The distal hereditary motor neuropathies

The distal hereditary motor neuropathies (dHMN) comprise a heterogenous group of diseases that share the common feature of a length-dependent predominantly motor neuropathy. Many forms of dHMN have minor sensory abnormalities and/or a significant upper-motor-neuron component, and there is often an o...

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Veröffentlicht in:	Journal of neurology, neurosurgery and psychiatry neurosurgery and psychiatry, 2012-01, Vol.83 (1), p.6-14
Hauptverfasser:	Rossor, Alexander M, Kalmar, Bernadett, Greensmith, Linda, Reilly, Mary M
Format:	Artikel
Sprache:	eng
Schlagworte:	Adenosine Triphosphatases - genetics Age ALS amyloid Amyotrophic lateral sclerosis Biological and medical sciences Cation Transport Proteins - genetics Charcot–Marie–Tooth disease Chromosomes Congenital diseases Copper-Transporting ATPases Cranial nerves. Spinal roots. Peripheral nerves. Autonomic nervous system. Gustation. Olfaction Disease distal hereditary motor neuropathy DNA-Binding Proteins - genetics Dynactin Complex Gene loci Genotype & phenotype Glycine-tRNA Ligase - genetics GTP-Binding Protein gamma Subunits - genetics Heat shock proteins Heat-Shock Proteins - genetics Hereditary Sensory and Motor Neuropathy - diagnosis Hereditary Sensory and Motor Neuropathy - genetics HMSN (Charcot–Marie–Tooth) HSP27 Heat-Shock Proteins - genetics Humans Medical sciences Microtubule-Associated Proteins - genetics motor neuron disease Muscular atrophy Mutation Nervous system (semeiology, syndromes) neurogenetics Neurology neuromuscular Paralysis peripheral neuropath peripheral neuropathology Protein-Serine-Threonine Kinases - genetics RNA Helicases - genetics spinal hereditary and sensory motor neuropathy Transcription Factors - genetics TRPV Cation Channels - genetics
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