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.
154 related articles for article (PubMed ID: 36476334)
1. Hyperinsulinism-hyperammonemia syndrome in two Peruvian children with refractory epilepsy. De Los Santos-La Torre MA; Del Águila-Villar CM; Lu-de Lama LR; Nuñez-Almache O; Chávez-Tejada EM; Espinoza-Robles OA; Pinto-Ibárcena PM; Calagua-Quispe MR; Azabache-Tafur PM; Tucto-Manchego RM J Pediatr Endocrinol Metab; 2023 Feb; 36(2):207-211. PubMed ID: 36476334 [TBL] [Abstract][Full Text] [Related]
2. Congenital Hyperinsulinemic Hypoglycemia and Hyperammonemia due to Pathogenic Variants in GLUD1. Roy K; Satapathy AK; Houhton JAL; Flanagan SE; Radha V; Mohan V; Sharma R; Jain V Indian J Pediatr; 2019 Nov; 86(11):1051-1053. PubMed ID: 31119523 [TBL] [Abstract][Full Text] [Related]
3. Hyperinsulinism hyperammonaemia (HI/HA) syndrome due to GLUD1 mutation: phenotypic variations ranging from late presentation to spontaneous resolution. Brandt A; Agarwal N; Giri D; Yung Z; Didi M; Senniappan S J Pediatr Endocrinol Metab; 2020 May; 33(5):675-679. PubMed ID: 32229669 [TBL] [Abstract][Full Text] [Related]
4. Hyperinsulinism-hyperammonemia syndrome: a de novo mutation of the GLUD1 gene in twins and a review of the literature. Ninković D; Sarnavka V; Bašnec A; Ćuk M; Ramadža DP; Fumić K; Kušec V; Santer R; Barić I J Pediatr Endocrinol Metab; 2016 Sep; 29(9):1083-8. PubMed ID: 27383869 [TBL] [Abstract][Full Text] [Related]
5. Biochemical evaluation of an infant with hypoglycemia resulting from a novel de novo mutation of the GLUD1 gene and hyperinsulinism-hyperammonemia syndrome. Balasubramaniam S; Kapoor R; Yeow JH; Lim PG; Flanagan S; Ellard S; Hussain K J Pediatr Endocrinol Metab; 2011; 24(7-8):573-7. PubMed ID: 21932603 [TBL] [Abstract][Full Text] [Related]
6. Hyperinsulinism/hyperammonemia (HI/HA) syndrome due to a mutation in the glutamate dehydrogenase gene. Corrêa-Giannella ML; Freire DS; Cavaleiro AM; Fortes MA; Giorgi RR; Pereira MA Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):485-9. PubMed ID: 23295286 [TBL] [Abstract][Full Text] [Related]
7. Hyperinsulinemic hypoglycemia: think of hyperinsulinism/hyperammonemia (HI/HA) syndrome caused by mutations in the GLUD1 gene. Tran C; Konstantopoulou V; Mecjia M; Perlman K; Mercimek-Mahmutoglu S; Kronick JB J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):873-6. PubMed ID: 25781533 [TBL] [Abstract][Full Text] [Related]
8. A novel mutation in the glutamate dehydrogenase (GLUD1) of a patient with congenital hyperinsulinism-hyperammonemia (HI/HA). Fang C; Ding X; Huang Y; Huang J; Zhao P; Hu J J Pediatr Endocrinol Metab; 2016 Mar; 29(3):385-8. PubMed ID: 26656609 [TBL] [Abstract][Full Text] [Related]
9. Seizures and diagnostic difficulties in hyperinsulinism-hyperammonemia syndrome. Aka S; Alanay Y; Boodhansingh KE; Stanley CA; Semiz S Turk J Pediatr; 2016; 58(5):541-544. PubMed ID: 28621098 [TBL] [Abstract][Full Text] [Related]
10. Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients. Sarajlija A; Milenkovic T; Djordjevic M; Mitrovic K; Todorovic S; Kecman B; Hussain K J Clin Res Pediatr Endocrinol; 2016 Jun; 8(2):228-31. PubMed ID: 26759084 [TBL] [Abstract][Full Text] [Related]
11. Familial hyperinsulinism-hyperammonemia syndrome in a family with seizures: case report. de las Heras J; Garin I; de Nanclares GP; Aguayo A; Rica I; Castaño L; Vela A J Pediatr Endocrinol Metab; 2010 Aug; 23(8):827-30. PubMed ID: 21073125 [TBL] [Abstract][Full Text] [Related]
12. The hyperinsulinism/hyperammonemia syndrome. Palladino AA; Stanley CA Rev Endocr Metab Disord; 2010 Sep; 11(3):171-8. PubMed ID: 20936362 [TBL] [Abstract][Full Text] [Related]
14. A novel mutation in GLUD1 causing hyperinsulinism-hyperammonemia in a patient with high density of homozygosity on microarray: a case report. Odom J; Gieron-Korthals M; Shulman D; Newkirk P; Prijoles E; Sanchez-Valle A J Med Case Rep; 2016 Feb; 10():25. PubMed ID: 26839063 [TBL] [Abstract][Full Text] [Related]
16. Hyperinsulinism-hyperammonemia Syndrome in an Infant with Seizures. Strajnar A; Tansek MZ; Podkrajsek KT; Battelino T; Groselj U Balkan J Med Genet; 2018 Jun; 21(1):77-81. PubMed ID: 30425915 [TBL] [Abstract][Full Text] [Related]
17. Two unrelated Chinese patients with hyperinsulinism /hyperammonemia (HI/HA) syndrome due to mutations in glutamate dehydrogenase gene. Diao C; Chen S; Xiao X; Wang T; Sun X; Wang O; Song H; Zhang Y; Yu M; Zhang Q; Wang H J Pediatr Endocrinol Metab; 2010 Jul; 23(7):733-8. PubMed ID: 20857847 [TBL] [Abstract][Full Text] [Related]
18. [Hyperinsulinism-hyperammonemia syndrome due to a de novo mutation in exon 7 (G979A) of the glutamate dehydrogenase gene with excellent response to diazoxide]. Montero Luis C; Pozo Román J; Muñoz Calvo MT; Martos Moreno G; Donoso MA; Rubio Cabezas O; Argente Oliver J An Pediatr (Barc); 2004 Nov; 61(5):433-7. PubMed ID: 15530324 [TBL] [Abstract][Full Text] [Related]
19. Mosaic GLUD1 Mutations Associated with Hyperinsulinism Hyperammonemia Syndrome. Boodhansingh KE; Rosenfeld E; Lord K; Adzick NS; Bhatti T; Ganguly A; De Leon DD; Stanley CA Horm Res Paediatr; 2022; 95(5):492-498. PubMed ID: 35952631 [TBL] [Abstract][Full Text] [Related]
20. Characterizing the neurological phenotype of the hyperinsulinism hyperammonemia syndrome. Rosenfeld E; Nanga RPR; Lucas A; Revell AY; Thomas A; Thomas NH; Roalf DR; Shinohara RT; Reddy R; Davis KA; De León DD Orphanet J Rare Dis; 2022 Jun; 17(1):248. PubMed ID: 35752848 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]