The Many Faces of Charcot-Marie-Tooth Disease
- 1 May 2000
- journal article
- editorial
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 57 (5) , 638-640
- https://doi.org/10.1001/archneur.57.5.638
Abstract
We shall not cease from exploration And the end of all our exploring Will be to arrive where we started And know the place for the first time.—T.S. EliotTHE WORKeywords
This publication has 8 references indexed in Scilit:
- Hereditary motor and sensory neuropathy type 2C is genetically distinct from types 2B and 2D.Archives of Neurology, 2000
- Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero geneJournal of Neurology, Neurosurgery & Psychiatry, 1999
- The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotypeBrain, 1999
- Charcot-Marie-Tooth disease: an intermediate formNeuromuscular Disorders, 1998
- X-linked dominant Charcot-Marie-Tooth disease: nerve biopsies allow morphological evaluation and detection of connexin32 mutations (Arg15Trp, Arg22Gln).Acta Neuropathologica, 1998
- Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24Human Molecular Genetics, 1996
- Hereditary motor and sensory neuropathy, X‐linkedNeurology, 1987
- Autosomal recessive forms of hereditary motor and sensory neuropathy.Journal of Neurology, Neurosurgery & Psychiatry, 1980