138 related articles for article (PubMed ID: 21624209)
1. [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]
2. 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]
3. 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]
4. 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]
5. 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]
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. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
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. Variable phenotype in five patients with Wolcott-Rallison syndrome due to the same EIF2AK3 (c.1259delA) mutation.
Al-Shawi M; Al Mutair A; Ellard S; Habeb AM
J Pediatr Endocrinol Metab; 2013; 26(7-8):757-60. PubMed ID: 23585173
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. Frequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review.
Habeb AM
Libyan J Med; 2013 Jun; 8(1):21137. PubMed ID: 23759358
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]