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Idiopathic Neuropathy

Known as: Unspecified idiopathic peripheral neuropathy 
Neuropathy, the cause of which is not known.
National Institutes of Health

Related topics

Related topics

9 relations

Narrower (3)

Charcot-Marie-Tooth DiseaseHereditary Sensory and Autonomic NeuropathiesRefsum Disease
Dejerine-Sottas Disease (disorder)Nervous system structurePeripheral Nerves

Broader (3)

Peripheral NeuropathyPolyneuropathynervous system disorder

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Reduced expression of Munc13-1 in human and porcine diabetic peripheral nerve.
2010
2010
Are anti-ganglioside antibodies of clinical value in multifocal motor neuropathy?
Pestronk and colleagues1 first reported antibodies to GMl ganglioside in a treatable form of multifocal motor neuropathy (MMN) in… 
2010
2010
Unilateral painful diaphragm paralysis as the only sign of amyotrophic neuralgia
2005
2005
APOE ε4 is not a susceptibility gene in idiopathic or diabetic sensory neuropathy
The presence of an APOE ε4 allele may be a risk factor for neuropathy severity in diabetes. The authors assessed the frequency of… 
2005
2005
APOE epsilon4 is not a susceptibility gene in idiopathic or diabetic sensory neuropathy.
The presence of an APOE epsilon4 allele may be a risk factor for neuropathy severity in diabetes. The authors assessed the… 
Highly Cited
2004
Highly Cited
2004
Prognostic ability of Tinel sign in determining outcome for decompression surgery in diabetic and nondiabetic neuropathy.
During the past 12 years, 6 studies reported restoration of sensation and relief of pain in the foot by decompression of the… 
2000
2000
Results of testing for anti-GM1 antibodies
We used an ELISA technique to measure IgG and IgM antibodies to the ganglioside GM1, with the results expressed in arbitrary… 
Review
1999
Review
1999
Charcot-Marie-Tooth disease type 2.
No unique genes have yet been found for CMT2, but both Cx32 and P0 appear to contribute to the phenotype. Not surprisingly, CMT2… 
1999
1999
Charcot‐Marie‐Tooth Disease Type 2
ABSTRACT: No unique genes have yet been found for CMT2, but both Cx32 and P0 appear to contribute to the phenotype. Not… 
1994
1994
Dysautonomia with acute sensory motor neuropathy. A new classification of acute autonomic neuropathy.
OBJECTIVES To characterize the dysautonomia associated with acute sensory motor neuropathy and to discuss the classification of… 
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