Clinical disease severity and axonal dysfunction in hereditary motor and sensory neuropathy Ia (Q81258363)

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7 January 2020

title

Clinical disease severity and axonal dysfunction in hereditary motor and sensory neuropathy Ia (English)

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hereditary motor and sensory neuropathy

7 January 2020

main subject

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author

Johannes H T M Koelman

3

object named as

Johannes H T M Koelman

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7 January 2020

author name string

Camiel Verhamme

1

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7 January 2020

Ivo N van Schaik

2

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7 January 2020

Rob J de Haan

4

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7 January 2020

Marinus Vermeulen

5

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7 January 2020

Marianne de Visser

6

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7 January 2020

publication date

1 December 2004

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7 January 2020

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7 January 2020

volume

251

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7 January 2020

issue

12

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7 January 2020

page(s)

1491-1497

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Scale development and Guy's Neurological Disability Scale

7 January 2020

cites work

1 reference

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Influence of recording site on CMAP amplitude on its variation over a length of nerve

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Large electrodes improve nerve conduction repeatability in controls as well as in patients with diabetic neuropathy

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Coexistent hereditary and inflammatory neuropathy

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Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance

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Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood: a longitudinal clinical and electrophysiologic study

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Effects of PMP22 duplication and deletions on the axonal cytoskeleton

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Altered slow axonal transport and regeneration in a myelin-deficient mutant mouse: the trembler as an in vivo model for Schwann cell-axon interactions

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No adjustments are needed for multiple comparisons

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

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

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PMP22 overexpression causes dysmyelination in mice.

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Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases

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

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Reference values for touch sensibility thresholds in healthy Nepalese volunteers.

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

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The Sickness Impact Profile: Development and Final Revision of a Health Status Measure

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Hand-held myometry: reference values

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

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Prednisone-responsive hereditary motor and sensory neuropathy

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