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Journal Abstract Search

271 related items for PubMed ID: 22996131

  • 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. PubMed ID: 22996131
    [Abstract] [Full Text] [Related]

  • 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 Dec; 6(1):54-8. PubMed ID: 23014256
    [Abstract] [Full Text] [Related]

  • 3. 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. PubMed ID: 21989597
    [Abstract] [Full Text] [Related]

  • 4. 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. PubMed ID: 22842804
    [Abstract] [Full Text] [Related]

  • 5. Monogenic Forms of Diabetes Mellitus.
    Gaál Z, Balogh I.
    Exp Suppl; 2019 Aug; 111():385-416. PubMed ID: 31588541
    [Abstract] [Full Text] [Related]

  • 6. [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 Aug; 14(1):45-9. PubMed ID: 18577347
    [Abstract] [Full Text] [Related]

  • 7. 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. PubMed ID: 19342262
    [Abstract] [Full Text] [Related]

  • 8. 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. PubMed ID: 21796147
    [Abstract] [Full Text] [Related]

  • 9. 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. PubMed ID: 17259376
    [Abstract] [Full Text] [Related]

  • 10. 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. PubMed ID: 22704848
    [Abstract] [Full Text] [Related]

  • 11. 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. PubMed ID: 20092027
    [Abstract] [Full Text] [Related]

  • 12. 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. PubMed ID: 22210575
    [Abstract] [Full Text] [Related]

  • 13. 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. PubMed ID: 22831748
    [Abstract] [Full Text] [Related]

  • 14. ATP-sensitive potassium channels--neonatal diabetes mellitus and beyond.
    Sperling MA.
    N Engl J Med; 2006 Aug 03; 355(5):507-10. PubMed ID: 16885555
    [No Abstract] [Full Text] [Related]

  • 15. Genetic causes and treatment of neonatal diabetes and early childhood diabetes.
    Barbetti F, D'Annunzio G.
    Best Pract Res Clin Endocrinol Metab; 2018 Aug 03; 32(4):575-591. PubMed ID: 30086875
    [Abstract] [Full Text] [Related]

  • 16. Effective treatment of diabetes caused by activating ABCC8/SUR1 mutation with glimepiride.
    Karges B, Schnur D, Ellard S, Kentrup H, Karges W.
    Diabet Med; 2012 May 03; 29(5):692-3. PubMed ID: 21992555
    [No Abstract] [Full Text] [Related]

  • 17. [Three-year observation of permanent neonatal diabetes].
    Noczyńska A, Zubkiewicz-Kucharska A, Salmonowicz B, Małecki M, Młynarski W.
    Pediatr Endocrinol Diabetes Metab; 2010 May 03; 16(1):50-4. PubMed ID: 20529607
    [Abstract] [Full Text] [Related]

  • 18. Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment.
    Greeley SA, Naylor RN, Philipson LH, Bell GI.
    Curr Diab Rep; 2011 Dec 03; 11(6):519-32. PubMed ID: 21993633
    [Abstract] [Full Text] [Related]

  • 19. Successful transfer to sulfonylurea therapy in an infant with developmental delay, epilepsy and neonatal diabetes (DEND) syndrome and a novel ABCC8 gene mutation.
    Zwaveling-Soonawala N, Hagebeuk EE, Slingerland AS, Ris-Stalpers C, Vulsma T, van Trotsenburg AS.
    Diabetologia; 2011 Feb 03; 54(2):469-71. PubMed ID: 21109997
    [No Abstract] [Full Text] [Related]

  • 20. Type 2 diabetes-associated missense polymorphisms KCNJ11 E23K and ABCC8 A1369S influence progression to diabetes and response to interventions in the Diabetes Prevention Program.
    Florez JC, Jablonski KA, Kahn SE, Franks PW, Dabelea D, Hamman RF, Knowler WC, Nathan DM, Altshuler D.
    Diabetes; 2007 Feb 03; 56(2):531-6. PubMed ID: 17259403
    [Abstract] [Full Text] [Related]

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