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.
8. 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 Dec; 59(6):693-695. PubMed ID: 30035403 [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 [Abstract] [Full Text] [Related]
11. 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 [Abstract] [Full Text] [Related]
14. [The Fanconi-Bickel syndrome: one more case]. Ruffa G, Ferrando M, Sbolgi P, Bartolozzi G, Lavia N. Minerva Pediatr; 1992 Jun; 44(6):313-8. PubMed ID: 1635533 [Abstract] [Full Text] [Related]
15. 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 [Abstract] [Full Text] [Related]
17. 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 [Abstract] [Full Text] [Related]
18. Fanconi-Bickel syndrome. Karande S, Kumbhare N, Kulkarni M. Indian Pediatr; 2007 Mar; 44(3):223-5. PubMed ID: 17413201 [Abstract] [Full Text] [Related]
19. Fanconi-Bickel syndrome in a 3-year-old Indian boy with a novel mutation in the GLUT2 gene. Gopalakrishnan A, Kumar M, Krishnamurthy S, Sakamoto O, Srinivasan S. Clin Exp Nephrol; 2011 Oct; 15(5):745-748. PubMed ID: 21625891 [Abstract] [Full Text] [Related]