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Hereditary liability to pressure palsies

Known as: Neuropathy, Hereditary, With Liability To Pressure Palsies, HNPP, Hereditary Pressure Sensitive Neuropathy 
National Institutes of Health

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7 relations

Broader (2)

ArthrogryposisHereditary Motor and Sensory Neuropathies
Autosomal dominant inheritanceEntrapment NeuropathiesNerve compression syndromePMP22 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
A Joint FED Watermarking System Using Spatial Fusion for Verifying the Security Issues of Teleradiology
Teleradiology allows transmission of medical images for clinical data interpretation to provide improved e-health care access… 
Review
2006
Review
2006
Molecular genetics of autosomal-dominant demyelinating Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease (CMT) is a clinically and genetically heterogeneous group of disorders and is the most common… 
2005
2005
Insurance and the tort system
This article examines Stapleton's view that insurance has lacked influence and been no more than a ‘makeweight’ argument in the… 
2003
2003
A rapid and definitive test for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies using multiplexed real-time PCR.
Alterations in gene copy number have been shown to cause disease in humans. Two of the most common inherited peripheral… 
1999
1999
Abundance and distribution of bacteria carrying sltII gene in natural river water
Direct in situ PCR with HNPP/Fast Red TR was used to enumerate bacteria carrying the sltII gene in river water. By direct in situ… 
1997
1997
A Transgenic Mouse Model for Human Hereditary Neuropathy with Liability to Pressure Palsies
Mutations in the gene encoding peripheral myelin protein 22 (PMP22) account for several inherited peripheral neuropathies in… 
1997
1997
Correlation between PMP‐22 messenger mRNA expression and phenotype in hereditary neuropathy with liability to pressure palsies
Hereditary neuropathy with liability to pressure palsies (HNPP) is associated with a deletion in chromosome 17p 11.2, which… 
1997
1997
Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2
Clinical and electrophysiological studies were performed in affected and unaffected individuals from five unrelated families… 
1996
1996
A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?
Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant neuropathy, most often associated with a… 
1989
1989
Tomaculous neuropathy presenting as acute recurrent polyneuropathy
Tomaculous neuropathy (TN) is classically associated with the inherited, recurrent focal neuropathies. We report a case of TN… 
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