(Q33629602)

28 July 2017

title

Autosomal recessive hereditary motor and sensory neuropathy with mental retardation, optic atrophy and pyramidal signs (English)

1 reference

hereditary motor and sensory neuropathy

28 July 2017

main subject

0 references

1 reference

MacDermot KD

1

1 reference

28 July 2017

Walker RW

series ordinal

2

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 October 1987

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

28 July 2017

published in

1 reference

28 July 2017

volume

50

1 reference

28 July 2017

issue

10

1 reference

28 July 2017

page(s)

1342-1347

1 reference

Peroneal muscular atrophy with pyramidal features

28 July 2017

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032462

The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting

21 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032462

X-linked motor-sensory neuropathy type-II with deafness and mental retardation: a new disorder.

21 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1032462

Familial opticoacoustic nerve degeneration and polyneuropathy

21 June 2018

1 reference

12 December 2020

Optic atrophy, neural deafness, and distal neurogenic amyotrophy; report of a family with two affected siblings

1 reference

12 December 2020

Hereditary polyneuropathy, oligophrenia, premature menopause and acromicria. A new syndrome

1 reference

12 December 2020

ON THE SUPRASPINAL EXTENSION OF LESIONS IN CHARCOT-MARIE-TOOTH 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

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

1 reference

12 December 2020

Charcot-Marie-Tooth disease with Leber optic atrophy

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.50.10.1342

1 reference

28 July 2017

1 reference

28 July 2017

1 reference