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Items: 1 to 20 of 143

1.

Spinal Charcot-Marie-Tooth disease: a reappraisal.

Devic P, Petiot P, Mauguière F.

Muscle Nerve. 2012 Oct;46(4):604-9. doi: 10.1002/mus.23456. Review.

PMID:
22987707
2.

Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease.

Pareyson D, Scaioli V, Laurà M.

Neuromolecular Med. 2006;8(1-2):3-22. Review.

PMID:
16775364
3.

Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy.

Solla P, Vannelli A, Bolino A, Marrosu G, Coviello S, Murru MR, Tranquilli S, Corongiu D, Benedetti S, Marrosu MG.

J Neurol Neurosurg Psychiatry. 2010 Sep;81(9):958-62. doi: 10.1136/jnnp.2009.181636. Epub 2010 Jul 26.

PMID:
20660910
4.

Charcot-Marie-Tooth disease.

Martel J, Mierau D, Donat J.

J Manipulative Physiol Ther. 1995 Mar-Apr;18(3):168-71.

PMID:
7790797
5.

Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience.

Luigetti M, Fabrizi GM, Bisogni G, Romano A, Taioli F, Ferrarini M, Bernardo D, Rossini PM, Sabatelli M.

Clin Neurol Neurosurg. 2016 May;144:67-71. doi: 10.1016/j.clineuro.2016.03.007. Epub 2016 Mar 9.

PMID:
26989944
6.

Charcot-Marie-Tooth disease and related inherited neuropathies.

Murakami T, Garcia CA, Reiter LT, Lupski JR.

Medicine (Baltimore). 1996 Sep;75(5):233-50. Review.

7.
10.

Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.

Sevilla T, Cuesta A, Chumillas MJ, Mayordomo F, Pedrola L, Palau F, Vílchez JJ.

Brain. 2003 Sep;126(Pt 9):2023-33. Epub 2003 Jun 23.

PMID:
12821518
11.

Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.

Bird TD, Kraft GH, Lipe HP, Kenney KL, Sumi SM.

Ann Neurol. 1997 Apr;41(4):463-9.

PMID:
9124803
12.

Comparison of CMT1A and CMT2: similarities and differences.

Bienfait HM, Verhamme C, van Schaik IN, Koelman JH, de Visser BW, de Haan RJ, Baas F, van Engelen BG, de Visser M.

J Neurol. 2006 Dec;253(12):1572-80. Epub 2006 Aug 28.

PMID:
16941080
13.

Neurofibromatosis, Charcot-Marie-Tooth disease, or both?

Roos KL, Pascuzzi RM, Dunn DW.

Neurofibromatosis. 1989;2(4):238-43.

PMID:
2517818
14.

MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families.

Braathen GJ, Sand JC, Lobato A, Høyer H, Russell MB.

BMC Med Genet. 2010 Mar 29;11:48. doi: 10.1186/1471-2350-11-48.

15.

[Hereditary motor and sensory neuropathy of Charcot-Marie-Tooth disease].

Sturtz F, Gonnaud PM, Besse JL, Chazot G, Vandenberghe A.

Arch Pediatr. 1995 Jan;2(1):70-8. Review. French.

PMID:
7735430
16.

Sensory manifestations in Charcot-Marie-Tooth disease.

Gemignani F, Melli G, Alfieri S, Inglese C, Marbini A.

J Peripher Nerv Syst. 2004 Mar;9(1):7-14.

PMID:
14871449
17.

Assessment of axonal loss in Charcot-Marie-Tooth neuropathies.

Lawson VH, Gordon Smith A, Bromberg MB.

Exp Neurol. 2003 Dec;184(2):753-7.

PMID:
14769367
18.
19.

[Sensory nerve conduction velocity determined by somatosensory evoked potentials in patients with hereditary motor and sensory neuropathy type I].

Takada H, Ozaki I, Kurihara A, Baba M, Matsunaga M.

Rinsho Shinkeigaku. 1995 Jan;35(1):76-9. Japanese.

PMID:
7781221
20.

HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients.

Capponi S, Geroldi A, Fossa P, Grandis M, Ciotti P, Gulli R, Schenone A, Mandich P, Bellone E.

J Peripher Nerv Syst. 2011 Dec;16(4):287-94. doi: 10.1111/j.1529-8027.2011.00361.x.

PMID:
22176143

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