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Inherited peripheral neuropathies.
Saporta MA, Shy ME. Saporta MA, et al. Neurol Clin. 2013 May;31(2):597-619. doi: 10.1016/j.ncl.2013.01.009. Epub 2013 Mar 5. Neurol Clin. 2013. PMID: 23642725 Free PMC article. Review.
Penetrance estimation of TTR familial amyloid polyneuropathy (type I) in Brazilian families.
Saporta MA, Zaros C, Cruz MW, André C, Misrahi M, Bonaïti-Pellié C, Planté-Bordeneuve V. Saporta MA, et al. Eur J Neurol. 2009 Mar;16(3):337-41. doi: 10.1111/j.1468-1331.2008.02429.x. Eur J Neurol. 2009. PMID: 19364362
Charcot-Marie-Tooth disease and other inherited neuropathies.
Saporta MA. Saporta MA. Continuum (Minneap Minn). 2014 Oct;20(5 Peripheral Nervous System Disorders):1208-25. doi: 10.1212/01.CON.0000455885.37169.4c. Continuum (Minneap Minn). 2014. PMID: 25299278 Review.
Cellular reprogramming and inherited peripheral neuropathies: perspectives and challenges.
Saporta MA. Saporta MA. Neural Regen Res. 2015 Jun;10(6):894-6. doi: 10.4103/1673-5374.158345. Neural Regen Res. 2015. PMID: 26199602 Free PMC article. No abstract available.
Human Tridimensional Neuronal Cultures for Phenotypic Drug Screening in Inherited Peripheral Neuropathies.
Maciel R, Correa R, Bosso Taniguchi J, Prufer Araujo I, Saporta MA. Maciel R, et al. Among authors: saporta ma. Clin Pharmacol Ther. 2020 May;107(5):1231-1239. doi: 10.1002/cpt.1718. Epub 2019 Dec 14. Clin Pharmacol Ther. 2020. PMID: 31715019
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
Saporta MA, Shy BR, Patzko A, Bai Y, Pennuto M, Ferri C, Tinelli E, Saveri P, Kirschner D, Crowther M, Southwood C, Wu X, Gow A, Feltri ML, Wrabetz L, Shy ME. Saporta MA, et al. Brain. 2012 Jul;135(Pt 7):2032-47. doi: 10.1093/brain/aws140. Epub 2012 Jun 10. Brain. 2012. PMID: 22689911 Free PMC article.
Acquired hepatocerebral degeneration without overt liver disease.
Saporta MA, André C, Bahia PR, Chimelli L, Pais PH, Silva TS, Correia AH, Nobre AB. Saporta MA, et al. Neurology. 2004 Nov 23;63(10):1981-2. doi: 10.1212/01.wnl.0000144193.62505.e6. Neurology. 2004. PMID: 15557536 No abstract available.
Hereditary motor neuropathies.
Dohrn MF, Saporta M. Dohrn MF, et al. Among authors: saporta m. Curr Opin Neurol. 2020 Oct;33(5):568-574. doi: 10.1097/WCO.0000000000000848. Curr Opin Neurol. 2020. PMID: 32796276
Yes, we can: Neuromuscular examination by telemedicine.
Saporta MA, Granit V, Lewis R, Benatar M. Saporta MA, et al. Muscle Nerve. 2020 Sep 1. doi: 10.1002/mus.27056. Online ahead of print. Muscle Nerve. 2020. PMID: 32875561 No abstract available.
Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.
Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, Herrmann DN, Day JW, Sumner CJ, Lloyd TE, Li J, Yum SW, Taroni F, Baas F, Choi BO, Pareyson D, Scherer SS, Reilly MM, Shy ME, Züchner S; Inherited Neuropathy Consortium. Tao F, et al. Among authors: saporta ma. J Neuromuscul Dis. 2019;6(2):201-211. doi: 10.3233/JND-190377. J Neuromuscul Dis. 2019. PMID: 30958311 Free PMC article.
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