(Q58183378)

4

object named as

Johannes H.T.M. Koelman

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author name string

Henriette M.E. Bienfait

1

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Camiel Verhamme

2

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Ivo N. Schaik

3

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Bram W. Ongerboer Visser

5

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Rob J. Haan

6

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Baziel G.M. Engelen

8

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Marianne Visser

https://scigraph.springernature.com/pub.10.1007/s00415-006-0260-6

9

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publication date

28 August 2006

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published in

Journal of Neurology

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volume

253

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issue

12

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page(s)

1572-1580

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exact match

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cites work

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00415-006-0260-6

Relation between size of compound sensory or muscle action potentials, and length of nerve segment

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00415-006-0260-6

Uniform slowing of conduction velocities in Charcot-Marie-Tooth polyneuropathy type 1

21 January 2018

1 reference

12 December 2020

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

1 reference

12 December 2020

Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities

1 reference

12 December 2020

Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy

1 reference

12 December 2020

2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot-Marie-Tooth Type 2 (CMT2-HMSN II) and Distal Hereditary Motor Neuropathy (distal HMN-Spinal CMT) 26-28 September 19

1 reference

12 December 2020

A model of the differing change in motor and sensory action potentials over distance

1 reference

12 December 2020

The clinical features of hereditary motor and sensory neuropathy types I and II

1 reference

12 December 2020

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

1 reference

12 December 2020

Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography

1 reference

12 December 2020

The phenotypic manifestations of chromosome 17p11.2 duplication.

1 reference

12 December 2020

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy

1 reference

12 December 2020

Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Conduction velocity distributions of the human median nerve: comparison of methods

1 reference

12 December 2020

Peroneal muscular atrophy. Part 1. Clinical and electrophysiological study

1 reference

12 December 2020

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

1 reference

12 December 2020

Assessment of axonal loss in Charcot-Marie-Tooth neuropathies

1 reference

12 December 2020

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Motor unit number estimate of distal and proximal muscles in Charcot-Marie-Tooth disease

1 reference

12 December 2020

The distribution of conduction velocities (DCV) in peripheral nerves: A review

1 reference

12 December 2020

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

1 reference

12 December 2020

Peroneal muscular atrophy (PMA) and related disorders. II. Histological findings in sural nerves

1 reference

12 December 2020

No adjustments are needed for multiple comparisons

1 reference

12 December 2020

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

1 reference

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

The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies

1 reference

12 December 2020

The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification

1 reference

12 December 2020

Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L

1 reference

12 December 2020

Effect of desynchronized inputs on compound sensory and muscle action potentials

1 reference

12 December 2020

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

1 reference

12 December 2020