| Year |
Citation |
Score |
| 2023 |
Elziny S, Sran S, Yoon H, Corrigan RR, Page J, Ringland A, Lanier A, Lapidus S, Foreman J, Heinzen EL, Iffland P, Crino PB, Bedrosian TA. Loss of alters development of the mouse cerebral cortex. Biorxiv : the Preprint Server For Biology. PMID 38077069 DOI: 10.1101/2023.11.29.569243 |
0.318 |
|
| 2022 |
Iffland PH, Everett ME, Cobb-Pitstick KM, Bowser LE, Barnes AE, Babus JK, Romanowski AJ, Baybis M, Elziny S, Puffenberger EG, Gonzaga-Jauregui C, Poulopoulos A, Carson VJ, Crino PB. NPRL3 loss alters neuronal morphology, mTOR localization, cortical lamination, and seizure threshold. Brain : a Journal of Neurology. PMID 35136953 DOI: 10.1093/brain/awac044 |
0.322 |
|
| 2022 |
Terry BK, Park R, Cho SH, Crino PB, Kim S. Abnormal activation of yap/Taz contributes to the pathogenesis of tuberous sclerosis complex. Human Molecular Genetics. PMID 34999833 DOI: 10.1093/hmg/ddab374 |
0.305 |
|
| 2021 |
Dang LT, Vaid S, Lin G, Swaminathan P, Safran J, Loughman A, Lee M, Glenn T, Majolo F, Crino PB, Parent JM. STRADA-mutant human cortical organoids model megalencephaly and exhibit delayed neuronal differentiation. Developmental Neurobiology. PMID 33619909 DOI: 10.1002/dneu.22816 |
0.312 |
|
| 2020 |
Dang LT, Glanowska KM, Iffland Ii PH, Barnes AE, Baybis M, Liu Y, Patino G, Vaid S, Streicher AM, Parker WE, Kim S, Moon UY, Henry FE, Murphy GG, Sutton M, ... ... Crino PB, et al. Multimodal Analysis of STRADA Function in Brain Development. Frontiers in Cellular Neuroscience. 14: 122. PMID 32457579 DOI: 10.3389/Fncel.2020.00122 |
0.658 |
|
| 2018 |
Iffland PH, Baybis M, Barnes AE, Leventer RJ, Lockhart PJ, Crino PB. DEPDC5 and NPRL3 modulate cell size, filopodial outgrowth, and localization of mTOR in neural progenitor cells and neurons. Neurobiology of Disease. PMID 29481864 DOI: 10.1016/j.nbd.2018.02.013 |
0.341 |
|
| 2017 |
Iffland PH, Crino PB. Focal Cortical Dysplasia: Gene Mutations, Cell Signaling, and Therapeutic Implications. Annual Review of Pathology. 12: 547-571. PMID 28135561 DOI: 10.1146/annurev-pathol-052016-100138 |
0.31 |
|
| 2016 |
Liu C, Russin J, Heck C, Kawata K, Adiga R, Yen W, Lambert J, Stear B, Law M, Marquez Y, Crino P, Millett D, Langford D. Dysregulation of PINCH signaling in mesial temporal epilepsy. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. PMID 27838154 DOI: 10.1016/j.jocn.2016.10.012 |
0.385 |
|
| 2016 |
Crino PB. The mTOR signalling cascade: paving new roads to cure neurological disease. Nature Reviews. Neurology. PMID 27340022 DOI: 10.1038/nrneurol.2016.81 |
0.308 |
|
| 2016 |
Bhoj EJ, Li D, Harr M, Edvardson S, Elpeleg O, Chisholm E, Juusola J, Douglas G, Guillen Sacoto MJ, Siquier-Pernet K, Saadi A, Bole-Feysot C, Nitschke P, Narravula A, Walke M, ... ... Crino P, et al. Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia. American Journal of Human Genetics. PMID 27040691 DOI: 10.1016/J.Ajhg.2016.03.016 |
0.374 |
|
| 2015 |
Jinks RN, Puffenberger EG, Baple E, Harding B, Crino P, Fogo AB, Wenger O, Xin B, Koehler AE, McGlincy MH, Provencher MM, Smith JD, Tran L, Al Turki S, Chioza BA, et al. Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73. Brain : a Journal of Neurology. 138: 2173-90. PMID 26070982 DOI: 10.1093/Brain/Awv153 |
0.333 |
|
| 2015 |
Crino PB. mTOR signaling in epilepsy: insights from malformations of cortical development. Cold Spring Harbor Perspectives in Medicine. 5. PMID 25833943 DOI: 10.1101/cshperspect.a022442 |
0.336 |
|
| 2014 |
Tsai V, Parker WE, Orlova KA, Baybis M, Chi AW, Berg BD, Birnbaum JF, Estevez J, Okochi K, Sarnat HB, Flores-Sarnat L, Aronica E, Crino PB. Fetal brain mTOR signaling activation in tuberous sclerosis complex. Cerebral Cortex (New York, N.Y. : 1991). 24: 315-27. PMID 23081885 DOI: 10.1093/Cercor/Bhs310 |
0.747 |
|
| 2013 |
Parker WE, Orlova KA, Parker WH, Birnbaum JF, Krymskaya VP, Goncharov DA, Baybis M, Helfferich J, Okochi K, Strauss KA, Crino PB. Rapamycin prevents seizures after depletion of STRADA in a rare neurodevelopmental disorder. Science Translational Medicine. 5: 182ra53. PMID 23616120 DOI: 10.1126/Scitranslmed.3005271 |
0.757 |
|
| 2012 |
Sarnat H, Flores-Sarnat L, Crino P, Hader W, Bello-Espinosa L. Hemimegalencephaly: foetal tauopathy with mTOR hyperactivation and neuronal lipidosis. Folia Neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences. 50: 330-45. PMID 23319189 DOI: 10.5114/fn.2012.32363 |
0.411 |
|
| 2012 |
Chen J, Tsai V, Parker WE, Aronica E, Baybis M, Crino PB. Detection of human papillomavirus in human focal cortical dysplasia type IIB. Annals of Neurology. 72: 881-92. PMID 23280839 DOI: 10.1002/Ana.23795 |
0.732 |
|
| 2012 |
Marcotte L, Aronica E, Baybis M, Crino PB. Cytoarchitectural alterations are widespread in cerebral cortex in tuberous sclerosis complex. Acta Neuropathologica. 123: 685-93. PMID 22327361 DOI: 10.1007/s00401-012-0950-3 |
0.341 |
|
| 2011 |
Parker WE, Orlova KA, Heuer GG, Baybis M, Aronica E, Frost M, Wong M, Crino PB. Enhanced epidermal growth factor, hepatocyte growth factor, and vascular endothelial growth factor expression in tuberous sclerosis complex. The American Journal of Pathology. 178: 296-305. PMID 21224066 DOI: 10.1016/J.Ajpath.2010.11.031 |
0.736 |
|
| 2011 |
Blümcke I, Thom M, Aronica E, Armstrong DD, Vinters HV, Palmini A, Jacques TS, Avanzini G, Barkovich AJ, Battaglia G, Becker A, Cepeda C, Cendes F, Colombo N, Crino P, et al. The clinicopathologic spectrum of focal cortical dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia. 52: 158-74. PMID 21219302 DOI: 10.1111/J.1528-1167.2010.02777.X |
0.316 |
|
| 2010 |
