These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
178 related articles for article (PubMed ID: 28766492)
1. MODY3, renal cysts, and Dandy-Walker variants with a microdeletion spanning the HNF1A gene. Matsukura H; Nagamori M; Miya K; Yorifuji T Clin Nephrol; 2017 Sep; 88(9):162-166. PubMed ID: 28766492 [TBL] [Abstract][Full Text] [Related]
2. The spectrum of HNF1A gene mutations in Greek patients with MODY3: relative frequency and identification of seven novel germline mutations. Tatsi C; Kanaka-Gantenbein C; Vazeou-Gerassimidi A; Chrysis D; Delis D; Tentolouris N; Dacou-Voutetakis C; Chrousos GP; Sertedaki A Pediatr Diabetes; 2013 Nov; 14(7):526-34. PubMed ID: 23517481 [TBL] [Abstract][Full Text] [Related]
3. Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young. Ellard S; Thomas K; Edghill EL; Owens M; Ambye L; Cropper J; Little J; Strachan M; Stride A; Ersoy B; Eiberg H; Pedersen O; Shepherd MH; Hansen T; Harries LW; Hattersley AT Diabetologia; 2007 Nov; 50(11):2313-7. PubMed ID: 17828387 [TBL] [Abstract][Full Text] [Related]
4. Clinical characteristics of HNF1B-related disorders in a Japanese population. Nagano C; Morisada N; Nozu K; Kamei K; Tanaka R; Kanda S; Shiona S; Araki Y; Ohara S; Matsumura C; Kasahara K; Mori Y; Seo A; Miura K; Washiyama M; Sugimoto K; Harada R; Tazoe S; Kourakata H; Enseki M; Aotani D; Yamada T; Sakakibara N; Yamamura T; Minamikawa S; Ishikura K; Ito S; Hattori M; Iijima K Clin Exp Nephrol; 2019 Sep; 23(9):1119-1129. PubMed ID: 31131422 [TBL] [Abstract][Full Text] [Related]
5. Maturity onset diabetes of the young: clinical characteristics and outcome after kidney and pancreas transplantation in MODY3 and RCAD patients: a single center experience. Poitou C; Francois H; Bellanne-Chantelot C; Noel C; Jacquet A; Clauin S; Beaudreuil S; Damieri H; Hebibi H; Hammoudi Y; Benoit G; Charpentier B; Durrbach A Transpl Int; 2012 May; 25(5):564-72. PubMed ID: 22432796 [TBL] [Abstract][Full Text] [Related]
6. Unexpected finding of a whole HNF1B gene deletion during the screening of rare MODY types in a series of Brazilian patients negative for GCK and HNF1A mutations. Dotto RP; Giuffrida FM; Franco L; Mathez AL; Weinert LS; Silveiro SP; Sa JR; Reis AF; Dias-da-Silva MR Diabetes Res Clin Pract; 2016 Jun; 116():100-4. PubMed ID: 27321323 [TBL] [Abstract][Full Text] [Related]
7. A case of digenic maturity onset diabetes of the young with heterozygous variants in both HNF1Α and HNF1Β genes. Patouni K; Cinek O; Pruhova S; Elblova L; Xatzipsalti M; Sertedaki A; Vazeou A Eur J Med Genet; 2021 Sep; 64(9):104264. PubMed ID: 34161864 [TBL] [Abstract][Full Text] [Related]
8. Expanded clinical spectrum in hepatocyte nuclear factor 1b-maturity-onset diabetes of the young. Raile K; Klopocki E; Holder M; Wessel T; Galler A; Deiss D; Müller D; Riebel T; Horn D; Maringa M; Weber J; Ullmann R; Grüters A J Clin Endocrinol Metab; 2009 Jul; 94(7):2658-64. PubMed ID: 19417042 [TBL] [Abstract][Full Text] [Related]
9. The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes. Sagen JV; Bjørkhaug L; Haukanes BI; Grevle L; Molnes J; Nedrebø BG; Søvik O; Njølstad PR; Johansson S; Molven A Diabetes Res Clin Pract; 2017 Nov; 133():142-149. PubMed ID: 28934671 [TBL] [Abstract][Full Text] [Related]
