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Year Number of Results
1987 1
1993 2
1994 1
1997 3
1998 4
1999 4
2000 7
2001 11
2002 6
2003 12
2004 33
2005 25
2006 31
2007 46
2008 36
2009 37
2010 42
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1,019 results

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Page 1
Congenital Hyperinsulinism: Diagnosis and Treatment Update.
Demirbilek H, Hussain K. Demirbilek H, et al. J Clin Res Pediatr Endocrinol. 2017 Dec 30;9(Suppl 2):69-87. doi: 10.4274/jcrpe.2017.S007. Epub 2017 Dec 27. J Clin Res Pediatr Endocrinol. 2017. PMID: 29280746 Free PMC article. Review.
Congenital Hyperinsulinism.
Sims K. Sims K. Neoreviews. 2021 Apr;22(4):e230-e240. doi: 10.1542/neo.22-4-e230. Neoreviews. 2021. PMID: 33795398 Review.
HH that persists despite these interventions should raise concern for congenital hyperinsulinism (CHI), prompting clinicians to perform a thorough evaluation. ...
HH that persists despite these interventions should raise concern for congenital hyperinsulinism (CHI), prompting clinicians t …
Congenital Hyperinsulinism: An Historical Perspective.
Thornton PS, Stanley CA, De Leon DD. Thornton PS, et al. Horm Res Paediatr. 2022;95(6):631-637. doi: 10.1159/000526442. Epub 2022 Nov 29. Horm Res Paediatr. 2022. PMID: 36446321 Free article. Review.
Congenital hyperinsulinism is the most common cause of persistent hypoglycemia in neonates, infants, and children. ...
Congenital hyperinsulinism is the most common cause of persistent hypoglycemia in neonates, infants, and children. ...
Update of variants identified in the pancreatic beta-cell K(ATP) channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes.
De Franco E, Saint-Martin C, Brusgaard K, Knight Johnson AE, Aguilar-Bryan L, Bowman P, Arnoux JB, Larsen AR, Sanyoura M, Greeley SAW, Calzada-León R, Harman B, Houghton JAL, Nishimura-Meguro E, Laver TW, Ellard S, Del Gaudio D, Christesen HT, Bellanné-Chantelot C, Flanagan SE. De Franco E, et al. Hum Mutat. 2020 May;41(5):884-905. doi: 10.1002/humu.23995. Epub 2020 Feb 17. Hum Mutat. 2020. PMID: 32027066 Free PMC article. Review.
Mutations in the two genes cause dysregulated insulin secretion; inactivating mutations cause an oversecretion of insulin, leading to congenital hyperinsulinism, whereas activating mutations cause the opposing phenotype, diabetes. ...
Mutations in the two genes cause dysregulated insulin secretion; inactivating mutations cause an oversecretion of insulin, leading to con …
Congenital hyperinsulinism disorders: Genetic and clinical characteristics.
Rosenfeld E, Ganguly A, De Leon DD. Rosenfeld E, et al. Am J Med Genet C Semin Med Genet. 2019 Dec;181(4):682-692. doi: 10.1002/ajmg.c.31737. Epub 2019 Aug 14. Am J Med Genet C Semin Med Genet. 2019. PMID: 31414570 Free PMC article. Review.
Congenital hyperinsulinism (HI) is the most frequent cause of persistent hypoglycemia in infants and children. ...
Congenital hyperinsulinism (HI) is the most frequent cause of persistent hypoglycemia in infants and children. ...
Congenital hyperinsulinism: recent updates on molecular mechanisms, diagnosis and management.
Giri D, Hawton K, Senniappan S. Giri D, et al. J Pediatr Endocrinol Metab. 2021 Sep 21;35(3):279-296. doi: 10.1515/jpem-2021-0369. Print 2022 Mar 28. J Pediatr Endocrinol Metab. 2021. PMID: 34547194 Review.
Congenital hyperinsulinism (CHI) is a rare disease characterized by an unregulated insulin release, leading to hypoglycaemia. ...
Congenital hyperinsulinism (CHI) is a rare disease characterized by an unregulated insulin release, leading to hypoglycaemia. …
Congenital hyperinsulinism.
Velde CD, Reigstad H, Tjora E, Guthe HJT, Hansen EV, Molven A, Njølstad PR. Velde CD, et al. Tidsskr Nor Laegeforen. 2023 Dec 11;143(18). doi: 10.4045/tidsskr.23.0425. Print 2023 Dec 12. Tidsskr Nor Laegeforen. 2023. PMID: 38088279 Free article. English, Norwegian.
This clinical review will give doctors who work with children and neonates an introduction to the diagnosis and treatment of congenital hyperinsulinism, the most common cause of persistent neonatal hypoglycaemia. ...Low levels of glucose and ketone bodies in the blo …
This clinical review will give doctors who work with children and neonates an introduction to the diagnosis and treatment of congenital …
Syndromic forms of congenital hyperinsulinism.
Zenker M, Mohnike K, Palm K. Zenker M, et al. Front Endocrinol (Lausanne). 2023 Mar 30;14:1013874. doi: 10.3389/fendo.2023.1013874. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37065762 Free PMC article. Review.
Congenital hyperinsulinism (CHI), also called hyperinsulinemic hypoglycemia (HH), is a very heterogeneous condition and represents the most common cause of severe and persistent hypoglycemia in infancy and childhood. ...
Congenital hyperinsulinism (CHI), also called hyperinsulinemic hypoglycemia (HH), is a very heterogeneous condition and repres …
Congenital hyperinsulinism.
Petraitienė I, Barauskas G, Gulbinas A, Malcius D, Hussain K, Verkauskas G, Verkauskienė R. Petraitienė I, et al. Medicina (Kaunas). 2014;50(3):190-5. doi: 10.1016/j.medici.2014.08.006. Epub 2014 Aug 13. Medicina (Kaunas). 2014. PMID: 25323548 Free article. Review.
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. Arnoux JB, et al. Early Hum Dev. 2010 May;86(5):287-94. doi: 10.1016/j.earlhumdev.2010.05.003. Epub 2010 Jun 13. Early Hum Dev. 2010. PMID: 20550977 Review.
Congenital hyperinsulinism (CHI or HI) is a condition leading to recurrent hypoglycemia due to an inappropriate insulin secretion by the pancreatic islet beta cells. ...
Congenital hyperinsulinism (CHI or HI) is a condition leading to recurrent hypoglycemia due to an inappropriate insulin secret …
1,019 results