Orlova KA, Tsai V, Baybis M, Heuer GG, Sisodiya S, Thom M, Strauss K, Aronica E, Storm PB, Crino PB. Early progenitor cell marker expression distinguishes type II from type I focal cortical dysplasias. Journal of Neuropathology and Experimental Neurology. 69: 850-63. PMID 20613634 DOI: 10.1097/Nen.0B013E3181Eac1F5 |
0.748 |
|
| 2010 |
Orlova KA, Parker WE, Heuer GG, Tsai V, Yoon J, Baybis M, Fenning RS, Strauss K, Crino PB. STRADalpha deficiency results in aberrant mTORC1 signaling during corticogenesis in humans and mice. The Journal of Clinical Investigation. 120: 1591-602. PMID 20424326 DOI: 10.1172/Jci41592 |
0.759 |
|
| 2010 |
Orlova KA, Crino PB. The tuberous sclerosis complex. Annals of the New York Academy of Sciences. 1184: 87-105. PMID 20146692 DOI: 10.1111/J.1749-6632.2009.05117.X |
0.749 |
|
| 2008 |
Boer K, Troost D, Jansen F, Nellist M, van den Ouweland AM, Geurts JJ, Spliet WG, Crino P, Aronica E. Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 28: 577-90. PMID 18410267 DOI: 10.1111/J.1440-1789.2008.00920.X |
0.391 |
|
| 2007 |
Crino PB. Focal brain malformations: a spectrum of disorders along the mTOR cascade. Novartis Foundation Symposium. 288: 260-72; discussion 2. PMID 18494264 DOI: 10.1002/9780470994030.ch18 |
0.321 |
|
| 2007 |
Gilby KL, Crino P, McIntyre DC. Neurodevelopment in seizure-prone and seizure-resistant rat strains: recognizing conflicts in management. Epilepsia. 48: 114-8. PMID 17910590 DOI: 10.1111/j.1528-1167.2007.01298.x |
0.326 |
|
| 2007 |
Lamparello P, Baybis M, Pollard J, Hol EM, Eisenstat DD, Aronica E, Crino PB. Developmental lineage of cell types in cortical dysplasia with balloon cells. Brain : a Journal of Neurology. 130: 2267-76. PMID 17711980 DOI: 10.1093/brain/awm175 |
0.327 |
|
| 2007 |
Boer K, Troost D, Spliet WG, Redeker S, Crino PB, Aronica E. A neuropathological study of two autopsy cases of syndromic hemimegalencephaly. Neuropathology and Applied Neurobiology. 33: 455-70. PMID 17617874 DOI: 10.1111/J.1365-2990.2006.00818.X |
0.302 |
|
| 2007 |
Aronica E, Boer K, Baybis M, Yu J, Crino P. Co-expression of cyclin D1 and phosphorylated ribosomal S6 proteins in hemimegalencephaly. Acta Neuropathologica. 114: 287-93. PMID 17483958 DOI: 10.1007/s00401-007-0225-6 |
0.382 |
|
| 2006 |
Marcotte L, Crino PB. The neurobiology of the tuberous sclerosis complex. Neuromolecular Medicine. 8: 531-46. PMID 17028374 DOI: 10.1385/NMM:8:4:531 |
0.329 |
|
| 2004 |
Crino PB. Molecular pathogenesis of tuber formation in tuberous sclerosis complex. Journal of Child Neurology. 19: 716-25. PMID 15563019 |
0.346 |
|
| 2004 |
Ess KC, Uhlmann EJ, Li W, Li H, Declue JE, Crino PB, Gutmann DH. Expression profiling in tuberous sclerosis complex (TSC) knockout mouse astrocytes to characterize human TSC brain pathology. Glia. 46: 28-40. PMID 14999811 DOI: 10.1002/Glia.10324 |
0.334 |
|
| 2003 |
Hua Y, Crino PB. Single cell lineage analysis in human focal cortical dysplasia. Cerebral Cortex (New York, N.Y. : 1991). 13: 693-9. PMID 12764046 DOI: 10.1093/cercor/13.6.693 |
0.302 |
|
| 2002 |
Onda H, Crino PB, Zhang H, Murphey RD, Rastelli L, Gould Rothberg BE, Kwiatkowski DJ. Tsc2 null murine neuroepithelial cells are a model for human tuber giant cells, and show activation of an mTOR pathway. Molecular and Cellular Neurosciences. 21: 561-74. PMID 12504590 DOI: 10.1006/mcne.2002.1184 |
0.343 |
|
| 2001 |
Eberwine J, Crino P. Analysis of mRNA populations from single live and fixed cells of the central nervous system. Current Protocols in Neuroscience / Editorial Board, Jacqueline N. Crawley ... [Et Al.]. Unit 5.3. PMID 18428502 DOI: 10.1002/0471142301.ns0503s00 |
0.565 |
|
| 2001 |
Taylor JP, Sater R, French J, Baltuch G, Crino PB. Transcription of intermediate filament genes is enhanced in focal cortical dysplasia. Acta Neuropathologica. 102: 141-8. PMID 11563628 |
0.307 |
|
| 2000 |
Kacharmina JE, Job C, Crino P, Eberwine J. Stimulation of glutamate receptor protein synthesis and membrane insertion within isolated neuronal dendrites. Proceedings of the National Academy of Sciences of the United States of America. 97: 11545-50. PMID 11027353 DOI: 10.1073/pnas.97.21.11545 |
0.572 |
|
| 2000 |
O'Dell DM, Raghupathi R, Crino PB, Eberwine JH, McIntosh TK. Traumatic brain injury alters the molecular fingerprint of TUNEL-positive cortical neurons In vivo: A single-cell analysis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 20: 4821-8. PMID 10864939 DOI: 10.1523/Jneurosci.20-13-04821.2000 |
0.573 |
|
| 1999 |
Kacharmina JE, Crino PB, Eberwine J. Preparation of cDNA from single cells and subcellular regions. Methods in Enzymology. 303: 3-18. PMID 10349635 DOI: 10.1016/S0076-6879(99)03003-7 |
0.568 |
|
| 1999 |
Ginsberg SD, Crino PB, Hemby SE, Weingarten JA, Lee VM, Eberwine JH, Trojanowski JQ. Predominance of neuronal mRNAs in individual Alzheimer's disease senile plaques. Annals of Neurology. 45: 174-81. PMID 9989619 DOI: 10.1002/1531-8249(199902)45:2<174::Aid-Ana7>3.0.Co;2-E |
0.686 |
|
| 1998 |
O'Dell DM, Raghupathi R, Crino PB, Morrison B, Eberwine JH, McIntosh TK. Amplification of mRNAs from single, fixed, TUNEL-positive cells. Biotechniques. 25: 566-8, 570. PMID 9793634 DOI: 10.2144/98254Bm04 |
0.507 |
|
| 1998 |
Crino P, Khodakhah K, Becker K, Ginsberg S, Hemby S, Eberwine J. Presence and phosphorylation of transcription factors in developing dendrites. Proceedings of the National Academy of Sciences of the United States of America. 95: 2313-8. PMID 9482882 DOI: 10.1073/pnas.95.5.2313 |
0.715 |
|
| 1997 |
Crino PB, Eberwine J. Cellular and molecular basis of cerebral dysgenesis. Journal of Neuroscience Research. 50: 907-16. PMID 9452005 DOI: 10.1002/(SICI)1097-4547(19971215)50:6<907::AID-JNR1>3.0.CO;2-H |
0.504 |
|
| 1997 |
