(Q48429094)

11 February 2018

title

The natural history of Charcot-Marie-Tooth type 1A in adults: a 5-year follow-up study (English)

1 reference

11 February 2018

author

Johannes H T M Koelman

3

object named as

Johannes H T M Koelman

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11 February 2018

author name string

Camiel Verhamme

1

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11 February 2018

Ivo N van Schaik

2

1 reference

11 February 2018

Rob J de Haan

4

1 reference

11 February 2018

Marianne de Visser

5

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11 February 2018

language of work or name

English

0 references

publication date

1 December 2009

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11 February 2018

published in

Brain

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11 February 2018

volume

132

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11 February 2018

issue

Pt 12

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11 February 2018

page(s)

3252-3262

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11 February 2018

Peripheral myelin protein 22 is in complex with alpha6beta4 integrin, and its absence alters the Schwann cell basal lamina.

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Hand involvement in children with Charcot-Marie-Tooth disease type 1A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Clinical evaluator reliability for quantitative and manual muscle testing measures of strength in children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

The formation of peripheral myelin protein 22 aggregates is hindered by the enhancement of autophagy and expression of cytoplasmic chaperones

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.

21 January 2018

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https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Psychometric evaluation of a new sensory scale in immune-mediated polyneuropathies. Inflammatory Neuropathy Cause and Treatment (INCAT) Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

PMP22 overexpression causes dysmyelination in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

The Timed "up and go" test: reliability and validity in persons with unilateral lower limb amputation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Motor unit number estimation in human neurological diseases and animal models

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Reliability and validity of the CMT neuropathy score as a measure of disability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Reliability of clinical outcome measures in Charcot-Marie-Tooth disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

The numbers of limb motor neurons in the human lumbosacral cord throughout life

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Hand-held myometry: reference values

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Maximum voluntary isometric contraction: Reference values and clinical application

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWP251

21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWP251

1 reference

11 February 2018

1 reference

11 February 2018