Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot–Marie–Tooth disease

By Dubourg O.  

Brain, Vol. 124, Iss. 10, 2001-10 ,pp. : 1958-1967

Oxford University Press

Access to resources Recommend Favorite

Clinical progression in Charcot–Marie-Tooth disease type 1A duplication: clinico-electrophysiological and MRI longitudinal study of a family

By Berciano José   Gallardo Elena   García Antonio   Ramón César   Infante Jon   Combarros Onofre  

Journal of Neurology, Vol. 257, Iss. 10, 2010-10 ,pp. : 1633-1641

Springer Publishing Company

Access to resources Recommend Favorite

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

By Sevilla T.  

Brain, Vol. 126, Iss. 9, 2003-09 ,pp. : 2023-2033

Oxford University Press

Access to resources Recommend Favorite

Pathomechanisms of Mutant Proteins in Charcot-Marie-Tooth Disease

By  

NeuroMolecular Medicine, Vol. 8, Iss. 1-2, 2006-03 ,pp. : 217-242

Humana Press, Inc

Access to resources Recommend Favorite

Molecular cell biology of Charcot-Marie-Tooth disease

By Berger Philipp   Young Peter   Suter Ueli  

Neurogenetics, Vol. 4, Iss. 1, 2002-03 ,pp. : 1-15

Springer Publishing Company

Access to resources Recommend Favorite