Crino PB, Trojanowski JQ, Eberwine J. Internexin, MAP1B, and nestin in cortical dysplasia as markers of developmental maturity. Acta Neuropathologica. 93: 619-27. PMID 9194902 DOI: 10.1007/S004010050660 |
0.562 |
|
| 1997 |
Ginsberg SD, Crino PB, Lee VM, Eberwine JH, Trojanowski JQ. Sequestration of RNA in Alzheimer's disease neurofibrillary tangles and senile plaques. Annals of Neurology. 41: 200-9. PMID 9029069 DOI: 10.1002/Ana.410410211 |
0.52 |
|
| 1996 |
Crino PB, Trojanowski JQ, Dichter MA, Eberwine J. Embryonic neuronal markers in tuberous sclerosis: single-cell molecular pathology. Proceedings of the National Academy of Sciences of the United States of America. 93: 14152-7. PMID 8943076 DOI: 10.1073/pnas.93.24.14152 |
0.6 |
|
| 1996 |
Crino P, Hemby S, Eberwine J. Utility of in situ transcription, single-cell nucleic acid amplification and expression profiling in the study of the central nervous system development Cell Vision - Journal of Analytical Morphology. 3: 203-206. |
0.594 |
|
| 1995 |
Eberwine J, Crino P, Dichter M. Review : Single-Cell mRNA Amplification: Implications for Basic and Clinical Neuroscience The Neuroscientist. 1: 200-211. DOI: 10.1177/107385849500100404 |
0.584 |
|
| 1991 |
Vogt BA, Crino PB, Volicer L. Laminar alterations in gamma-aminobutyric acidA, muscarinic, and beta adrenoceptors and neuron degeneration in cingulate cortex in Alzheimer's disease. Journal of Neurochemistry. 57: 282-90. PMID 1675662 DOI: 10.1111/j.1471-4159.1991.tb02126.x |
0.436 |
|
| 1990 |
Volicer L, Crino PB. Involvement of free radicals in dementia of the Alzheimer type: a hypothesis. Neurobiology of Aging. 11: 567-71. PMID 2146522 DOI: 10.1016/0197-4580(90)90119-K |
0.415 |
|
| 1990 |
Crino PB, Vogt BA, Volicer L, Wiley RG. Cellular localization of serotonin 1A, 1B and uptake sites in cingulate cortex of the rat. The Journal of Pharmacology and Experimental Therapeutics. 252: 651-6. PMID 2138221 |
0.434 |
|
| 1989 |
Crino PB, Ullman MD, Vogt BA, Bird ED, Volicer L. Brain gangliosides in dementia of the Alzheimer type. Archives of Neurology. 46: 398-401. PMID 2705899 DOI: 10.1001/archneur.1989.00520400054019 |
0.466 |
|
| 1989 |
Crino PB, Vogt BA, Chen JC, Volicer L. Neurotoxic effects of partially oxidized serotonin: tryptamine-4,5-dione. Brain Research. 504: 247-57. PMID 2598027 DOI: 10.1016/0006-8993(89)91364-4 |
0.582 |
|
| 1989 |
Volicer L, Seltzer B, Rheaume Y, Karner J, Glennon M, Riley ME, Crino P. Eating difficulties in patients with probable dementia of the Alzheimer type. Journal of Geriatric Psychiatry and Neurology. 2: 188-95. PMID 2483945 DOI: 10.1177/089198878900200404 |
0.45 |
|
| 1989 |
Volicer L, Chen JC, Crino PB, Vogt BA, Fishman J, Rubins J, Schenepper PW, Wolfe N. Neurotoxic properties of a serotonin oxidation product: possible role in Alzheimer's disease. Progress in Clinical and Biological Research. 317: 453-65. PMID 2481322 DOI: 10.1097/00002093-198802030-00090 |
0.564 |
|
| 1989 |
Chen JC, Crino PB, Schnepper PW, To AC, Volicer L. Increased serotonin efflux by a partially oxidized serotonin: tryptamine-4,5-dione. The Journal of Pharmacology and Experimental Therapeutics. 250: 141-8. PMID 2473186 |
0.519 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2007 |
Samadani U, Judkins AR, Akpalu A, Aronica E, Crino PB. Differential cellular gene expression in ganglioglioma. Epilepsia. 48: 646-53. PMID 17437409 DOI: 10.1111/J.1528-1167.2007.00925.X |
0.299 |
|
| 2004 |
Baybis M, Yu J, Lee A, Golden JA, Weiner H, McKhann G, Aronica E, Crino PB. mTOR cascade activation distinguishes tubers from focal cortical dysplasia. Annals of Neurology. 56: 478-87. PMID 15455405 DOI: 10.1002/Ana.20211 |
0.298 |
|
| 2012 |
Wong M, Crino PB. Tuberous sclerosis and epilepsy: role of astrocytes. Glia. 60: 1244-50. PMID 22438024 DOI: 10.1002/glia.22326 |
0.297 |
|
| 2016 |
Mühlebner A, van Scheppingen J, Hulshof HM, Scholl T, Iyer AM, Anink JJ, van den Ouweland AM, Nellist MD, Jansen FE, Spliet WG, Krsek P, Benova B, Zamecnik J, Crino PB, Prayer D, et al. Novel Histopathological Patterns in Cortical Tubers of Epilepsy Surgery Patients with Tuberous Sclerosis Complex. Plos One. 11: e0157396. PMID 27295297 DOI: 10.1371/journal.pone.0157396 |
0.293 |
|
| 2009 |
Crino PB. Focal brain malformations: seizures, signaling, sequencing. Epilepsia. 50: 3-8. PMID 19761448 DOI: 10.1111/j.1528-1167.2009.02289.x |
0.292 |
|
| 2011 |
Crino PB. mTOR: A pathogenic signaling pathway in developmental brain malformations. Trends in Molecular Medicine. 17: 734-42. PMID 21890410 DOI: 10.1016/j.molmed.2011.07.008 |
0.291 |
|
| 2002 |
Ryzhova EV, Crino P, Shawver L, Westmoreland SV, Lackner AA, González-Scarano F. Simian immunodeficiency virus encephalitis: analysis of envelope sequences from individual brain multinucleated giant cells and tissue samples. Virology. 297: 57-67. PMID 12083836 DOI: 10.1006/Viro.2002.1395 |
0.29 |
|
| 2013 |
Lim KC, Crino PB. Focal malformations of cortical development: new vistas for molecular pathogenesis. Neuroscience. 252: 262-76. PMID 23892008 DOI: 10.1016/j.neuroscience.2013.07.037 |
0.29 |
|
| 2008 |
Sosunov AA, Wu X, Weiner HL, Mikell CB, Goodman RR, Crino PD, McKhann GM. Tuberous sclerosis: a primary pathology of astrocytes? Epilepsia. 49: 53-62. PMID 18226172 DOI: 10.1111/J.1528-1167.2008.01493.X |
0.289 |
|
| 2001 |
Scherer SS, Xu T, Crino P, Arroyo EJ, Gutmann DH. Ezrin, radixin, and moesin are components of Schwann cell microvilli. Journal of Neuroscience Research. 65: 150-64. PMID 11438984 DOI: 10.1002/Jnr.1138 |
0.289 |
|
| 2019 |
Iffland PH, Carson V, Bordey A, Crino PB. GATORopathies: The role of amino acid regulatory gene mutations in epilepsy and cortical malformations. Epilepsia. PMID 31625153 DOI: 10.1111/epi.16370 |
