(Q81258363)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15645349%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15645349%20AND%20SRC:MED&resulttype=core&format=json

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15645349%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

author name string

Camiel Verhamme

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15645349%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

Ivo N van Schaik

2

1 reference

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7 January 2020

Rob J de Haan

4

1 reference

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7 January 2020

Marinus Vermeulen

5

1 reference

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7 January 2020

Marianne de Visser

6

1 reference

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7 January 2020

publication date

1 December 2004

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15645349%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15645349%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

251

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15645349%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

issue

12

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7 January 2020

page(s)

1491-1497

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00415-004-0578-x

7 January 2020

exact match

0 references

cites work

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

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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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12 December 2020

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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12 December 2020

Hereditary motor and sensory neuropathies: a biological perspective

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12 December 2020

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

1 reference

12 December 2020

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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12 December 2020