185 related articles for article (PubMed ID: 32104032)
1. Recent Advances in Neonatal Diabetes.
Dahl A; Kumar S
Diabetes Metab Syndr Obes; 2020; 13():355-364. PubMed ID: 32104032
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Three cases of permanent neonatal diabetes mellitus: genotypes and management outcome.
Ooi HL; Wu LL
Singapore Med J; 2012 Jul; 53(7):e142-4. PubMed ID: 22815030
[TBL] [Abstract][Full Text] [Related]
5. 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]
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. 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]
8. Successful transition to sulfonylurea therapy in two Iraqi siblings with neonatal diabetes mellitus and iDEND syndrome due to ABCC8 mutation.
Ozsu E; Giri D; Seymen Karabulut G; Senniappan S
J Pediatr Endocrinol Metab; 2016 Dec; 29(12):1403-1406. PubMed ID: 27849623
[TBL] [Abstract][Full Text] [Related]
9. Neonatal Diabetes Mellitus.
Beltrand J; Busiah K; Vaivre-Douret L; Fauret AL; Berdugo M; Cavé H; Polak M
Front Pediatr; 2020; 8():540718. PubMed ID: 33102403
[TBL] [Abstract][Full Text] [Related]
10. Transient Neonatal Diabetes Mellitus in a Very Preterm Infant due to ABCC8 Mutation.
Piccini B; Coviello C; Drovandi L; Rosangela A; Monzali F; Casalini E; Giglio S; Toni S; Dani C
AJP Rep; 2018 Jan; 8(1):e39-e42. PubMed ID: 29527407
[TBL] [Abstract][Full Text] [Related]
11. Personalized medicine switching from insulin to sulfonylurea in permanent neonatal diabetes mellitus dictated by a novel activating ABCC8 mutation.
Mak CM; Lee CY; Lam CW; Siu WK; Hung VC; Chan AY
Diagn Mol Pathol; 2012 Mar; 21(1):56-9. PubMed ID: 22306677
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. Successful transfer from insulin to oral sulfonylurea in a 3-year-old girl with a mutation in the KCNJ11 gene.
Al-Mahdi M; Al Mutair A; Al Balwi M; Hussain K
Ann Saudi Med; 2010; 30(2):162-4. PubMed ID: 20220270
[TBL] [Abstract][Full Text] [Related]
16. Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children.
Jahnavi S; Poovazhagi V; Mohan V; Bodhini D; Raghupathy P; Amutha A; Suresh Kumar P; Adhikari P; Shriraam M; Kaur T; Das AK; Molnes J; Njolstad PR; Unnikrishnan R; Radha V
Clin Genet; 2013 May; 83(5):439-45. PubMed ID: 22831748
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism.
Gloyn AL; Siddiqui J; Ellard S
Hum Mutat; 2006 Mar; 27(3):220-31. PubMed ID: 16416420
[TBL] [Abstract][Full Text] [Related]
18. Diabetes and hypoglycaemia in young children and mutations in the Kir6.2 subunit of the potassium channel: therapeutic consequences.
Flechtner I; de Lonlay P; Polak M
Diabetes Metab; 2006 Dec; 32(6):569-80. PubMed ID: 17296510
[TBL] [Abstract][Full Text] [Related]
19. Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy.
Biagiotti L; Proverbio MC; Bosio L; Gervasi F; Rovida E; Cerioni V; Bove M; Valin PS; Albarello L; Zamproni I; Grassi S; Doglioni C; Mora S; Chiumello G; Biunno I
Exp Mol Pathol; 2007 Aug; 83(1):59-64. PubMed ID: 17316607
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