0.286 |
|
| 2020 |
Iffland PH, Barnes AE, Baybis M, Crino PB. Dynamic analysis of 4E-BP1 phosphorylation in neurons with Tsc2 or Depdc5 knockout. Experimental Neurology. 113432. PMID 32781001 DOI: 10.1016/j.expneurol.2020.113432 |
0.282 |
|
| 2023 |
Elziny S, Crino PB, Winawer M. SLC35A2 somatic variants in drug resistant epilepsy: FCD and MOGHE. Neurobiology of Disease. 187: 106299. PMID 37739137 DOI: 10.1016/j.nbd.2023.106299 |
0.279 |
|
| 2002 |
Crino PB, Jin H, Shumate MD, Robinson MB, Coulter DA, Brooks-Kayal AR. Increased expression of the neuronal glutamate transporter (EAAT3/EAAC1) in hippocampal and neocortical epilepsy. Epilepsia. 43: 211-8. PMID 11906504 DOI: 10.1046/J.1528-1157.2002.35001.X |
0.278 |
|
| 2015 |
Moon UY, Park JY, Park R, Cho JY, Hughes LJ, McKenna J, Goetzl L, Cho SH, Crino PB, Gambello MJ, Kim S. Impaired Reelin-Dab1 Signaling Contributes to Neuronal Migration Deficits of Tuberous Sclerosis Complex. Cell Reports. PMID 26235615 DOI: 10.1016/J.Celrep.2015.07.013 |
0.276 |
|
| 2013 |
Prabowo AS, Anink JJ, Lammens M, Nellist M, van den Ouweland AM, Adle-Biassette H, Sarnat HB, Flores-Sarnat L, Crino PB, Aronica E. Fetal brain lesions in tuberous sclerosis complex: TORC1 activation and inflammation. Brain Pathology (Zurich, Switzerland). 23: 45-59. PMID 22805177 DOI: 10.1111/j.1750-3639.2012.00616.x |
0.275 |
|
| 2015 |
Crino PB. Focal Cortical Dysplasia. Seminars in Neurology. 35: 201-8. PMID 26060899 DOI: 10.1055/s-0035-1552617 |
0.274 |
|
| 1992 |
Grossman M, Crino P, Reivich M, Stern MB, Hurtig HI. Attention and sentence processing deficits in Parkinson's disease: the role of anterior cingulate cortex. Cerebral Cortex (New York, N.Y. : 1991). 2: 513-25. PMID 1477527 DOI: 10.1093/Cercor/2.6.513 |
0.273 |
|
| 2022 |
Korotkov A, Luinenburg MJ, Romagnolo A, Zimmer TS, van Scheppingen J, Bongaarts A, Broekaart DWM, Anink JJ, Mijnsbergen C, Jansen FE, van Hecke W, Spliet WG, van Rijen PC, Feucht M, Hainfellner JA, ... ... Crino PB, et al. Down-regulation of the brain-specific cell-adhesion molecule contactin-3 in tuberous sclerosis complex during the early postnatal period. Journal of Neurodevelopmental Disorders. 14: 8. PMID 35030990 DOI: 10.1186/s11689-022-09416-2 |
0.271 |
|
| 2003 |
Maldonado M, Baybis M, Newman D, Kolson DL, Chen W, McKhann G, Gutmann DH, Crino PB. Expression of ICAM-1, TNF-alpha, NF kappa B, and MAP kinase in tubers of the tuberous sclerosis complex. Neurobiology of Disease. 14: 279-90. PMID 14572449 DOI: 10.1016/S0969-9961(03)00127-X |
0.267 |
|
| 2001 |
White R, Hua Y, Scheithauer B, Lynch DR, Henske EP, Crino PB. Selective alterations in glutamate and GABA receptor subunit mRNA expression in dysplastic neurons and giant cells of cortical tubers. Annals of Neurology. 49: 67-78. PMID 11198298 DOI: 10.1002/1531-8249(200101)49:1<67::Aid-Ana10>3.0.Co;2-L |
0.266 |
|
| 2011 |
Tobochnik S, Gutierrez C, Crino P, Connolly P. Refractory Nonlesional Neocortical Epilepsy: Current Trends Journal of Neurology and Neurophysiology. 2013: 1-8. DOI: 10.4172/2155-9562.S2-004 |
0.265 |
|
| 2004 |
Telfeian AE, Judkins A, Younkin D, Pollock AN, Crino P. Subependymal giant cell astrocytoma with cranial and spinal metastases in a patient with tuberous sclerosis. Case report. Journal of Neurosurgery. 100: 498-500. PMID 15287462 DOI: 10.3171/Ped.2004.100.5.0498 |
0.261 |
|
| 2001 |
Sheen VL, Dixon PH, Fox JW, Hong SE, Kinton L, Sisodiya SM, Duncan JS, Dubeau F, Scheffer IE, Schachter SC, Wilner A, Henchy R, Crino P, Kamuro K, DiMario F, et al. Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. Human Molecular Genetics. 10: 1775-83. PMID 11532987 DOI: 10.1093/Hmg/10.17.1775 |
0.259 |
|
| 2013 |
Crino PB. Evolving neurobiology of tuberous sclerosis complex. Acta Neuropathologica. 125: 317-32. PMID 23386324 DOI: 10.1007/s00401-013-1085-x |
0.257 |
|
| 2004 |
Kolson DL, Sabnekar P, Baybis M, Crino PB. Gene expression in TUNEL-positive neurons in human immunodeficiency virus-infected brain. Journal of Neurovirology. 10: 102-7. PMID 14982747 DOI: 10.1080/753312760 |
0.256 |
|
| 1999 |
Crino PB, Henske EP. New developments in the neurobiology of the tuberous sclerosis complex. Neurology. 53: 1384-90. PMID 10534239 |
0.256 |
|
| 2001 |
Kyin R, Hua Y, Baybis M, Scheithauer B, Kolson D, Uhlmann E, Gutmann D, Crino PB. Differential cellular expression of neurotrophins in cortical tubers of the tuberous sclerosis complex. The American Journal of Pathology. 159: 1541-54. PMID 11583980 DOI: 10.1016/S0002-9440(10)62539-4 |
0.255 |
|
| 2007 |
Rüegg S, Baybis M, Juul H, Dichter M, Crino PB. Effects of rapamycin on gene expression, morphology, and electrophysiological properties of rat hippocampal neurons. Epilepsy Research. 77: 85-92. PMID 17983731 DOI: 10.1016/J.Eplepsyres.2007.09.009 |
0.254 |
|
| 2015 |
Srivastava IN, Shperdheja J, Baybis M, Ferguson T, Crino PB. mTOR pathway inhibition prevents neuroinflammation and neuronal death in a mouse model of cerebral palsy. Neurobiology of Disease. 85: 144-154. PMID 26459113 DOI: 10.1016/j.nbd.2015.10.001 |
0.252 |
|
| 2022 |
Lai D, Gade M, Yang E, Koh HY, Lu J, Walley NM, Buckley AF, Sands TT, Akman CI, Mikati MA, McKhann GM, Goldman JE, Canoll P, Alexander AL, Park KL, ... ... Crino PB, et al. Somatic variants in diverse genes leads to a spectrum of focal cortical malformations. Brain : a Journal of Neurology. PMID 35441233 DOI: 10.1093/brain/awac117 |
0.251 |
|
| 2001 |
Crino P. New RELN Mutation Associated with Lissencephaly and Epilepsy. Epilepsy Currents / American Epilepsy Society. 1: 72. PMID 15309195 DOI: 10.1046/j.1535-7597.2001.00017.x |
0.251 |
|
| 2001 |
