CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles

Addison's disease: a survey on 633 patients in Padova

(2013) Corrado Betterle et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Congenital adrenal hyperplasia

(2011) Anna Wedell   CLINICAL BIOCHEMISTRY

Multiple Loci in the HLA Complex Are Associated with Addison's Disease

(2011) Beate Skinningsrud et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Insulin gene VNTR genotype associates with frequency and phenotype of the autoimmune response to proinsulin

(2010) I Durinovic-Belló et al.   GENES AND IMMUNITY

Haplotype Analysis Discriminates Genetic Risk for DR3-Associated Endocrine Autoimmunity and Helps Define Extreme Risk for Addison’s Disease

(2010) Peter R. Baker et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline

(2010) Phyllis W. Speiser et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Cytotoxic T lymphocyte antigen-4 Ala17 polymorphism is a genetic marker of autoimmune adrenal insufficiency: Italian association study and meta-analysis of European studies

(2009) Annalisa Brozzetti et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Autoantibodies to adrenal cytochrome P450 antigens in isolated Addison's disease and autoimmune polyendocrine syndrome type II

(2009) J. Seissler et al.   EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES

Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease

(2009) O. J. Brand et al.   HUMAN MOLECULAR GENETICS

Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison’s Disease and Graves’ Disease Susceptibility

(2009) Anna L. Mitchell et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Homozygosity of the Polymorphism MICA5.1 Identifies Extreme Risk of Progression to Overt Adrenal Insufficiency among 21-Hydroxylase Antibody-Positive Patients with Type 1 Diabetes

(2009) Taylor M. Triolo et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Clinical, Immunological, and Genetic Features of Autoimmune Primary Adrenal Insufficiency: Observations from a Norwegian Registry

(2009) Martina M. Erichsen et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Clinical manifestations and management of patients with autoimmune polyendocrine syndrome type I

(2009) E. S. Husebye et al.   JOURNAL OF INTERNAL MEDICINE

Linkage analysis of the C4A/C4B copy number variation and polymorphisms of the adjacent steroid 21-hydroxylase gene in a healthy population

(2009) Bernadett Blaskó et al.   MOLECULAR IMMUNOLOGY

The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease

(2008) Matthew Roycroft et al.   CLINICAL ENDOCRINOLOGY

A Common Nonsynonymous Single Nucleotide Polymorphism in the SLC30A8 Gene Determines ZnT8 Autoantibody Specificity in Type 1 Diabetes

(2008) J. M. Wenzlau et al.   DIABETES

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease

(2008) Beate Skinningsrud et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Likelihood-Based Association Analysis for Nuclear Families and Unrelated Subjects with Missing Genotype Data

(2008) Frank Dudbridge   HUMAN HEREDITY

Polymorphisms inCLEC16AandCIITAat 16p13 Are Associated with Primary Adrenal Insufficiency

(2008) Beate Skinningsrud et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM