Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with charcot-marie-tooth disease 1A duplication (Q74015122)

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scientific article published on 01 August 2000

Language	Label	Description	Also known as
English	Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with charcot-marie-tooth disease 1A duplication	scientific article published on 01 August 2000

Statements

scholarly article

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8 November 2019

Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with charcot-marie-tooth disease 1A duplication (English)

1 reference

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8 November 2019

author name string

J Berciano

1

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8 November 2019

A García

2

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8 November 2019

J Calleja

3

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8 November 2019

O Combarros

4

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8 November 2019

publication date

1 August 2000

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8 November 2019

Neuromuscular Disorders

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8 November 2019

10

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8 November 2019

6

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8 November 2019

419-424

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8 November 2019

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900114-5

7 January 2021

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From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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Longitudinal study of neuropathic deficits and nerve conduction abnormalities in hereditary motor and sensory neuropathy type 1

1 reference

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7 January 2021

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Longitudinal studies of the duplication form of Charcot-Marie-Tooth polyneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900114-5

7 January 2021

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Axonal pathology in demyelinating diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900114-5

7 January 2021

based on heuristic

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Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1.

1 reference

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Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtype

1 reference

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Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I)

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Prevalence of hereditary motor and sensory neuropathy in Cantabria

1 reference

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7 January 2021

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The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy type I

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900114-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900114-5

7 January 2021

based on heuristic

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Motor and sensory conduction in infancy and childhood: reappraisal

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900114-5

7 January 2021

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Electrophysiologic correlates of peripheral nervous system maturation in infancy and childhood

1 reference

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7 January 2021

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Detection of hereditary motor sensory neuropathy type I in childhood

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7 January 2021

based on heuristic

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The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies

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7 January 2021

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Nerve conduction and biopsy correlation in over 100 consecutive patients with suspected polyneuropathy

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Effects of PMP22 duplication and deletions on the axonal cytoskeleton

1 reference

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7 January 2021

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Distal axonopathy in peripheral nerves of PMP22-mutant mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2899%2900114-5

7 January 2021

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Identifiers

10.1016/S0960-8966(99)00114-5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899448%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10899448%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

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