(Q58184730)

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Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2

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scholarly article

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Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2 (English)

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hereditary neuropathy with liability to pressure palsies

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object named as

F. Palau

5

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author name string

A. Cruz-Martínez

1

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S. Bort

2

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J. Arpa

3

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J. Duarte

4

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publication date

May 1997

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European Journal of Neurology

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4

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3

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274-286

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Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological aspects.

1 reference

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Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies

1 reference

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Brachial plexus involvement in familial pressure-sensitive neuropathy: electrophysiological and morphological findings.

1 reference

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21 January 2018

Electrophysiological aspects of sensory conduction velocity in healthy adults. 1. Conduction velocity from digit to palm, from palm to wrist, and across the elbow, as a function of age

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

21 January 2018

Electrophysiological aspects of sensory conduction velocity in healthy adults. 2. Ratio between the amplitude of sensory evoked potentials at the wrist on stimulating different fingers in both hands

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

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Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies

1 reference

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Recurrent familial brachial plexus palsies as the only clinical expression of 'tomaculous' neuropathy

1 reference

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21 January 2018

COMPRESSION OF THE LATERAL POPLITEAL (COMMON PERONEAL) NERVE.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

21 January 2018

Hereditary neuropathy with liability to pressure palsies. Report of two families and review of the literature

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

21 January 2018

A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

21 January 2018

Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

21 January 2018

Central motor conduction times using transcranial stimulation and F wave latencies.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

21 January 2018

Familial recurrent polyneuropathy. A family and a survey

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

21 January 2018

DNA analysis in Finnish patients with hereditary neuropathy with liability to pressure palsies (HNPP).

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

21 January 2018

Slimmer's paralysis--peroneal neuropathy during weight reduction

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.1997.TB00347.X

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Hereditary compression syndrome of peripheral nerves.

1 reference

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21 January 2018

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10.1111/J.1468-1331.1997.TB00347.X

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