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 *

137 related articles for article (PubMed ID: 28493372)

  • 1. Glycosuria and hyperglycemia in the neonatal period as the first clinical sign of Fanconi-Bickel syndrome.
    Bahíllo-Curieses MP; Garrote-Molpeceres R; Miñambres-Rodríguez M; Del Real-Llorente MR; Tobar-Mideros C; Rellán-Rodríguez S
    Pediatr Diabetes; 2018 Feb; 19(1):180-183. PubMed ID: 28493372
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Fanconi-Bickel syndrome: a case of neonatal onset.
    Riva S; Ghisalberti C; Parini R; Furlan F; Bettinelli A; Somaschini M
    J Perinatol; 2004 May; 24(5):322-3. PubMed ID: 15116130
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [The Fanconi-Bickel syndrome].
    Velásquez L; Portillo VH; Sanjinés R; Gamboa JD; Feria-Kaiser C; Valencia P
    Bol Med Hosp Infant Mex; 1991 Apr; 48(4):255-60. PubMed ID: 1867746
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fanconi-Bickel syndrome.
    Karande S; Kumbhare N; Kulkarni M
    Indian Pediatr; 2007 Mar; 44(3):223-5. PubMed ID: 17413201
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fanconi Bickel Syndrome with Hypercalciuria due to GLUT 2 Mutation.
    Shah R; Rao S; Parikh R; Sophia T; Khalid H
    Indian Pediatr; 2016 Sep; 53(9):829-830. PubMed ID: 27771652
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diabetes-like renal glomerular disease in Fanconi-Bickel syndrome.
    Berry GT; Baker L; Kaplan FS; Witzleben CL
    Pediatr Nephrol; 1995 Jun; 9(3):287-91. PubMed ID: 7632512
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transient neonatal diabetes as a presentation of Fanconi- Bickel Syndrome.
    Setoodeh A; Rabbani A
    Acta Med Iran; 2012; 50(12):836-8. PubMed ID: 23456528
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical, genetic profile and therapy evaluation of 11 Chinese pediatric patients with Fanconi-Bickel syndrome.
    Du T; Xia Y; Sun C; Gong Z; Liang L; Gong Z; Wang R; Lu D; Zhang K; Yang Y; Sun Y; Sun M; Sun Y; Xiao B; Qiu W
    Orphanet J Rare Dis; 2024 Feb; 19(1):75. PubMed ID: 38365697
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fanconi-Bickel Syndrome: Two Pakistani Patients Presenting with Hypophosphatemic Rickets.
    Afroze B; Chen M
    J Pediatr Genet; 2016 Sep; 5(3):161-6. PubMed ID: 27617158
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical Features and Genetic Sequencing of Children with Fanconi-Bickel Syndrome.
    Govindarajan S; Khandelwal P; Sharma S; Agarwala A; Sinha A; Hari P; Bagga A
    Indian J Pediatr; 2023 Feb; 90(2):178-180. PubMed ID: 36324017
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hyperglycemia and hypoinsulinemia in patients with Fanconi-Bickel syndrome.
    Taha D; Al-Harbi N; Al-Sabban E
    J Pediatr Endocrinol Metab; 2008 Jun; 21(6):581-6. PubMed ID: 18717244
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations.
    Şeker-Yılmaz B; Kör D; Bulut FD; Yüksel B; Karabay-Bayazıt A; Topaloğlu AK; Ceylaner G; Önenli-Mungan N
    Turk J Pediatr; 2017; 59(4):434-441. PubMed ID: 29624224
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Segregation of a novel homozygous 6 nucleotide deletion in GLUT2 gene in a Fanconi-Bickel syndrome family.
    Abbasi F; Azizi F; Javaheri M; Mosallanejad A; Ebrahim-Habibi A; Ghafouri-Fard S
    Gene; 2015 Feb; 557(1):103-5. PubMed ID: 25523092
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fanconi-Bickel syndrome: GLUT2 mutations associated with a mild phenotype.
    Grünert SC; Schwab KO; Pohl M; Sass JO; Santer R
    Mol Genet Metab; 2012 Mar; 105(3):433-7. PubMed ID: 22214819
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Fanconi-Bickel syndrome patient with a novel mutation and accompanying situs inversus totalis.
    Taştemel-Öztürk T; Bilginer-Gürbüz B; Tekşam Ö; Sivri S
    Turk J Pediatr; 2017; 59(6):693-695. PubMed ID: 30035403
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fanconi-Bickel syndrome.
    Manz F; Bickel H; Brodehl J; Feist D; Gellissen K; Geschöll-Bauer B; Gilli G; Harms E; Helwig H; Nützenadel W
    Pediatr Nephrol; 1987 Jul; 1(3):509-18. PubMed ID: 3153325
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fanconi-Bickel syndrome in two Palestinian children: marked phenotypic variability with identical mutation.
    Dweikat IM; Alawneh IS; Bahar SF; Sultan MI
    BMC Res Notes; 2016 Aug; 9():387. PubMed ID: 27487919
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fanconi-Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia.
    Sharari S; Abou-Alloul M; Hussain K; Ahmad Khan F
    Int J Mol Sci; 2020 Aug; 21(17):. PubMed ID: 32877990
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Bilateral nuclear cataracts as the first neonatal sign of Fanconi-Bickel syndrome.
    Furlan F; Santer R; Vismara E; Santus F; Sersale G; Menni F; Parini R
    J Inherit Metab Dis; 2006 Oct; 29(5):685. PubMed ID: 16906471
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An Indian girl with Fanconi-Bickel syndrome without SLC2A2 gene mutation.
    Dayal D; Dekate P; Sharda S; Das A; Attri S
    J Pediatr Genet; 2013 Jun; 2(2):109-12. PubMed ID: 27625848
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.