| Year |
Citation |
Score |
| 2023 |
Biancardi V, Yang X, Ding X, Passi D, Funk GD, Pagliardini S. Cholinergic projections to the preBötzinger complex. The Journal of Comparative Neurology. PMID 37211631 DOI: 10.1002/cne.25497 |
0.653 |
|
| 2020 |
Biancardi V, Saini J, Pageni A, Hema Prashaad M, Funk GD, Pagliardini S. Mapping of the excitatory, inhibitory, and modulatory afferent projections to the anatomically defined active expiratory oscillator in adult male rats. The Journal of Comparative Neurology. PMID 32656849 DOI: 10.1002/Cne.24984 |
0.68 |
|
| 2020 |
Biancardi V, Saini J, Pageni A, Mani HP, Funk GD, Pagliardini S. Retrograde projections to the expiratory oscillator, the parafacial respiratory group, in adult male rats The Faseb Journal. 34: 1-1. DOI: 10.1096/Fasebj.2020.34.S1.07231 |
0.597 |
|
| 2019 |
Pisanski A, Ding X, Koch NA, Pagliardini S. Chemogenetic modulation of the parafacial respiratory group influences the recruitment of abdominal activity during REM sleep. Sleep. PMID 31747042 DOI: 10.1093/sleep/zsz283 |
0.369 |
|
| 2019 |
Reklow RJ, Alvares TS, Zhang Y, Miranda Tapia AP, Biancardi V, Katzell AK, Frangos SM, Hansen MA, Toohey AW, Cass CE, Young JD, Pagliardini S, Boison D, Funk GD. The Purinome and the preBötzinger Complex - A Ménage of Unexplored Mechanisms That May Modulate/Shape the Hypoxic Ventilatory Response. Frontiers in Cellular Neuroscience. 13: 365. PMID 31496935 DOI: 10.3389/Fncel.2019.00365 |
0.613 |
|
| 2018 |
Pisanski A, Pagliardini S. The parafacial respiratory group and the control of active expiration. Respiratory Physiology & Neurobiology. PMID 29933053 DOI: 10.1016/j.resp.2018.06.010 |
0.413 |
|
| 2017 |
Saini JK, Pagliardini S. Breathing During Sleep in the Postnatal Period of Rats: The Contribution of Active Expiration. Sleep. 40. PMID 29294135 DOI: 10.1093/sleep/zsx172 |
0.333 |
|
| 2017 |
da Silva GSF, Sabino JPJ, Rajani V, Alvares TS, Pagliardini S, Branco LGS, Funk GD. Excitatory Modulation of the preBötzinger Complex Inspiratory Rhythm Generating Network by Endogenous Hydrogen Sulfide. Frontiers in Physiology. 8: 452. PMID 28713283 DOI: 10.3389/Fphys.2017.00452 |
0.619 |
|
| 2017 |
Rajani V, Zhang Y, Jalubula V, Rancic V, SheikhBahaei S, Zwicker JD, Pagliardini S, Dickson CT, Ballanyi K, Kasparov S, Gourine AV, Funk GD. Release of ATP by preBötzinger complex astrocytes contributes to the hypoxic ventilatory response via a Ca(2+) -dependent P2Y1 receptor mechanism. The Journal of Physiology. PMID 28678385 DOI: 10.1113/Jp274727 |
0.635 |
|
| 2016 |
Boutin RC, Alsahafi Z, Pagliardini S. Cholinergic modulation of the paraFacial respiratory group. The Journal of Physiology. PMID 27808424 DOI: 10.1113/JP273012 |
0.452 |
|
| 2016 |
Li P, Janczewski WA, Yackle K, Kam K, Pagliardini S, Krasnow MA, Feldman JL. The peptidergic control circuit for sighing. Nature. PMID 26855425 DOI: 10.1038/nature16964 |
0.721 |
|
| 2015 |
Andrews CG, Pagliardini S. Expiratory activation of abdominal muscle is associated with improved respiratory stability and an increase in minute ventilation in REM epochs of adult rats. Journal of Applied Physiology (Bethesda, Md. : 1985). 119: 968-74. PMID 26338455 DOI: 10.1152/japplphysiol.00420.2015 |
0.344 |
|
| 2015 |
Alsahafi Z, Dickson CT, Pagliardini S. Optogenetic excitation of preBötzinger Complex neurons potently drives inspiratory activity in vivo. The Journal of Physiology. PMID 26010654 DOI: 10.1113/JP270471 |
0.387 |
|
| 2015 |
