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Journal Abstract Search

391 related items for PubMed ID: 27329029

  • 21. Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study.
    Bowman P, Sulen Å, Barbetti F, Beltrand J, Svalastoga P, Codner E, Tessmann EH, Juliusson PB, Skrivarhaug T, Pearson ER, Flanagan SE, Babiker T, Thomas NJ, Shepherd MH, Ellard S, Klimes I, Szopa M, Polak M, Iafusco D, Hattersley AT, Njølstad PR, Neonatal Diabetes International Collaborative Group.
    Lancet Diabetes Endocrinol; 2018 Aug; 6(8):637-646. PubMed ID: 29880308
    [Abstract] [Full Text] [Related]

  • 22. Long-term Follow-up of Glycemic and Neurological Outcomes in an International Series of Patients With Sulfonylurea-Treated ABCC8 Permanent Neonatal Diabetes.
    Bowman P, Mathews F, Barbetti F, Shepherd MH, Sanchez J, Piccini B, Beltrand J, Letourneau-Freiberg LR, Polak M, Greeley SAW, Rawlins E, Babiker T, Thomas NJ, De Franco E, Ellard S, Flanagan SE, Hattersley AT, Neonatal Diabetes International Collaborative Group.
    Diabetes Care; 2021 Jan; 44(1):35-42. PubMed ID: 33184150
    [Abstract] [Full Text] [Related]

  • 23. [Neonatal diabetes: a disease linked to multiple mechanisms].
    Flechtner I, Vaxillaire M, Cavé H, Froguel P, Polak M.
    Arch Pediatr; 2007 Nov; 14(11):1356-65. PubMed ID: 17931842
    [Abstract] [Full Text] [Related]

  • 24. 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; 11(6):519-32. PubMed ID: 21993633
    [Abstract] [Full Text] [Related]

  • 25. Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes.
    Babiker T, Vedovato N, Patel K, Thomas N, Finn R, Männikkö R, Chakera AJ, Flanagan SE, Shepherd MH, Ellard S, Ashcroft FM, Hattersley AT.
    Diabetologia; 2016 Jun; 59(6):1162-6. PubMed ID: 27033559
    [Abstract] [Full Text] [Related]

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

  • 27.
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  • 28. Functional characterization of activating mutations in the sulfonylurea receptor 1 (ABCC8) causing neonatal diabetes mellitus in Asian Indian children.
    Balamurugan K, Kavitha B, Yang Z, Mohan V, Radha V, Shyng SL.
    Pediatr Diabetes; 2019 Jun; 20(4):397-407. PubMed ID: 30861254
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  • 30. Genetic and clinical features of neonatal and early onset diabetes mellitus in a tertiary center cohort in Brazil.
    Costa-Riquetto AD, de Santana LS, Franco PC, Jr ACS, Martio AE, Lisboa HRK, Kohara SK, Teles MG.
    Clin Genet; 2023 Apr; 103(4):434-447. PubMed ID: 36510364
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  • 32. Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study [corrected].
    Busiah K, Drunat S, Vaivre-Douret L, Bonnefond A, Simon A, Flechtner I, Gérard B, Pouvreau N, Elie C, Nimri R, De Vries L, Tubiana-Rufi N, Metz C, Bertrand AM, Nivot-Adamiak S, de Kerdanet M, Stuckens C, Jennane F, Souchon PF, Le Tallec C, Désirée C, Pereira S, Dechaume A, Robert JJ, Phillip M, Scharfmann R, Czernichow P, Froguel P, Vaxillaire M, Polak M, Cavé H, French NDM study group.
    Lancet Diabetes Endocrinol; 2013 Nov; 1(3):199-207. PubMed ID: 24622368
    [Abstract] [Full Text] [Related]

  • 33. Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period.
    Patch AM, Flanagan SE, Boustred C, Hattersley AT, Ellard S.
    Diabetes Obes Metab; 2007 Nov; 9 Suppl 2(Suppl 2):28-39. PubMed ID: 17919176
    [Abstract] [Full Text] [Related]

  • 34. Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene.
    Tonini G, Bizzarri C, Bonfanti R, Vanelli M, Cerutti F, Faleschini E, Meschi F, Prisco F, Ciacco E, Cappa M, Torelli C, Cauvin V, Tumini S, Iafusco D, Barbetti F, Early-Onset Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology.
    Diabetologia; 2006 Sep; 49(9):2210-3. PubMed ID: 16816952
    [No Abstract] [Full Text] [Related]

  • 35. Clinical presentation and long-term outcome of patients with KCNJ11/ABCC8 variants: Neonatal diabetes or MODY in the DPV registry from Germany and Austria.
    Warncke K, Eckert A, Kapellen T, Kummer S, Raile K, Dunstheimer D, Grulich-Henn J, Woelfle J, Wenzel S, Hofer SE, Dost A, Holl RW.
    Pediatr Diabetes; 2022 Nov; 23(7):999-1008. PubMed ID: 35822653
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  • 37. The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities.
    Rica I, Luzuriaga C, Pérez de Nanclares G, Estalella I, Aragonés A, Barrio R, Bilbao JR, Carlés C, Fernández C, Fernández JM, Fernández-Rebollo E, Gastaldo E, Giralt P, Gomez Vida JM, Gutiérrez A, López Siguero JP, Martínez-Aedo MJ, Muñoz M, Prieto J, Rodrigo J, Vargas F, Castano L.
    Diabet Med; 2007 Jul; 24(7):707-13. PubMed ID: 17490422
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  • 39. Permanent diabetes during the first year of life: multiple gene screening in 54 patients.
    Russo L, Iafusco D, Brescianini S, Nocerino V, Bizzarri C, Toni S, Cerutti F, Monciotti C, Pesavento R, Iughetti L, Bernardini L, Bonfanti R, Gargantini L, Vanelli M, Aguilar-Bryan L, Stazi MA, Grasso V, Colombo C, Barbetti F, ISPED Early Diabetes Study Group.
    Diabetologia; 2011 Jul; 54(7):1693-701. PubMed ID: 21544516
    [Abstract] [Full Text] [Related]

  • 40. Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience.
    Laimon W, El-Ziny M, El-Hawary A, Elsharkawy A, Salem NA, Aboelenin HM, Awad MH, Flanagan SE, De Franco E.
    Acta Diabetol; 2021 Dec; 58(12):1689-1700. PubMed ID: 34426871
    [Abstract] [Full Text] [Related]

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