152 related articles for article (PubMed ID: 16813601)
21. 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]
22. Wolcott-Rallison Syndrome With Different Clinical Presentations and Genetic Patterns in 2 Infants.
Davoodi MA; Karamizadeh Z; Ghobadi F; Shokrpour N
Health Care Manag (Frederick); 2018; 37(4):354-357. PubMed ID: 30234637
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. 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]
26. Primary hypothyroidism: an unusual manifestation of Wolcott-Rallison syndrome.
Ersoy B; Özhan B; Kiremitçi S; Rubio-Cabezas O; Ellard S
Eur J Pediatr; 2014 Dec; 173(12):1565-8. PubMed ID: 23933668
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Microscopic and ultrastructural features in Wolcott-Rallison syndrome, a permanent neonatal diabetes mellitus: about two autopsy cases.
Collardeau-Frachon S; Vasiljevic A; Jouvet A; Bouvier R; Senée V; Nicolino M
Pediatr Diabetes; 2015 Nov; 16(7):510-20. PubMed ID: 25131821
[TBL] [Abstract][Full Text] [Related]
29. Wolcott-Rallison syndrome due to the same mutation in EIF2AK3 (c.205G>T) in two unrelated families: A case report.
Huang A; Wei H
Exp Ther Med; 2019 Apr; 17(4):2765-2768. PubMed ID: 30906465
[TBL] [Abstract][Full Text] [Related]
30. Identification of Two Novel Compound Heterozygous
Zhao N; Yang Y; Li P; Xiong Q; Xiao H; Wu C
Front Pediatr; 2021; 9():679646. PubMed ID: 34123975
[No Abstract] [Full Text] [Related]
31. Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott-Rallison syndrome.
Spehar Uroić A; Mulliqi Kotori V; Rojnić Putarek N; Kušec V; Dumić M
Eur J Pediatr; 2014 Apr; 173(4):529-31. PubMed ID: 24194294
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Liver disease and other comorbidities in Wolcott-Rallison syndrome: different phenotype and variable associations in a large cohort.
Habeb AM; Deeb A; Johnson M; Abdullah M; Abdulrasoul M; Al-Awneh H; Al-Maghamsi MS; Al-Murshedi F; Al-Saif R; Al-Sinani S; Ramadan D; Tfayli H; Flanagan SE; Ellard S
Horm Res Paediatr; 2015; 83(3):190-7. PubMed ID: 25659842
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. An Infant With Neonatal Diabetes and Double Outlet Right Ventricle - Wolcott- Rallison syndrome.
Bejiqi R; Retkoceri R; Zeka N; Bejiqi R; Bejic S
Med Arch; 2018 Oct; 72(4):289-291. PubMed ID: 30514997
[TBL] [Abstract][Full Text] [Related]
36. [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]
37. Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3.
Brickwood S; Bonthron DT; Al-Gazali LI; Piper K; Hearn T; Wilson DI; Hanley NA
J Med Genet; 2003 Sep; 40(9):685-9. PubMed ID: 12960215
[No Abstract] [Full Text] [Related]
38. Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome.
Behnam B; Shakiba M; Ahani A; Razzaghy Azar M
Hepat Mon; 2013; 13(6):e10124. PubMed ID: 24032041
[TBL] [Abstract][Full Text] [Related]
39. The EIF2AK3 gene region and type I diabetes in subjects from South India.
Allotey RA; Mohan V; McDermott MF; Deepa R; Premalatha G; Hassan Z; Cassell PG; North BV; Vaxillaire M; Mein CA; Swan DC; O'Grady E; Ramachandran A; Snehalatha C; Sinnot PJ; Hemmatpour SK; Froguel P; Hitman GA
Genes Immun; 2004 Dec; 5(8):648-52. PubMed ID: 15483661
[TBL] [Abstract][Full Text] [Related]
40. Short stature in child with early-onset diabetes.
Hawkes CP; McGlacken-Byrne SM; Murphy NP
Eur J Pediatr; 2013 Sep; 172(9):1255-7. PubMed ID: 23644647
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
