic uremic syndrome, Italy, 1988-2000 Emerging Infectious Diseases. 9: 106-108. PMID 12533290 |
0.043 |
|
| 2005 |
Peratoner L, Pennesi M, Bordugo A, Melega R, Sorce P, Travan L, Minisini S, Zennaro F, Da Ronch L. Kidney length and scarring in children with urinary tract infection: importance of ultrasound scans. Abdominal Imaging. 30: 780-5. PMID 16252147 DOI: 10.1007/s00261-005-0324-6 |
0.043 |
|
| 2012 |
Foschini MP, Baldovini C, Pennesi MG, Cocchi R, Simpson RH. Signet ring cell tumor of the minor salivary gland exhibiting benign behavior. Human Pathology. 43: 303-6. PMID 21813157 DOI: 10.1016/j.humpath.2011.04.025 |
0.04 |
|
| 2008 |
Pennesi M, Travan L, Peratoner L, Bordugo A, Cattaneo A, Ronfani L, Minisini S, Ventura A. Is antibiotic prophylaxis in children with vesicoureteral reflux effective in preventing pyelonephritis and renal scars? A randomized, controlled trial. Pediatrics. 121: e1489-94. PMID 18490378 DOI: 10.1542/peds.2007-2652 |
0.04 |
|
| 2006 |
Foschini MP, Cocchi R, Marucci G, Pennesi MG, Magrini E, Ligorio C, Lombardini F, Tosi AL, Marchetti C. High DeltaN p63 isoform expression favours recurrences in odontogenic keratocyst--odontogenic keratocystic tumour. International Journal of Oral and Maxillofacial Surgery. 35: 673-5. PMID 16687239 DOI: 10.1016/j.ijom.2006.02.021 |
0.04 |
|
| 2018 |
Pennesi ME, Birch DG, Jayasundera KT, Parker M, Tan O, Gurses-Ozden R, Reichley C, Beasley KN, Yang P, Weleber RG, Bennett LD, Heckenlively JR, Kothapalli K, Chulay JD, For The Xlrs-Study Group. Prospective Evaluation of Patients With X-Linked Retinoschisis During 18 Months. Investigative Ophthalmology & Visual Science. 59: 5941-5956. PMID 30551202 DOI: 10.1167/Iovs.18-24565 |
0.039 |
|
| 2016 |
Ku CA, Hariprasad SM, Pennesi ME. Gene Therapy Trial Update: A Primer for Vitreoretinal Specialists. Ophthalmic Surgery, Lasers & Imaging Retina. 47: 6-12. PMID 26731203 DOI: 10.3928/23258160-20151214-01 |
0.039 |
|
| 2018 |
Alberici I, La Manna A, Pennesi M, Starc M, Scozzola F, Nicolini G, Toffolo A, Marra G, Chimenz R, Sica F, Maringhini S, Monasta L, Montini G. First urinary tract infections in children: the role of the risk factors proposed by the Italian recommendations. Acta Paediatrica (Oslo, Norway : 1992). PMID 30028535 DOI: 10.1111/apa.14506 |
0.039 |
|
| 2012 |
Pennesi M, L'erario I, Travan L, Ventura A. Managing children under 36 months of age with febrile urinary tract infection: a new approach. Pediatric Nephrology (Berlin, Germany). 27: 611-5. PMID 22234625 DOI: 10.1007/s00467-011-2087-3 |
0.038 |
|
| 2013 |
Ruggiero B, Vivarelli M, Gianviti A, Benetti E, Peruzzi L, Barbano G, Corona F, Ventura G, Pecoraro C, Murer L, Ghiggeri GM, Pennesi M, Edefonti A, Coppo R, Emma F. Lupus nephritis in children and adolescents: results of the Italian Collaborative Study. Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. 28: 1487-96. PMID 23345627 DOI: 10.1093/ndt/gfs589 |
0.038 |
|
| 2004 |
Pennesi M, Pitter M, Bordugo A, Minisini S, Peratoner L. Behavioral therapy for primary nocturnal enuresis. The Journal of Urology. 171: 408-10. PMID 14665944 DOI: 10.1097/01.ju.0000097497.75022.e8 |
