126 related articles for article (PubMed ID: 29675256)
1. A case with relapsed transient neonatal diabetes mellitus treated with sulfonylurea, ending chronic insulin requirement.
Ando A; Nagasaka S; Ishibashi S
Endocrinol Diabetes Metab Case Rep; 2018; 2018():. PubMed ID: 29675256
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Successful sulfonylurea treatment in a patient with permanent neonatal diabetes mellitus with a novel KCNJ11 mutation.
Ahn SY; Kim GH; Yoo HW
Korean J Pediatr; 2015 Aug; 58(8):309-12. PubMed ID: 26388896
[TBL] [Abstract][Full Text] [Related]
4. Neonatal Diabetes: Case Report of a 9-Week-Old Presenting Diabetic Ketoacidosis Due to an Activating
Sood S; Landreth H; Bustinza J; Chalmers L; Thukaram R
J Investig Med High Impact Case Rep; 2017; 5(1):2324709617698718. PubMed ID: 28540314
[No Abstract] [Full Text] [Related]
5. Diabetes in very young children and mutations in the insulin-secreting cell potassium channel genes: therapeutic consequences.
Flechtner I; Vaxillaire M; Cavé H; Scharfmann R; Froguel P; Polak M
Endocr Dev; 2007; 12():86-98. PubMed ID: 17923772
[TBL] [Abstract][Full Text] [Related]
6. Successful switching from insulin to sulfonylurea in a 3-month-old infant with diabetes due to p.G53D mutation in KCNJ11.
Yoon JS; Park KJ; Sohn YB; Lee HS; Hwang JS
Ann Pediatr Endocrinol Metab; 2018 Sep; 23(3):154-157. PubMed ID: 30286572
[TBL] [Abstract][Full Text] [Related]
7. Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk.
Vedovato N; Cliff E; Proks P; Poovazhagi V; Flanagan SE; Ellard S; Hattersley AT; Ashcroft FM
Diabetologia; 2016 Jul; 59(7):1430-1436. PubMed ID: 27118464
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Patterns of postmeal insulin secretion in individuals with sulfonylurea-treated
Bowman P; McDonald TJ; Knight BA; Flanagan SE; Leveridge M; Spaull SR; Shields BM; Hammersley S; Shepherd MH; Andrews RC; Patel KA; Hattersley AT
BMJ Open Diabetes Res Care; 2019; 7(1):e000721. PubMed ID: 31908791
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [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]
13. Neonatal diabetes mellitus due to a new KCNJ11 mutation - 10 years of the patient`s follow-up.
Ješić MD; Stock H; Zdravković V; Kovačević S; Savić M; Ješić MM
Turk J Pediatr; 2021; 63(3):490-494. PubMed ID: 34254494
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Non classic presentations of a genetic mutation typically associated with transient neonatal diabetes.
Devaraja J; Elder C; Scott A
Endocrinol Diabetes Metab Case Rep; 2020 Feb; 2020():. PubMed ID: 32101525
[TBL] [Abstract][Full Text] [Related]
16. A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults.
Tarasov AI; Nicolson TJ; Riveline JP; Taneja TK; Baldwin SA; Baldwin JM; Charpentier G; Gautier JF; Froguel P; Vaxillaire M; Rutter GA
Diabetes; 2008 Jun; 57(6):1595-604. PubMed ID: 18346985
[TBL] [Abstract][Full Text] [Related]
17. Genotype-phenotype correlation of K
Gopi S; Kavitha B; Kanthimathi S; Kannan A; Kumar R; Joshi R; Kanodia S; Arya AD; Pendsey S; Pendsey S; Raghupathy P; Mohan V; Radha V
Pediatr Diabetes; 2021 Feb; 22(1):82-92. PubMed ID: 32893419
[TBL] [Abstract][Full Text] [Related]
18. Permanent neonatal diabetes by a new mutation in KCNJ11: unsuccessful switch to sulfonylurea.
Lau E; Correia C; Freitas P; Nogueira C; Costa M; Saavedra A; Costa C; Carvalho D; Fontoura M
Arch Endocrinol Metab; 2015 Dec; 59(6):559-61. PubMed ID: 26331221
[TBL] [Abstract][Full Text] [Related]
19. 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; 93(7-8):423-432. PubMed ID: 33498041
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]