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Hereditary Motor and Sensory Neuropathies

Known as: HMSN, Herditary Sensory and Motor Neuropathy, Hereditary Sensory and Motor Neuropathy 
A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both… 
National Institutes of Health

Related topics

Related topics

30 relations

Narrower (18)

Cardioneuromyopathy with Hyaline Masses and Nemaline RodsCharcot-Marie-Tooth DiseaseHagemoser Weinstein Bresnick syndromeHereditary Motor and Sensory Neuropathy Type I
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Congenital Pain InsensitivityDejerine-Sottas Disease (disorder)Hanel's syndromeHereditary peripheral neuropathy
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Broader (1)

Sensory neuropathy

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2004
Highly Cited
2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy
Distal hereditary motor neuropathies are pure motor disorders of the peripheral nervous system resulting in severe atrophy and… 
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Review
2002
Review
2002
Hereditary motor and sensory neuropathies: a biological perspective
Mutations in genes expressed in Schwann cells and the axons they ensheath cause the hereditary motor and sensory neuropathies… 
Highly Cited
2000
Highly Cited
2000
N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom.
Hereditary motor and sensory neuropathies, to which Charcot-Marie-Tooth (CMT) disease belongs, are a common cause of disability… 
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Highly Cited
1995
Highly Cited
1995
Strength training in patients with myotonic dystrophy and hereditary motor and sensory neuropathy: a randomized clinical trial.
A randomized clinical trial on the effects of strength training was performed in myotonic dystrophy (MyD) patients and patients… 
Review
1991
Review
1991
Hereditary motor and sensory neuropathies.
  • J. Vance
  • Journal of medical genetics
  • 1991
  • Corpus ID: 8473784
The hereditary motor and sensory neuropathies (HMSN) represent a genetically heterogeneous collection of disorders in which… 
Highly Cited
1991
Highly Cited
1991
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
Hereditary motor and sensory neuropathy type I (HMSN I) or Charcot-Marie-Tooth disease type 1 (CMT 1) is an autosomal dominant… 
Highly Cited
1990
Highly Cited
1990
X-linked dominant hereditary motor and sensory neuropathy.
Modern techniques have defined the hereditary motor and sensory neuropathies (HMSN) as a genetically heterogeneous group of… 
Highly Cited
1982
Highly Cited
1982
Prednisone-responsive hereditary motor and sensory neuropathy.
Neurologic improvement with use of prednisone, in some cases on several occasions, was demonstrated in seven patients who had a… 
Highly Cited
1980
Highly Cited
1980
The clinical features of hereditary motor and sensory neuropathy types I and II.
Observations have been made on a series of 228 patients with hereditary motor and sensory neuropathy, comprising 120 index cases… 
Highly Cited
1980
Highly Cited
1980
Genetic aspects of hereditary motor and sensory neuropathy (types I and II)
The genetic features of a series of 227 patients with hereditary motor and sensory neuropathy (HMSN) have been analysed. The… 
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