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Items: 20

1.

Challenges in modelling the Charcot-Marie-Tooth neuropathies for therapy development.

Juneja M, Burns J, Saporta MA, Timmerman V.

J Neurol Neurosurg Psychiatry. 2018 Jul 17. pii: jnnp-2018-318834. doi: 10.1136/jnnp-2018-318834. [Epub ahead of print]

2.

The human motor neuron axonal transcriptome is enriched for transcripts related to mitochondrial function and microtubule-based axonal transport.

Maciel R, Bis DM, Rebelo AP, Saghira C, Züchner S, Saporta MA.

Exp Neurol. 2018 Sep;307:155-163. doi: 10.1016/j.expneurol.2018.06.008. Epub 2018 Jun 20.

PMID:
29935168
3.

Analysis of Myelinating Schwann Cells in Human Skin Biopsies.

Saporta MA, de Moraes Maciel R.

Methods Mol Biol. 2018;1739:359-369. doi: 10.1007/978-1-4939-7649-2_24.

PMID:
29546720
4.

A human cellular model to study peripheral myelination and demyelinating neuropathies.

Saporta MA, Shy ME.

Brain. 2017 Apr 1;140(4):856-859. doi: 10.1093/brain/awx048. No abstract available.

5.

Cellular reprogramming and inherited peripheral neuropathies: perspectives and challenges.

Saporta MA.

Neural Regen Res. 2015 Jun;10(6):894-6. doi: 10.4103/1673-5374.158345. No abstract available.

6.

Axonal Charcot-Marie-Tooth disease patient-derived motor neurons demonstrate disease-specific phenotypes including abnormal electrophysiological properties.

Saporta MA, Dang V, Volfson D, Zou B, Xie XS, Adebola A, Liem RK, Shy M, Dimos JT.

Exp Neurol. 2015 Jan;263:190-9. doi: 10.1016/j.expneurol.2014.10.005. Epub 2014 Oct 30.

7.

Charcot-Marie-Tooth disease and other inherited neuropathies.

Saporta MA.

Continuum (Minneap Minn). 2014 Oct;20(5 Peripheral Nervous System Disorders):1208-25. doi: 10.1212/01.CON.0000455885.37169.4c. Review.

PMID:
25299278
8.

Inherited peripheral neuropathies.

Saporta MA, Shy ME.

Neurol Clin. 2013 May;31(2):597-619. doi: 10.1016/j.ncl.2013.01.009. Epub 2013 Mar 5. Review.

9.

Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice.

Patzkó A, Bai Y, Saporta MA, Katona I, Wu X, Vizzuso D, Feltri ML, Wang S, Dillon LM, Kamholz J, Kirschner D, Sarkar FH, Wrabetz L, Shy ME.

Brain. 2012 Dec;135(Pt 12):3551-66. doi: 10.1093/brain/aws299. Erratum in: Brain. 2014 Dec;137(Pt 12):e316.

10.

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.

Brain. 2012 Jul;135(Pt 7):2032-47. doi: 10.1093/brain/aws140. Epub 2012 Jun 10.

11.

Induced pluripotent stem cells in the study of neurological diseases.

Saporta MA, Grskovic M, Dimos JT.

Stem Cell Res Ther. 2011 Sep 21;2(5):37. doi: 10.1186/scrt78. Review.

12.

Neuropathy in a human without the PMP22 gene.

Saporta MA, Katona I, Zhang X, Roper HP, McClelland L, Macdonald F, Brueton L, Blake J, Suter U, Reilly MM, Shy ME, Li J.

Arch Neurol. 2011 Jun;68(6):814-21. doi: 10.1001/archneurol.2011.110.

13.

Conduction block in PMP22 deficiency.

Bai Y, Zhang X, Katona I, Saporta MA, Shy ME, O'Malley HA, Isom LL, Suter U, Li J.

J Neurosci. 2010 Jan 13;30(2):600-8. doi: 10.1523/JNEUROSCI.4264-09.2010.

14.

Shortened internodal length of dermal myelinated nerve fibres in Charcot-Marie-Tooth disease type 1A.

Saporta MA, Katona I, Lewis RA, Masse S, Shy ME, Li J.

Brain. 2009 Dec;132(Pt 12):3263-73. doi: 10.1093/brain/awp274.

15.

Isolated posterior cerebral artery infarction caused by carotid artery dissection.

de Christoph DH, Souza-Lima F, da Saporta MA, de Freitas GR.

Arch Neurol. 2009 Aug;66(8):1034-5. doi: 10.1001/archneurol.2009.147. No abstract available.

PMID:
19667228
16.

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.

Eur J Neurol. 2009 Mar;16(3):337-41. doi: 10.1111/j.1468-1331.2008.02429.x.

PMID:
19364362
17.

Discordant expression of familial amyloid polyneuropathy in monozygotic Brazilian twins.

Saporta MA, Plante-Bordeneuve V, Misrahi M, Cruz MW.

Amyloid. 2009 Mar;16(1):38-41. doi: 10.1080/13506120802676955.

PMID:
19291513
18.

On the origin of the transthyretin Val30Met familial amyloid polyneuropathy.

Zaros C, Genin E, Hellman U, Saporta MA, Languille L, Wadington-Cruz M, Suhr O, Misrahi M, Planté-Bordeneuve V.

Ann Hum Genet. 2008 Jul;72(Pt 4):478-84. doi: 10.1111/j.1469-1809.2008.00439.x. Epub 2008 May 5.

19.

Acquired hepatocerebral degeneration without overt liver disease.

Saporta MA, André C, Bahia PR, Chimelli L, Pais PH, Silva TS, Correia AH, Nobre AB.

Neurology. 2004 Nov 23;63(10):1981-2. No abstract available.

PMID:
15557536
20.

[Prevalence and indirect costs of headache in a Brazilian Company].

Vincent M, Rodrigues Ade J, De Oliveira GV, De Souza KF, Doi LM, Rocha MB, Saporta MA, Orleans RB, Kotecki R, Estrela VV, De Medeiros VA, Borges WI.

Arq Neuropsiquiatr. 1998 Dec;56(4):734-43. Portuguese.

PMID:
10029875

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