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Items: 1 to 20 of 112

1.

Reclassification of diabetes etiology in a family with multiple diabetes phenotypes.

Kavvoura FK, Raimondo A, Thanabalasingham G, Barrett A, Webster AL, Shears D, Mann NP, Ellard S, Gloyn AL, Owen KR.

J Clin Endocrinol Metab. 2014 Jun;99(6):E1067-71. doi: 10.1210/jc.2013-3641. Epub 2014 Feb 27.

2.

The 0.1% of the population with glucokinase monogenic diabetes can be recognized by clinical characteristics in pregnancy: the Atlantic Diabetes in Pregnancy cohort.

Chakera AJ, Spyer G, Vincent N, Ellard S, Hattersley AT, Dunne FP.

Diabetes Care. 2014;37(5):1230-6. doi: 10.2337/dc13-2248. Epub 2014 Feb 18.

PMID:
24550216
3.

Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase Mutation.

Chakera AJ, Steele AM, Gloyn AL, Shepherd MH, Shields B, Ellard S, Hattersley AT.

Diabetes Care. 2015 Jul;38(7):1383-92. doi: 10.2337/dc14-2769. Review.

PMID:
26106223
4.

A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousins.

Esquiaveto-Aun AM, De Mello MP, Paulino MF, Minicucci WJ, Guerra-Júnior G, De Lemos-Marini SH.

Diabetol Metab Syndr. 2015 Nov 18;7:101. doi: 10.1186/s13098-015-0101-9. eCollection 2015.

5.

A novel genetic mutation in a Portuguese family with GCK-MODY.

Almeida C, Silva SR, Garcia E, Leite AL, Teles A, Campos RA.

J Pediatr Endocrinol Metab. 2014 Jan;27(1-2):129-33. doi: 10.1515/jpem-2013-0056.

PMID:
23843579
6.

Impact of Type 2 diabetes on Glucokinase diabetes (GCK-MODY) phenotype in a Roma (Gypsy) family - case report.

Stanik J, Kusekova M, Huckova M, Valentinova L, Masindova I, Stanikova D, Ferenczova J, Gasperikova D, Klimes I.

Endocr Regul. 2012 Apr;46(2):99-105.

PMID:
22540858
7.

Glucokinase gene mutations (MODY 2) in Asian Indians.

Kanthimathi S, Jahnavi S, Balamurugan K, Ranjani H, Sonya J, Goswami S, Chowdhury S, Mohan V, Radha V.

Diabetes Technol Ther. 2014 Mar;16(3):180-5. doi: 10.1089/dia.2013.0244. Epub 2014 Jan 9.

PMID:
24405491
8.

Update on mutations in glucokinase (GCK), which cause maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemic hypoglycemia.

Osbak KK, Colclough K, Saint-Martin C, Beer NL, Bellanné-Chantelot C, Ellard S, Gloyn AL.

Hum Mutat. 2009 Nov;30(11):1512-26. doi: 10.1002/humu.21110. Review.

PMID:
19790256
9.

The clinical management of hyperglycemia in pregnancy complicated by maturity-onset diabetes of the young.

Bacon S, Schmid J, McCarthy A, Edwards J, Fleming A, Kinsley B, Firth R, Byrne B, Gavin C, Byrne MM.

Am J Obstet Gynecol. 2015 Aug;213(2):236.e1-7. doi: 10.1016/j.ajog.2015.04.037. Epub 2015 Apr 30.

PMID:
25935773
10.

Molecular and clinical characterization of glucokinase maturity-onset diabetes of the young (GCK-MODY) in Japanese patients.

Kawakita R, Hosokawa Y, Fujimaru R, Tamagawa N, Urakami T, Takasawa K, Moriya K, Mizuno H, Maruo Y, Takuwa M, Nagasaka H, Nishi Y, Yamamoto Y, Aizu K, Yorifuji T.

Diabet Med. 2014 Nov;31(11):1357-62. doi: 10.1111/dme.12487. Epub 2014 May 24.

