GLUCOSURIA

作品数：4被引量：7H指数：1
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相关期刊：《World Journal of Gastroenterology》《Case Reports in Clinical Medicine》《World Journal of Clinical Pediatrics》《China Medical Abstracts(Internal Medicine)》更多>>
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Renal glucosuria in children
《World Journal of Clinical Pediatrics》2025年第1期46-54,共9页Meral Torun Bayram Salih Kavukcu 
The kidneys play a critical role in maintaining glucose homeostasis.Under normal renal tubular function,most of the glucose filtered from the glomeruli is re-absorbed in the proximal tubules,leaving only trace amounts...
关键词：Sodium-glucose cotransporters Basolateral glucose transporters Familial renal glucosuria Intestinal glucose-galactose malabsorption Fanconi-Bickel syndrome Sodium-glucose cotransporter 2 inhibitors 
2019096 Mutation analysis of SLC5A2 gene and determination of the renal threshold for glucose excretion in Chinese patients with familial renal glucosuria
《China Medical Abstracts(Internal Medicine)》2019年第1期51-52,共2页WANG Sai 
Objective To analyze and identify the mutations in SGLT2 gene of nine Chinese families with FRG,and determine the renal threshold for glucose excretion (RTG),so as to explore the association of genotype and RTG.Method...
关键词：analyze SGLT2 
Latent Autoimmune Diabetes in Adults Complicated by Persistent Isolated Glucosuria in the Absence of Hyperglycemia
《Case Reports in Clinical Medicine》2017年第5期133-136,共4页Kosuke Inoue Yuya Tsurutani Chiho Sugisawa Sachiko Suematsu Jun Saito Masao Omura Tetsuo Nishikawa 
Latent autoimmune diabetes in adults (LADA) is an autoimmune diabetes of adult-onset with the presence of diabetes associated autoantibodies. Familial renal glucosuria (FRG) is an inherited renal tubular disorder that...
关键词：Latent Autoimmune Diabetes in Adults (LADA) FAMILIAL Renal GLUCOSURIA (FRG) SLC5A2 Mutation Sodium-Glucose COTRANSPORTER 2 (SGLT2) Insulin Therapy 
ARC syndrome with high GGT cholestasis caused by VPS33B mutations被引量：7
《World Journal of Gastroenterology》2014年第16期4830-4834,共5页Jian-She Wang Jing Zhao Li-Ting Li 
Supported by National Natural Science Foundation of China,No.81070281
Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome (OMIM 208085) is an autosomal recessive disorder that is caused by mutations in 2 interacting genes VPS33B and VIPAS39. Mutations in VPS33B gene account...
关键词：Arthrogryposis  renal dysfunction and cholestasis syndrome CHOLESTASIS Gamma-glutamyl-transpeptidase VPS33B Renal dysfunction GLUCOSURIA 
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