171 related articles for article (PubMed ID: 28652565)
1. 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]
2. 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]
3. 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]
4. 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]
5. Wolcott Rallison syndrome: a rare inherited diabetes mellitus.
Khare S; Goroshi MR; Budyal S; Bandgar T; Lila A; Shah N
Indian J Pediatr; 2014 Nov; 81(11):1225-7. PubMed ID: 24710710
[TBL] [Abstract][Full Text] [Related]
6. Wolcott-Rallison syndrome.
Julier C; Nicolino M
Orphanet J Rare Dis; 2010 Nov; 5():29. PubMed ID: 21050479
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. Os odontoideum in wolcott-rallison syndrome: a case series of 4 patients.
Dias RP; Buchanan CR; Thomas N; Lim S; Solanki G; Connor SE; Barrett TG; Kapoor RR
Orphanet J Rare Dis; 2016 Feb; 11():14. PubMed ID: 26860746
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]