PMID:
24804978
11.

Insights into the pathogenicity of rare missense GCK variants from the identification and functional characterization of compound heterozygous and double mutations inherited in cis.

Beer NL, Osbak KK, van de Bunt M, Tribble ND, Steele AM, Wensley KJ, Edghill EL, Colcough K, Barrett A, Valentínová L, Rundle JK, Raimondo A, Grimsby J, Ellard S, Gloyn AL.

Diabetes Care. 2012 Jul;35(7):1482-4. doi: 10.2337/dc11-2420. Epub 2012 May 18.

12.

Identification and functional characterisation of novel glucokinase mutations causing maturity-onset diabetes of the young in Slovakia.

Valentínová L, Beer NL, Staník J, Tribble ND, van de Bunt M, Hučková M, Barrett A, Klimeš I, Gašperíková D, Gloyn AL.

PLoS One. 2012;7(4):e34541. doi: 10.1371/journal.pone.0034541. Epub 2012 Apr 6.

13.

Co-inheritance of HNF1a and GCK mutations in a family with maturity-onset diabetes of the young (MODY): implications for genetic testing.

López-Garrido MP, Herranz-Antolín S, Alija-Merillas MJ, Giralt P, Escribano J.

Clin Endocrinol (Oxf). 2013 Sep;79(3):342-7. doi: 10.1111/cen.12050. Epub 2013 Apr 1.

PMID:
23009393
15.

GCK monogenic diabetes and gestational diabetes: possible diagnosis on clinical grounds.

Flack JR, Ross GP, Cheung NW.

Diabet Med. 2015 Dec;32(12):1596-601. doi: 10.1111/dme.12830. Epub 2015 Jul 2.

PMID:
26043405
16.

Identifying Glucokinase Monogenic Diabetes in a Multiethnic Gestational Diabetes Mellitus Cohort: New Pregnancy Screening Criteria and Utility of HbA1c.

Rudland VL, Hinchcliffe M, Pinner J, Cole S, Mercorella B, Molyneaux L, Constantino M, Yue DK, Ross GP, Wong J.

Diabetes Care. 2016 Jan;39(1):50-2. doi: 10.2337/dc15-1001. Epub 2015 Jun 24.

PMID:
26109503
17.

The glucokinase mutation p.T206P is common among MODY patients of Jewish Ashkenazi descent.

Gozlan Y, Tenenbaum A, Shalitin S, Lebenthal Y, Oron T, Cohen O, Phillip M, Gat-Yablonski G.

Pediatr Diabetes. 2012 Sep;13(6):e14-21. doi: 10.1111/j.1399-5448.2011.00822.x. Epub 2011 Oct 7.

PMID:
21978167
18.

Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry.

Sagen JV, Bjørkhaug L, Molnes J, Raeder H, Grevle L, Søvik O, Molven A, Njølstad PR.

Pediatr Diabetes. 2008 Oct;9(5):442-9. doi: 10.1111/j.1399-5448.2008.00399.x. Epub 2008 Apr 9.

PMID:
18399931
19.

Systematic assessment of etiology in adults with a clinical diagnosis of young-onset type 2 diabetes is a successful strategy for identifying maturity-onset diabetes of the young.

Thanabalasingham G, Pal A, Selwood MP, Dudley C, Fisher K, Bingley PJ, Ellard S, Farmer AJ, McCarthy MI, Owen KR.

Diabetes Care. 2012 Jun;35(6):1206-12. doi: 10.2337/dc11-1243. Epub 2012 Mar 19.

20.

Four novel cases of permanent neonatal diabetes mellitus caused by homozygous mutations in the glucokinase gene.

Bennett K, James C, Mutair A, Al-Shaikh H, Sinani A, Hussain K.

Pediatr Diabetes. 2011 May;12(3 Pt 1):192-6. doi: 10.1111/j.1399-5448.2010.00683.x. Epub 2010 Sep 6.

PMID:
21518409

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