ElMallah MK, Pagliardini S, Turner SM, Cerreta AJ, Falk DJ, Byrne BJ, Greer JJ, Fuller DD. Ampakines Stimulate Respiratory Motor Output and Ventilation in a Murine Model of Pompe Disease. American Journal of Respiratory Cell and Molecular Biology. PMID 25569118 DOI: 10.1165/Rcmb.2014-0374Oc |
0.7 |
|
| 2014 |
Viczko J, Sharma AV, Pagliardini S, Wolansky T, Dickson CT. Lack of respiratory coupling with neocortical and hippocampal slow oscillations. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 3937-46. PMID 24623771 DOI: 10.1523/JNEUROSCI.3581-13.2014 |
0.341 |
|
| 2013 |
Pagliardini S, Gosgnach S, Dickson CT. Spontaneous sleep-like brain state alternations and breathing characteristics in urethane anesthetized mice. Plos One. 8: e70411. PMID 23936201 DOI: 10.1371/Journal.Pone.0070411 |
0.371 |
|
| 2013 |
Pagliardini S, Funk GD, Dickson CT. Breathing and brain state: urethane anesthesia as a model for natural sleep. Respiratory Physiology & Neurobiology. 188: 324-32. PMID 23751523 DOI: 10.1016/J.Resp.2013.05.035 |
0.59 |
|
| 2012 |
Pagliardini S, Greer JJ, Funk GD, Dickson CT. State-dependent modulation of breathing in urethane-anesthetized rats. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 11259-70. PMID 22895710 DOI: 10.1523/Jneurosci.0948-12.2012 |
0.723 |
|
| 2011 |
Pagliardini S, Janczewski WA, Tan W, Dickson CT, Deisseroth K, Feldman JL. Active expiration induced by excitation of ventral medulla in adult anesthetized rats. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 2895-905. PMID 21414911 DOI: 10.1523/JNEUROSCI.5338-10.2011 |
0.662 |
|
| 2011 |
Zwicker J, Pagliardini S, Kasparov S, Gourine A, Funk G. Purinergic modulation of preBötzinger Complex inspiratory rhythm generating networks Autonomic Neuroscience. 163: 77. DOI: 10.1016/J.Autneu.2011.05.111 |
0.582 |
|
| 2010 |
Tan W, Pagliardini S, Yang P, Janczewski WA, Feldman JL. Projections of preBötzinger complex neurons in adult rats. The Journal of Comparative Neurology. 518: 1862-78. PMID 20235095 DOI: 10.1002/cne.22308 |
0.693 |
|
| 2009 |
Huxtable AG, Zwicker JD, Poon BY, Pagliardini S, Vrouwe SQ, Greer JJ, Funk GD. Tripartite purinergic modulation of central respiratory networks during perinatal development: the influence of ATP, ectonucleotidases, and ATP metabolites. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 14713-25. PMID 19940166 DOI: 10.1523/Jneurosci.2660-09.2009 |
0.735 |
|
| 2008 |
Pagliardini S, Ren J, Gray PA, Vandunk C, Gross M, Goulding M, Greer JJ. Central respiratory rhythmogenesis is abnormal in lbx1- deficient mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 11030-41. PMID 18945911 DOI: 10.1523/Jneurosci.1648-08.2008 |
0.76 |
|
| 2008 |
Buccafusca R, Venditti CP, Kenyon LC, Johanson RA, Van Bockstaele E, Ren J, Pagliardini S, Minarcik J, Golden JA, Coady MJ, Greer JJ, Berry GT. Characterization of the null murine sodium/myo-inositol cotransporter 1 (Smit1 or Slc5a3) phenotype: myo-inositol rescue is independent of expression of its cognate mitochondrial ribosomal protein subunit 6 (Mrps6) gene and of phosphatidylinositol levels in neonatal brain. Molecular Genetics and Metabolism. 95: 81-95. PMID 18675571 DOI: 10.1016/J.Ymgme.2008.05.008 |
0.668 |
|
| 2008 |
Pagliardini S, Rent J, Wevrick R, Greer JJ. Neurodevelopmental abnormalities in the brainstem of prenatal mice lacking the Prader-Willi syndrome gene Necdin. Advances in Experimental Medicine and Biology. 605: 139-43. PMID 18085261 DOI: 10.1007/978-0-387-73693-8_24 |
0.657 |
|
| 2008 |
