Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero

Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype

Vincent Timmerman, Peter De Jonghe, C. Ceuterick et al. · Neurology · 1999 · 153 citations

Medicine, Genetics, Neurology +17

Two divergent types of nerve pathology in patients with different P sub 0 mutations in Charcot-Marie-Tooth disease

Anneke Gabreëls-Festen, Jessica E. Hoogendijk, P.H.S. Meijerink et al. · Neurology · 1996 · 149 citations

Medicine, Neurology, Pathology +17

Charcot-Marie-Tooth disease and related peripheral neuropathies.

Peter De Jonghe, Vincent Timmerman, Eva Nelis et al. · PubMed · 1997 · 115 citations

Medicine, Genetics, Molecular Genetics +17

Molecular bases of myelin formation as revealed by investigations on mice deficient in glial cell surface molecules

Rudolf Martini, M. Schachner · Glia · 1997 · 110 citations

Medicine, Neurobiology, Neuroscience +16

Autosornal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths

Aldo Quattrone, Antonio Gambardella, Francesco Bono et al. · Neurology · 1996 · 110 citations

Medicine, Neurology, Neuroscience +17