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Items: 1 to 20 of 145

1.

Charcot-Marie-Tooth disease: emerging mechanisms and therapies.

d'Ydewalle C, Benoy V, Van Den Bosch L.

Int J Biochem Cell Biol. 2012 Aug;44(8):1299-304. doi: 10.1016/j.biocel.2012.04.020. Epub 2012 Apr 30. Review.

PMID:
22575637
2.

Axonal Charcot-Marie-Tooth disease.

Shy ME, Patzkó A.

Curr Opin Neurol. 2011 Oct;24(5):475-83. doi: 10.1097/WCO.0b013e32834aa331. Review.

PMID:
21892080
3.

Mechanisms of disease: inherited demyelinating neuropathies--from basic to clinical research.

Nave KA, Sereda MW, Ehrenreich H.

Nat Clin Pract Neurol. 2007 Aug;3(8):453-64. Review.

PMID:
17671523
4.

Charcot-Marie-Tooth disease: an update.

Shy ME.

Curr Opin Neurol. 2004 Oct;17(5):579-85. Review.

PMID:
15367862
5.

The various Charcot-Marie-Tooth diseases.

Vallat JM, Mathis S, Funalot B.

Curr Opin Neurol. 2013 Oct;26(5):473-80. doi: 10.1097/WCO.0b013e328364c04b. Review.

PMID:
23945280
6.

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.

De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Lévy N.

Am J Hum Genet. 2002 Mar;70(3):726-36. Epub 2002 Jan 17. Erratum in: Am J Hum Genet 2002 Apr;70(4):1075.

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.

HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth disease.

d'Ydewalle C, Krishnan J, Chiheb DM, Van Damme P, Irobi J, Kozikowski AP, Vanden Berghe P, Timmerman V, Robberecht W, Van Den Bosch L.

Nat Med. 2011 Jul 24;17(8):968-74. doi: 10.1038/nm.2396.

PMID:
21785432
9.

A rat model of Charcot-Marie-Tooth disease 1A recapitulates disease variability and supplies biomarkers of axonal loss in patients.

Fledrich R, Schlotter-Weigel B, Schnizer TJ, Wichert SP, Stassart RM, Meyer zu Hörste G, Klink A, Weiss BG, Haag U, Walter MC, Rautenstrauss B, Paulus W, Rossner MJ, Sereda MW.

Brain. 2012 Jan;135(Pt 1):72-87. doi: 10.1093/brain/awr322. Epub 2011 Dec 20.

10.

Update on Charcot-Marie-Tooth disease.

Patzkó A, Shy ME.

Curr Neurol Neurosci Rep. 2011 Feb;11(1):78-88. doi: 10.1007/s11910-010-0158-7. Review.

11.

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.

12.

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
13.

The Wlds transgene reduces axon loss in a Charcot-Marie-Tooth disease 1A rat model and nicotinamide delays post-traumatic axonal degeneration.

Meyer zu Horste G, Miesbach TA, Muller JI, Fledrich R, Stassart RM, Kieseier BC, Coleman MP, Sereda MW.

Neurobiol Dis. 2011 Apr;42(1):1-8. doi: 10.1016/j.nbd.2010.12.006. Epub 2010 Dec 16.

PMID:
21168501
14.

Myelin disorders: Causes and perspectives of Charcot-Marie-Tooth neuropathy.

Meyer zu Hörste G, Prukop T, Nave KA, Sereda MW.

J Mol Neurosci. 2006;28(1):77-88. Review.

PMID:
16632877
15.

Disease mechanisms and potential therapeutic strategies in Charcot-Marie-Tooth disease.

Young P, Suter U.

Brain Res Brain Res Rev. 2001 Oct;36(2-3):213-21. Review.

PMID:
11690618
16.

Murine therapeutic models for Charcot-Marie-Tooth (CMT) disease.

Fledrich R, Stassart RM, Sereda MW.

Br Med Bull. 2012 Jun;102:89-113. doi: 10.1093/bmb/lds010. Epub 2012 May 2. Review.

PMID:
22551516
17.

Charcot-Marie-Tooth neuropathies: diagnosis and management.

Jani-Acsadi A, Krajewski K, Shy ME.

Semin Neurol. 2008 Apr;28(2):185-94. doi: 10.1055/s-2008-1062264. Review.

PMID:
18351520
18.

Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease.

Fabrizi GM, Ferrarini M, Cavallaro T, Cabrini I, Cerini R, Bertolasi L, Rizzuto N.

Neurology. 2007 Jul 17;69(3):291-5.

PMID:
17636067
19.

Animal models of inherited neuropathies.

Meyer Zu Hörste G, Nave KA.

Curr Opin Neurol. 2006 Oct;19(5):464-73. Review.

PMID:
16969156
20.

The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene.

Chaouch M, Allal Y, De Sandre-Giovannoli A, Vallat JM, Amer-el-Khedoud A, Kassouri N, Chaouch A, Sindou P, Hammadouche T, Tazir M, Lévy N, Grid D.

Neuromuscul Disord. 2003 Jan;13(1):60-7.

PMID:
12467734
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