Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 192

1.

Diseases of connexins expressed in myelinating glia.

Abrams CK.

Neurosci Lett. 2017 May 23. pii: S0304-3940(17)30433-0. doi: 10.1016/j.neulet.2017.05.037. [Epub ahead of print] Review.

PMID:
28545922
2.

Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.

Berciano J, García A, Gallardo E, Peeters K, Pelayo-Negro AL, Álvarez-Paradelo S, Gazulla J, Martínez-Tames M, Infante J, Jordanova A.

J Neurol. 2017 Mar 31. doi: 10.1007/s00415-017-8474-3. [Epub ahead of print] Review.

PMID:
28364294
3.

GDAP1-Related Hereditary Motor and Sensory Neuropathy.

Bird TD.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2004 May 11 [updated 2017 Mar 30].

4.

Defective axonal transport: A common pathological mechanism in inherited and acquired peripheral neuropathies.

Prior R, Van Helleputte L, Benoy V, Van Den Bosch L.

Neurobiol Dis. 2017 Feb 24. pii: S0969-9961(17)30032-3. doi: 10.1016/j.nbd.2017.02.009. [Epub ahead of print] Review.

5.

Rab7 may be a novel therapeutic target for neurologic diseases as a key regulator in autophagy.

Wen H, Zhan L, Chen S, Long L, Xu E.

J Neurosci Res. 2017 Feb 10. doi: 10.1002/jnr.24034. [Epub ahead of print] Review.

PMID:
28186670
6.

Charcot Marie Tooth 2B Peripheral Sensory Neuropathy: How Rab7 Mutations Impact NGF Signaling?

Liu H, Wu C.

Int J Mol Sci. 2017 Feb 4;18(2). pii: E324. doi: 10.3390/ijms18020324. Review.

7.

Endoplasmic Reticulum Protein Quality Control Failure in Myelin Disorders.

Volpi VG, Touvier T, D'Antonio M.

Front Mol Neurosci. 2017 Jan 4;9:162. doi: 10.3389/fnmol.2016.00162. eCollection 2016. Review.

8.

Axonal neuropathy with neuromyotonia: there is a HINT.

Peeters K, Chamova T, Tournev I, Jordanova A.

Brain. 2017 Apr 1;140(4):868-877. doi: 10.1093/brain/aww301. Review.

9.

Advances in myelinating glial cell development.

Herbert AL, Monk KR.

Curr Opin Neurobiol. 2017 Feb;42:53-60. doi: 10.1016/j.conb.2016.11.003. Epub 2016 Dec 6. Review.

PMID:
27930937
10.

Towards a functional pathology of hereditary neuropathies.

Weis J, Claeys KG, Roos A, Azzedine H, Katona I, Schröder JM, Senderek J.

Acta Neuropathol. 2017 Apr;133(4):493-515. doi: 10.1007/s00401-016-1645-y. Epub 2016 Nov 28. Review.

PMID:
27896434
11.

Dynamin Functions and Ligands: Classical Mechanisms Behind.

Singh M, Jadhav HR, Bhatt T.

Mol Pharmacol. 2017 Feb;91(2):123-134. doi: 10.1124/mol.116.105064. Epub 2016 Nov 22. Review.

PMID:
27879341
12.

Predicting the pathogenicity of aminoacyl-tRNA synthetase mutations.

Oprescu SN, Griffin LB, Beg AA, Antonellis A.

Methods. 2017 Jan 15;113:139-151. doi: 10.1016/j.ymeth.2016.11.013. Epub 2016 Nov 20. Review.

PMID:
27876679
13.

Hereditary neuropathies: An update.

Stojkovic T.

Rev Neurol (Paris). 2016 Dec;172(12):775-778. doi: 10.1016/j.neurol.2016.06.007. Epub 2016 Nov 17. Review.

PMID:
27866730
14.

WANTED - Dead or alive: Myotubularins, a large disease-associated protein family.

Raess MA, Friant S, Cowling BS, Laporte J.

Adv Biol Regul. 2017 Jan;63:49-58. doi: 10.1016/j.jbior.2016.09.001. Epub 2016 Sep 15. Review.

PMID:
27666502
15.

ATP7A-Related Copper Transport Disorders.

Kaler SG.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2003 May 9 [updated 2016 Aug 18].

16.

Gait in children and adolescents with Charcot-Marie-Tooth disease: a systematic review.

Kennedy RA, Carroll K, McGinley JL.

J Peripher Nerv Syst. 2016 Dec;21(4):317-328. doi: 10.1111/jns.12183. Review.

PMID:
27513454
17.

Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish.

Kozol RA, Abrams AJ, James DM, Buglo E, Yan Q, Dallman JE.

Front Mol Neurosci. 2016 Jul 7;9:55. doi: 10.3389/fnmol.2016.00055. eCollection 2016. Review.

18.

What's New in Severe Deformity Correction: The German Perspective.

Schmitt S, Peak AC, Berrsche G, Wenz W.

Foot Ankle Clin. 2016 Jun;21(2):219-36. doi: 10.1016/j.fcl.2016.01.002. Epub 2016 Mar 31. Review.

PMID:
27261803
19.

Classifications of neurogenetic diseases: An increasingly complex problem.

Vallat JM, Goizet C, Tazir M, Couratier P, Magy L, Mathis S.

Rev Neurol (Paris). 2016 Jun-Jul;172(6-7):339-49. doi: 10.1016/j.neurol.2016.04.005. Epub 2016 May 27. Review.

PMID:
27240993
20.

Connexinopathies: a structural and functional glimpse.

García IE, Prado P, Pupo A, Jara O, Rojas-Gómez D, Mujica P, Flores-Muñoz C, González-Casanova J, Soto-Riveros C, Pinto BI, Retamal MA, González C, Martínez AD.

BMC Cell Biol. 2016 May 24;17 Suppl 1:17. doi: 10.1186/s12860-016-0092-x. Review.

Supplemental Content

Loading ...
Support Center