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.
4. 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 31; 21(17):. PubMed ID: 32877990 [Abstract] [Full Text] [Related]
6. The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome. Santer R, Groth S, Kinner M, Dombrowski A, Berry GT, Brodehl J, Leonard JV, Moses S, Norgren S, Skovby F, Schneppenheim R, Steinmann B, Schaub J. Hum Genet; 2002 Jan 31; 110(1):21-9. PubMed ID: 11810292 [Abstract] [Full Text] [Related]
7. Genetic testing of two Pakistani patients affected with rare autosomal recessive Fanconi-Bickel syndrome and identification of a novel SLC2A2 splice site variant. Batool H, Zubaida B, Hashmi MA, Naeem M. J Pediatr Endocrinol Metab; 2019 Nov 26; 32(11):1229-1233. PubMed ID: 31473689 [Abstract] [Full Text] [Related]
8. Functional and structural analysis of rare SLC2A2 variants associated with Fanconi-Bickel syndrome and metabolic traits. Enogieru OJ, Ung PMU, Yee SW, Schlessinger A, Giacomini KM. Hum Mutat; 2019 Jul 26; 40(7):983-995. PubMed ID: 30950137 [Abstract] [Full Text] [Related]
9. [SLC2A2 gene analysis in three Chinese children with Fanconi-Bickel syndrome]. Wang W, Wei M, Song HM, Qiu ZQ, Zhang LJ, Li Z, Tang XY. Zhongguo Dang Dai Er Ke Za Zhi; 2015 Apr 26; 17(4):362-6. PubMed ID: 25919556 [Abstract] [Full Text] [Related]
10. 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 Apr 26; 59(4):434-441. PubMed ID: 29624224 [Abstract] [Full Text] [Related]
11. Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi-Bickel Syndrome. Sharari S, Kabeer B, Mohammed I, Haris B, Pavlovski I, Hawari I, Bhat AA, Toufiq M, Tomei S, Mathew R, Syed N, Nisar S, Maacha S, Grivel JC, Chaussabel D, Ericsson J, Hussain K. Biomedicines; 2022 Aug 29; 10(9):. PubMed ID: 36140215 [Abstract] [Full Text] [Related]
12. Mutations in SLC2A2 gene reveal hGLUT2 function in pancreatic β cell development. Michau A, Guillemain G, Grosfeld A, Vuillaumier-Barrot S, Grand T, Keck M, L'Hoste S, Chateau D, Serradas P, Teulon J, De Lonlay P, Scharfmann R, Brot-Laroche E, Leturque A, Le Gall M. J Biol Chem; 2013 Oct 25; 288(43):31080-92. PubMed ID: 23986439 [Abstract] [Full Text] [Related]
18. Transient neonatal diabetes as a presentation of Fanconi- Bickel Syndrome. Setoodeh A, Rabbani A. Acta Med Iran; 2012 Nov 25; 50(12):836-8. PubMed ID: 23456528 [Abstract] [Full Text] [Related]
19. GLUT2, glucose sensing and glucose homeostasis. Thorens B. Diabetologia; 2015 Feb 25; 58(2):221-32. PubMed ID: 25421524 [Abstract] [Full Text] [Related]
20. Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience. Laimon W, El-Ziny M, El-Hawary A, Elsharkawy A, Salem NA, Aboelenin HM, Awad MH, Flanagan SE, De Franco E. Acta Diabetol; 2021 Dec 25; 58(12):1689-1700. PubMed ID: 34426871 [Abstract] [Full Text] [Related] Page: [Next] [New Search]