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.
130 related articles for article (PubMed ID: 23263430)
21. Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation. Gürbüz F; Yüksel B; Topaloğlu AK J Clin Res Pediatr Endocrinol; 2016 Dec; 8(4):496-497. PubMed ID: 27145240 [No Abstract] [Full Text] [Related]
22. Wolcott-Rallison syndrome: a case series of three patients. Memon F; Arif M; Kirmani S; Humayun K Pediatr Endocrinol Diabetes Metab; 2022; 28(3):238-240. PubMed ID: 36106422 [TBL] [Abstract][Full Text] [Related]
23. A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes. Abbasi F; Habibi M; Enayati S; Bitarafan F; Razzaghy-Azar M; Sotodeh A; Omran SP; Maroofian R; Amoli MM Can J Diabetes; 2018 Jun; 42(3):272-275. PubMed ID: 28843469 [TBL] [Abstract][Full Text] [Related]
24. Ketoacidosis in Neonatal Diabetes Mellitus, Part of Wolcott-Rallison Syndrome. Sreeramaneni PGA; Ambula SRV Am J Case Rep; 2017 Jun; 18():719-722. PubMed ID: 28652565 [TBL] [Abstract][Full Text] [Related]
25. Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome. Reis AF; Kannengiesser C; Jennane F; Manna TD; Cheurfa N; Oudin C; Savoldelli RD; Oliveira C; Grandchamp B; Kok F; Velho G Pediatr Diabetes; 2011 May; 12(3 Pt 1):187-91. PubMed ID: 21518408 [TBL] [Abstract][Full Text] [Related]
26. [Two novel EIF2AK3 mutations in a Chinese boy with Wolcott-Rallison syndrome]. Feng DR; Meng Y; Zhao SM; Shi HP; Wang WC; Huang SZ Zhonghua Er Ke Za Zhi; 2011 Apr; 49(4):301-5. PubMed ID: 21624209 [TBL] [Abstract][Full Text] [Related]
28. Novel splice site mutation in EIF2AK3 gene causes Wolcott-Rallison syndrome in a consanguineous family from Saudi Arabia. Al-Aama JY; Al-Zahrani HS; Jelani M; Sabir HS; Al-Saeedi SA; Ahmed S Congenit Anom (Kyoto); 2018 Jan; 58(1):39-40. PubMed ID: 28220546 [No Abstract] [Full Text] [Related]
29. A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungary. Sümegi A; Hendrik Z; Gáll T; Felszeghy E; Szakszon K; Antal-Szalmás P; Beke L; Papp Á; Méhes G; Balla J; Balla G BMC Med Genet; 2020 Mar; 21(1):61. PubMed ID: 32216767 [TBL] [Abstract][Full Text] [Related]
30. Long-term follow-up of a child with Wolcott-Rallison syndrome. Shah N; Karguppikar MB; Khadilkar V; Khadilkar A BMJ Case Rep; 2021 May; 14(5):. PubMed ID: 33986015 [TBL] [Abstract][Full Text] [Related]
31. Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literature. Iyer S; Korada M; Rainbow L; Kirk J; Brown RM; Shaw N; Barrett TG Acta Paediatr; 2004 Sep; 93(9):1195-201. PubMed ID: 15384883 [TBL] [Abstract][Full Text] [Related]
32. A novel EIF2AK3 mutation leading to Wolcott-Rallison syndrome in a Chinese child. Sang Y; Liu M; Yang W; Yan J; Chengzhu ; Ni G J Pediatr Endocrinol Metab; 2011; 24(3-4):181-4. PubMed ID: 21648287 [TBL] [Abstract][Full Text] [Related]
33. [A case report of EIF2AK3-related Wolcott-Rallison syndrome and literature review]. Zhang HJ; Wang SB; Guo XF; Weng B; Lin L; Hao Y Zhongguo Dang Dai Er Ke Za Zhi; 2019 Feb; 21(2):176-179. PubMed ID: 30782283 [TBL] [Abstract][Full Text] [Related]
34. EIF2AK3 novel mutation in a child with early-onset diabetes mellitus, a case report. Fatani TH BMC Pediatr; 2019 Mar; 19(1):85. PubMed ID: 30922274 [TBL] [Abstract][Full Text] [Related]
35. First European Case of Simultaneous Liver and Pancreas Transplantation as Treatment of Wolcott-Rallison Syndrome in a Small Child. Nordström J; Lundgren M; Jorns C; Fischler B; Arnell H; Dlugosz R; Sandberg J; Wennberg L; Nowak G Transplantation; 2020 Mar; 104(3):522-525. PubMed ID: 31335762 [TBL] [Abstract][Full Text] [Related]
36. Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy. Castelnau P; Le Merrer M; Diatloff-Zito C; Marquis E; Tête MJ; Robert JJ Eur J Pediatr; 2000 Aug; 159(8):631-3. PubMed ID: 10968248 [TBL] [Abstract][Full Text] [Related]
37. Wolcott-Rallison syndrome associated with congenital malformations and a mosaic deletion 15q 11-12. Stewart FJ; Carson DJ; Thomas PS; Humphreys M; Thornton C; Nevin NC Clin Genet; 1996 Mar; 49(3):152-5. PubMed ID: 8737981 [TBL] [Abstract][Full Text] [Related]
39. Lissencephaly-pachygyria spectrum in a North Indian boy with Wolcott-Rallison syndrome due to homozygous deletion of exon 1 in the EIF2AK3 gene. Gupta A; Reddy C; Saini L; Yadav J; Kumar R; Houghton J; Ellard S; Dayal D Pediatr Endocrinol Diabetes Metab; 2021; 27(4):287-290. PubMed ID: 34928108 [TBL] [Abstract][Full Text] [Related]
40. EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome. Delépine M; Nicolino M; Barrett T; Golamaully M; Lathrop GM; Julier C Nat Genet; 2000 Aug; 25(4):406-9. PubMed ID: 10932183 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]