Hurd PL, Bailey AA, Gongal PA, Yan RH, Greer JJ, Pagliardini S. Intrauterine position effects on anogenital distance and digit ratio in male and female mice. Archives of Sexual Behavior. 37: 9-18. PMID 18080736 DOI: 10.1007/S10508-007-9259-Z |
0.628 |
|
| 2007 |
Wolansky T, Pagliardini S, Greer JJ, Dickson CT. Immunohistochemical characterization of substance P receptor (NK(1)R)-expressing interneurons in the entorhinal cortex. The Journal of Comparative Neurology. 502: 427-41. PMID 17366610 DOI: 10.1002/cne.21338 |
0.678 |
|
| 2005 |
Pagliardini S, Ren J, Wevrick R, Greer JJ. Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin. The American Journal of Pathology. 167: 175-91. PMID 15972963 DOI: 10.1016/S0002-9440(10)62964-1 |
0.714 |
|
| 2005 |
Pagliardini S, Adachi T, Ren J, Funk GD, Greer JJ. Fluorescent tagging of rhythmically active respiratory neurons within the pre-Bötzinger complex of rat medullary slice preparations. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 2591-6. PMID 15758169 DOI: 10.1523/Jneurosci.4930-04.2005 |
0.768 |
|
| 2003 |
Pagliardini S, Ren J, Greer JJ. Ontogeny of the pre-Bötzinger complex in perinatal rats. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 9575-84. PMID 14573537 DOI: 10.1523/Jneurosci.23-29-09575.2003 |
0.725 |
|
| 2003 |
Gardoni F, Pagliardini S, Setola V, Bassanini S, Cattabeni F, Battaglia G, Di Luca M. The NMDA receptor complex is altered in an animal model of human cerebral heterotopia. Journal of Neuropathology and Experimental Neurology. 62: 662-75. PMID 12834111 DOI: 10.1093/Jnen/62.6.662 |
0.367 |
|
| 2003 |
Battaglia G, Pagliardini S, Saglietti L, Cattabeni F, Di Luca M, Bassanini S, Setola V. Neurogenesis in cerebral heterotopia induced in rats by prenatal methylazoxymethanol treatment. Cerebral Cortex (New York, N.Y. : 1991). 13: 736-48. PMID 12816889 DOI: 10.1093/cercor/13.7.736 |
0.334 |
|
| 2003 |
Ren J, Lee S, Pagliardini S, Gérard M, Stewart CL, Greer JJ, Wevrick R. Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 1569-73. PMID 12629158 DOI: 10.1523/Jneurosci.23-05-01569.2003 |
0.734 |
|
| 2001 |
Hwang SJ, Pagliardini S, Rustioni A, Valtschanoff JG. Presynaptic kainate receptors in primary afferents to the superficial laminae of the rat spinal cord. The Journal of Comparative Neurology. 436: 275-89. PMID 11438930 DOI: 10.1002/cne.1067 |
0.302 |
|
| 2001 |
Hwang SJ, Pagliardini S, Boukhelifa M, Parast MM, Otey CA, Rustioni A, Valtschanoff JG. Palladin is expressed preferentially in excitatory terminals in the rat central nervous system. The Journal of Comparative Neurology. 436: 211-24. PMID 11438925 DOI: 10.1002/Cne.1062 |
0.331 |
|
| 2000 |
Pagliardini S, Giavazzi A, Setola V, Lizier C, Di Luca M, DeBiasi S, Battaglia G. Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cord. Human Molecular Genetics. 9: 47-56. PMID 10587577 DOI: 10.1093/HMG/9.1.47 |
0.353 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2022 |
Cardani S, Janes TA, Saini JK, Di Lascio S, Benfante R, Fornasari D, Pagliardini S. Etonogestrel Administration Reduces the Expression of PHOX2B and Its Target Genes in the Solitary Tract Nucleus. International Journal of Molecular Sciences. 23. PMID 35563209 DOI: 10.3390/ijms23094816 |
0.295 |
|
| 2018 |
Hauer BE, Negash B, Chan K, Vuong W, Colbourne F, Pagliardini S, Dickson CT. Hyperoxia Enhances Slow-wave Forebrain States in Urethane Anesthetized and Naturally Sleeping Rats. Journal of Neurophysiology. PMID 29947598 DOI: 10.1152/jn.00373.2018 |
0.293 |
|
| 2001 |
Di Luca M, Gardoni F, Finardi A, Pagliardini S, Cattabeni F, Battaglia G, Missale C. NMDA receptor subunits are phosphorylated by activation of neurotrophin receptors in PSD of rat spinal cord. Neuroreport. 12: 1301-5. PMID 11338211 DOI: 10.1097/00001756-200105080-00049 |