Crino PB, Duhaime AC, Baltuch G, White R. Differential expression of glutamate and GABA-A receptor subunit mRNA in cortical dysplasia. Neurology. 56: 906-13. PMID 11294928 |
0.25 |
|
| 1997 |
Paulson HL, Das SS, Crino PB, Perez MK, Patel SC, Gotsdiner D, Fischbeck KH, Pittman RN. Machado-Joseph disease gene product is a cytoplasmic protein widely expressed in brain. Annals of Neurology. 41: 453-62. PMID 9124802 DOI: 10.1002/ana.410410408 |
0.249 |
|
| 2003 |
Lee A, Maldonado M, Baybis M, Walsh CA, Scheithauer B, Yeung R, Parent J, Weiner HL, Crino PB. Markers of cellular proliferation are expressed in cortical tubers. Annals of Neurology. 53: 668-73. PMID 12731003 DOI: 10.1002/Ana.10579 |
0.248 |
|
| 2009 |
Baybis M, Aronica E, Nathanson KL, Crino PB. Deletion of 15q11.2-15q13.1 in isolated human hemimegalencephaly. Acta Neuropathologica. 118: 821-3. PMID 19851776 DOI: 10.1007/S00401-009-0603-3 |
0.246 |
|
| 2002 |
Crino PB, Miyata H, Vinters HV. Neurodevelopmental disorders as a cause of seizures: neuropathologic, genetic, and mechanistic considerations. Brain Pathology (Zurich, Switzerland). 12: 212-33. PMID 11958376 DOI: 10.1111/J.1750-3639.2002.Tb00437.X |
0.245 |
|
| 2017 |
Caban C, Khan N, Hasbani DM, Crino PB. Genetics of tuberous sclerosis complex: implications for clinical practice. The Application of Clinical Genetics. 10: 1-8. PMID 28053551 DOI: 10.2147/Tacg.S90262 |
0.239 |
|
| 2004 |
Crino PB. Malformations of cortical development: molecular pathogenesis and experimental strategies. Advances in Experimental Medicine and Biology. 548: 175-91. PMID 15250594 |
0.238 |
|
| 2018 |
Hasbani DM, Crino PB. Tuberous sclerosis complex. Handbook of Clinical Neurology. 148: 813-822. PMID 29478616 DOI: 10.1016/B978-0-444-64076-5.00052-1 |
0.235 |
|
| 2023 |
Levitin MO, Rawlins LE, Sanchez-Andrade G, Arshad OA, Collins SC, Sawiak SJ, Iffland PH, Andersson MHL, Bupp C, Cambridge EL, Coomber EL, Ellis I, Herkert JC, Ironfield H, Jory L, ... ... Crino PB, et al. Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes. Brain : a Journal of Neurology. PMID 37437211 DOI: 10.1093/brain/awad231 |
0.232 |
|
| 2018 |
Winawer MR, Griffin NG, Samanamud J, Baugh EH, Rathakrishnan D, Ramalingam S, Zagzag D, Schevon CA, Dugan P, Hegde M, Sheth SA, McKhann GM, Doyle WK, Grant GA, Porter BE, ... ... Crino PB, et al. Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy. Annals of Neurology. PMID 29679388 DOI: 10.1002/Ana.25243 |
0.23 |
|
| 2003 |
Telfeian AE, Tseng HC, Baybis M, Crino PB, Dichter MA. Differential expression of GABA and glutamate-receptor subunits and enzymes involved in GABA metabolism between electrophysiologically identified hippocampal CA1 pyramidal cells and interneurons. Epilepsia. 44: 143-9. PMID 12558566 DOI: 10.1046/J.1528-1157.2003.06102.X |
0.228 |
|
| 2010 |
Boer K, Crino PB, Gorter JA, Nellist M, Jansen FE, Spliet WG, van Rijen PC, Wittink FR, Breit TM, Troost D, Wadman WJ, Aronica E. Gene expression analysis of tuberous sclerosis complex cortical tubers reveals increased expression of adhesion and inflammatory factors. Brain Pathology (Zurich, Switzerland). 20: 704-19. PMID 19912235 DOI: 10.1111/J.1750-3639.2009.00341.X |
0.227 |
|
| 2015 |
Scerri T, Riseley JR, Gillies G, Pope K, Burgess R, Mandelstam SA, Dibbens L, Chow CW, Maixner W, Simon Harvey A, Jackson GD, Amor DJ, Delatycki MB, Crino PB, Berkovic SF, et al. Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5. Annals of Clinical and Translational Neurology. 2: 575-80. PMID 26000329 DOI: 10.1002/acn3.191 |
0.226 |
|
| 2016 |
Iffland PH, Crino PB. Sending Mixed Signals: The Expanding Role of Molecular Cascade Mutations in Malformations of Cortical Development and Epilepsy. Epilepsy Currents / American Epilepsy Society. 16: 158-63. PMID 27330441 DOI: 10.5698/1535-7511-16.3.158 |
0.222 |
|
| 2019 |
Iffland PH, Crino PB. The role of somatic mutational events in the pathogenesis of epilepsy. Current Opinion in Neurology. PMID 30762606 DOI: 10.1097/WCO.0000000000000667 |
0.221 |
|
| 2000 |
Choe W, Albright A, Sulcove J, Jaffer S, Hesselgesser J, Lavi E, Crino P, Kolson DL. Functional expression of the seven-transmembrane HIV-1 co-receptor APJ in neural cells. Journal of Neurovirology. 6: S61-9. PMID 10871767 |
0.218 |
|
| 2015 |
Sim JC, Scerri T, Fanjul-Fernández M, Riseley JR, Gillies G, Pope K, van Roozendaal H, Heng JI, Mandelstam SA, McGillivray G, MacGregor D, Kannan L, Maixner W, Harvey AS, Amor DJ, ... ... Crino PB, et al. Familial cortical dysplasia caused by mutation in the mTOR regulator NPRL3. Annals of Neurology. PMID 26285051 DOI: 10.1002/Ana.24502 |
0.215 |
|
| 2007 |
Puffenberger EG, Strauss KA, Ramsey KE, Craig DW, Stephan DA, Robinson DL, Hendrickson CL, Gottlieb S, Ramsay DA, Siu VM, Heuer GG, Crino PB, Morton DH. Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5. Brain : a Journal of Neurology. 130: 1929-41. PMID 17522105 DOI: 10.1093/brain/awm100 |
0.212 |
|
| 2005 |
Jansen LA, Uhlmann EJ, Crino PB, Gutmann DH, Wong M. Epileptogenesis and reduced inward rectifier potassium current in tuberous sclerosis complex-1-deficient astrocytes. Epilepsia. 46: 1871-80. PMID 16393152 DOI: 10.1111/J.1528-1167.2005.00289.X |
0.208 |
|
| 2005 |
Yu J, Baybis M, Lee A, McKhann G, Chugani D, Kupsky WJ, Aronica E, Crino PB. Targeted gene expression analysis in hemimegalencephaly: activation of beta-catenin signaling. Brain Pathology (Zurich, Switzerland). 15: 179-86. PMID 16196383 DOI: 10.1111/J.1750-3639.2005.Tb00518.X |
0.208 |
|
| 2017 |
Griffin NG, Cronin KD, Walley NM, Hulette CM, Grant GA, Mikati MA, LaBreche HG, Rehder CW, Allen AS, Crino PB, Heinzen EL. Somatic uniparental disomy of Chromosome 16p in hemimegalencephaly. Cold Spring Harbor Molecular Case Studies. 3. PMID 28864461 DOI: 10.1101/mcs.a001735 |
