(Q33680138)

28 July 2017

Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p. (English)

1 reference

28 July 2017

8

Weissenbach J

1 reference

28 July 2017

Heinzlef O

1

1 reference

28 July 2017

Paternotte C

2

1 reference

28 July 2017

Mahieux F

3

1 reference

28 July 2017

Prud'homme JF

4

1 reference

28 July 2017

Dien J

5

1 reference

28 July 2017

Madigand M

6

1 reference

28 July 2017

Pouget J

7

1 reference

28 July 2017

Roullet E

9

1 reference

28 July 2017

Hazan J

10

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 February 1998

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

35

1 reference

28 July 2017

2

1 reference

28 July 2017

89-93

1 reference

Pure hereditary spastic paraplegia.

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Incorrect specification of marker allele frequencies: effects on linkage analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Classification of the hereditary ataxias and paraplegias

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Familial spastic paraplegia with epilepsy.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Etiological heterogeneity in X-linked spastic paraplegia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

FAMILIAL AMYOTROPHIC DYSTONIC PARAPLEGIA

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Hereditary spastic paraplegia associated with epilepsy, mental retardation and hearing impairment.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Familial spastic paraplegia with mental impairment and thin corpus callosum

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

The phenotype of "pure" autosomal dominant spastic paraplegia

10 December 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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

Hereditary Spastic Paraplegia with Dementia

1 reference

12 December 2020

Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.35.2.89

1 reference

28 July 2017

1 reference

28 July 2017

1 reference