Autoimmune Polyglandular Syndrome Type 1
What's New
Last Posted: Mar 04, 2023
- Genetic Screening in a Large Chinese Cohort of Childhood Onset Hypoparathyroidism by Next-Generation Sequencing Combined with TBX1-MLPA.
Wang Yabing, et al. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2019 0 (12) 2254-2263 - Monocytic Cytokines in Autoimmune Polyglandular Syndrome Type 2 Are Modulated by Vitamin D and HLA-DQ.
Kraus Anna U, et al. Frontiers in immunology 2020 0 583709 - Severe weight loss in a hypothyroid patient as an acute presentation of autoimmune polyglandular syndrome type II.
Silajdzija Elvira, et al. Hormones (Athens, Greece) 2022 0 (2) 317-322 - Autoimmune Regulator Gene Polymorphisms in Egyptian Systemic Lupus Erythematosus Patients: Preliminary Results.
Attia Doaa Hs, et al. International journal of rheumatology 2021 0 5546639 - Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.
Tomer Yaron, et al. Journal of autoimmunity 2015 6 32-9 - HLA-DQB1 Position 57 Defines Susceptibility to Isolated and Polyglandular Autoimmunity in Adults: Interaction With Gender.
Kraus Anna U, et al. The Journal of clinical endocrinology and metabolism 2019 6 (6) 1907-1916 - Human Leukocyte Antigen class II polymorphisms among Croatian patients with type 1 diabetes and autoimmune polyglandular syndrome type 3 variant.
Grubic Zorana, et al. Gene 2018 6 - A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans.
Pazderska Agnieszka, et al. The Journal of clinical endocrinology and metabolism 2016 9 jc20162368 - Association Studies of the GPR103 and BCL2L15 Genes in Autoimmune Thyroid Disease in the Japanese Population.
Ban Yoshiyuki, et al. Frontiers in endocrinology 2016 0 92 - Association of TNF-a, CTLA4, and PTPN22 polymorphisms with type 1 diabetes and other autoimmune diseases in Brazil.
Tavares N A C, et al. Genetics and molecular research : GMR 2015 0 (4) 18936-44
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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