0.289 |
|
| 2002 |
Battaglia G, Pagliardini S, Ferrario A, Gardoni F, Tassi L, Setola V, Garbelli R, LoRusso G, Spreafico R, Di Luca M, Avanzini G. AlphaCaMKII and NMDA-receptor subunit expression in epileptogenic cortex from human periventricular nodular heterotopia. Epilepsia. 43: 209-16. PMID 12121323 DOI: 10.1046/j.1528-1157.43.s.5.38.x |
0.286 |
|
| 2003 |
Battaglia G, Bassanini S, Granata T, Setola V, Giavazzi A, Pagliardini S. The genesis of epileptogenic cerebral heterotopia: clues from experimental models. Epileptic Disorders : International Epilepsy Journal With Videotape. 5: S51-8. PMID 14617421 |
0.263 |
|
| 2024 |
Janes TA, Cardani S, Saini JK, Pagliardini S. Etonogestrel promotes respiratory recovery in an in vivo rat model of central chemoreflex impairment. Acta Physiologica (Oxford, England). e14093. PMID 38258900 DOI: 10.1111/apha.14093 |
0.251 |
|
| 2019 |
Agarwal J, Saad E, Fontaine G, Pagliardini S, Dafoe W, Killian K, Gibney RTN, Huston J, Vethanayagam D. Routine use of post-bronchodilator testing in pulmonary function testing labs. Clinical and Investigative Medicine. Medecine Clinique Et Experimentale. 41: E204-E210. PMID 30737980 DOI: 10.25011/cim.v41i4.32224 |
0.236 |
|
| 2022 |
Hauer BE, Pagliardini S, Dickson CT. Tonic excitation of nucleus reuniens decreases prefrontal-hippocampal coordination during slow-wave states. Hippocampus. PMID 35522233 DOI: 10.1002/hipo.23420 |
0.227 |
|
| 2019 |
Hauer BE, Pagliardini S, Dickson CT. The Reuniens Nucleus of the Thalamus has an Essential Role in Coordinating Slow Wave Activity between Neocortex and Hippocampus. Eneuro. PMID 31548369 DOI: 10.1523/ENEURO.0365-19.2019 |
0.226 |
|
| 2021 |
Baddam P, Biancardi V, Roth DM, Eaton F, Thereza-Bussolaro C, Mandal R, Wishart DS, Barr A, MacLean J, Flores-Mir C, Pagliardini S, Graf D. Neural crest-specific deletion of leads to midfacial hypoplasia, nasal airway obstruction, and disordered breathing modelling Obstructive Sleep Apnea. Disease Models & Mechanisms. PMID 33431521 DOI: 10.1242/dmm.047738 |
0.213 |
|
| 2022 |
Hauer BE, Pagliardini S, Dickson CT. Prefrontal-Hippocampal Pathways Through the Nucleus Reuniens Are Functionally Biased by Brain State. Frontiers in Neuroanatomy. 15: 804872. PMID 35173588 DOI: 10.3389/fnana.2021.804872 |
0.211 |
|
| 2021 |
Saini JK, Janes TA, MacLean JE, Pagliardini S. Expiratory activity during sleep in children. Journal of Sleep Research. e13539. PMID 34921704 DOI: 10.1111/jsr.13539 |
0.196 |
|
| 2022 |
Joseph V, Pagliardini S, Belaidi E. Editorial: Causes and Consequences of Sleep Apnea: Spotlights on the Roles of Sex and Sex Hormones. Frontiers in Physiology. 13: 857627. PMID 35283785 DOI: 10.3389/fphys.2022.857627 |
0.138 |
|
| 2010 |
Miranda C, Fumagalli T, Anania MC, Vizioli MG, Pagliardini S, Pierotti MA, Greco A. Role of STAT3 in in vitro transformation triggered by TRK oncogenes. Plos One. 5: e9446. PMID 20209132 DOI: 10.1371/journal.pone.0009446 |
0.122 |
|
| 1993 |
Greco A, Orlandi R, Mariani C, Miranda C, Borrello MG, Cattaneo A, Pagliardini S, Pierotti MA. Expression of TRK-T1 oncogene induces differentiation of PC12 cells. Cell Growth & Differentiation : the Molecular Biology Journal of the American Association For Cancer Research. 4: 539-46. PMID 8398895 |
0.115 |
|
| 2011 |
Anania MC, Sensi M, Radaelli E, Miranda C, Vizioli MG, Pagliardini S, Favini E, Cleris L, Supino R, Formelli F, Borrello MG, Pierotti MA, Greco A. TIMP3 regulates migration, invasion and in vivo tumorigenicity of thyroid tumor cells. Oncogene. 30: 3011-23. PMID 21339735 DOI: 10.1038/onc.2011.18 |
0.115 |
|
| 2002 |
Miranda C, Di Virgilio M, Selleri S, Zanotti G, Pagliardini S, Pierotti MA, Greco A. Novel pathogenic mechanisms of congenital insensitivity to pain with anhidrosis genetic disorder unveiled by functional analysis of neurotrophic tyrosine receptor kinase type 1/nerve growth factor receptor mutations. The Journal of Biological Chemistry. 277: 6455-62. PMID 11719521 DOI: 10.1074/jbc.M110016200 |
0.106 |
|
| 1995 |
Greco A, Mariani C, Miranda C, Lupas A, Pagliardini S, Pomati M, Pierotti MA. The DNA rearrangement that generates the TRK-T3 oncogene involves a novel gene on chromosome 3 whose product has a potential coiled-coil domain. Molecular and Cellular Biology. 15: 6118-27. PMID 7565764 |
0.099 |
|
| 2011 |
Vizioli MG, Possik PA, Tarantino E, Meissl K, Borrello MG, Miranda C, Anania MC, Pagliardini S, Seregni E, Pierotti MA, Pilotti S, Peeper DS, Greco A. Evidence of oncogene-induced senescence in thyroid carcinogenesis. Endocrine-Related Cancer. 18: 743-57. PMID 21937739 DOI: 10.1530/ERC-11-0240 |
0.098 |
|
| 2018 |
Gazzaz M, Saini J, Pagliardini S, Tsui B, Jeffery C, El-Hakim H. Comparison of inhaled versus intravenous anesthesia for laryngoscopy and laryngeal electromyography in a rat model. Journal of Otolaryngology - Head & Neck Surgery = Le Journal D'Oto-Rhino-Laryngologie Et De Chirurgie Cervico-Faciale. 47: 64. PMID 30342558 DOI: 10.1186/s40463-018-0312-9 |
0.097 |
|
| 1999 |
Capra V, Ravasi S, Bolla M, Viappiani S, Pagliardini S, Belloni PA, Mezzetti M, Folco GC, Nicosia S, Rovati GE. Evaluation of the pharmacological activity of the pure cysteinyl-leukotriene receptor antagonists CGP 45715A (iralukast) and CGP 57698 in human airways. Advances in Experimental Medicine and Biology. 469: 313-8. PMID 10667347 |
0.096 |
|
| 2023 |
Ward-Flanagan R, Pagliardini S, Dickson CT. Urethane provides an unparalleled anaesthetic model for natural sleep: Commentary on Mondino et al., 2022. The European Journal of Neuroscience. PMID 37041120 DOI: 10.1111/ejn.15985 |
0.095 |
|
| 2006 |
Spada M, Pagliardini S, Yasuda M, Tukel T, Thiagarajan G, Sakuraba H, Ponzone A, Desnick RJ. High incidence of later-onset fabry disease revealed by newborn screening. American Journal of Human Genetics. 79: 31-40. PMID 16773563 DOI: 10.1086/504601 |
0.094 |
|
| 1998 |
Greco A, Fusetti L, Miranda C, Villa R, Zanotti S, Pagliardini S, Pierotti MA. Role of the TFG N-terminus and coiled-coil domain in the transforming activity of the thyroid TRK-T3 oncogene. Oncogene. 16: 809-16. PMID 9488046 DOI: 10.1038/sj.onc.1201596 |
0.092 |
|
| 2006 |
Miranda C, Roccato E, Raho G, Pagliardini S, Pierotti MA, Greco A. The TFG protein, involved in oncogenic rearrangements, interacts with TANK and NEMO, two proteins involved in the NF-kappaB pathway. Journal of Cellular Physiology. 208: 154-60. PMID 16547966 DOI: 10.1002/jcp.20644 |
0.089 |
|
| 1993 |
Greco A, Mariani C, Miranda C, Pagliardini S, Pierotti MA. Characterization of the NTRK1 genomic region involved in chromosomal rearrangements generating TRK oncogenes. Genomics. 18: 397-400. PMID 8288244 DOI: 10.1006/geno.1993.1482 |
0.087 |
|
| 2002 |
Miranda C, Zanotti G, Pagliardini S, Ponzetto C, Pierotti MA, Greco A. Gain of function mutations of RTK conserved residues display differential effects on NTRK1 kinase activity. Oncogene. 21: 8334-9. PMID 12447696 DOI: 10.1038/sj.onc.1206052 |
0.087 |
|
| 2003 |
