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8. HNF4A-related Fanconi syndrome in a Chinese patient: a case report and review of the literature. Liu J; Shen Q; Li G; Xu H J Med Case Rep; 2018 Jul; 12(1):203. PubMed ID: 30005691 [TBL] [Abstract][Full Text] [Related]
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12. Prolonged episodes of hypoglycaemia in HNF4A-MODY mutation carriers with IGT. Evidence of persistent hyperinsulinism into early adulthood. Bacon S; Kyithar MP; Condron EM; Vizzard N; Burke M; Byrne MM Acta Diabetol; 2016 Dec; 53(6):965-972. PubMed ID: 27552834 [TBL] [Abstract][Full Text] [Related]
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15. Identification of HNF1A-MODY and HNF4A-MODY in Irish families: phenotypic characteristics and therapeutic implications. Kyithar MP; Bacon S; Pannu KK; Rizvi SR; Colclough K; Ellard S; Byrne MM Diabetes Metab; 2011 Dec; 37(6):512-9. PubMed ID: 21683639 [TBL] [Abstract][Full Text] [Related]
16. Congenital hyperinsulinism due to mutations in HNF1A. Yau D; Colclough K; Natarajan A; Parikh R; Canham N; Didi M; Senniappan S; Banerjee I Eur J Med Genet; 2020 Jun; 63(6):103928. PubMed ID: 32325224 [TBL] [Abstract][Full Text] [Related]
17. Congenital hyperinsulinism due to mutations in HNF4A and HADH. Kapoor RR; Heslegrave A; Hussain K Rev Endocr Metab Disord; 2010 Sep; 11(3):185-91. PubMed ID: 20931292 [TBL] [Abstract][Full Text] [Related]
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19. Clinical heterogeneity of hyperinsulinism due to HNF1A and HNF4A mutations. Tung JY; Boodhansingh K; Stanley CA; De León DD Pediatr Diabetes; 2018 Aug; 19(5):910-916. PubMed ID: 29493090 [TBL] [Abstract][Full Text] [Related]
20. Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism. Johnson SR; Leo PJ; McInerney-Leo AM; Anderson LK; Marshall M; McGown I; Newell F; Brown MA; Conwell LS; Harris M; Duncan EL Pediatr Diabetes; 2018 Jun; 19(4):656-662. PubMed ID: 29417725 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]