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.
136 related articles for article (PubMed ID: 38963811)
21. Novel Compound Heterozygous Variants of the Al Balwi R; Bubshait D; Al Nefily R; Al Ghamdi O Children (Basel); 2021 Sep; 8(10):. PubMed ID: 34682101 [TBL] [Abstract][Full Text] [Related]
22. 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]
23. Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia. Jahnavi S; Poovazhagi V; Kanthimathi S; Balamurugan K; Bodhini D; Yadav J; Jain V; Khadgawat R; Sikdar M; Bhavatharini A; Das AK; Kaur T; Mohan V; Radha V Ann Hum Genet; 2014 Sep; 78(5):311-9. PubMed ID: 25117148 [TBL] [Abstract][Full Text] [Related]
24. Genotype and phenotype analysis of a cohort of patients with congenital hyperinsulinism based on DOPA-PET CT scanning. Ni J; Ge J; Zhang M; Hussain K; Guan Y; Cheng R; Xi L; Zheng Z; Ren S; Luo F Eur J Pediatr; 2019 Aug; 178(8):1161-1169. PubMed ID: 31218401 [TBL] [Abstract][Full Text] [Related]
25. A novel mutation of Park JS; Lee HJ; Park CH Korean J Pediatr; 2016 Nov; 59(Suppl 1):S116-S120. PubMed ID: 28018462 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. The molecular mechanisms, diagnosis and management of congenital hyperinsulinism. Senniappan S; Arya VB; Hussain K Indian J Endocrinol Metab; 2013 Jan; 17(1):19-30. PubMed ID: 23776849 [TBL] [Abstract][Full Text] [Related]
28. Congenital hyperinsulinism: clinical and molecular characterisation of compound heterozygous ABCC8 mutation responsive to Diazoxide therapy. Arya VB; Aziz Q; Nessa A; Tinker A; Hussain K Int J Pediatr Endocrinol; 2014; 2014(1):24. PubMed ID: 25584046 [TBL] [Abstract][Full Text] [Related]
29. Clinical heterogeneity of hyperinsulinism due to HNF1A and HNF4A mutations. Tung JY; Boodhansingh K; Stanley CA; De León DD Pediatr Diabetes; 2018 Aug; 19(5):910-916. PubMed ID: 29493090 [TBL] [Abstract][Full Text] [Related]
31. Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital Hyperinsulinism. Razzaghy-Azar M; Saeedi S; Dayani SB; Enayati S; Abbasi F; Hashemian S; Eshraghi P; Karimdadi S; Tajdini P; Vakili R; Amoli MM; Yaghootkar H J Clin Res Pediatr Endocrinol; 2022 Mar; 14(1):87-95. PubMed ID: 34927408 [TBL] [Abstract][Full Text] [Related]
32. Targeted gene panel analysis of Japanese patients with maturity-onset diabetes of the young-like diabetes mellitus: Roles of inactivating variants in the ABCC8 and insulin resistance genes. Yorifuji T; Watanabe Y; Kitayama K; Yamada Y; Higuchi S; Mori J; Kato M; Takahashi T; Okuda T; Aoyama T J Diabetes Investig; 2023 Mar; 14(3):387-403. PubMed ID: 36504295 [TBL] [Abstract][Full Text] [Related]
33. Genetics and Natural History of Non-pancreatectomized Patients With Congenital Hyperinsulinism Due to Variants in ABCC8. Clemente M; Cobo P; Antolín M; Campos A; Yeste D; Tomasini R; Caimari M; Masas M; García-Arumí E; Fernández-Cancio M; Baz-Redón N; Camats-Tarruella N J Clin Endocrinol Metab; 2023 Oct; 108(11):e1316-e1328. PubMed ID: 37216904 [TBL] [Abstract][Full Text] [Related]
34. Challenging diagnosis of congenital hyperinsulinism in two infants of diabetic mothers with rare pathogenic Huerta-Saenz L; Saunders C; Yan Y Int J Pediatr Endocrinol; 2018; 2018():5. PubMed ID: 30026763 [TBL] [Abstract][Full Text] [Related]
35. Congenital Hyperinsulinism Caused by Novel Homozygous KATP Channel Gene Variants May Be Linked to Unexplained Neonatal Deaths among Kurdish Consanguineous Families. Amaratunga SA; Hussein Tayeb T; Rozenkova K; Kucerova P; Pruhova S; Lebl J Horm Res Paediatr; 2020; 93(1):58-65. PubMed ID: 32203961 [TBL] [Abstract][Full Text] [Related]
36. Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism. Proverbio MC; Mangano E; Gessi A; Bordoni R; Spinelli R; Asselta R; Valin PS; Di Candia S; Zamproni I; Diceglie C; Mora S; Caruso-Nicoletti M; Salvatoni A; De Bellis G; Battaglia C PLoS One; 2013; 8(7):e68740. PubMed ID: 23869231 [TBL] [Abstract][Full Text] [Related]
37. 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]