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Journal Abstract Search

350 related items for PubMed ID: 26463504

  • 1. Genetic characteristics, clinical spectrum, and incidence of neonatal diabetes in the Emirate of AbuDhabi, United Arab Emirates.
    Deeb A, Habeb A, Kaplan W, Attia S, Hadi S, Osman A, Al-Jubeh J, Flanagan S, DeFranco E, Ellard S.
    Am J Med Genet A; 2016 Mar; 170(3):602-9. PubMed ID: 26463504
    [Abstract] [Full Text] [Related]

  • 2. Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.
    Demirbilek H, Arya VB, Ozbek MN, Houghton JA, Baran RT, Akar M, Tekes S, Tuzun H, Mackay DJ, Flanagan SE, Hattersley AT, Ellard S, Hussain K.
    Eur J Endocrinol; 2015 Jun; 172(6):697-705. PubMed ID: 25755231
    [Abstract] [Full Text] [Related]

  • 3. Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience.
    Abali ZY, De Franco E, Karakilic Ozturan E, Poyrazoglu S, Bundak R, Bas F, Flanagan SE, Darendeliler F.
    Horm Res Paediatr; 2020 Jun; 93(7-8):423-432. PubMed ID: 33498041
    [Abstract] [Full Text] [Related]

  • 4. Permanent neonatal diabetes mellitus: prevalence and genetic diagnosis in the SEARCH for Diabetes in Youth Study.
    Kanakatti Shankar R, Pihoker C, Dolan LM, Standiford D, Badaru A, Dabelea D, Rodriguez B, Black MH, Imperatore G, Hattersley A, Ellard S, Gilliam LK, SEARCH for Diabetes in Youth Study Group.
    Pediatr Diabetes; 2013 May; 14(3):174-80. PubMed ID: 23050777
    [Abstract] [Full Text] [Related]

  • 5. Clinical and genetic features of Argentinian children with diabetes-onset before 12months of age: Successful transfer from insulin to oral sulfonylurea.
    Taberner P, Flanagan SE, Mackay DJ, Ellard S, Taverna MJ, Ferraro M.
    Diabetes Res Clin Pract; 2016 Jul; 117():104-10. PubMed ID: 27329029
    [Abstract] [Full Text] [Related]

  • 6. Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia.
    Habeb AM, Al-Magamsi MS, Eid IM, Ali MI, Hattersley AT, Hussain K, Ellard S.
    Pediatr Diabetes; 2012 Sep; 13(6):499-505. PubMed ID: 22060631
    [Abstract] [Full Text] [Related]

  • 7. Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of KATP-Channel Neonatal Diabetes Mellitus in Vietnam National Children's Hospital.
    Ngoc CTB, Dien TM, De Franco E, Ellard S, Houghton JAL, Lan NN, Thao BP, Khanh NN, Flanagan SE, Craig ME, Dung VC.
    Front Endocrinol (Lausanne); 2021 Sep; 12():727083. PubMed ID: 34566892
    [Abstract] [Full Text] [Related]

  • 8. Permanent neonatal diabetes: different aetiology in Arabs compared to Europeans.
    Habeb AM, Flanagan SE, Deeb A, Al-Alwan I, Alawneh H, Balafrej AA, Mutair A, Hattersley AT, Hussain K, Ellard S.
    Arch Dis Child; 2012 Aug; 97(8):721-3. PubMed ID: 22859427
    [Abstract] [Full Text] [Related]

  • 9. Neonatal diabetes mellitus: a disease linked to multiple mechanisms.
    Polak M, Cavé H.
    Orphanet J Rare Dis; 2007 Mar 09; 2():12. PubMed ID: 17349054
    [Abstract] [Full Text] [Related]

  • 10. 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 09; 58(12):1689-1700. PubMed ID: 34426871
    [Abstract] [Full Text] [Related]

  • 11. Molecular and clinical features of KATP -channel neonatal diabetes mellitus in Japan.
    Hashimoto Y, Dateki S, Hirose M, Satomura K, Sawada H, Mizuno H, Sugihara S, Maruyama K, Urakami T, Sugawara H, Shirai K, Yorifuji T.
    Pediatr Diabetes; 2017 Nov 09; 18(7):532-539. PubMed ID: 27681997
    [Abstract] [Full Text] [Related]

  • 12. Differences between transient neonatal diabetes mellitus subtypes can guide diagnosis and therapy.
    Bonfanti R, Iafusco D, Rabbone I, Diedenhofen G, Bizzarri C, Patera PI, Reinstadler P, Costantino F, Calcaterra V, Iughetti L, Savastio S, Favia A, Cardella F, Lo Presti D, Girtler Y, Rabbiosi S, D'Annunzio G, Zanfardino A, Piscopo A, Casaburo F, Pintomalli L, Russo L, Grasso V, Minuto N, Mucciolo M, Novelli A, Marucci A, Piccini B, Toni S, Silvestri F, Carrera P, Rigamonti A, Frontino G, Trada M, Tinti D, Delvecchio M, Rapini N, Schiaffini R, Mammì C, Barbetti F, Diabetes Study Group of ISPED.
    Eur J Endocrinol; 2021 Apr 09; 184(4):575-585. PubMed ID: 33606663
    [Abstract] [Full Text] [Related]

  • 13. Permanent neonatal diabetes mellitus in Jordan.
    Abujbara MA, Liswi MI, El-Khateeb MS, Flanagan SE, Ellard S, Ajlouni KM.
    J Pediatr Endocrinol Metab; 2014 Sep 09; 27(9-10):879-83. PubMed ID: 24825091
    [Abstract] [Full Text] [Related]

  • 14. The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar.
    Al-Khawaga S, Mohammed I, Saraswathi S, Haris B, Hasnah R, Saeed A, Almabrazi H, Syed N, Jithesh P, El Awwa A, Khalifa A, AlKhalaf F, Petrovski G, Abdelalim EM, Hussain K.
    Mol Genet Genomic Med; 2019 Oct 09; 7(10):e00753. PubMed ID: 31441606
    [Abstract] [Full Text] [Related]

  • 15. 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 09; 9 Suppl 2(Suppl 2):28-39. PubMed ID: 17919176
    [Abstract] [Full Text] [Related]

  • 16. Molecular basis of neonatal diabetes in Japanese patients.
    Suzuki S, Makita Y, Mukai T, Matsuo K, Ueda O, Fujieda K.
    J Clin Endocrinol Metab; 2007 Oct 09; 92(10):3979-85. PubMed ID: 17635943
    [Abstract] [Full Text] [Related]

  • 17. Sulfonylurea in the treatment of neonatal diabetes mellitus children with heterogeneous genetic backgrounds.
    Zhang M, Chen X, Shen S, Li T, Chen L, Hu M, Cao L, Cheng R, Zhao Z, Luo F.
    J Pediatr Endocrinol Metab; 2015 Jul 09; 28(7-8):877-84. PubMed ID: 25781672
    [Abstract] [Full Text] [Related]

  • 18. 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 09; 24(7):707-13. PubMed ID: 17490422
    [Abstract] [Full Text] [Related]

  • 19. 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 09; 1(3):199-207. PubMed ID: 24622368
    [Abstract] [Full Text] [Related]

  • 20. [Neonatal diabetes: a disease linked to multiple mechanisms].
    Flechtner I, Vaxillaire M, Cavé H, Froguel P, Polak M.
    Arch Pediatr; 2007 Nov 09; 14(11):1356-65. PubMed ID: 17931842
    [Abstract] [Full Text] [Related]

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