(Q40807240)

23 September 2017

1 reference

title

Hereditary motor and sensory neuropathy: HMSN type II (neuronal type) and X-linked HMSN. (English)

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hereditary motor and sensory neuropathy

23 September 2017

main subject

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author name string

Hahn AF

series ordinal

1

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23 September 2017

publication date

1 April 1993

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23 September 2017

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23 September 2017

volume

3

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23 September 2017

issue

2

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23 September 2017

page(s)

147-155

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

23 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

Hereditary motor and sensory neuropathy type I and type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

Peripheral and central sensory nerve conduction in Charcot-Marie-Tooth disease and comparison with Friedreich's ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

Hereditary motor sensory neuropathy type II with neurofilament accumulation: new finding or new disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

Murine motor neuron disease (the wobbler mouse): degeneration and regeneration of the lower motor neuron.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

The peroneal muscular atrophy syndrome. Clinical, genetic, electrophysiological and nerve biopsy studies. Part 2. Observations on pathological changes in sural nerve biopsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

Polyneuropathies in paediatrics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

X-linked dominant hereditary motor and sensory neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

X-linked dominant charcot-marie-tooth neuropathy with 15 cases in a family genetic linkage study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1750-3639.1993.TB00739.X

10.1111/J.1750-3639.1993.TB00739.X

21 January 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference