Sensory Neuropathy, Hereditary

Known as: Neurogenic Acroosteolysis, Neurogenic Acroosteolyses, Neuropathies, Congenital Sensory 
 
National Institutes of Health

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Highly Cited
2011
Highly Cited
2011
DNA methyltransferase 1 (DNMT1) is crucial for maintenance of methylation, gene regulation and chromatin stability. DNA mismatch… (More)
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Highly Cited
2010
Highly Cited
2010
Neuropathic pain is accompanied by both positive and negative sensory signs. To explore the spectrum of sensory abnormalities… (More)
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Highly Cited
2009
Highly Cited
2009
CONTEXT Persistent pain and sensory disturbances following surgical treatment for breast cancer is a significant clinical problem… (More)
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Highly Cited
2004
Highly Cited
2004
One prominent feature of sensory responses in neocortex is that they rapidly adapt to increases in frequency, a process called… (More)
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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… (More)
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Highly Cited
2001
Highly Cited
2001
Hereditary sensory neuropathy type I (HSN1) is the most common hereditary disorder of peripheral sensory neurons. HSN1 is an… (More)
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Highly Cited
2001
Highly Cited
2001
Phantom limb pain is a frequent consequence of the amputation of a body part. Based on the finding that phantom limb pain is… (More)
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Highly Cited
1998
Highly Cited
1998
PURPOSE The Swedish Rectal Cancer Trial has unequivocally demonstrated that preoperative high-dose (5 x 5 Gy) radiotherapy… (More)
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Highly Cited
1998
Highly Cited
1998
The relationship between phantom limb phenomena and cortical reorganization was examined in five subjects with congenital absence… (More)
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Highly Cited
1995
Highly Cited
1995
OBJECTIVE To use punch skin biopsies to evaluate the loss of intra-epidermal nerve fibers in sensory neuropathies. BACKGROUND… (More)
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