10. Hepatic phenotypes of HNF1B gene mutations: a case of neonatal cholestasis requiring portoenterostomy and literature review. Kotalova R; Dusatkova P; Cinek O; Dusatkova L; Dedic T; Seeman T; Lebl J; Pruhova S World J Gastroenterol; 2015 Feb; 21(8):2550-7. PubMed ID: 25741167 [TBL] [Abstract][Full Text] [Related]
11. Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha (HNF1A) and 4 alpha (HNF4A) in maturity-onset diabetes of the young. Ellard S; Colclough K Hum Mutat; 2006 Sep; 27(9):854-69. PubMed ID: 16917892 [TBL] [Abstract][Full Text] [Related]
12. Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study). Eide SA; Raeder H; Johansson S; Midthjell K; Søvik O; Njølstad PR; Molven A Diabet Med; 2008 Jul; 25(7):775-81. PubMed ID: 18513305 [TBL] [Abstract][Full Text] [Related]
13. Screening of HNF1A and HNF4A mutation and clinical phenotype analysis in a large cohort of Chinese patients with maturity-onset diabetes of the young. Wang X; Wang T; Yu M; Zhang H; Ping F; Zhang Q; Xu J; Feng K; Xiao X Acta Diabetol; 2019 Mar; 56(3):281-288. PubMed ID: 30293189 [TBL] [Abstract][Full Text] [Related]
14. Primary hepatocellular neoplasms in a MODY3 family with a novel HNF1A germline mutation. Willson JS; Godwin TD; Wiggins GA; Guilford PJ; McCall JL J Hepatol; 2013 Oct; 59(4):904-7. PubMed ID: 23707370 [TBL] [Abstract][Full Text] [Related]
15. Novel insights into genetics and clinics of the HNF1A-MODY. Valkovicova T; Skopkova M; Stanik J; Gasperikova D Endocr Regul; 2019 Apr; 53(2):110-134. PubMed ID: 31517624 [TBL] [Abstract][Full Text] [Related]
16. Structure-function studies of HNF1A (MODY3) gene mutations in South Indian patients with monogenic diabetes. Balamurugan K; Bjørkhaug L; Mahajan S; Kanthimathi S; Njølstad PR; Srinivasan N; Mohan V; Radha V Clin Genet; 2016 Dec; 90(6):486-495. PubMed ID: 26853433 [TBL] [Abstract][Full Text] [Related]
17. A Korean Family Presenting with Renal Cysts and Maturity-Onset Diabetes of the Young Caused by a Novel In-Frame Deletion of Han JY; Gwack J; Kim TY; Park J Int J Mol Sci; 2024 Sep; 25(18):. PubMed ID: 39337310 [TBL] [Abstract][Full Text] [Related]
18. Towards a new point of view on the phenotype of patients with a 17q12 microdeletion syndrome. Laffargue F; Bourthoumieu S; Llanas B; Baudouin V; Lahoche A; Morin D; Bessenay L; De Parscau L; Cloarec S; Delrue MA; Taupiac E; Dizier E; Laroche C; Bahans C; Yardin C; Lacombe D; Guigonis V Arch Dis Child; 2015 Mar; 100(3):259-64. PubMed ID: 25324567 [TBL] [Abstract][Full Text] [Related]
19. Novel presentations of congenital hyperinsulinism due to mutations in the MODY genes: HNF1A and HNF4A. Stanescu DE; Hughes N; Kaplan B; Stanley CA; De León DD J Clin Endocrinol Metab; 2012 Oct; 97(10):E2026-30. PubMed ID: 22802087 [TBL] [Abstract][Full Text] [Related]
20. Spectrum of HNF1A somatic mutations in hepatocellular adenoma differs from that in patients with MODY3 and suggests genotoxic damage. Jeannot E; Mellottee L; Bioulac-Sage P; Balabaud C; Scoazec JY; Tran Van Nhieu J; Bacq Y; Michalak S; Buob D; ; Laurent-Puig P; Rusyn I; Zucman-Rossi J Diabetes; 2010 Jul; 59(7):1836-44. PubMed ID: 20393147 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]