HLA in coeliac disease families: a novel test of risk modification by the 'other' haplotype when at least one DQA105-DQB102 haplotype is carried (Q28209245)

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scientific article (publication date: August 2002)

Language	Label	Description	Also known as
English	HLA in coeliac disease families: a novel test of risk modification by the 'other' haplotype when at least one DQA105-DQB102 haplotype is carried	scientific article (publication date: August 2002)

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scholarly article

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HLA in coeliac disease families: a novel test of risk modification by the 'other' haplotype when at least one DQA1*05-DQB1*02 haplotype is carried (English)

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Staffan Nilsson

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object named as

S Nilsson

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author name string

A S Louka

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M Olsson

3

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B Talseth

4

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B A Lie

5

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J Ek

6

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A H Gudjónsdóttir

7

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H Ascher

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L M Sollid

9

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language of work or name

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publication date

August 2002

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Tissue Antigens

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60

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2

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147-54

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Current approaches to diagnosis and treatment of celiac disease: an evolving spectrum

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Molecular basis of celiac disease

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Genome search in celiac disease.

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Genomewide linkage analysis of celiac disease in Finnish families

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Evidence for a primary association of celiac disease to a particular HLA-DQ alpha/beta heterodimer

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Gliadin-specific, HLA-DQ(alpha 1*0501,beta 1*0201) restricted T cells isolated from the small intestinal mucosa of celiac disease patients

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Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups

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Reevaluation of the relative risk for susceptibility to celiac disease of HLA-DRB1, -DQA1, -DQB1, -DPB1, and -TAP2 alleles in a French population.

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HLA class II alleles associated with celiac disease susceptibility in a southern European population

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HLA-DR phenotypes in Spanish coeliac children: their contribution to the understanding of the genetics of the disease

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Different HLA associated gene combinations contribute to susceptibility for coeliac disease and dermatitis herpetiformis

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Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11

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Genetic contribution of the HLA region to the familial clustering of coeliac disease.

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A study of Italian pediatric celiac disease patients confirms that the primary HLA association is to the DQ(alpha 1*0501, beta 1*0201) heterodimer

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On the HLA-DQ(α1*0501, β1*0201)-associated susceptibility in celiac disease: A possible gene dosage effect ofDQB1*0201

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HLA-DQB1*0602 homozygosity increases relative risk for narcolepsy but not disease severity in two ethnic groups. US Modafinil in Narcolepsy Multicenter Study Group

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Revised criteria for diagnosis of coeliac disease. Report of Working Group of European Society of Paediatric Gastroenterology and Nutrition

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HLA Genotypes and the Increased Incidence of Coeliac Disease in Sweden

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Distribution of HLA-DRB1, -DQA1 and -DQB1 alleles and DQA1-DQB1 genotypes among Norwegian patients with insulin-dependent diabetes mellitus

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Histocompatibility determinants in Israeli Jewish patients with coeliac disease: population and family study

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Family and population studies of HLA and coeliac disease in the West of Ireland

1 reference

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HLA and diseases: involvement of more than one HLA-linked determinant of disease susceptibility

1 reference

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inferred from DOI database lookup

HLA-DR typing in coeliac disease: evidence for genetic heterogeneity

1 reference

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Identifiers

10.1034/J.1399-0039.2002.600205.X

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release_b3y4lzhvcfgdpbxl7bczplqm5q

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https://api.fatcat.wiki/v0/release/b3y4lzhvcfgdpbxl7bczplqm5q

24 November 2022

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