0.037 |
|
| 2003 |
Bruno I, Pennesi M, Marchetti F. ACE-inhibitors-induced metabolic acidosis in a child with nephrotic syndrome. Pediatric Nephrology (Berlin, Germany). 18: 1293-4. PMID 14579142 DOI: 10.1007/s00467-003-1282-2 |
0.036 |
|
| 2001 |
Peratoner L, Pennesi M. Progress and disappointments in nephrourology | Progressi e delusioni in nefro-urologia Medico E Bambino. 20: 51-55. |
0.036 |
|
| 2021 |
Ciulla T, Pennesi ME, Kiss S, Cunningham ET. DNA- and RNA-based Gene Therapies in Ophthalmology. International Ophthalmology Clinics. 61: 3-16. PMID 34196315 DOI: 10.1097/IIO.0000000000000359 |
0.035 |
|
| 1996 |
Lepore L, Rabusin M, Pennesi M, Randi M, Brizzi F. Bilateral Baker's cyst in a patient with psoriatic arthritis of pediatric onset. Clinical and Experimental Rheumatology. 14: 109-10. PMID 8697649 |
0.035 |
|
| 1999 |
Bartolucci C, Campofiloni S, Luchetti G, Pennesi M. Utilizzazione di una procedura latex free nelle ecografie endovaginali Giornale Italiano Di Ostetricia E Ginecologia. 21: 387-388. |
0.032 |
|
| 2012 |
Porciani MC, Ricceri I, Attanà P, Pennesi M, Michelotti F, Mascia G, Sacchi S, Hashtroudi L, Padeletti L. Discordant electrical and mechanical atrial delays affect intracavitary electrogram-based cardiac resynchronization therapy optimization. Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups On Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology. 14: 593-8. PMID 22041885 DOI: 10.1093/europace/eur335 |
0.032 |
|
| 2013 |
Patti G, Naviglio S, Pennesi M, Gregori M, Moressa V, Ventura A. Normal voiding does not exclude posterior urethral valves. Archives of Disease in Childhood. 98: 634. PMID 23645814 DOI: 10.1136/archdischild-2013-304114 |
0.03 |
|
| 2020 |
Ielasi A, Moscarella E, Testa L, Gioffrè G, Morabito G, Cortese B, Colangelo S, Tomai F, Arioli F, Maioli M, Leoncini M, Tumminello G, Benedetto S, Lucchina PG, Pennesi M, et al. IntravaScular lithotripsy for the Management of undILatable coronary stEnt: The SMILE Registry. Cardiovascular Revascularization Medicine : Including Molecular Interventions. PMID 32580881 DOI: 10.1016/j.carrev.2020.05.020 |
0.027 |
|
| 2008 |
De Cunto A, Pennesi M, Salierno P. Re: Antibiotic prophylaxis for the prevention of recurrent urinary tract infection in children with low grade vesicoureteral reflux: results from a prospective randomized study: G. Roussey-Kesler, V. Gadjos, N. Idres, B. Horen, L. Ichay, M. D. Leclair, F. Raymond, A. Grellier, I. Hazart, L. De parscau, R. Salomon, G. Champion, V. Leroy, V. Guigonis, D. Siret, J. B. Palcoux,S. Taque, A. Lemoigne, J. M. Nguyen and C. Guyot. J Urol 2008; 179: 674-679. The Journal of Urology. 180: 2258-9. PMID 18804797 DOI: 10.1016/j.juro.2008.07.080 |
0.027 |
|
| 2002 |
Pennesi M, Torre G, Del Santo M, Sonzogni A. Glomerulonephritis after recombinant hepatitis B vaccine. The Pediatric Infectious Disease Journal. 21: 172-3. PMID 11840090 DOI: 10.1097/00006454-200202000-00020 |
0.027 |
|
| 1996 |
