Recurrent polyradiculoneuropathy with the 17p11.2 deletion-Reference-Cited by-同舟云学术

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Recurrent polyradiculoneuropathy with the 17p11.2 deletion

Published:1997-09 Issue:9 Volume:20 Page:1184-1186
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Le Forestier Nadine,LeGuern Eric,Coullin Philippe,Birouk Nazha,Maisonobe Thierry,Brice Alexis,L�ger Jean Marc,Bouche Pierre

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference11 articles.

1. Tomaculous neuropathy: A clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p<11.2

2. DNA deletion associated with hereditary neuropathy with liability to pressure palsies

3. Hereditary Neuropathy with Liability to Pressure Palsies Masquerading as Slowly Progressive Polyneuropathy

4. Clinical, electrophysiologic, and molecular correlations in 13 families with hereditary neuropathy with liability to pressure palsies and a chromosome 17p11.2 deletion

5. : Guillain-Barré Syndrome. London, Springer-Verlag, 1990.

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1. Hereditary neuropathy with liability to pressure palsies;Journal of Neurology;2019-04-15

2. Neuropatie ereditarie da ipersensibilità alla pressione (neuropatia tomaculare o allantoidea);EMC - Neurologia;2018-04

3. Hereditary and inflammatory neuropathies: a review of reported associations, mimics and misdiagnoses;Journal of Neurology, Neurosurgery & Psychiatry;2016-03-23

4. Unusual presentation of hereditary neuropathy with liability to pressure palsies;Journal of Brachial Plexus and Peripheral Nerve Injury;2014-09-17

5. Hereditary neuropathy with liability to pressure palsy;Peripheral nerve disorders;2014-08-11

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