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Items: 1 to 20 of 33

1.

The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases.

Planté-Bordeneuve V, Parman Y, Guiochon-Mantel A, Alj Y, Deymeer F, Serdaroglu P, Eraksoy M, Said G.

J Neurol. 2001 Sep;248(9):795-803.

PMID:
11596785
2.

Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.

Plante-Bordeneuve V, Said G.

Muscle Nerve. 2002 Nov;26(5):608-21. Review.

PMID:
12402282
3.

Inherited neuropathies: from gene to disease.

Keller MP, Chance PF.

Brain Pathol. 1999 Apr;9(2):327-41. Review.

PMID:
10219749
4.

Genetic evaluation of inherited motor/sensory neuropathy.

Chance PF.

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

PMID:
16106622
5.

Phenotypic clustering in MPZ mutations.

Shy ME, Jáni A, Krajewski K, Grandis M, Lewis RA, Li J, Shy RR, Balsamo J, Lilien J, Garbern JY, Kamholz J.

Brain. 2004 Feb;127(Pt 2):371-84. Review.

PMID:
14711881
6.

[Mutation of the myelin Po gene in hereditary motor and sensory neuropathy].

Hayasaka K.

Rinsho Shinkeigaku. 1995 Dec;35(12):1444-6. Review. Japanese.

PMID:
8752425
7.

[Molecular genetics of inherited neuropathies].

Takashima H.

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

PMID:
16541790
8.

Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies.

Nelis E, Haites N, Van Broeckhoven C.

Hum Mutat. 1999;13(1):11-28. Review.

PMID:
9888385
9.

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G; Study Group for Hereditary Neuropathy in Japan..

Brain. 2003 Jan;126(Pt 1):134-51. Review.

PMID:
12477701
10.

Molecular basis of hereditary neuropathies.

Chance PF.

Phys Med Rehabil Clin N Am. 2001 May;12(2):277-91. Review.

PMID:
11345007
11.

Congenital hypomyelinating neuropathy: two patients with long-term follow-up.

Phillips JP, Warner LE, Lupski JR, Garg BP.

Pediatr Neurol. 1999 Mar;20(3):226-32. Review.

PMID:
10207934
12.

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
13.

Corticosteroid- responsive asymmetric neuropathy with a myelin protein zero gene mutation.

Watanabe M, Yamamoto N, Ohkoshi N, Nagata H, Kohno Y, Hayashi A, Tamaoka A, Shoji S.

Neurology. 2002 Sep 10;59(5):767-9. Review.

PMID:
12221176
16.

Hereditary demyelinating motor and sensory neuropathy.

Gabreëls-Festen A, Gabreëls F.

Brain Pathol. 1993 Apr;3(2):135-46. Review.

PMID:
8293175
17.

Four novel cases of periaxin-related neuropathy and review of the literature.

Marchesi C, Milani M, Morbin M, Cesani M, Lauria G, Scaioli V, Piccolo G, Fabrizi GM, Cavallaro T, Taroni F, Pareyson D.

Neurology. 2010 Nov 16;75(20):1830-8. doi: 10.1212/WNL.0b013e3181fd6314. Review.

PMID:
21079185
18.

[Molecular biology and genetics of hereditary motor and sensory neuropathies].

Stögbauer F, Halfter H, Young P, Ringelstein EB.

Nervenarzt. 1996 Dec;67(12):987-97. Review. German.

PMID:
9082200
19.

Molecular genetics of inherited peripheral neuropathies: who are the actors?

Meuleman J, Timmerman V, Nelis E, De Jonghe P.

Acta Neurol Belg. 2000 Sep;100(3):171-80. Review.

PMID:
11098291
20.

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