Coexistence of hereditary motor and sensory neuropathy type IA and IGM paraproteinemic neuropathy-Reference-Cited by-同舟云学术

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Coexistence of hereditary motor and sensory neuropathy type IA and IGM paraproteinemic neuropathy

Published:1993-06 Issue:6 Volume:33 Page:649-652
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Gregory R.,Thomas P. K.,King R. H. M.,Hallam P. L. J.,Malcolm S.,Hughes R. A. C.,Harding A. E.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference13 articles.

1. THE CLINICAL FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I AND II

2. Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

3. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

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

5. Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)

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1. Diagnosis and treatment of chronic acquired demyelinating polyneuropathies;Nature Reviews Neurology;2014-07-01

2. Genetically Determined Neuropathies;Biopsy Diagnosis of Peripheral Neuropathy;2014-06-23

3. Coexistence of Charcot-Marie-Tooth disease type 1A and anti-MAG neuropathy;Journal of the Peripheral Nervous System;2013-06

4. Immune-mediated components of hereditary demyelinating neuropathies: lessons from animal models and patients;The Lancet Neurology;2004-08

5. Differential diagnosis of Charcot-Marie-Tooth disease and related neuropathies;Neurological Sciences;2004-06

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