Lv1
70 积分 2026-01-07 加入
Literature review on genotype–phenotype correlation in patients with hereditary spherocytosis
4个月前
已完结
Erythropoietic Protoporphyria with cirrhosis with late onset dermatological manifestations in an Indian patient- The first report
4个月前
已关闭
Unearthing TULP3 Mutation as a Rare Cause of Cryptogenic Cirrhosis: A Case Report and Review of the Literature
4个月前
已完结
First Indian Case of Wilson's Disease With a Chinese-specific ATP7B Variant: Clinical and Genetic Insights
4个月前
已完结
Bile Duct Paucity in a Case of Neonatal Intrahepatic Cholestasis Due to Citrin Deficiency: Finding the Missing Piece of the Puzzle!
4个月前
已关闭
皖公网安备34019202002308
