Hepatocyte Nuclear Factor-4 Alfa Mutation Associated with Hyperinsulinaemic Hypoglycaemia and Atypical Renal Fanconi Syndrome: Expanding the Clinical Phenotype-Reference-Cited by-同舟云学术

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Hepatocyte Nuclear Factor-4 Alfa Mutation Associated with Hyperinsulinaemic Hypoglycaemia and Atypical Renal Fanconi Syndrome: Expanding the Clinical Phenotype

Published:2016 Issue:5 Volume:86 Page:337-341
ISSN:1663-2818
Container-title:Hormone Research in Paediatrics
language:en
Short-container-title:Horm Res Paediatr

Author:

Improda Nicola,Shah Pratik,Güemes Maria,Gilbert Clare,Morgan Kate,Sebire Neil,Bockenhauer Detlef,Hussain Khalid

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Band-shaped keratopathy in HNF4A -related Fanconi syndrome: a case report and review of the literature;Ophthalmic Genetics;2023-11-24

2. De novo HNF4A-associated atypical Fanconi renal tubulopathy syndrome;Journal of Nephrology;2023-06-13

3. Expanding the p.(Arg85Trp) Variant-Specific Phenotype of HNF4A: Features of Glycogen Storage Disease, Liver Cirrhosis, Impaired Mitochondrial Function, and Glomerular Changes;Molecular Syndromology;2023

4. Renal Fanconi Syndromes and Other Proximal Tubular Disorders;Pediatric Kidney Disease;2023

5. Hepatocyte nuclear factors play an important role in the pathogenesis of nephropathy;Clinical and Translational Discovery;2022-06

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