Hereditary motor and sensory neuropathies
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),General Medicine,Surgery
Reference109 articles.
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3. Localization of X-linked dominant Charcot-Marie-Tooth disease (CMT 2) to Xq 13;Beckett;J. Neurogenet.,1986
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1. PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies;Orphanet Journal of Rare Diseases;2014
2. Hand strength and fatigue in patients with hereditary motor and sensory neuropathy (types I and II);Archives of Physical Medicine and Rehabilitation;2002-09
3. Peripheral nerve extracellular matrix remodeling in Charcot-Marie-Tooth type I disease;Acta Neuropathologica;2002-09
4. Molecular genetic analysis of Charcot–Marie–Tooth 1A duplication in Norwegian patients by quantitative photostimulated luminescence imaging;Journal of the Neurological Sciences;2001-07
5. EGR2 mutation R359W causes a spectrum of Dejerine-Sottas neuropathy;Neurogenetics;2001-03-15
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