128 related articles for article (PubMed ID: 21910811)
1. Early-onset, severe lipoatrophy in a patient with permanent neonatal diabetes mellitus secondary to a recessive mutation in the INS gene.
Rachmiel M; Rubio-Cabezas O; Ellard S; Hattersley AT; Perlman K
Pediatr Diabetes; 2012 Sep; 13(6):e26-9. PubMed ID: 21910811
[TBL] [Abstract][Full Text] [Related]
2. [Permanent neonatal diabetes and recessive mutation in the INS gene: a familial history].
Di Benedetto M; Richard O; Pélissier P; Darteyre S; Cavé H; Stéphan JL
Arch Pediatr; 2013 Feb; 20(2):199-202. PubMed ID: 23245869
[TBL] [Abstract][Full Text] [Related]
3. Permanent neonatal diabetes mellitus due to a C96Y heterozygous mutation in the insulin gene. A case report.
Ahamed A; Unnikrishnan AG; Pendsey SS; Nampoothiri S; Bhavani N; Praveen VP; Kumar H; Jayakumar RV; Nair V; Ellard S; Edghill EL
JOP; 2008 Nov; 9(6):715-8. PubMed ID: 18981553
[TBL] [Abstract][Full Text] [Related]
4. Novel homozygous likely-pathogenic intronic variant in INS causing permanent neonatal diabetes in siblings.
Courtney R; Gamble C; Arango ML; Shah A; Rubio NI; Nguyen J; Rodriguez-Buritica D
J Pediatr Endocrinol Metab; 2016 Sep; 29(9):1089-93. PubMed ID: 27487489
[TBL] [Abstract][Full Text] [Related]
5. Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.
Molven A; Ringdal M; Nordbø AM; Raeder H; Støy J; Lipkind GM; Steiner DF; Philipson LH; Bergmann I; Aarskog D; Undlien DE; Joner G; Søvik O; ; Bell GI; Njølstad PR
Diabetes; 2008 Apr; 57(4):1131-5. PubMed ID: 18192540
[TBL] [Abstract][Full Text] [Related]
6. Rare types of diabetes mellitus.
Mihai B; Mihai C; Cijevschi-Prelipcean C; Lăcătuşu C
Rev Med Chir Soc Med Nat Iasi; 2012; 116(3):700-7. PubMed ID: 23272513
[TBL] [Abstract][Full Text] [Related]
7. Molecular scanning of beta-3-adrenergic receptor gene in total congenital lipoatrophic diabetes mellitus.
Silver K; Walston J; Plotnick L; Taylor SI; Kahn CR; Shuldiner AR
J Clin Endocrinol Metab; 1997 Oct; 82(10):3395-8. PubMed ID: 9329375
[TBL] [Abstract][Full Text] [Related]
8. KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.
Massa O; Iafusco D; D'Amato E; Gloyn AL; Hattersley AT; Pasquino B; Tonini G; Dammacco F; Zanette G; Meschi F; Porzio O; Bottazzo G; Crinó A; Lorini R; Cerutti F; Vanelli M; Barbetti F;
Hum Mutat; 2005 Jan; 25(1):22-7. PubMed ID: 15580558
[TBL] [Abstract][Full Text] [Related]
9. Outpatient transition of an infant with permanent neonatal diabetes due to a KCNJ11 activating mutation from subcutaneous insulin to oral glyburide.
Bremer AA; Ranadive S; Lustig RH
Pediatr Diabetes; 2008 Jun; 9(3 Pt 1):236-9. PubMed ID: 18221420
[TBL] [Abstract][Full Text] [Related]
10. Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.