0.206 |
|
| 2014 |
Aronica E, Crino PB. Epilepsy related to developmental tumors and malformations of cortical development. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 11: 251-68. PMID 24481729 DOI: 10.1007/s13311-013-0251-0 |
0.205 |
|
| 2005 |
Crino PB. Molecular pathogenesis of focal cortical dysplasia and hemimegalencephaly. Journal of Child Neurology. 20: 330-6. PMID 15921235 |
0.203 |
|
| 2004 |
Baybis M, Lynch D, Lee A, Patel A, McKhann G, Chugani D, J Kupsky W, Aronica E, Crino PB. Altered expression of neurotransmitter-receptor subunit and uptake site mRNAs in hemimegalencephaly. Epilepsia. 45: 1517-24. PMID 15571509 DOI: 10.1111/J.0013-9580.2004.16204.X |
0.201 |
|
| 1996 |
Crino PB, Eberwine J. Molecular characterization of the dendritic growth cone: regulated mRNA transport and local protein synthesis. Neuron. 17: 1173-87. PMID 8982164 DOI: 10.1016/S0896-6273(00)80248-2 |
0.198 |
|
| 2017 |
Mills JD, Iyer AM, van Scheppingen J, Bongaarts A, Anink JJ, Janssen B, Zimmer TS, Spliet WG, van Rijen PC, Jansen FE, Feucht M, Hainfellner JA, Krsek P, Zamecnik J, Kotulska K, ... ... Crino PB, et al. Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment. Scientific Reports. 7: 8089. PMID 28808237 DOI: 10.1038/s41598-017-06145-8 |
0.197 |
|
| 2008 |
Boer K, Jansen F, Nellist M, Redeker S, van den Ouweland AM, Spliet WG, van Nieuwenhuizen O, Troost D, Crino PB, Aronica E. Inflammatory processes in cortical tubers and subependymal giant cell tumors of tuberous sclerosis complex. Epilepsy Research. 78: 7-21. PMID 18023148 DOI: 10.1016/J.Eplepsyres.2007.10.002 |
0.196 |
|
| 2021 |
Campion TJ, Sheikh IS, Smit RD, Iffland PH, Chen J, Junker IP, Krynska B, Crino PB, Smith GM. Viral expression of constitutively active AKT3 induces CST axonal sprouting and regeneration, but also promotes seizures. Experimental Neurology. 113961. PMID 34953897 DOI: 10.1016/j.expneurol.2021.113961 |
0.195 |
|
| 2015 |
Sosunov AA, McGovern RA, Mikell CB, Wu X, Coughlin DG, Crino PB, Weiner HL, Ghatan S, Goldman JE, McKhann GM. Epileptogenic but MRI-normal perituberal tissue in Tuberous Sclerosis Complex contains tuber-specific abnormalities. Acta Neuropathologica Communications. 3: 17. PMID 25853525 DOI: 10.1186/S40478-015-0191-5 |
0.188 |
|
| 1992 |
Vogt BA, Crino PB, Vogt LJ. Reorganization of cingulate cortex in Alzheimer's disease: neuron loss, neuritic plaques, and muscarinic receptor binding. Cerebral Cortex (New York, N.Y. : 1991). 2: 526-35. PMID 1477528 DOI: 10.1093/cercor/2.6.526 |
0.186 |
|
| 2010 |
Wong M, Crino PB. MTOR and epileptogenesis in developmental brain malformations Epilepsia. 51: 72. DOI: 10.1111/j.1528-1167.2010.02858.x |
0.184 |
|
| 2003 |
Wong M, Ess KC, Uhlmann EJ, Jansen LA, Li W, Crino PB, Mennerick S, Yamada KA, Gutmann DH. Impaired glial glutamate transport in a mouse tuberous sclerosis epilepsy model. Annals of Neurology. 54: 251-6. PMID 12891680 DOI: 10.1002/Ana.10648 |
0.18 |
|
| 2009 |
Bishay V, Stavropoulos SW, Soulen MC, Wein AJ, Maldowicz SB, Trerotola SO, Crino P. Abstract No. 172: Giant Renal Angiomyolipoma Embolization: Technique and Results Journal of Vascular and Interventional Radiology. 20. DOI: 10.1016/J.Jvir.2008.12.160 |
0.176 |
|
| 2011 |
Vincent A, Crino PB. Systemic and neurologic autoimmune disorders associated with seizures or epilepsy. Epilepsia. 52: 12-7. PMID 21542840 DOI: 10.1111/j.1528-1167.2011.03030.x |
0.169 |
|
| 2015 |
Leventer RJ, Scerri T, Marsh AP, Pope K, Gillies G, Maixner W, MacGregor D, Harvey AS, Delatycki MB, Amor DJ, Crino P, Bahlo M, Lockhart PJ. Hemispheric cortical dysplasia secondary to a mosaic somatic mutation in MTOR. Neurology. 84: 2029-32. PMID 25878179 DOI: 10.1212/WNL.0000000000001594 |
0.169 |
|
| 1996 |
Crino PB, Galetta SL, Sater RA, Raps EC, Witte A, Roby D, Rosenquist AC. Clinicopathologic study of paraneoplastic brainstem encephalitis and ophthalmoparesis. Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society. 16: 44-8. PMID 8963420 DOI: 10.1097/00041327-199603000-00011 |
0.164 |
|
| 2010 |
Crino PB, Aronica E, Baltuch G, Nathanson KL. Biallelic TSC gene inactivation in tuberous sclerosis complex. Neurology. 74: 1716-23. PMID 20498439 DOI: 10.1212/Wnl.0B013E3181E04325 |
0.164 |
|
| 2007 |
Crino PB. Gene expression, genetics, and genomics in epilepsy: some answers, more questions. Epilepsia. 48: 42-50. PMID 17571352 DOI: 10.1111/j.1528-1167.2007.01066.x |
0.162 |
|
| 2023 |
Farach LS, Northrup H, Nellist M, van Unen L, Hillman P, Klonowska K, Ekong R, Crino PB, Sing Au K. Mild TSC Phenotype and Non-Penetrance Associated with a Frameshift Variant in TSC2 Prompts Caution in Evaluating Pathogenicity of Frameshift Variants. Gene. 147566. PMID 37311496 DOI: 10.1016/j.gene.2023.147566 |
0.162 |
|
| 2000 |
Crino PB, Chou K. Epilepsy and Cortical Dysplasias. Current Treatment Options in Neurology. 2: 543-552. PMID 11096778 |
0.161 |
|
| 2009 |
Franz DN, de Vries PJ, Crino PB. Giant cell astrocytomas in tuberous sclerosis complex. Archives of Disease in Childhood. 94: 75-6. PMID 19103791 |
0.16 |
|
| 2022 |
Barba C, Blumcke I, Winawer MR, Hartlieb T, Kang HC, Grisotto L, Chipaux M, Bien CG, Heřmanovská B, Porter BE, Lidov HGW, Cetica V, Woermann FG, Lopez-Rivera JA, Canoll PD, ... ... Crino PB, et al. Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the Gene. Neurology. PMID 36307217 DOI: 10.1212/WNL.0000000000201471 |
0.158 |
|
| 2010 |
Crino PB, Mehta R, Vinters HV. Pathogenesis of TSC in the Brain Tuberous Sclerosis Complex: Genes, Clinical Features and Therapeutics. 159-185. DOI: 10.1002/9783527630073.ch9 |
0.154 |
|
| 2019 |
Crino PB. Mechanistic target of rapamycin (mTOR) signaling in status epilepticus. Epilepsy & Behavior : E&B. 106550. PMID 31732331 DOI: 10.1016/j.yebeh.2019.106550 |
