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Results: 1 to 20 of 28

Related Articles by Review for PubMed (Select 12690580)

1.

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

Antonellis A, Ellsworth RE, Sambuughin N, Puls I, Abel A, Lee-Lin SQ, Jordanova A, Kremensky I, Christodoulou K, Middleton LT, Sivakumar K, Ionasescu V, Funalot B, Vance JM, Goldfarb LG, Fischbeck KH, Green ED.

Am J Hum Genet. 2003 May;72(5):1293-9. Epub 2003 Apr 10.

2.

Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.

Bird TD.

Neurol Clin. 1989 Feb;7(1):9-23. Review.

PMID:
2646524
3.

Genetic evaluation of inherited motor/sensory neuropathy.

Chance PF.

Suppl Clin Neurophysiol. 2004;57:228-42. Review.

PMID:
16106622
4.

Dominantly inherited peripheral neuropathies.

Vallat JM.

J Neuropathol Exp Neurol. 2003 Jul;62(7):699-714. Review.

PMID:
12901697
5.

Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease.

Houlden H, Reilly MM.

Neuromolecular Med. 2006;8(1-2):43-62. Review.

PMID:
16775366
6.

Molecular basis of neuromuscular diseases.

Chance PF, Ashizawa T, Hoffman EP, Crawford TO.

Phys Med Rehabil Clin N Am. 1998 Feb;9(1):49-81, vi. Review.

PMID:
9894134
7.

[Nephropathy and Charcot-Marie-Tooth disease. A case report].

Fillod I, Cochat P, Colon S, Wright C, David L.

Pediatrie. 1990;45(5):319-22. Review. French.

PMID:
2165244
9.

[Charcot-Marie-Tooth disease].

Lee YC, Chang MH, Lin KP.

Acta Neurol Taiwan. 2008 Sep;17(3):203-13. Review. Chinese.

10.

Benign autosomal dominant syndrome of neuronal Charcot-Marie-Tooth disease, ptosis, parkinsonism, and dementia.

Tandan R, Taylor R, Adesina A, Sharma K, Fries T, Pendlebury W.

Neurology. 1990 May;40(5):773-9. Review.

PMID:
2184381
11.

[Molecular genetics of inherited neuropathies].

Takashima H.

Rinsho Shinkeigaku. 2006 Jan;46(1):1-18. Review. Japanese.

PMID:
16541790
12.

[From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].

Verhamme C, Baas F.

Ned Tijdschr Geneeskd. 2005 Jul 2;149(27):1505-9. Review. Dutch.

PMID:
16032995
13.

[Type 2 Charcot-Marie-Tooth disease?].

Combarros-Pascual O.

Rev Neurol. 2000 Jan 1-15;30(1):79-81. Review. Spanish.

PMID:
10743002
14.

[Distal spinal muscular atrophy].

Sevilla T.

Neurologia. 1996 Dec;11 Suppl 5:58-65. Review. Spanish.

PMID:
9044574
15.

[Carbamazepine-sensitive neuromyotonia and Charcot-Marie-Tooth disease of the neuronal type].

Serratrice G, Pouget J, Pellissier JF, Cros D.

Rev Neurol (Paris). 1989;145(12):867-8. Review. French.

PMID:
2694289
16.

To charge or not to charge: mechanistic insights into neuropathy-associated tRNA synthetase mutations.

Wallen RC, Antonellis A.

Curr Opin Genet Dev. 2013 Jun;23(3):302-9. doi: 10.1016/j.gde.2013.02.002. Epub 2013 Mar 4. Review.

17.

Hereditary motor and sensory neuropathy: evolution of the concept and present status.

Thomas PK.

Electroencephalogr Clin Neurophysiol Suppl. 1987;39:115-20. Review. No abstract available.

PMID:
2820690
18.

Emerging pathways for hereditary axonopathies.

Züchner S, Vance JM.

J Mol Med (Berl). 2005 Dec;83(12):935-43. Epub 2005 Aug 31. Review.

PMID:
16133422
19.

DNA diagnostics for Charcot-Marie-Tooth disease and related inherited neuropathies.

Lupski JR.

Clin Chem. 1996 Jul;42(7):995-8. Review. No abstract available.

20.

GARS-Associated Axonal Neuropathy.

Goldfarb LG, Sivakumar K.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2006 Nov 08 [updated 2011 Aug 25].

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