Gloyn AL; Pearson ER; Antcliff JF; Proks P; Bruining GJ; Slingerland AS; Howard N; Srinivasan S; Silva JM; Molnes J; Edghill EL; Frayling TM; Temple IK; Mackay D; Shield JP; Sumnik Z; van Rhijn A; Wales JK; Clark P; Gorman S; Aisenberg J; Ellard S; Njølstad PR; Ashcroft FM; Hattersley AT
N Engl J Med; 2004 Apr; 350(18):1838-49. PubMed ID: 15115830
[TBL] [Abstract][Full Text] [Related]
11. Identification of insulin gene variants in patients with neonatal diabetes in the Chinese population.
Fu J; Wang T; Li M; Xiao X
J Diabetes Investig; 2020 May; 11(3):578-584. PubMed ID: 31605659
[TBL] [Abstract][Full Text] [Related]
12. A family with permanent neonatal diabetes due to a novel mutation in INS gene.
Dimova R; Tankova T; Gergelcheva I; Tournev I; Konstantinova M
Diabetes Res Clin Pract; 2015 May; 108(2):e28-30. PubMed ID: 25765664
[TBL] [Abstract][Full Text] [Related]
13. Bilateral cataracts in a 6-yr-old with new onset diabetes: a novel presentation of a known INS gene mutation.
Wasserman H; Hufnagel RB; Miraldi Utz V; Zhang K; Valencia CA; Leslie ND; Crimmins NA
Pediatr Diabetes; 2016 Nov; 17(7):535-539. PubMed ID: 26530398
[TBL] [Abstract][Full Text] [Related]
14. Case report: A 10-year prognosis of neonatal diabetes caused by a novel
Tian M; Feng Y; Liu Y; Wang H
Front Endocrinol (Lausanne); 2022; 13():1086785. PubMed ID: 36686471
[TBL] [Abstract][Full Text] [Related]
15. Permanent neonatal diabetes caused by a homozygous nonsense mutation in the glucokinase gene.
Rubio-Cabezas O; Díaz González F; Aragonés A; Argente J; Campos-Barros A
Pediatr Diabetes; 2008 Jun; 9(3 Pt 1):245-9. PubMed ID: 18298419
[TBL] [Abstract][Full Text] [Related]
16. A Novel c.125 T>G (p.Val42Gly) Mutation in The Human INS Gene Leads to Neonatal Diabetes Mellitus via a Decrease in Insulin Synthesis.
Sun F; Du W; Ma J; Gu M; Wang J; Zhu H; Song H; Gao G
Exp Clin Endocrinol Diabetes; 2020 Mar; 128(3):182-189. PubMed ID: 29890547
[TBL] [Abstract][Full Text] [Related]
17. Emergence of insulin resistance following empirical glibenclamide therapy: a case report of neonatal diabetes with a recessive INS gene mutation.
Yildiz M; Akcay T; Aydin B; Akgun A; Dogan BB; De Franco E; Ellard S; Onal H
J Pediatr Endocrinol Metab; 2018 Mar; 31(3):345-348. PubMed ID: 29305569
[TBL] [Abstract][Full Text] [Related]
18. A new variant of a known mutation in two siblings with permanent neonatal diabetes mellitus.
Aycan Z; Cetinkaya S; Oğuz SS; Ceylaner S
J Pediatr Endocrinol Metab; 2011; 24(5-6):373-5. PubMed ID: 21823539
[TBL] [Abstract][Full Text] [Related]
19. Neonatal diabetes due to homozygous INS gene promoter mutations: Highly variable phenotype, remission and early relapse during the first 3 years of life.
Demiral M; Demirbilek H; Çelik K; Okur N; Hussain K; Ozbek MN
Pediatr Diabetes; 2020 Nov; 21(7):1169-1175. PubMed ID: 32656923
[TBL] [Abstract][Full Text] [Related]
20. Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.
Shaw-Smith C; Flanagan SE; Patch AM; Grulich-Henn J; Habeb AM; Hussain K; Pomahacova R; Matyka K; Abdullah M; Hattersley AT; Ellard S
Pediatr Diabetes; 2012 Jun; 13(4):314-21. PubMed ID: 22369132
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]