Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy (Q36507166)

14 August 2017

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title

Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy (English)

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hereditary neuropathy with liability to pressure palsies

14 August 2017

main subject

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author name string

Phillip F Chance

series ordinal

1

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14 August 2017

publication date

1 January 2006

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14 August 2017

published in

NeuroMolecular Medicine

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14 August 2017

volume

8

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14 August 2017

issue

1-2

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14 August 2017

page(s)

159-174

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https://scigraph.springernature.com/pub.10.1385/nmm:8:1-2:159

14 August 2017

exact match

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12 December 2020

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12 December 2020

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Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion

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12 December 2020

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12 December 2020

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Hereditary neuropathy with liability to pressure palsies is not a major cause of idiopathic carpal tunnel syndrome

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12 December 2020

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12 December 2020

Tomaculous neuropathy with unusual clinical aspects

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12 December 2020

A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies

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12 December 2020

HEREDITARY NEUROPATHY, WITH LIABILITY TO PRESSURE PALSIES; A CLINICAL AND ELECTROPHYSIOLOGICAL STUDY OF FOUR FAMILIES

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12 December 2020

A novel 3'-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies

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12 December 2020

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12 December 2020

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12 December 2020

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

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Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage

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12 December 2020

Filament formation of MSF-A, a mammalian septin, in human mammary epithelial cells depends on interactions with microtubules

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12 December 2020

Hereditary Neuropathy With Liability to Pressure Palsies and Inherited Brachial Plexus Neuropathy-Two Genetically Distinct Disorders

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Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit

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Fulminant case of hereditary neuropathy with liability to pressure palsy

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12 December 2020

A novel PMP22 point mutation causing HNPP phenotype: studies on nerve xenografts

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12 December 2020

Immune brachial plexus neuropathy: suggestive evidence for an inflammatory-immune pathogenesis

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12 December 2020

Hereditary recurrent brachial plexus neuropathy with dysmorphic features

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12 December 2020

Surgical treatment of a tomaculous neuropathy

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12 December 2020

Heredofamilial neuritis with brachial predilection

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12 December 2020

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

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12 December 2020

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities

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12 December 2020

Human peripheral myelin protein-22 carries the L2/HNK-1 carbohydrate adhesion epitope

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12 December 2020

The Septin 9 (MSF) gene is amplified and overexpressed in mouse mammary gland adenocarcinomas and human breast cancer cell lines

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12 December 2020

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

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12 December 2020

Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies

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12 December 2020

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12 December 2020

Unusual association of multiple sclerosis and tomaculous neuropathy

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12 December 2020

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Heredofamilial Brachial Plexus Neuropathy (Hereditary Neuralgic Amyotrophy with Brachial Predilection) in Childhood

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12 December 2020

Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A

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12 December 2020

Deletion of the PMP22 gene and hereditary neuropathy with liability to pressure palsies

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12 December 2020

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12 December 2020

Microsatellite mapping of the deletion in patients with hereditary neuropathy with liability to pressure palsies (HNPP): new molecular tools for the study of the region 17p12 --> p11 and for diagnosis

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3rd workshop of the European CMT consortium: 54th ENMC International Workshop on genotype/phenotype correlations in Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies 28-30 November 1997, Naarden, The Netherlands

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12 December 2020

The natural history of hereditary neuralgic amyotrophy in the Dutch population: two distinct types?

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12 December 2020

Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by interphase fluorescence in situ hybridization

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12 December 2020

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disorders

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12 December 2020

Underexpression of messenger RNA for peripheral myelin protein 22 in hereditary neuropathy with liability to pressure palsies

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12 December 2020

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study

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Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice

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12 December 2020

Identifiers

DOI

10.1385/NMM:8:1-2:159

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Dimensions Publication ID

14 August 2017

1053061647

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1 reference