Autoimmune Enteropathy
What's New
Last Posted: Jul 24, 2023
- Analysis of a series of Italian APECED patients with autoimmune hepatitis and gastro-enteropathies.
Giorgia Paldino, et al. Frontiers in immunology 2023 0 1172369 - Genetics, environment, and asthma associated with celiac disease in the extended family of an affected child.
Sigala-Robles R, et al. Revista de gastroenterologia de Mexico (English) 2017 0 (2) 79-85 - PREVALENCE OF CELIAC DISEASE PREDISPOSING GENOTYPES, INCLUDING HLA-DQ2.2 VARIANT, IN BRAZILIAN CHILDREN.
Selleski Nicole, et al. Arquivos de gastroenterologia 2018 0 (1) 82-85 - Celiac disease serology and gut microbiome following proton pump inhibitor treatment.
Jang Sophie, et al. Medicine 2020 0 (35) e21488 - Human Leucocyte Antigen Genotyping in Celiac Disease: Reasons for Inappropriate Use.
Kav Taylan, et al. Clinical laboratory 2021 0 (10) - Celiac disease in pediatric patients according to HLA genetic risk classes: a retrospective observational study.
Tolone Carlo, et al. Italian journal of pediatrics 2021 0 (1) 107 - Human leukocyte antigen (HLA)-DQ2 and -DQ8 haplotypes in celiac, celiac with type 1 diabetic, and celiac suspected pediatric cases.
Siddiqui Komal, et al. Medicine 2021 0 (11) e24954 - Determination of High-Resolution HLA-DQB1 Suballeles and IL-17 Polymorphisms in Turkish Pediatric Patients.
Eldem Asl?, et al. Journal of pediatric genetics 2022 0 (3) 192-197 - High rates of variation in HLA-DQ2/DQ8 testing for coeliac disease: results from an RCPAQAP pilot program.
Horan Martin Patrick et al. Journal of clinical pathology 2018 Oct 71(10) 900-905 - Simplifying celiac disease predisposing HLA-DQ alleles determination by the real time PCR method.
Selleski Nicole, et al. Arquivos de gastroenterologia 0 0 (2) 143-6 - The role of HLA DQ2 and DQ8 in dissecting celiac-like disease in common variable immunodeficiency.
Venhoff Nils, et al. Journal of clinical immunology 2013 7 (5) 909-16 - Autoimmune enteropathy
From NCATS Genetic and Rare Diseases Information Center - HLA-DQB1*02 dose effect on RIA anti-tissue transglutaminase autoantibody levels and clinicopathological expressivity of celiac disease.
Nenna Raffaella, et al. Journal of pediatric gastroenterology and nutrition 2008 9 (3) 288-92
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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
- Content source: