Progression of multiple sclerosis is associated with exon 1 CTLA‐4 gene polymorphism

No abstract is available for this paper.

• Publication year

  2004

• Venue

  Acta Neurologica Scandinavica

• Publication date

  2004-07-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1111/j.1600-0404.2004.00271.xPMID 15180809
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• Homeostasis and self-tolerance in the immune system: turning lymphocytes off.

  1998cited by this paper
• Autoimmunity: The pathogen connection

  1998cited by this paper
• HLA associations with multiple sclerosis in the Canary Islands.

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• CTLA4 codon 17 dimorphism in patients with rheumatoid arthritis.

  1998cited by this paper
• CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus.

  1997cited by this paper
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  1997cited by this paper
• Epitope spreading

  1996cited by this paper
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  1996cited by this paper
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  1996cited by this paper
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  1996cited by this paper
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  1995cited by this paper
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  1995cited by this paper
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  1995cited by this paper
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  1995cited by this paper
• CD28-B7 interactions in T-cell activation.

  1994cited by this paper
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  1994cited by this paper
• Induction of relapsing paralysis in experimental autoimmune encephalomyelitis by bacterial superantigen

  1993cited by this paper
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  1992cited by this paper
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  1991cited by this paper
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  1991cited by this paper
• The natural history of multiple sclerosis: a geographically based study. 3. Multivariate analysis of predictive factors and models of outcome.

  1991cited by this paper
• HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation.

  1991cited by this paper
• The natural history of multiple sclerosis: a geographically based study. I. Clinical course and disability.

  1989cited by this paper
• Course and prognosis of chronic progressive multiple sclerosis: Results of an epidemiological study

  1988cited by this paper
• New diagnostic criteria for multiple sclerosis: Guidelines for research protocols

  1983cited by this paper
• Rating neurologic impairment in multiple sclerosis

  1983influential reference

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  2014cites this paper
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  2013cites this paper
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  2012cites this paper
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  2011cites this paper
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  2011cites this paper
• CTLA‐4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients

  2011influential citation
• CTLA4 exon 1 and promoter polymorphisms in patients with multiple sclerosis

  2009cites this paper
• The CTLA‐4 gene polymorphisms are associated with CTLA‐4 protein expression levels in multiple sclerosis patients and with susceptibility to disease

  2009cites this paper
• Association Between Genotypes and Phenotypes in Coeliac Disease

  2009cites this paper
• Zaburzenia odporności komórkowej u chorych na stwardnienie rozsiane

  2008cites this paper
• Clinical and genetical aspects of Celiac Disease

  2008cites this paper
• CTLA-4 and multiple sclerosis: the A49G single nucleotide polymorphism shows no association with multiple sclerosis in a Southern Australian population.

  2008cites this paper
• The genetics of clinical outcome in multiple sclerosis.

  2008influential citation
• No evidence for association of CTLA-4 gene polymorphisms with the risk of developing multiple sclerosis: a meta-analysis

  2007cites this paper
• CTLA4 gene polymorphisms and multiple sclerosis in Northern Ireland.

  2007cites this paper
• Recent advances in genetic analysis of multiple sclerosis: genetic associations and therapeutic implications

  2007cites this paper
• Non-HLA associations with autoimmune diseases.

  2006cites this paper
• Association of CTLA-4 gene polymorphism with oral squamous cell carcinoma.

  2006cites this paper
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  2005cites this paper