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.
532 related articles for article (PubMed ID: 10932183)
1. 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]
2. 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]
3. Early-onset diabetes mellitus and neurodevelopmental retardation: the first Greek case of Wolcott-Rallison syndrome. Triantafyllou P; Vargiami E; Vagianou I; Badouraki M; Julier C; Zafeiriou DI J Pediatr Endocrinol Metab; 2014 Sep; 27(9-10):967-70. PubMed ID: 24859506 [TBL] [Abstract][Full Text] [Related]
4. THE 3rd W522X MUTATION IN EIF2AK3 GENE FROM TURKEY: A NEW PATIENT WITH WOLCOTT-RALLISON SYNDROME. Bahsi T; Unal A; Bakir A; Perçin EF Genet Couns; 2016; 27(3):411-418. PubMed ID: 30204972 [TBL] [Abstract][Full Text] [Related]
5. EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndrome. Jahnavi S; Poovazhagi V; Kanthimathi S; Gayathri V; Mohan V; Radha V Pediatr Diabetes; 2014 Jun; 15(4):313-8. PubMed ID: 24168455 [TBL] [Abstract][Full Text] [Related]
6. Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity. Senée V; Vattem KM; Delépine M; Rainbow LA; Haton C; Lecoq A; Shaw NJ; Robert JJ; Rooman R; Diatloff-Zito C; Michaud JL; Bin-Abbas B; Taha D; Zabel B; Franceschini P; Topaloglu AK; Lathrop GM; Barrett TG; Nicolino M; Wek RC; Julier C Diabetes; 2004 Jul; 53(7):1876-83. PubMed ID: 15220213 [TBL] [Abstract][Full Text] [Related]
7. Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature. Ozbek MN; Senée V; Aydemir S; Kotan LD; Mungan NO; Yuksel B; Julier C; Topaloglu AK Pediatr Diabetes; 2010 Jun; 11(4):279-85. PubMed ID: 20202148 [TBL] [Abstract][Full Text] [Related]
8. Loss of kinase activity in a patient with Wolcott-Rallison syndrome caused by a novel mutation in the EIF2AK3 gene. Biason-Lauber A; Lang-Muritano M; Vaccaro T; Schoenle EJ Diabetes; 2002 Jul; 51(7):2301-5. PubMed ID: 12086964 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. 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]
12. 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]
13. A novel mutation in the EIF2AK3 gene with variable expressivity in two patients with Wolcott-Rallison syndrome. Durocher F; Faure R; Labrie Y; Pelletier L; Bouchard I; Laframboise R Clin Genet; 2006 Jul; 70(1):34-8. PubMed ID: 16813601 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Wolcott-Rallison syndrome in Iran: a common cause of neonatal diabetes. Asl SN; Vakili R; Vakili S; Soheilipour F; Hashemipour M; Ghahramani S; De Franco E; Yaghootkar H J Pediatr Endocrinol Metab; 2019 Jun; 32(6):607-613. PubMed ID: 31141482 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene. Mihci E; Türkkahraman D; Ellard S; Akçurin S; Bircan I J Clin Res Pediatr Endocrinol; 2012 Jun; 4(2):101-3. PubMed ID: 22672868 [TBL] [Abstract][Full Text] [Related]
18. Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families. Rubio-Cabezas O; Patch AM; Minton JA; Flanagan SE; Edghill EL; Hussain K; Balafrej A; Deeb A; Buchanan CR; Jefferson IG; Mutair A; ; Hattersley AT; Ellard S J Clin Endocrinol Metab; 2009 Nov; 94(11):4162-70. PubMed ID: 19837917 [TBL] [Abstract][Full Text] [Related]