Roccato E, Pagliardini S, Cleris L, Canevari S, Formelli F, Pierotti MA, Greco A. Role of TFG sequences outside the coiled-coil domain in TRK-T3 oncogenic activation. Oncogene. 22: 807-18. PMID 12584559 DOI: 10.1038/sj.onc.1206189 |
0.085 |
|
| 2014 |
Vizioli MG, Santos J, Pilotti S, Mazzoni M, Anania MC, Miranda C, Pagliardini S, Pierotti MA, Gil J, Greco A. Oncogenic RAS-induced senescence in human primary thyrocytes: molecular effectors and inflammatory secretome involved. Oncotarget. 5: 8270-83. PMID 25268744 |
0.082 |
|
| 2005 |
Roccato E, Miranda C, Raho G, Pagliardini S, Pierotti MA, Greco A. Analysis of SHP-1-mediated down-regulation of the TRK-T3 oncoprotein identifies Trk-fused gene (TFG) as a novel SHP-1-interacting protein. The Journal of Biological Chemistry. 280: 3382-9. PMID 15557341 DOI: 10.1074/jbc.M407522200 |
0.077 |
|
| 2012 |
Paciotti S, Persichetti E, Pagliardini S, Deganuto M, Rosano C, Balducci C, Codini M, Filocamo M, Menghini AR, Pagliardini V, Pasqui S, Bembi B, Dardis A, Beccari T. First pilot newborn screening for four lysosomal storage diseases in an Italian region: identification and analysis of a putative causative mutation in the GBA gene. Clinica Chimica Acta; International Journal of Clinical Chemistry. 413: 1827-31. PMID 22820396 DOI: 10.1016/j.cca.2012.07.011 |
0.077 |
|
| 2008 |
Ferrero GB, Pagliardini S, Veljkovic A, Porta F, Bena C, Tardivo I, Restagno G, Silengo MC, Bignamini E. In vivo specific reduction of arylsulfatase B enzymatic activity in children with cystic fibrosis. Molecular Genetics and Metabolism. 94: 139. PMID 18299243 DOI: 10.1016/j.ymgme.2007.10.010 |
0.074 |
|
| 1997 |
Greco A, Miranda C, Pagliardini S, Fusetti L, Bongarzone I, Pierotti MA. Chromosome 1 rearrangements involving the genes TPR and NTRK1 produce structurally different thyroid-specific TRK oncogenes. Genes, Chromosomes & Cancer. 19: 112-23. PMID 9172002 DOI: 10.1002/(SICI)1098-2264(199706)19:2<112::AID-GCC7>3.0.CO;2-1 |
0.073 |
|
| 1993 |
Einaudi S, Lala R, Corrias A, Matarazzo P, Pagliardini S, de Sanctis C. Auxological and biochemical parameters in assessing treatment of infants and toddlers with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. The Journal of Pediatric Endocrinology. 6: 173-8. PMID 8348221 |
0.073 |
|
| 1984 |
Ponzone A, Ricca V, Ferraris S, Guardamagna O, Bracco G, Pagliardini S, Levis F, Giovannini M, Riva E, Longhi R. DHPR deficiency in Italy. The Journal of Pediatrics. 105: 1008. PMID 6502332 DOI: 10.1016/S0022-3476(84)80104-3 |
0.073 |
|
| 2013 |
Porta F, Pagliardini V, Barbera C, Calvo P, Pagliardini S, Lualdi S, Filocamo M, Spada M. Neonatal chitotriosidase activity is not predictive for Niemann-Pick disease type A/B: implications for newborn screening for lysosomal storage disorders. Molecular Genetics and Metabolism. 108: 106. PMID 23228552 DOI: 10.1016/j.ymgme.2012.11.004 |
0.07 |
|
| 2006 |
Mandato C, Brive L, Miura Y, Davis JA, Di Cosmo N, Lucariello S, Pagliardini S, Seo NS, Parenti G, Vecchione R, Freeze HH, Vajro P. Cryptogenic liver disease in four children: a novel congenital disorder of glycosylation. Pediatric Research. 59: 293-8. PMID 16439595 DOI: 10.1203/01.pdr.0000196378.30165.26 |
0.068 |
|
| 2015 |
Anania M, Gasparri F, Cetti E, Fraietta I, Todoerti K, Miranda C, Mazzoni M, Re C, Colombo R, Ukmar G, Camisasca S, Pagliardini S, Pierotti M, Neri A, Galvani A, et al. Identification of thyroid tumor cell vulnerabilities through a siRNA-based functional screening. Oncotarget. 6: 34629-48. PMID 26431489 DOI: 10.18632/oncotarget.5282 |