Pennesi M, Peratoner L. Acute renal failure in the course of toxic shock sindrome | Insufficienza renale acuta in corso di sindrome da shock tossico Rivista Italiana Di Pediatria. 22: 93-96. |
0.026 |
|
| 2001 |
Pennesi M. Acute poststreptococcal glomerulonephritis | Glomerulonefrite acuta post-streptococcica Medico E Bambino. 20: 457-460. |
0.026 |
|
| 2017 |
Hewitt IK, Pennesi M, Morello W, Ronfani L, Montini G. Antibiotic Prophylaxis for Urinary Tract Infection-Related Renal Scarring: A Systematic Review. Pediatrics. 139. PMID 28557737 DOI: 10.1542/peds.2016-3145 |
0.025 |
|
| 2012 |
Ammenti A, Cataldi L, Chimenz R, Fanos V, La Manna A, Marra G, Materassi M, Pecile P, Pennesi M, Pisanello L, Sica F, Toffolo A, Montini G. Febrile urinary tract infections in young children: recommendations for the diagnosis, treatment and follow-up. Acta Paediatrica (Oslo, Norway : 1992). 101: 451-7. PMID 22122295 DOI: 10.1111/j.1651-2227.2011.02549.x |
0.025 |
|
| 2012 |
Ardissino G, Testa S, Daccò V, Paglialonga F, Viganò S, Felice-Civitillo C, Battaglino F, Bettinelli A, Bordugo A, Cecchetti V, De Pascale S, La Manna A, Li Volti S, Maringhini S, Montini G, ... Pennesi M, et al. Puberty is associated with increased deterioration of renal function in patients with CKD: data from the ItalKid Project. Archives of Disease in Childhood. 97: 885-8. PMID 22833407 DOI: 10.1136/archdischild-2011-300685 |
0.024 |
|
| 1998 |
Pennesi M, Salvatore CM, Peratoner L. Different clinical presentations of pyelonephritis in children with and without vesicoureteral reflux: an Italian Multicenter Study. Pediatrics. 102: 1493-4. PMID 9882229 |
0.024 |
|
| 1996 |
Lepore L, Martelossi S, Pennesi M, Falcini F, Ermini ML, Ferrari R, Perticarari S, Presani G, Lucchesi A, Lapini M, Ventura A. Prevalence of celiac disease in patients with juvenile chronic arthritis. The Journal of Pediatrics. 129: 311-3. PMID 8765635 DOI: 10.1016/S0022-3476(96)70262-7 |
0.023 |
|
| 2011 |
Foschini MP, Morandi L, Marchetti C, Cocchi R, Eusebi LH, Farnedi A, Badiali G, Gissi DB, Pennesi MG, Montebugnoli L. Cancerization of cutaneous flap reconstruction for oral squamous cell carcinoma: report of three cases studied with the mtDNA D-loop sequence analysis. Histopathology. 58: 361-7. PMID 21255069 DOI: 10.1111/j.1365-2559.2011.03754.x |
0.019 |
|
| 2014 |
De Carlo M, Cortese B, Pennesi M, Misuraca L, Conte L, Pitì A, Petronio AS, Balbarini A. Design of the rosuvastatin pretreatment to reduce embolization during Carotid Artery Stenting trial. Journal of Cardiovascular Medicine (Hagerstown, Md.). 15: 595-600. PMID 24922046 DOI: 10.2459/01.JCM.0000446384.42103.a3 |
0.017 |
|
| 2004 |
Marchetti F, Pennesi M, Pecile P, Ellero S, Brondello C, Peratoner L. Antibiotic treatment of acute pyelonephritis | La terapia antibiotica della pielonefrite acuta Medico E Bambino. 23: 316-319. |
0.017 |
|
| 1974 |
Bartolini R, Busoni P, Pennesi MA. Analgesia during labor by intermittent administration of methoxyflurane (Penthrane) | L'ANALGESIA IN TRAVAGLIO DI PARTO MEDIANTE SOMMINISTRAZIONE INTERMITTENTE DI METOSSIFLURANO (PENTRANO) Riv.Ostet.Ginec.Prat.. 54: 541-548. |
