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Items: 1 to 20 of 175

1.

Monogenic models: what have the single gene disorders taught us?

Klupa T, Skupien J, Malecki MT.

Curr Diab Rep. 2012 Dec;12(6):659-66. doi: 10.1007/s11892-012-0325-0. Review.

2.

Genetics of type 2 diabetes mellitus and other specific types of diabetes; its role in treatment modalities.

Kota SK, Meher LK, Jammula S, Kota SK, Modi KD.

Diabetes Metab Syndr. 2012 Jan-Mar;6(1):54-8. doi: 10.1016/j.dsx.2012.05.014. Review.

PMID:
23014256
3.

[Permanent neonatal diabetes with known genetic background: oral drugs in treatment of childhood diabetes].

Gach A, Gadzicka A, Młynarski W.

Pediatr Endocrinol Diabetes Metab. 2008;14(1):45-9. Review. Polish.

PMID:
18577347
4.

Heterozygous ABCC8 mutations are a cause of MODY.

Bowman P, Flanagan SE, Edghill EL, Damhuis A, Shepherd MH, Paisey R, Hattersley AT, Ellard S.

Diabetologia. 2012 Jan;55(1):123-7. doi: 10.1007/s00125-011-2319-x.

PMID:
21989597
5.

Effects of single nucleotide polymorphisms in K(ATP) channel genes on type 2 diabetes in a Turkish population.

Gonen MS, Arikoglu H, Erkoc Kaya D, Ozdemir H, Ipekci SH, Arslan A, Kayis SA, Gogebakan B.

Arch Med Res. 2012 May;43(4):317-23. doi: 10.1016/j.arcmed.2012.06.001.

PMID:
22704848
6.

Clinical and metabolic features of adult-onset diabetes caused by ABCC8 mutations.

Riveline JP, Rousseau E, Reznik Y, Fetita S, Philippe J, Dechaume A, Hartemann A, Polak M, Petit C, Charpentier G, Gautier JF, Froguel P, Vaxillaire M.

Diabetes Care. 2012 Feb;35(2):248-51. doi: 10.2337/dc11-1469.

7.

A pathway to insulin independence in newborns and infants with diabetes.

Shahawy S, Chan NK, Ellard S, Young E, Shahawy H, Mace J, Peverini R, Chinnock R, Njolstad PR, Hattersley AT, Hathout E.

J Perinatol. 2011 Aug;31(8):567-70. doi: 10.1038/jp.2011.4.

PMID:
21796147
8.

Mutations in the ABCC8 gene can cause autoantibody-negative insulin-dependent diabetes.

Hartemann-Heurtier A, Simon A, Bellanné-Chantelot C, Reynaud R, Cavé H, Polak M, Vaxillaire M, Grimaldi A.

Diabetes Metab. 2009 Jun;35(3):233-5. doi: 10.1016/j.diabet.2009.01.003.

9.

Successful sulfonylurea treatment of a neonate with neonatal diabetes mellitus due to a novel missense mutation, p.P1199L, in the ABCC8 gene.

Oztekin O, Durmaz E, Kalay S, Flanagan SE, Ellard S, Bircan I.

J Perinatol. 2012 Aug;32(8):645-7. doi: 10.1038/jp.2012.46.

PMID:
22842804
10.

An ATP-binding mutation (G334D) in KCNJ11 is associated with a sulfonylurea-insensitive form of developmental delay, epilepsy, and neonatal diabetes.

Masia R, Koster JC, Tumini S, Chiarelli F, Colombo C, Nichols CG, Barbetti F.

Diabetes. 2007 Feb;56(2):328-36.

11.

Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children.

Jahnavi S, Poovazhagi V, Mohan V, Bodhini D, Raghupathy P, Amutha A, Suresh Kumar P, Adhikari P, Shriraam M, Kaur T, Das AK, Molnes J, Njolstad PR, Unnikrishnan R, Radha V.

Clin Genet. 2013 May;83(5):439-45. doi: 10.1111/j.1399-0004.2012.01939.x.

PMID:
22831748
12.

Transient neonatal diabetes due to activating mutation in the ABCC8 gene encoding SUR1.

Batra CM, Gupta N, Atwal G, Gupta V.

Indian J Pediatr. 2009 Nov;76(11):1169-72.

PMID:
20092027
13.

Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes.

Murphy R, Ellard S, Hattersley AT.

Nat Clin Pract Endocrinol Metab. 2008 Apr;4(4):200-13. doi: 10.1038/ncpendmet0778. Review.

PMID:
18301398
14.

[Progress in diabetes genetics].

Njølstad PR, Hertel JK, Søvik O, Raeder H, Johansson S, Molven A.

Tidsskr Nor Laegeforen. 2010 Jun 3;130(11):1145-9. doi: 10.4045/tidsskr.09.1035. Review. Norwegian.

16.

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus.

Babenko AP, Polak M, Cavé H, Busiah K, Czernichow P, Scharfmann R, Bryan J, Aguilar-Bryan L, Vaxillaire M, Froguel P.

N Engl J Med. 2006 Aug 3;355(5):456-66.

17.

[Three-year observation of permanent neonatal diabetes].

Noczyńska A, Zubkiewicz-Kucharska A, Salmonowicz B, Małecki M, Młynarski W.

Pediatr Endocrinol Diabetes Metab. 2010;16(1):50-4. Polish.

PMID:
20529607
18.

Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Diabetes) Study Group.

Polak M, Dechaume A, Cavé H, Nimri R, Crosnier H, Sulmont V, de Kerdanet M, Scharfmann R, Lebenthal Y, Froguel P, Vaxillaire M; French ND (Neonatal Diabetes) Study Group..

Diabetes. 2008 Apr;57(4):1115-9. doi: 10.2337/db07-1358.

19.

Effect of genetic variants in KCNJ11, ABCC8, PPARG and HNF4A loci on the susceptibility of type 2 diabetes in Chinese Han population.

Wang F, Han XY, Ren Q, Zhang XY, Han LC, Luo YY, Zhou XH, Ji LN.

Chin Med J (Engl). 2009 Oct 20;122(20):2477-82.

PMID:
20079163
20.
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