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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 23644647)

  • 1. 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]  

  • 2. 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]  

  • 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. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 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]  

  • 11. 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]  

  • 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. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Wolcott-Rallison syndrome.
    Julier C; Nicolino M
    Orphanet J Rare Dis; 2010 Nov; 5():29. PubMed ID: 21050479
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.