(Q33596441)

28 July 2017

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title

Hereditary motor and sensory neuropathies (English)

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28 July 2017

J M Vance

1

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PubMed ID

1999826

28 July 2017

language of work or name

English

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publication date

1 January 1991

1 reference

Journal of Medical Genetics

28 July 2017

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28 July 2017

28

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28 July 2017

1-5

1 reference

28 July 2017

1

1 reference

Sequential tests for the detection of linkage

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Autosomal recessive forms of hereditary motor and sensory neuropathy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Genetic aspects of hereditary motor and sensory neuropathy (types I and II)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Alpha 1-antitrypsin: apparent molecular weight heterogeneity shown by two-dimensional electrophoresis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

The hypertrophic forms of hereditary motor and sensory neuropathy. A study of hypertrophic Charcot-Marie-Tooth disease (HMSN type I) and Dejerine-Sottas disease (HMSN type III) in childhood

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type I.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and human.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Charcot-Marie-Tooth disease: data for genetic counseling relating age to risk

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016739

Pooled European series of hereditary peripheral neuropathies in infancy and childhood. A "correspondence work shop" report of the European Federation of Child Neurology Societies (EFCNS)

28 July 2018

1 reference

12 December 2020

Linkage evidence for genetic heterogeneity among kinships with hereditary motor and sensory neuropathy, type I

1 reference

12 December 2020

Evolution of nerve conduction abnormalities in children with dominant hypertrophic neuropathy of the Charcot-Marie-Tooth type

1 reference

12 December 2020

X-linked neuropathy: gene localization with DNA probes

1 reference

12 December 2020

Linkage analysis of Charcot-Marie-Tooth neuropathy (HMSN type I)

1 reference

12 December 2020

Hereditary motor and sensory neuropathy, X-linked: a half century follow-up

1 reference

12 December 2020

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

1 reference

12 December 2020

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

1 reference

12 December 2020

Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy)

1 reference

12 December 2020

The clinical features of hereditary motor and sensory neuropathy types I and II

1 reference

12 December 2020

Linkage between the loci for autosomal dominant neuronal Charcot-Marie-Tooth neuropathy (CMT1) and serum amyloid P component (APCS) on human chromosome 1.

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.28.1.1

1 reference

28 July 2017

1 reference

28 July 2017

1 reference

PubMed ID

1999826