(Q33733242)

English

Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

hereditary motor and sensory neuropathy

0 references

neurophysiology

1 reference

based on heuristic

inferred from title

muscular atrophy

1 reference

based on heuristic

inferred from title

author name string

Frith JA

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

McLeod JG

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Nicholson GA

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Yang F

4

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Europe PubMed Central

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29 July 2017

language of work or name

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publication date

1 November 1994

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Europe PubMed Central

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29 July 2017

Journal of Neurology, Neurosurgery and Psychiatry

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Europe PubMed Central

PubMed publication ID

29 July 2017

57

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Europe PubMed Central

PubMed publication ID

29 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1343-1346

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Hereditary spastic paraplegia with amyotrophy and pes cavus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073184

21 June 2018

Peroneal muscular atrophy with pyramidal features

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073184

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073184

21 June 2018

Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073184

21 June 2018

Central motor conduction in a family with hereditary motor and sensory neuropathy with pyramidal signs (HMSN V)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073184

21 June 2018

Peroneal muscular atrophy (PMA) and related disorders. II. Histological findings in sural nerves

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073184

21 June 2018

Hypertrophic Charcot-Marie-Tooth disease. Light and electron microscope studies of the sural nerve

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073184

21 June 2018

Charcot-Marie-Tooth neuropathy type 1A mutation: apparent crossovers with D17S122 are due to a duplication

1 reference

https://pubmed.ncbi.nlm.nih.gov/7964809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary spastic paraplegia; report of a family with associated extrapyramidal signs

1 reference

https://pubmed.ncbi.nlm.nih.gov/7964809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7964809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peripheral neuropathy associated with polycythemia Vera

1 reference

https://pubmed.ncbi.nlm.nih.gov/7964809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7964809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JNNP.57.11.1343

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

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