These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
70 related articles for article (PubMed ID: 22289760)
1. [Neonatal diabetes mellitus caused by KCNJ11 mutation: a case report]. Wang SY; Zhang LJ; He ZQ; Tian Q; Li XD Zhongguo Dang Dai Er Ke Za Zhi; 2012 Jan; 14(1):73-5. PubMed ID: 22289760 [No Abstract] [Full Text] [Related]
2. 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]
3. Successful sulfonylurea treatment of a neonate with neonatal diabetes mellitus due to a new KCNJ11 mutation. Ješić MM; Ješić MD; Maglajlić S; Sajić S; Necić S Diabetes Res Clin Pract; 2011 Jan; 91(1):e1-3. PubMed ID: 21056492 [TBL] [Abstract][Full Text] [Related]
4. Neonatal diabetes mellitus: description of two Puerto Rican children with KCNJ11 activating gene mutation. Nieves-Rivera F; González-Pijem L P R Health Sci J; 2011 Jun; 30(2):87-9. PubMed ID: 21682153 [TBL] [Abstract][Full Text] [Related]
5. Transfer to sulphonylurea therapy in adult subjects with permanent neonatal diabetes due to KCNJ11-activating [corrected] mutations: evidence for improvement in insulin sensitivity. Malecki MT; Skupien J; Klupa T; Wanic K; Mlynarski W; Gach A; Solecka I; Sieradzki J Diabetes Care; 2007 Jan; 30(1):147-9. PubMed ID: 17192350 [No Abstract] [Full Text] [Related]
6. KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features. Gloyn AL; Diatloff-Zito C; Edghill EL; Bellanné-Chantelot C; Nivot S; Coutant R; Ellard S; Hattersley AT; Robert JJ Eur J Hum Genet; 2006 Jul; 14(7):824-30. PubMed ID: 16670688 [TBL] [Abstract][Full Text] [Related]
7. Sulphonylurea treatment does not improve psychomotor development in children with KCNJ11 mutations causing permanent neonatal diabetes mellitus accompanied by developmental delay and epilepsy (DEND syndrome). Sumnik Z; Kolouskova S; Wales JK; Komarek V; Cinek O Diabet Med; 2007 Oct; 24(10):1176-8. PubMed ID: 17888143 [No Abstract] [Full Text] [Related]
8. Variable phenotypic spectrum of diabetes mellitus in a family carrying a novel KCNJ11 gene mutation. D'Amato E; Tammaro P; Craig TJ; Tosi A; Giorgetti R; Lorini R; Ashcroft FM Diabet Med; 2008 Jun; 25(6):651-6. PubMed ID: 18544102 [TBL] [Abstract][Full Text] [Related]
10. 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]
12. Sulfonylurea-responsive diabetes in childhood. Landau Z; Wainstein J; Hanukoglu A; Tuval M; Lavie J; Glaser B J Pediatr; 2007 May; 150(5):553-5. PubMed ID: 17452235 [TBL] [Abstract][Full Text] [Related]
13. Transition from insulin to glyburide in a 4-month-old girl with neonatal diabetes mellitus caused by a mutation in KCNJ11. Chan YM; Laffel LM Pediatr Diabetes; 2007 Aug; 8(4):235-8. PubMed ID: 17659066 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Islet-specific antibody seroconversion in patients with long duration of permanent neonatal diabetes caused by mutations in the KCNJ11 gene. Gach A; Wyka K; Malecki MT; Noczynska A; Skupien J; Nazim J; Szalecki M; Bodalski J; Sieradzki J; Mlynarski W Diabetes Care; 2007 Aug; 30(8):2080-2. PubMed ID: 17475937 [No Abstract] [Full Text] [Related]
17. Mutations at the same residue (R50) of Kir6.2 (KCNJ11) that cause neonatal diabetes produce different functional effects. Shimomura K; Girard CA; Proks P; Nazim J; Lippiat JD; Cerutti F; Lorini R; Ellard S; Hattersley AT; Barbetti F; Ashcroft FM Diabetes; 2006 Jun; 55(6):1705-12. PubMed ID: 16731833 [TBL] [Abstract][Full Text] [Related]
18. A novel mutation of KCNJ11 gene in a patient with permanent neonatal diabetes mellitus. Chang WL; Huang CJ; Lei TH; Niu DM; Chiu CY; Jap TS Diabetes Res Clin Pract; 2014 Apr; 104(1):e29-32. PubMed ID: 24468099 [TBL] [Abstract][Full Text] [Related]
19. [Low doses of sulphonyluria as a successful replacement for insulin therapy in a patient with neonatal diabetes due to a mutation of KCNJ11 gene encoding Kir6.2]. Ille J; Putarek NR; Radica A; Hattersley A; Ellard S; Dumić M Lijec Vjesn; 2010; 132(3-4):90-3. PubMed ID: 20540435 [TBL] [Abstract][Full Text] [Related]
20. Neonatal diabetes in a child positive for islet cell antibodies at onset and Kir6.2 activating mutation. Gach A; Wyka K; Pietrzak I; Wegner O; Malecki MT; Mlynarski W Diabetes Res Clin Pract; 2009 Nov; 86(2):e25-7. PubMed ID: 19692135 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]