(Q57728135)

English

Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity

scientific article published on 01 January 2000

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677858%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677858%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Mustafa A. Salih

1

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4 November 2019

author name string

T Maisonobe

2

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Europe PubMed Central

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4 November 2019

M Kabiraj

3

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4 November 2019

M Akbar

6

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4 November 2019

A Tahan

7

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4 November 2019

D Grid

9

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4 November 2019

T Hamadouche

10

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4 November 2019

A Guilbot

11

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4 November 2019

A Brice

12

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4 November 2019

E Leguern

13

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4 November 2019

M al Rayess

4

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4 November 2019

M H al-Turaiki

5

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4 November 2019

J A Urtizberea

8

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4 November 2019

publication date

1 January 2000

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4 November 2019

Neuromuscular Disorders

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4 November 2019

10

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4 November 2019

1

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4 November 2019

10-15

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4 November 2019

Autosomal recessive forms of hereditary motor and sensory neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal recessive form of hereditary motor and sensory neuropathy type I.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary demyelinating motor and sensory neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

A clinical, electrophysiologic, neuropathologic, and genetic study of two large Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary motor and sensory neuropathy--Lom, a novel demyelinating neuropathy associated with deafness in gypsies. Clinical, electrophysiological and nerve biopsy findings

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Globular neuropathy. A disorder of axons and Schwann cells

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Variability of morphological features in early infantile polyneuropathy with defective myelination

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital hypo- and hypermyelination neuropathy. Two cases

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary motor and sensory neuropathy with myelin outfolding: Clinical, genetic and neuropathological study of three cases

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal recessive motor and sensory neuropathy with excessive myelin outfolding in two siblings

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

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Autosomal recessive hypermyelinating neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B).

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900057-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0960-8966(99)00057-7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677858%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10677858%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

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