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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

190 related articles for article (PubMed ID: 20686794)

  • 21. A syndrome of congenital hyperinsulinism and rhabdomyolysis is caused by KCNJ11 mutation.
    Albaqumi M; Alhabib FA; Shamseldin HE; Mohammed F; Alkuraya FS
    J Med Genet; 2014 Apr; 51(4):271-4. PubMed ID: 24421282
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Congenital hyperinsulinism in Brazilian neonates: a study of histology, KATP channel genes, and proliferation of β cells.
    Lovisolo SM; Mendonça BB; Pinto EM; Manna TD; Saldiva PH; Zerbini MC
    Pediatr Dev Pathol; 2010; 13(5):375-84. PubMed ID: 20482375
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Therapies and outcomes of congenital hyperinsulinism-induced hypoglycaemia.
    Banerjee I; Salomon-Estebanez M; Shah P; Nicholson J; Cosgrove KE; Dunne MJ
    Diabet Med; 2019 Jan; 36(1):9-21. PubMed ID: 30246418
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genotype-phenotype associations in patients with severe hyperinsulinism of infancy.
    Greer RM; Shah J; Jeske YW; Brown D; Walker RM; Cowley D; Bowling FG; Liaskou D; Harris M; Thomsett MJ; Choong C; Bell JR; Jack MM; Cotterill AM
    Pediatr Dev Pathol; 2007; 10(1):25-34. PubMed ID: 17378627
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Hyperinsulinemic hypoglycemia evolving to gestational diabetes and diabetes mellitus in a family carrying the inactivating ABCC8 E1506K mutation.
    Vieira TC; Bergamin CS; Gurgel LC; Moisés RS
    Pediatr Diabetes; 2010 Nov; 11(7):505-8. PubMed ID: 20042013
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Clinical and genetic evaluation of patients with KATP channel mutations from the German registry for congenital hyperinsulinism.
    Mohnike K; Wieland I; Barthlen W; Vogelgesang S; Empting S; Mohnike W; Meissner T; Zenker M
    Horm Res Paediatr; 2014; 81(3):156-68. PubMed ID: 24401662
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Congenital hyperinsulinism in Chinese patients: 5-yr treatment outcome of 95 clinical cases with genetic analysis of 55 cases.
    Gong C; Huang S; Su C; Qi Z; Liu F; Wu D; Cao B; Gu Y; Li W; Liang X; Liu M
    Pediatr Diabetes; 2016 May; 17(3):227-34. PubMed ID: 25639667
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cognitive and developmental outcome of conservatively treated children with congenital hyperinsulinism.
    Levy-Shraga Y; Pinhas-Hamiel O; Kraus-Houminer E; Landau H; Mazor-Aronovitch K; Modan-Moses D; Gillis D; Koren I; Dollberg D; Gabis LV
    J Pediatr Endocrinol Metab; 2013; 26(3-4):301-8. PubMed ID: 23327786
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Octreotide-induced hepatitis in a child with persistent hyperinsulinemia hypoglycemia of infancy.
    Ben-Ari J; Greenberg M; Nemet D; Edelstein E; Eliakim A
    J Pediatr Endocrinol Metab; 2013; 26(1-2):179-82. PubMed ID: 23327813
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Efficacy and safety of long-term, continuous subcutaneous octreotide infusion for patients with different subtypes of KATP-channel hyperinsulinism.
    Yorifuji T; Kawakita R; Hosokawa Y; Fujimaru R; Matsubara K; Aizu K; Suzuki S; Nagasaka H; Nishibori H; Masue M
    Clin Endocrinol (Oxf); 2013 Jun; 78(6):891-7. PubMed ID: 23067144
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A multidisciplinary approach to the focal form of congenital hyperinsulinism leads to successful treatment by partial pancreatectomy.
    Adzick NS; Thornton PS; Stanley CA; Kaye RD; Ruchelli E
    J Pediatr Surg; 2004 Mar; 39(3):270-5. PubMed ID: 15017536
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Characterization of the ABCC8 gene mutation and phenotype in patients with congenital hyperinsulinism in western Saudi Arabia.
    Al-Agha AE; Ahmad IA
    Saudi Med J; 2013 Oct; 34(10):1002-6. PubMed ID: 24145932
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The surgical management of congenital hyperinsulinemic hypoglycemia in infancy.
    Fékété CN; de Lonlay P; Jaubert F; Rahier J; Brunelle F; Saudubray JM
    J Pediatr Surg; 2004 Mar; 39(3):267-9. PubMed ID: 15017535
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations.
    Demirbilek H; Arya VB; Ozbek MN; Akinci A; Dogan M; Demirel F; Houghton J; Kaba S; Guzel F; Baran RT; Unal S; Tekkes S; Flanagan SE; Ellard S; Hussain K
    Eur J Endocrinol; 2014 Jun; 170(6):885-92. PubMed ID: 24686051
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical characteristics, outcome, and predictors of neurological sequelae of persistent congenital hyperinsulinism: A single tertiary center experience.
    Laimon W; Aboelenin HM; El Tantawi NT
    Pediatr Diabetes; 2021 May; 22(3):388-399. PubMed ID: 33528087
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Congenital hyperinsulinism in the north-east Netherlands. Clinical features and DNA diagnostics in 22 children].
    Verheul JC; Ris-Stalpers C; Bikker H; Bakker-van Waarde WM; Noordam C
    Ned Tijdschr Geneeskd; 2011; 155(32):A3343. PubMed ID: 21835061
    [TBL] [Abstract][Full Text] [Related]  

  • 38. High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.
    Rozenkova K; Malikova J; Nessa A; Dusatkova L; Bjørkhaug L; Obermannova B; Dusatkova P; Kytnarova J; Aukrust I; Najmi LA; Rypackova B; Sumnik Z; Lebl J; Njølstad PR; Hussain K; Pruhova S
    J Clin Endocrinol Metab; 2015 Dec; 100(12):E1540-9. PubMed ID: 26431509
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The difficult management of persistent, non-focal congenital hyperinsulinism: A retrospective review from a single, tertiary center.
    Rasmussen AG; Melikian M; Globa E; Detlefsen S; Rasmussen L; Petersen H; Brusgaard K; Rasmussen AH; Mortensen MB; Christesen HT
    Pediatr Diabetes; 2020 May; 21(3):441-455. PubMed ID: 31997554
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Successful treatment of congenital hyperinsulinism with long-acting release octreotide.
    Le Quan Sang KH; Arnoux JB; Mamoune A; Saint-Martin C; Bellanné-Chantelot C; Valayannopoulos V; Brassier A; Kayirangwa H; Barbier V; Broissand C; Fabreguettes JR; Charron B; Thalabard JC; de Lonlay P
    Eur J Endocrinol; 2012 Feb; 166(2):333-9. PubMed ID: 22048969
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.