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Hereditary Sensory Autonomic Neuropathy, Type 1

Known as: Hereditary Sensory and Autonomic Neuropathy Type I, HSN Type I, HSAN IA 
 
National Institutes of Health

Papers overview

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Review
2012
Review
2012
BACKGROUND Patients with neuropathic pain present with various pain-related sensory abnormalities. These sensory features form… Expand
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Highly Cited
2011
Highly Cited
2011
Hereditary sensory and autonomic neuropathy type 1 (HSAN1) causes sensory loss that predominantly affects the lower limbs, often… Expand
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Highly Cited
2007
Highly Cited
2007
Patterns of sensory abnormalities in children and adults with autism were examined using the Diagnostic Interview for Social and… Expand
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Highly Cited
2006
Highly Cited
2006
Hereditary sensory and autonomic neuropathy type I (HSAN I) is the most frequent type of hereditary neuropathy that primarily… Expand
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Highly Cited
2002
Highly Cited
2002
&NA; Our preliminary observations on a small group of burning mouth syndrome (BMS) patients indicated a change in the non… Expand
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Highly Cited
2001
Highly Cited
2001
Hereditary sensory neuropathy type 1 (HSN1, MIM 162400; ref. 1) genetically maps to human chromosome 9q22 (refs. 2–4). We report… Expand
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Review
1997
Review
1997
Sensory-perceptual abnormalities in people with autism are discussed from two perspectives: published firsthand accounts and… Expand
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Review
1994
Review
1994
The characteristic form and development of sensory disturbances during migraine auras suggests that the underlying mechanism is a… Expand
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Highly Cited
1992
Highly Cited
1992
We studied 71 patients with "paraneoplastic" encephalomyelitis, sensory neuronopathy, or both associated with the presence of the… Expand
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Highly Cited
1959
Highly Cited
1959
 
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