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Items: 1 to 20 of 28

1.

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.

Züchner S, Noureddine M, Kennerson M, Verhoeven K, Claeys K, De Jonghe P, Merory J, Oliveira SA, Speer MC, Stenger JE, Walizada G, Zhu D, Pericak-Vance MA, Nicholson G, Timmerman V, Vance JM.

Nat Genet. 2005 Mar;37(3):289-94. Epub 2005 Jan 30.

PMID:
15731758
2.

[Molecular genetics of inherited neuropathies].

Takashima H.

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

PMID:
16541790
3.

Intermediate forms of Charcot-Marie-Tooth neuropathy: a review.

Nicholson G, Myers S.

Neuromolecular Med. 2006;8(1-2):123-30. Review.

PMID:
16775371
4.
5.

Dynamin 2 and human diseases.

Durieux AC, Prudhon B, Guicheney P, Bitoun M.

J Mol Med (Berl). 2010 Apr;88(4):339-50. doi: 10.1007/s00109-009-0587-4. Epub 2010 Feb 3. Review.

PMID:
20127478
6.

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
7.

Charcot-Marie-Tooth disease: a clinico-genetic confrontation.

Barisic N, Claeys KG, Sirotković-Skerlev M, Löfgren A, Nelis E, De Jonghe P, Timmerman V.

Ann Hum Genet. 2008 May;72(Pt 3):416-41. doi: 10.1111/j.1469-1809.2007.00412.x. Epub 2008 Jan 23. Review.

8.

The genetic convergence of Charcot-Marie-Tooth disease types 1 and 2 and the role of genetics in sporadic neuropathy.

Boerkoel CF, Takashima H, Lupski JR.

Curr Neurol Neurosci Rep. 2002 Jan;2(1):70-7. Review.

PMID:
11898586
9.

[Charcot-Marie-Tooth disease].

Lee YC, Chang MH, Lin KP.

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

PMID:
18975529
10.

Dynamin 2 in Charcot-Marie-Tooth disease.

Tanabe K, Takei K.

Acta Med Okayama. 2012;66(3):183-90. Review.

11.

Genetic evaluation of inherited motor/sensory neuropathy.

Chance PF.

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

PMID:
16106622
12.
13.

[Molecular genetics of Charcot-Marie-Tooth disease].

Zhang YZ, Zhong N.

Beijing Da Xue Xue Bao. 2005 Feb 18;37(1):100-5. Review. Chinese.

14.

Autosomal-recessive Charcot-Marie-Tooth diseases.

Vallat JM, Tazir M, Magdelaine C, Sturtz F, Grid D.

J Neuropathol Exp Neurol. 2005 May;64(5):363-70. Review.

PMID:
15892292
15.

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
16.

Intermediate Charcot-Marie-Tooth disease.

Liu L, Zhang R.

Neurosci Bull. 2014 Dec;30(6):999-1009. doi: 10.1007/s12264-014-1475-7. Epub 2014 Oct 17. Review.

PMID:
25326399
17.

The dominantly inherited motor and sensory neuropathies: clinical and molecular advances.

Nicholson GA.

Muscle Nerve. 2006 May;33(5):589-97. Review.

PMID:
16392117
18.

Molecular genetics of autosomal-recessive axonal Charcot-Marie-Tooth neuropathies.

Bernard R, De Sandre-Giovannoli A, Delague V, Lévy N.

Neuromolecular Med. 2006;8(1-2):87-106. Review.

PMID:
16775369
19.

Role of dynamin 2 in the disassembly of focal adhesions.

Briñas L, Vassilopoulos S, Bonne G, Guicheney P, Bitoun M.

J Mol Med (Berl). 2013 Jul;91(7):803-9. doi: 10.1007/s00109-013-1040-2. Epub 2013 Apr 23. Review.

PMID:
23609221
20.

Charcot-Marie-tooth disease.

Casasnovas C, Cano LM, Albertí A, Céspedes M, Rigo G.

Foot Ankle Spec. 2008 Dec;1(6):350-4. doi: 10.1177/1938640008326247. Epub 2008 Oct 22. Review.

PMID:
19825739

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