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 *

484 related articles for article (PubMed ID: 21967988)

  • 1. Congenital hyperinsulinism: current trends in diagnosis and therapy.
    Arnoux JB; Verkarre V; Saint-Martin C; Montravers F; Brassier A; Valayannopoulos V; Brunelle F; Fournet JC; Robert JJ; Aigrain Y; Bellanné-Chantelot C; de Lonlay P
    Orphanet J Rare Dis; 2011 Oct; 6():63. PubMed ID: 21967988
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Congenital hyperinsulinism in newborn and infant].
    Giurgea I; Ribeiro MJ; Boddaert N; Touati G; Robert JJ; Saudubray JM; Jaubert F; Bellanné-Chantelot C; Brunelle F; Nihoul-Fékété C; de Lonlay P
    Arch Pediatr; 2005 Nov; 12(11):1628-35. PubMed ID: 16198094
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital hyperinsulinism.
    Arnoux JB; de Lonlay P; Ribeiro MJ; Hussain K; Blankenstein O; Mohnike K; Valayannopoulos V; Robert JJ; Rahier J; Sempoux C; Bellanné C; Verkarre V; Aigrain Y; Jaubert F; Brunelle F; Nihoul-Fékété C
    Early Hum Dev; 2010 May; 86(5):287-94. PubMed ID: 20550977
    [TBL] [Abstract][Full Text] [Related]  

  • 4. ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism.
    Bellanné-Chantelot C; Saint-Martin C; Ribeiro MJ; Vaury C; Verkarre V; Arnoux JB; Valayannopoulos V; Gobrecht S; Sempoux C; Rahier J; Fournet JC; Jaubert F; Aigrain Y; Nihoul-Fékété C; de Lonlay P
    J Med Genet; 2010 Nov; 47(11):752-9. PubMed ID: 20685672
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinism.
    Chandran S; Peng FY; Rajadurai VS; Lu YT; Chang KT; Flanagan SE; Ellard S; Hussain K
    Endocrinol Diabetes Metab Case Rep; 2013; 2013():130041. PubMed ID: 24616771
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations.
    Arya VB; Guemes M; Nessa A; Alam S; Shah P; Gilbert C; Senniappan S; Flanagan SE; Ellard S; Hussain K
    Eur J Endocrinol; 2014 Dec; 171(6):685-95. PubMed ID: 25201519
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The diagnosis of ectopic focal hyperinsulinism of infancy with [18F]-dopa positron emission tomography.
    Hussain K; Seppänen M; Näntö-Salonen K; Adzick NS; Stanley CA; Thornton P; Minn H
    J Clin Endocrinol Metab; 2006 Aug; 91(8):2839-42. PubMed ID: 16684819
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital hyperinsulinism: pancreatic [18F]fluoro-L-dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochemistry study of DOPA decarboxylase and insulin secretion.
    de Lonlay P; Simon-Carre A; Ribeiro MJ; Boddaert N; Giurgea I; Laborde K; Bellanné-Chantelot C; Verkarre V; Polak M; Rahier J; Syrota A; Seidenwurm D; Nihoul-Fékété C; Robert JJ; Brunelle F; Jaubert F
    J Clin Endocrinol Metab; 2006 Mar; 91(3):933-40. PubMed ID: 16403819
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hyperinsulinism in the Neonate.
    Lord K; De León DD
    Clin Perinatol; 2018 Mar; 45(1):61-74. PubMed ID: 29406007
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The heterogeneity of focal forms of congenital hyperinsulinism.
    Ismail D; Kapoor RR; Smith VV; Ashworth M; Blankenstein O; Pierro A; Flanagan SE; Ellard S; Hussain K
    J Clin Endocrinol Metab; 2012 Jan; 97(1):E94-9. PubMed ID: 22031516
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rapid genetic analysis, imaging with 18F-DOPA-PET/CT scan and laparoscopic surgery in congenital hyperinsulinism.
    Cherubini V; Bagalini LS; Ianilli A; Marigliano M; Biagioni M; Carnielli V; Iasonni V; Berbellini A; Hussain K; Gabrielli O
    J Pediatr Endocrinol Metab; 2010; 23(1-2):171-7. PubMed ID: 20432820
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Perspective on the Genetics and Diagnosis of Congenital Hyperinsulinism Disorders.
    Stanley CA
    J Clin Endocrinol Metab; 2016 Mar; 101(3):815-26. PubMed ID: 26908106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital Hyperinsulinism Caused by Mutations in
    Butnariu LI; Bizim DA; Păduraru G; Păduraru L; Moisă ȘM; Popa S; Gimiga N; Ghiga G; Bădescu MC; Lupu A; Vasiliu I; Trandafir LM
    Int J Mol Sci; 2024 May; 25(10):. PubMed ID: 38791571
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A specialized team approach to diagnosis and medical versus surgical treatment of infants with congenital hyperinsulinism.
    Palladino AA; Stanley CA
    Semin Pediatr Surg; 2011 Feb; 20(1):32-7. PubMed ID: 21186002
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Noninvasive diagnosis of focal hyperinsulinism of infancy with [18F]-DOPA positron emission tomography.
    Otonkoski T; Näntö-Salonen K; Seppänen M; Veijola R; Huopio H; Hussain K; Tapanainen P; Eskola O; Parkkola R; Ekström K; Guiot Y; Rahier J; Laakso M; Rintala R; Nuutila P; Minn H
    Diabetes; 2006 Jan; 55(1):13-8. PubMed ID: 16380471
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism.
    Saint-Martin C; Zhou Q; Martin GM; Vaury C; Leroy G; Arnoux JB; de Lonlay P; Shyng SL; Bellanné-Chantelot C
    Clin Genet; 2015 May; 87(5):448-54. PubMed ID: 24814349
    [TBL] [Abstract][Full Text] [Related]  

  • 20. In vitro insulin secretion by pancreatic tissue from infants with diazoxide-resistant congenital hyperinsulinism deviates from model predictions.
    Henquin JC; Nenquin M; Sempoux C; Guiot Y; Bellanné-Chantelot C; Otonkoski T; de Lonlay P; Nihoul-Fékété C; Rahier J
    J Clin Invest; 2011 Oct; 121(10):3932-42. PubMed ID: 21968111
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.