0.017 |
|
| 2019 |
Ammenti A, Alberici I, Brugnara M, Chimenz R, Guarino S, La Manna A, La Scola C, Maringhini S, Marra G, Materassi M, Morello W, Nicolini G, Pennesi M, Pisanello L, Pugliese F, et al. Updated Italian recommendations for the diagnosis, treatment and follow up of the first febrile urinary tract infection in young children. Acta Paediatrica (Oslo, Norway : 1992). PMID 31454101 DOI: 10.1111/apa.14988 |
0.015 |
|
| 2015 |
Esposito G, Pennesi M, Bichi S, Patrini D, Pellegrino P, Redaelli M, Poloni C, Gerometta P, Gentinetta F, Cappabianca G. Hybrid multistep approach to mega-aortic syndrome: the Lupiae technique. European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association For Cardio-Thoracic Surgery. 47: 126-33; discussion 1. PMID 24674908 DOI: 10.1093/ejcts/ezu102 |
0.014 |
|
| 2005 |
Marchetti F, Bua J, Demarini S, Devescovi R, Germani C, Mergoni P, Messi G, Pennesi M, Rabusin M, Sarti A, Ventura A, Arrighini A, Chirico G, Duse M, Miguetti N, et al. Priorities among off-label prescriptions: Paediatricians' perspective | Le priorità associate all'uso dei farmaci "off-label": Il punto di vista del pediatra ospedaliero Medico E Bambino. 24: 527-531. |
0.014 |
|
| 2014 |
Bassanese G, Norbedo S, Pennesi M. The salt of life: Blood test in urinary tract infection? | Il sale della vita: Esami di laboratorio nelle infezioni delle vie urinarie? Medico E Bambino. 33: 330. |
0.014 |
|
| 2011 |
Genead MA, Fishman GA, Landeman M, Pennesi ME, Traboulsi EI. Diagnostic and therapeutic challenges. Retina (Philadelphia, Pa.). 31: 413-8. PMID 20458258 DOI: 10.1097/IAE.0b013e3181dc58db |
0.013 |
|
| 2012 |
Pennesi M, L'Erario I, Barbi E. Endoscopic treatment of primary vesicoureteral reflux. The New England Journal of Medicine. 367: 88; author reply 89. PMID 22762335 DOI: 10.1056/NEJMc1204964#SA1 |
0.011 |
|
| 2021 |
Pulido JS, Procopio R, Davila HJ, Bello N, Ku C, Pennesi ME, Yang P, Nagiel A, Mahroo OA, Aleman TS, Salido EM, Reynolds M. IRD panels-caveat emptor-truly know your IRD panel. Retina (Philadelphia, Pa.). PMID 34690342 DOI: 10.1097/IAE.0000000000003319 |
0.011 |
|
| 2018 |
Selekman RE, Shapiro DJ, Boscardin J, Williams G, Craig JC, Brandström P, Pennesi M, Roussey-Kesler G, Hari P, Copp HL. Uropathogen Resistance and Antibiotic Prophylaxis: A Meta-analysis. Pediatrics. PMID 29954832 DOI: 10.1542/peds.2018-0119 |
0.011 |
|
| 2014 |
Assandro P, Ferrara G, Zerqueni G, Pennesi M, Barbi E. Practical guidelines for the correct use of urinary catheter in children | Consigli pratici per il corretto utilizzo del catetere vescicale in pediatria Medico E Bambino. 33: 369-376. |
0.011 |
|
| 2021 |
Ciulla T, Pennesi ME, Kiss S, Cunningham ET. Preface. International Ophthalmology Clinics. 61: 1-2. PMID 34196314 DOI: 10.1097/IIO.0000000000000371 |
0.01 |
|
| 2012 |
Giurici N, Pennesi M. Importance of bladder bowel dysfunction in patients with urinary tract infection. The Journal of Pediatrics. 161: 370; author reply 37. PMID 22608904 DOI: 10.1016/j.jpeds.2012.04.014 |