0.151 |
|
| 2017 |
Ortiz-González XR, Tintos-Hernández JA, Keller K, Li X, Foley AR, Bharucha-Goebel DX, Kessler SK, Yum SW, Crino PB, He M, Wallace DC, Bönnemann CG. Homozygous Boricua TBCK Mutation Causes Neurodegeneration and Aberrant Autophagy. Annals of Neurology. PMID 29283439 DOI: 10.1002/ana.25130 |
0.148 |
|
| 2014 |
Leventer RJ, Jansen FE, Mandelstam SA, Ho A, Mohamed I, Sarnat HB, Kato M, Fukasawa T, Saitsu H, Matsumoto N, Itoh M, Kalnins RM, Chow CW, Harvey AS, Jackson GD, ... Crino PB, et al. Is focal cortical dysplasia sporadic? Family evidence for genetic susceptibility. Epilepsia. 55: e22-6. PMID 24502525 DOI: 10.1111/epi.12533 |
0.146 |
|
| 2008 |
Crino PB. Rapamycin and tuberous sclerosis complex: from Easter Island to epilepsy. Annals of Neurology. 63: 415-7. PMID 18360828 DOI: 10.1002/ana.21369 |
0.146 |
|
| 2005 |
Detre JA, Crino PB. A multilayered approach to studying cortical malformations: EEG-fMRI. Neurology. 64: 1108-10. PMID 15824328 DOI: 10.1212/01.WNL.0000161078.53641.12 |
0.144 |
|
| 2004 |
Najm I, Ying Z, Babb T, Crino PB, Macdonald R, Mathern GW, Spreafico R. Mechanisms of epileptogenicity in cortical dysplasias. Neurology. 62: S9-13. PMID 15037672 DOI: 10.1212/01.Wnl.0000114506.49267.Bb |
0.143 |
|
| 2015 |
Crino PB. The enlarging spectrum of focal cortical dysplasias. Brain : a Journal of Neurology. 138: 1446-8. PMID 26013804 DOI: 10.1093/brain/awv098 |
0.142 |
|
| 2023 |
Robertson CD, Davis P, Richardson RR, Iffland PH, Vieira DCO, Steyert M, McKeon PN, Romanowski AJ, Crutcher G, Jašarević E, Wolff SBE, Mathur BN, Crino PB, Bale TL, Dick IE, et al. Modeling an ultra-rare epilepsy variant in wildtype mice with in utero prime editing. Biorxiv : the Preprint Server For Biology. PMID 38106154 DOI: 10.1101/2023.12.06.570164 |
0.139 |
|
| 1995 |
Crino PB, Sater RA, Sperling M, Katsetos CD. Renal cell carcinomatous meningitis: pathologic and immunohistochemical features. Neurology. 45: 189-91. PMID 7529900 DOI: 10.1212/WNL.45.1.189 |
0.138 |
|
| 2011 |
Aronica E, Crino PB. Inflammation in epilepsy: clinical observations. Epilepsia. 52: 26-32. PMID 21542843 DOI: 10.1111/j.1528-1167.2011.03033.x |
0.134 |
|
| 2021 |
Korotkov A, Sim NS, Luinenburg MJ, Anink JJ, van Scheppingen J, Zimmer TS, Bongaarts A, Broekaart DWM, Mijnsbergen C, Jansen FE, Van Hecke W, Spliet WGM, van Rijen PC, Feucht M, Hainfellner JA, ... ... Crino PB, et al. MicroRNA-34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesis. Neuropathology and Applied Neurobiology. PMID 33942341 DOI: 10.1111/nan.12717 |
0.131 |
|
| 2022 |
Park SM, Roache CE, Iffland PH, Moldenhauer HJ, Matychak KK, Plante AE, Lieberman AG, Crino PB, Meredith A. BK channel properties correlate with neurobehavioral severity in three -linked channelopathy mouse models. Elife. 11. PMID 35819138 DOI: 10.7554/eLife.77953 |
0.13 |
|
| 2021 |
Gledhill J, Brand E, Pollard J, Clair RS, Wallach T, Crino P. Association of Epileptic and Non-epileptic Seizures and Changes in Circulating Plasma Proteins Linked to Neuroinflammation. Neurology. PMID 33495377 DOI: 10.1212/WNL.0000000000011552 |
0.127 |
|
| 2007 |
Sisodiya S, Cross JH, Blümcke I, Chadwick D, Craig J, Crino PB, Debenham P, Delanty N, Elmslie F, Gardiner M, Golden J, Goldstein D, Greenberg DA, Guerrini R, Hanna M, et al. Genetics of epilepsy: epilepsy research foundation workshop report. Epileptic Disorders : International Epilepsy Journal With Videotape. 9: 194-236. PMID 17525034 DOI: 10.1684/Epd.2007.0107 |
0.125 |
|
| 2001 |
Crino PB. Reelin' in Genes for Cortical Dysplasia. Epilepsy Currents / American Epilepsy Society. 1: 61-65. PMID 15309192 DOI: 10.1046/j.1535-7597.2001.00014.x |
0.121 |
|
| 2006 |
Crino PB, Becker AJ. Gene profiling in temporal lobe epilepsy tissue and dysplastic lesions. Epilepsia. 47: 1608-16. PMID 17054681 DOI: 10.1111/j.1528-1167.2006.00712.x |
0.118 |
|
| 2012 |
Pollard JR, Eidelman O, Mueller GP, Dalgard CL, Crino PB, Anderson CT, Brand EJ, Burakgazi E, Ivaturi SK, Pollard HB. The TARC/sICAM5 Ratio in Patient Plasma is a Candidate Biomarker for Drug Resistant Epilepsy. Frontiers in Neurology. 3: 181. PMID 23293627 DOI: 10.3389/Fneur.2012.00181 |
0.112 |
|
| 2001 |
Telfeian AE, Philips MF, Crino PB, Judy KD. Postoperative epilepsy in patients undergoing craniotomy for glioblastoma multiforme. Journal of Experimental & Clinical Cancer Research : Cr. 20: 5-10. PMID 11370829 |
0.111 |
|
| 1992 |
Vogt BA, Crino PB, Jensen EL. Multiple heteroreceptors on limbic thalamic axons: M2 acetylcholine, serotonin1B, beta 2-adrenoceptors, mu-opioid, and neurotensin. Synapse (New York, N.Y.). 10: 44-53. PMID 1311129 DOI: 10.1002/syn.890100107 |
0.111 |
|
| 1990 |
Vogt BA, Plager MD, Crino PB, Bird ED. Laminar distributions of muscarinic acetylcholine, serotonin, GABA and opioid receptors in human posterior cingulate cortex. Neuroscience. 36: 165-74. PMID 1977100 DOI: 10.1016/0306-4522(90)90359-C |
0.111 |
|
| 2000 |
Crino PB. Tuberous sclerosis complex: Developmental perspectives in psychiatry Annals of Neurology. 48: 133-133. DOI: 10.1002/1531-8249(200007)48:1<133::AID-ANA31>3.0.CO;2-M |
0.11 |
|
| 2003 |
Crino PB. Knockout of a Tuberous Sclerosis Gene Highlights Role of Glia in Epileptogenesis. Epilepsy Currents / American Epilepsy Society. 3: 139-141. PMID 15309059 DOI: 10.1046/j.1535-7597.2003.03411.x |
0.104 |
|
| 2022 |
Moss A, Moss E, Moss R, Moss L, Chiang S, Crino P. A Patient Perspective on Seizure Detection and Forecasting. Frontiers in Neurology. 13: 779551. PMID 35222243 DOI: 10.3389/fneur.2022.779551 |
0.104 |
|
| 2002 |
