(Q33931313)

30 July 2017

1 reference

title

The genetics of multiple sclerosis. (English)

1 reference

30 July 2017

A Compston

1

1 reference

30 July 2017

publication date

1 February 2000

1 reference

Clinical Chemistry and Laboratory Medicine

30 July 2017

published in

1 reference

30 July 2017

volume

38

1 reference

30 July 2017

issue

2

1 reference

30 July 2017

page(s)

133-135

1 reference

Multiple sclerosis: updated risks for relatives

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Age-adjusted recurrence risks for relatives of patients with multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Risks of multiple sclerosis in relatives of patients in Flanders, Belgium

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

A population-based study of multiple sclerosis in twins: update.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Evidence for genetic basis of multiple sclerosis. The Canadian Collaborative Study Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

HLA associations with multiple sclerosis in the Canary Islands

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

HLA-DR and -DQ associations with multiple sclerosis in Turkey

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Multiple sclerosis: the increased frequency of the ICAM-1 exon 6 gene point mutation genetic type K469.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Combined effect of HLA-DRB1*1501 and interleukin-1 receptor antagonist gene allele 2 in susceptibility to relapsing/remitting multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Occurrence and clinical relevance of an interleukin-4 gene polymorphism in patients with multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Linkage and association analysis of genes encoding cytokines and myelin proteins in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

The CCR5 deletion mutation fails to protect against multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Genetic susceptibility to multiple sclerosis linked to myelin basic protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Identification of a Val I 45 IIe substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach. French Multiple Sclerosis Genetics Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Genomewide scan of multiple sclerosis in Finnish multiplex families

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

HLA typing in the United Kingdom multiple sclerosis genome screen

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

A full genome search in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

Linkage analysis of multiple sclerosis with candidate region markers in Sardinian and Continental Italian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2000.020

21 January 2018

Identifiers

DOI

10.1515/CCLM.2000.020

1 reference

30 July 2017

1 reference