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4. Low prevalence of MODY2 and MODY3 mutations in Brazilian individuals with clinical MODY phenotype. Furuzawa GK; Giuffrida FM; Oliveira CS; Chacra AR; Dib SA; Reis AF Diabetes Res Clin Pract; 2008 Sep; 81(3):e12-4. PubMed ID: 18672310 [TBL] [Abstract][Full Text] [Related]
5. Identification of novel and recurrent glucokinase mutations in Belgian and Luxembourg maturity onset diabetes of the young patients. Vits L; Beckers D; Craen M; de Beaufort C; Vanfleteren E; Dahan K; Nollet A; Vanhaverbeke G; Imschoot SV; Bourguignon JP; Beauloye V; Storm K; Massa G; Giri M; Nobels F; De Schepper J; Rooman R; Van den Bruel A; Mathieu C; Wuyts W Clin Genet; 2006 Oct; 70(4):355-9. PubMed ID: 16965331 [No Abstract] [Full Text] [Related]
6. Three novel missense mutations in the glucokinase gene (G80S; E221K; G227C) in Italian subjects with maturity-onset diabetes of the young (MODY). Mutations in brief no. 162. Online. Guazzini B; Gaffi D; Mainieri D; Multari G; Cordera R; Bertolini S; Pozza G; Meschi F; Barbetti F Hum Mutat; 1998; 12(2):136. PubMed ID: 10694920 [TBL] [Abstract][Full Text] [Related]
7. Novel mutations in GCK and HNF1A genes in Italian families with MODY phenotype. Cappelli A; Tumini S; Consoli A; Carinci S; Piersanti C; Ruggiero G; Simonella G; Soletti F; Staffolani P; Pianese L Diabetes Res Clin Pract; 2009 Mar; 83(3):e72-4. PubMed ID: 19150152 [TBL] [Abstract][Full Text] [Related]
9. Identification of eight novel glucokinase mutations in Italian children with maturity-onset diabetes of the young. Mantovani V; Salardi S; Cerreta V; Bastia D; Cenci M; Ragni L; Zucchini S; Parente R; Cicognani A Hum Mutat; 2003 Oct; 22(4):338. PubMed ID: 12955723 [TBL] [Abstract][Full Text] [Related]
10. Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy. Gloyn AL Hum Mutat; 2003 Nov; 22(5):353-62. PubMed ID: 14517946 [TBL] [Abstract][Full Text] [Related]
11. A defective beta-cell glucose sensor as a cause of diabetes. Weir GC N Engl J Med; 1993 Mar; 328(10):729-31. PubMed ID: 8433735 [No Abstract] [Full Text] [Related]
12. Prevalence and clinical phenotype of the p.Val226Met glucokinase gene mutation in French Canadians in Quebec, Canada. Henderson M; Levy E; Delvin E; Losekoot M; Lambert M Mol Genet Metab; 2007 Jan; 90(1):87-92. PubMed ID: 17079173 [TBL] [Abstract][Full Text] [Related]
13. A new missense mutation in the glucokinase gene in an Italian Mody family. Bertini C; Maioli M; Fresu P; Tonolo G; Pirastu M; Maioli M Diabetologia; 1996 Nov; 39(11):1413-4. PubMed ID: 8933019 [No Abstract] [Full Text] [Related]
14. [Swiss journey through the clinical and genetic characteristics of diabetes in young patients]. Dussoix P; Tappy L; Philippe J Schweiz Med Wochenschr; 1998 Jan; 128(5):162-6. PubMed ID: 9522422 [TBL] [Abstract][Full Text] [Related]
15. [Glucokinase and non-insulin-dependent diabetes: from gene to disease]. Froguel P; Velho G Journ Annu Diabetol Hotel Dieu; 1993; ():51-61. PubMed ID: 8331876 [No Abstract] [Full Text] [Related]
16. [Mutation screening of GCK gene in Chinese early-onset diabetes population]. Zheng TS; Wu SH; Yang Z; Lu HJ; Xiang KS Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):671-4. PubMed ID: 16331569 [TBL] [Abstract][Full Text] [Related]
17. A novel nonsense mutation in GCK exon 9 co-segregates with diabetes phenotype. Knebel B; Jacob S; Boxberg CV; Müller-Wieland D; Kotzka J Exp Clin Endocrinol Diabetes; 2004 Jun; 112(6):298-301. PubMed ID: 15216446 [TBL] [Abstract][Full Text] [Related]
18. Clinical characteristics of mutation carriers in a large family with glucokinase diabetes (MODY2). Shehadeh N; Bakri D; Njølstad PR; Gershoni-Baruch R Diabet Med; 2005 Aug; 22(8):994-8. PubMed ID: 16026363 [TBL] [Abstract][Full Text] [Related]
20. [Glucokinase: the first hit in the hunt for a gene in late-onset diabetes]. Laakso M Duodecim; 1994; 110(1):13-5. PubMed ID: 7555744 [No Abstract] [Full Text] [Related] [Next] [New Search]