Crino PB. Gene expression analysis as a strategy to understand the molecular pathogenesis of infantile spasms. International Review of Neurobiology. 49: 367-89. PMID 12040902 |
0.104 |
|
| 2010 |
Crino PB. The pathophysiology of tuberous sclerosis complex. Epilepsia. 51: 27-9. PMID 20331708 DOI: 10.1111/j.1528-1167.2009.02438.x |
0.103 |
|
| 2015 |
Crino PB. Reply: HPV in focal cortical dysplasia. Annals of Neurology. 77: 353; discussion 353. PMID 25523244 DOI: 10.1002/ana.24333 |
0.103 |
|
| 2007 |
Crino PB. Is focal cortical dysplasia genetic in origin? Epileptic Disorders. 9: 225-227. |
0.099 |
|
| 2022 |
Mills JD, Iyer AM, van Scheppingen J, Bongaarts A, Anink JJ, Janssen B, Zimmer TS, Spliet WG, van Rijen PC, Jansen FE, Feucht M, Hainfellner JA, Krsek P, Zamecnik J, Kotulska K, ... ... Crino PB, et al. Author Correction: Coding and small non-coding transcriptional landscape of tuberous sclerosis complex cortical tubers: implications for pathophysiology and treatment. Scientific Reports. 12: 15457. PMID 36104396 DOI: 10.1038/s41598-022-20109-7 |
0.099 |
|
| 2008 |
Nass R, Crino PB. Tuberous sclerosis complex: a tale of two genes. Neurology. 70: 904-5. PMID 18347312 DOI: 10.1212/01.wnl.0000305964.52343.8f |
0.094 |
|
| 2014 |
Crino PB. Viral infection and focal cortical dysplasia. Reply. Annals of Neurology. 75: 616-7. PMID 24122905 DOI: 10.1002/ana.24032 |
0.092 |
|
| 2006 |
Crino PB, Nathanson KL, Henske EP. The tuberous sclerosis complex. The New England Journal of Medicine. 355: 1345-56. PMID 17005952 DOI: 10.1056/Nejmra055323 |
0.091 |
|
| 2008 |
Crino PB. Do we have a cure for tuberous sclerosis complex? Epilepsy Currents / American Epilepsy Society. 8: 159-62. PMID 19127311 DOI: 10.1111/j.1535-7511.2008.00279.x |
0.089 |
|
| 1995 |
Crino PB, Martin JA, Hill WD, Greenberg B, Lee VM, Trojanowski JQ. Beta-Amyloid peptide and amyloid precursor proteins in olfactory mucosa of patients with Alzheimer's disease, Parkinson's disease, and Down syndrome. The Annals of Otology, Rhinology, and Laryngology. 104: 655-61. PMID 7639477 DOI: 10.1177/000348949510400812 |
0.088 |
|
| 2000 |
French J, Crino P, Porter RJ. Antiepileptic drugs in the treatment of neocortical epilepsies. Advances in Neurology. 84: 525-31. PMID 11091894 |
0.084 |
|
| 2018 |
Crino PB. Polymicrogyria and GRIN1 mutations: altered connections, altered excitability. Brain : a Journal of Neurology. 141: 622-623. PMID 30753417 DOI: 10.1093/brain/awy047 |
0.079 |
|
| 2023 |
Elziny S, Crino PB. Vascularization in mTOR Mouse Mutants: An Effort Not in Vein. Eneuro. 10. PMID 37479502 DOI: 10.1523/ENEURO.0122-23.2023 |
0.074 |
|
| 2010 |
Crino PB. Single Cell Genomic DNA Analysis Encyclopedia of Neuroscience. 831-835. DOI: 10.1016/B978-008045046-9.00880-9 |
0.066 |
|
| 1995 |
Crino PB, Zimmerman R, Laskowitz D, Raps E, Rostami A. Re: MRI in Guillain-barré syndrome Neurology. 45: 1024. |
0.064 |
|
| 2005 |
Kothary N, Soulen MC, Clark TW, Wein AJ, Shlansky-Goldberg RD, Crino PB, Stavropoulos SW. Renal angiomyolipoma: long-term results after arterial embolization. Journal of Vascular and Interventional Radiology : Jvir. 16: 45-50. PMID 15640409 DOI: 10.1097/01.RVI.0000143769.79774.70 |
0.061 |
|
| 1988 |
Mirabelli F, Salis A, Vairetti MP, Crino P, Finardi G, Richelmi P, Bellomo G. Surface blebbing and cytoskeletal abnormalities caused by sulfhydryl reagents in isolated hepatocytes. I. Alkylating reagents Medecine Biologie Environment. 16: 187-197. |
0.057 |
|
| 2010 |
Bishay VL, Crino PB, Wein AJ, Malkowicz SB, Trerotola SO, Soulen MC, Stavropoulos SW. Embolization of giant renal angiomyolipomas: technique and results. Journal of Vascular and Interventional Radiology : Jvir. 21: 67-72. PMID 20123192 DOI: 10.1016/j.jvir.2009.09.020 |
0.052 |
|
| 2004 |
Crino PB. New Candidate Genes for Infantile Spasms and Mental Retardation. Epilepsy Currents / American Epilepsy Society. 4: 11-12. PMID 15346135 DOI: 10.1111/j.1535-7597.2004.04104.x |
0.051 |
|
| 2000 |
Stamigna C, Crino P, Saccardo F. Wild relatives of chickpea: Multiple disease resistance and problems to introgression in the cultigen Journal of Genetics and Breeding. 54: 213-219. |
0.047 |
|
| 1994 |
Crino PB, Zimmerman R, Laskowitz D, Raps EC, Rostami AM. Magnetic resonance imaging of the cauda equina in Guillain-Barré syndrome. Neurology. 44: 1334-6. PMID 8035942 DOI: 10.1212/WNL.44.7.1334 |
0.045 |
|
| 1993 |
Crino PB, Grossman RI, Rostami A. Magnetic resonance imaging of the cauda equina in chronic inflammatory demyelinating polyneuropathy. Annals of Neurology. 33: 311-3. PMID 8388677 DOI: 10.1002/ana.410330314 |
0.031 |
|
| 2002 |
Crino PB. Bourneville and Taylor: a developing story? Annals of Neurology. 52: 6-9. PMID 12112041 DOI: 10.1002/ana.10306 |
0.023 |
|
| 2004 |
Stamigna C, Crino P, Chatelet P, Saccardo F. Induction of Embryogenesis in isolated microspores of artichoke (cynara scolymus L.) Acta Horticulturae. 660: 139-143. |
0.017 |
|
| 2020 |
Crino PB. "mTORopathies: A Road Well-Traveled". Epilepsy Currents. 1535759720959320. PMID 33052752 DOI: 10.1177/1535759720959320 |
0.01 |
|
| 2007 |
Crino PB, Nathanson KL, Henske EP. The authors reply [17] New England Journal of Medicine. 356: 93-94. |
0.01 |
|
| 2005 |
Crino PB. Give PEAF a chance. Epilepsy Currents / American Epilepsy Society. 5: 35-6. PMID 16059454 DOI: 10.1111/j.1535-7597.2005.05110.x |
0.01 |
|
| 1995 |
Crino PB, Zimmerman R, Laskowitz D, Raps E, Rostami A. Reply from the Authors Neurology. 45: 1024-1024. DOI: 10.1212/wnl.45.5.1024-c |
0.01 |
|
| 1994 |
Crino P, Lai A, Di Bonito R, Veronese P, Saccardo F. Genetic variability in tomato plants regenerated from irradiated cotyledons Journal of Genetics and Breeding. 48: 281-290. |
0.01 |
|
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