Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study (Q36317599)

13 August 2017

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

1 reference

13 August 2017

3

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13 August 2017

Nielsen JE

1

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13 August 2017

Krabbe K

2

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13 August 2017

Koefoed P

4

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13 August 2017

Jensen LN

5

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13 August 2017

Fenger K

6

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13 August 2017

Eiberg H

7

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13 August 2017

Hasholt L

8

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13 August 2017

Werdelin L

9

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13 August 2017

Sørensen SA

10

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13 August 2017

language of work or name

English

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publication date

1 January 1998

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

13 August 2017

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13 August 2017

64

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13 August 2017

1

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13 August 2017

61-66

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Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group

13 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

A comprehensive genetic map of the human genome based on 5,264 microsatellites

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Hereditary "pure" spastic paraplegia: a study of nine families

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Magnetic resonance imaging in degenerative ataxic disorders

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Unstable triplet repeat diseases.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

X-linked pure familial spastic paraparesis. Characterization of a large kindred with magnetic resonance imaging studies

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Correlation between CAG repeat length and clinical features in Machado-Joseph disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Classification of the hereditary ataxias and paraplegias

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Strümpell's familial spastic paraplegia: genetics and neuropathology

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Motor and somatosensory evoked potentials in hereditary spastic paraplegia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Central motor conduction studies in hereditary spastic paraplegia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

The neuropathology of hereditary spastic paraparesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation Danish family.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

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

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Multisystem involvement of the central nervous system in Strümpell's disease. A neurophysiological and neuropsychological study

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Age dependent white matter lesions and brain volume changes in healthy volunteers.

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Avoiding recomputation in linkage analysis.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

A quantitative study of sensory function in hereditary spastic paraplegia

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2169895

Visual, auditory and somatosensory pathway involvement in hereditary cerebellar ataxia, Friedreich's ataxia and familial spastic paraplegia

22 September 2018

1 reference

12 December 2020

The phenotype of "pure" autosomal dominant spastic paraplegia

1 reference

12 December 2020

Clinically silent dysfunction of dorsal columns and dorsal spinocerebellar tracts in hereditary spastic paraparesis

1 reference

12 December 2020

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p

1 reference

12 December 2020

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.64.1.61

1 reference

13 August 2017

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13 August 2017

1 reference