0.068 |
|
| 1992 |
Greco A, Pierotti MA, Bongarzone I, Pagliardini S, Lanzi C, Della Porta G. TRK-T1 is a novel oncogene formed by the fusion of TPR and TRK genes in human papillary thyroid carcinomas. Oncogene. 7: 237-42. PMID 1532241 |
0.067 |
|
| 2015 |
Pagliardini V, Pagliardini S, Corrado L, Lucenti A, Panigati L, Bersano E, Servo S, Cantello R, D'Alfonso S, Mazzini L. Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: a survey clinic-based study. Journal of the Neurological Sciences. 348: 245-50. PMID 25563799 DOI: 10.1016/j.jns.2014.12.016 |
0.067 |
|
| 2008 |
Calvo PL, Pagliardini S, Baldi M, Pucci A, Sturiale L, Garozzo D, Vinciguerra T, Barbera C, Jaeken J. Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx. Journal of Inherited Metabolic Disease. 31: S437-40. PMID 19067230 DOI: 10.1007/s10545-008-1004-9 |
0.063 |
|
| 2011 |
Porta F, Pagliardini S, Pagliardini V, Dotta A, Mussa A, Spada M. Lysosomal enzyme activities in phenylketonuria. Molecular Genetics and Metabolism. 102: 508. PMID 21316999 DOI: 10.1016/j.ymgme.2011.01.014 |
0.062 |
|
| 2015 |
Porta F, Pagliardini S, Pagliardini V, Ponzone A, Spada M. Newborn screening for galactosemia: a 30-year single center experience. World Journal of Pediatrics : Wjp. 11: 160-4. PMID 25754754 DOI: 10.1007/s12519-015-0017-3 |
0.056 |
|
| 2013 |
Spada M, Porta F, Vercelli L, Pagliardini V, Chiadò-Piat L, Boffi P, Pagliardini S, Remiche G, Ronchi D, Comi G, Mongini T. Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemia. Molecular Genetics and Metabolism. 109: 171-3. PMID 23566438 DOI: 10.1016/j.ymgme.2013.03.002 |
0.05 |
|
| 1999 |
Enrico Rovati G, Ravasi S, Capra V, Pagliardini S, Mezzetti M, Nicosia S. Characterization of a distinctive pharmacologial profile for LTC4 binding sites in human lung parenchyma using a kinetic approach Prostaglandins & Other Lipid Mediators. 59: 44. DOI: 10.1016/S0090-6980(99)90279-4 |
0.049 |
|
| 2009 |
Olivieri A, Altamura R, Angeloni U, Antonozzi I, Baserga M, Berardi R, Bernasconi S, Bona G, Bucci I, Burroni M, Calaciura F, Caldarera R, Cappa M, Caruso U, Casini MR, ... ... Pagliardini S, et al. The Italian National Register of infants with congenital hypothyroidism: Twenty years of surveillance and study of congenital hypothyroidism Italian Journal of Pediatrics. 35. DOI: 10.1186/1824-7288-35-2 |
0.047 |
|
| 1983 |
Bracco G, Pagliardini S. [Method of eliminating inhibition by antibiotics in the Guthrie test for phenylketonuria]. Pathologica. 75: 72-4. PMID 6440108 |
0.046 |
|
| 2014 |
Mussa A, Pagliardini S, Pagliardini V, Molinatto C, Baldassarre G, Corrias A, Silengo MC, Ferrero GB. α-Fetoprotein assay on dried blood spot for hepatoblastoma screening in children with overgrowth-cancer predisposition syndromes. Pediatric Research. 76: 544-8. PMID 25167201 DOI: 10.1038/pr.2014.126 |
0.046 |
|
| 2009 |
Kleinert J, Kotanko P, Spada M, Pagliardini S, Paschke E, Paul K, Voigtländer T, Wallner M, Kramar R, Stummvoll HK, Schwarz C, Horn S, Holzer H, Födinger M, Sunder-Plassmann G. Anderson-Fabry disease: a case-finding study among male kidney transplant recipients in Austria. Transplant International : Official Journal of the European Society For Organ Transplantation. 22: 287-92. PMID 18954370 DOI: 10.1111/j.1432-2277.2008.00791.x |
0.041 |
|
| 2013 |
Anania MC, Miranda C, Vizioli MG, Mazzoni M, Cleris L, Pagliardini S, Manenti G, Borrello MG, Pierotti MA, Greco A. S100A11 overexpression contributes to the malignant phenotype of papillary thyroid carcinoma. The Journal of Clinical Endocrinology and Metabolism. 98: E1591-600. PMID 23928665 DOI: 10.1210/jc.2013-1652 |
