(Q33668220)

28 July 2017

title

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

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hereditary motor and sensory neuropathy

28 July 2017

main subject

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author name string

Harding AE

series ordinal

1

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28 July 2017

Thomas PK

series ordinal

2

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28 July 2017

language of work or name

English

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publication date

1 October 1980

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

17

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28 July 2017

issue

5

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28 July 2017

page(s)

329-336

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Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literature

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

A distal form of chronic spinal muscular atrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

Distal muscular dystrophy in an English family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

A recessively inherited mixed polyneuropathy of early onset.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

Linkage relations of locus for X-borne type of Charcot-Marie-Tooth muscular atrophy and that for Xg blood groups

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

Possible maternal effect on severity of neurofibromatosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048594

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

21 June 2018

1 reference

12 December 2020

Nerve conduction studies in Charcot-Marie-Tooth disease

1 reference

12 December 2020

Onion bulbs in a nerve biopsy specimen from an original case of Roussy-Lévy disease

1 reference

12 December 2020

Wide spectrum of motor conduction velocity in Charcot-Marie-Tooth disease. An anatomico-physiological interpretation

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 peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification

1 reference

12 December 2020

Observations on the syndrome of hypertrophic neuritis (the hypertrophic interstitial radiculo-neuropathies)

1 reference

12 December 2020

Extreme slowing of nerve conduction in peroneal muscular atrophy

1 reference

12 December 2020

Identifiers

0 references

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28 July 2017

1 reference