(Q43650936)

25 November 2017

title

Increased intracortical facilitation in patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p. (English)

1 reference

25 November 2017

2

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Anders Fuglsang-Frederiksen

25 November 2017

series ordinal

5

object named as

A Fuglsang-Frederiksen

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25 November 2017

J E Nielsen

1

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25 November 2017

K Fenger

series ordinal

3

1 reference

25 November 2017

S A Sørensen

series ordinal

4

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25 November 2017

publication date

1 July 2001

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European Journal of Neurology

25 November 2017

published in

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25 November 2017

volume

8

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25 November 2017

issue

4

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25 November 2017

page(s)

335-339

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Intracortical inhibition and facilitation are abnormal in Huntington's disease: a paired magnetic stimulation study

25 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Strümpell's familial spastic paraplegia: genetics and neuropathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

The neuropathology of hereditary spastic paraparesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Classification of the hereditary ataxias and paraplegias

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Strumpell's pure familial spastic paraplegia: case study and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Molecular genetics of familial spastic paraplegia: a multitude of responsible genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Corticocortical inhibition in human motor cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Analysis of serial measurements in medical research

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Electrophysiological studies in familial spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Urodynamic evaluation of patients with autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Motor and somatosensory evoked potentials in hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

A quantitative study of sensory function in hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Double cortical stimulation in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Dextromethorphan decreases the excitability of the human motor cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

Effects of antiepileptic drugs on motor cortex excitability in humans: a transcranial magnetic stimulation study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2001.00249.X

10.1046/J.1468-1331.2001.00249.X

21 January 2018

Identifiers

DOI

1 reference

25 November 2017

1 reference