0.039 |
|
| 2005 |
Di Rocco M, Hennet T, Grubenmann CE, Pagliardini S, Allegri AE, Frank CG, Aebi M, Vignola S, Jaeken J. Congenital disorder of glycosylation (CDG) Ig: report on a patient and review of the literature. Journal of Inherited Metabolic Disease. 28: 1162-4. PMID 16435218 DOI: 10.1007/S10545-005-0137-3 |
0.038 |
|
| 2003 |
Silengo M, Valenzise M, Pagliardini S, Spada M. Hair changes in congenital disorders of glycosylation (CDG type 1). European Journal of Pediatrics. 162: 114-5. PMID 12607543 |
0.037 |
|
| 1983 |
Bracco G, Pagliardini S. Guthrie test recalls due to antibiotic inhibition. Lancet (London, England). 1: 1331-2. PMID 6134115 DOI: 10.1016/S0140-6736(83)92438-8 |
0.036 |
|
| 2001 |
Girardi E, Ravà L, Pezzotti P, Puro V, Ippolito G, Antonozzi I, Beghini R, Burroni M, Caruso U, Ciannamea R, Chiovato L, Cioni M, Corbetta C, Costa F, Damato VD, ... ... Pagliardini S, et al. Monitoring the trend of the transmission rate of vertically acquired HIV infection: A simple method applied to Italian data Journal of Biological Regulators and Homeostatic Agents. 15: 229-234. PMID 11693429 |
0.032 |
|
| 2005 |
Medda E, Olivieri A, Stazi MA, Grandolfo ME, Fazzini C, Baserga M, Burroni M, Cacciari E, Calaciura F, Cassio A, Chiovato L, Costa P, Leonardi D, Martucci M, Moschini L, ... Pagliardini S, et al. Risk factors for congenital hypothyroidism: results of a population case-control study (1997-2003). European Journal of Endocrinology / European Federation of Endocrine Societies. 153: 765-73. PMID 16322381 DOI: 10.1530/eje.1.02048 |
0.03 |
|
| 2015 |
Musumeci O, la Marca G, Spada M, Mondello S, Danesino C, Comi GP, Pegoraro E, Antonini G, Marrosu G, Liguori R, Morandi L, Moggio M, Massa R, Ravaglia S, Di Muzio A, ... ... Pagliardini S, et al. LOPED study: Looking for an early diagnosis in a late-onset Pompe disease high-risk population Journal of Neurology, Neurosurgery and Psychiatry. DOI: 10.1136/jnnp-2014-310164 |
0.028 |
|
| 2007 |
Olivieri A, Medda E, De Angelis S, Valensise H, De Felice M, Fazzini C, Cascino I, Cordeddu V, Sorcini M, Stazi MA, Altamura R, Angeloni U, Antonozzi I, Baserga M, Berardi R, ... ... Pagliardini S, et al. High risk of congenital hypothyroidism in multiple pregnancies Journal of Clinical Endocrinology and Metabolism. 92: 3141-3147. PMID 17488789 DOI: 10.1210/jc.2007-0238 |
0.022 |
|
| 1978 |
Campagnoli C, Fessia L, Gilli V, Pagliardini S, Peris C, Richetta R, Rustichelli S. [Changes induced with L-dopa in the serum levels of prolactin and somatotropin in the diagnosis of amenorrhea-galactorrhea]. Minerva Ginecologica. 30: 135-8. PMID 566402 |
0.016 |
|
| 1997 |
Romano C, Balsamo A, Burroni M, Cardillo A, Carnevale F, Caruso U, Cerone R, Ciatti R, Cioni M, Corbetta C, Dotti L, Impellizzeri A, Lelli A, Leuzzi V, Lilliu F, ... Pagliardini S, et al. Diagnosis, classification, basis of treatment of hyperphenylalaninemias | Accertamento diagnostico, nosografia, principi di trattamento delle iperfenilalaninemie Rivista Italiana Di Pediatria. 23: 1040-1044. |
0.015 |
|
| 2004 |
Kotanko P, Kramar R, Devrnja D, Paschke E, Voigtländer T, Auinger M, Pagliardini S, Spada M, Demmelbauer K, Lorenz M, Hauser AC, Kofler HJ, Lhotta K, Neyer U, Pronai W, et al. Results of a nationwide screening for Anderson-Fabry disease among dialysis patients. Journal of the American Society of Nephrology : Jasn. 15: 1323-9. PMID 15100373 |
0.012 |
|
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