BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 17635943)

  • 1. 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; 92(10):3979-85. PubMed ID: 17635943
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood.
    Flanagan SE; Patch AM; Mackay DJ; Edghill EL; Gloyn AL; Robinson D; Shield JP; Temple K; Ellard S; Hattersley AT
    Diabetes; 2007 Jul; 56(7):1930-7. PubMed ID: 17446535
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Relapsing diabetes can result from moderately activating mutations in KCNJ11.
    Gloyn AL; Reimann F; Girard C; Edghill EL; Proks P; Pearson ER; Temple IK; Mackay DJ; Shield JP; Freedenberg D; Noyes K; Ellard S; Ashcroft FM; Gribble FM; Hattersley AT
    Hum Mol Genet; 2005 Apr; 14(7):925-34. PubMed ID: 15718250
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriers.
    Stanik J; Gasperikova D; Paskova M; Barak L; Javorkova J; Jancova E; Ciljakova M; Hlava P; Michalek J; Flanagan SE; Pearson E; Hattersley AT; Ellard S; Klimes I
    J Clin Endocrinol Metab; 2007 Apr; 92(4):1276-82. PubMed ID: 17213273
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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;
    Eur J Endocrinol; 2021 Apr; 184(4):575-585. PubMed ID: 33606663
    [TBL] [Abstract][Full Text] [Related]  

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

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular and clinical features of K
    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; 18(7):532-539. PubMed ID: 27681997
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of K
    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; 12():727083. PubMed ID: 34566892
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mosaic paternal uniparental isodisomy and an ABCC8 gene mutation in a patient with permanent neonatal diabetes and hemihypertrophy.
    Shield JP; Flanagan SE; Mackay DJ; Harries LW; Proks P; Girard C; Ashcroft FM; Temple IK; Ellard S
    Diabetes; 2008 Jan; 57(1):255-8. PubMed ID: 17942821
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. AV59M KCNJ11 gene mutation leading to intermediate DEND syndrome in a Chinese child.
    Sang Y; Ni G; Gu Y; Liu M
    J Pediatr Endocrinol Metab; 2011; 24(9-10):763-6. PubMed ID: 22145471
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Incidence of neonatal diabetes in Austria-calculation based on the Austrian Diabetes Register.
    Wiedemann B; Schober E; Waldhoer T; Koehle J; Flanagan SE; Mackay DJ; Steichen E; Meraner D; Zimmerhackl LB; Hattersley AT; Ellard S; Hofer S
    Pediatr Diabetes; 2010 Feb; 11(1):18-23. PubMed ID: 19496964
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Case report: Better late than never, but sooner is better: switch from CSII to sulfonylureas in two patients with neonatal diabetes due to KCNJ11 variants.
    Mancioppi V; Pozzi E; Zanetta S; Missineo A; Savastio S; Barbetti F; Mellone S; Giordano M; Rabbone I
    Front Endocrinol (Lausanne); 2023; 14():1143736. PubMed ID: 37251668
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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;
    Lancet Diabetes Endocrinol; 2013 Nov; 1(3):199-207. PubMed ID: 24622368
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.