Autoimmune Pancreatitis
What's New
Last Posted: Feb 24, 2023
- Long-term yield of pancreatic cancer surveillance in high-risk individuals.
Overbeek Kasper A, et al. Gut 2021 0 (6) 1152-1160 - HLA-DRB1?16 and -DQB1?05 alleles are strongly associated with autoimmune pancreatitis in a cohort of hundred patients.
Goni Elisabetta, et al. Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2022 0 (4) 466-471 - Artificial Intelligence Implementation in Pancreaticobiliary Endoscopy.
Low Daniel J et al. Expert review of gastroenterology & hepatology 2022 - Association of autoimmune hepatitis with Src homology 2 adaptor protein 3 gene polymorphisms in Japanese patients.
Umemura Takeji, et al. Journal of human genetics 2017 11 (11) 963-967 - Extensive molecular analysis suggested the strong genetic heterogeneity of idiopathic chronic pancreatitis.
Sofia Valentina Maria, et al. Molecular medicine (Cambridge, Mass.) 2016 5 - Investigation of susceptibility genes triggering lachrymal/salivary gland lesion complications in Japanese patients with type 1 autoimmune pancreatitis.
Oguchi Takaya, et al. PloS one 2015 0 (5) e0127078 - Cystic fibrosis transmembrane conductance regulator gene variants are associated with autoimmune pancreatitis and slow response to steroid treatment.
Chang Ming-Chu, et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2015 9 (5) 661-7 - Human cationic trypsinogen but not serine peptidase inhibitor, Kazal type 1 variants increase the risk of type 1 autoimmune pancreatitis.
Chang Ming-Chu, et al. Journal of gastroenterology and hepatology 2014 12 (12) 2038-42 - PRSS1_p.Leu81Met mutation results in autoimmune pancreatitis.
Gao F, et al. World journal of gastroenterology : WJG 2013 6 (21) 21 - Polymorphism in the KCNA3 gene is associated with susceptibility to autoimmune pancreatitis in the Japanese population.
Ota Masao, et al. Disease markers 2011 0 (4) 223-9
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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 the CDC Office of Public Health Genomics 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, 2023
- Page last updated:Mar 21, 2023
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