Genetic Predisposition to Coronary Artery Disease
Seung Hoan Choi +7 more
openaire +2 more sources
Ceftriaxone‐associated immune haemolytic anaemia: A patient‐level systematic review
Abstract Ceftriaxone can cause acute haemolysis. Its clinical presentation, risk factors, and outcomes remain incompletely characterized. We conducted a systematic review of published cases with patient‐level data, following international guidelines and with registration in PROSPERO (CRD420261338709). Reports were identified through three bibliographic
Sonja Miotti +9 more
wiley +1 more source
Genotype-Specific Clinical Response to a Lactose-Free Diet in Adult Patients Evaluated for Lactose Intolerance: Implications for Clinical Assessment. [PDF]
Mirică RE +5 more
europepmc +1 more source
Comprehensive Genomic Analysis in Hereditary Adrenal and Extra-Adrenal Paragangliomas. [PDF]
Purnaghshband H +13 more
europepmc +1 more source
Genetic and autoimmune predispositions to fulminant viral hepatitis in children. [PDF]
Bousfiha M +6 more
europepmc +1 more source
Support for Disclosure of Hereditary Tumor Risk to Children and Adolescents: A Scoping Review. [PDF]
Sugima K +4 more
europepmc +1 more source
Insights from GWAS, TWAS, and DEG analysis: CDKN2B-AS1, MAP3K4, and P2RX2-encoded P2X2 receptor identified as potential therapeutic targets for ischemic heart disease in Russian adults and long-living individuals. [PDF]
Daniel V +27 more
europepmc +1 more source
Epigenetic and genetic factors modifying the association between diet quality and incident type 2 diabetes: the EPIC-Potsdam cohort. [PDF]
El-Khoury C +3 more
europepmc +1 more source