0.01 |
|
| 2012 |
Giurici N, Pennesi M. Re: Urinary tract infections in children and the risk of ESRF. Acta Paediatrica (Oslo, Norway : 1992). 101: e196; author reply e. PMID 22296520 DOI: 10.1111/j.1651-2227.2012.02621.x |
0.01 |
|
| 2012 |
Giurici N, Pennesi M. Urinary tract infections in children and the risk of ESRF Acta Paediatrica, International Journal of Paediatrics. 101: e196. DOI: 10.1111/j.1651-2227.2012.02600.x |
0.01 |
|
| 2009 |
Montini G, Ammenti A, Cataldi L, Chimenz R, Fanos V, La Manna A, Marra G, Materassi M, Pecile P, Pennesi M, Pisanello L, Sica F, Toffolo A. Febrile urinary tract infections | Le infezioni febbrili delle vie urinarie Medico E Bambino. 28: 359-370. |
0.01 |
|
| 2008 |
Travan L, Pennesi M, Ronfani L. In reply Pediatrics. 122: 1410-1411. DOI: 10.1542/peds.2008-2831 |
0.01 |
|
| 2008 |
De Cunto A, Maschio M, Pennesi M, Benettoni A. Management of hypertension in children and adolescents: From diagnosis to treatment | L'ipertensione arteriosa in età pediatrica: Dall'inquadramento diagnostico alla terapia Medico E Bambino. 27: 226-234. |
0.01 |
|
| 2006 |
Pennesi M, Giacomini A, Franzil A, Travan L. Prediction of vesicoureteral reflux: sibilla or more? Archives of Disease in Childhood. 91: 716. PMID 16861498 |
0.01 |
|
| 2006 |
Pennesi M, Biasotto E, Saccari A. Schönlein-Henoch purpura involving the penis. Archives of Disease in Childhood. 91: 603. PMID 16790720 DOI: 10.1136/adc.2005.072652 |
0.01 |
|
| 2005 |
Franzil A, Taddio A, Lepore L, Pennesi M, Furlan C. Foot pain in a child with chronic glomerulonephritis | Dolore al piede in bambina con glomerulonefrite cronica Medico E Bambino. 24: 679-680. |
0.01 |
|
| 2004 |
Pennesi M. Continuous changing of policies on urinary tract infections | Seguendo i cambiamenti nelle politiche sulla infezione urinaria Medico E Bambino. 23: 608-609. |
0.01 |
|
| 2002 |
Pennesi M. Enuresis and desmopressin: Why should we not use it? | Enuresi e desmopressina: Le ragioni del no Medico E Bambino. 21: 320-322. |
0.01 |
|
| 2001 |
Barbi E, Pennesi M, Sarti A, Bruno I, Neri E, Pahor T, Torre G, Martelossi S, Tamaro P, Rabusin M, Balsemin F, Filaferro M, Ventura A. Paediatric task force for sedation in painful diagnostic procedures | Unità di sedazione pediatrica: Per procedure diagnostiche dolorose Medico E Bambino. 20: 369-375. |
0.01 |
|
| 2000 |
Pennesi M, Torre G. Angiotensin converting enzyme inhibition in non-diabetic nephropathy with non-nephrotic proteinuria. Pediatric Nephrology (Berlin, Germany). 14: 438. PMID 10805476 |
0.01 |
|
| 2000 |
Pennesi M. Antibiotic prophylaxis in children with vesicouretheral reflux | Profilassi antibiotica nei bambini con RVU. Necessità di una revisione critica Medico E Bambino. 19: 638-641. |
0.01 |
|
| 1985 |
Brianzoni E, Berbellini A, Pennesi M, Centioni G, Tacconi R, Trognoni A, Marsili G. Serum myoglobin in athletes after physical activity. Quaderni Sclavo Di Diagnostica Clinica E Di Laboratorio. 21: 257-63. PMID 3835572 |
0.01 |
|
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