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23. The Fanconi syndrome of cystinosis: insights into the pathophysiology. Sakarcan A Turk J Pediatr; 2002; 44(4):279-82. PubMed ID: 12458800 [TBL] [Abstract][Full Text] [Related]
24. Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome. Sakamoto O; Ogawa E; Ohura T; Igarashi Y; Matsubara Y; Narisawa K; Iinuma K Pediatr Res; 2000 Nov; 48(5):586-9. PubMed ID: 11044475 [TBL] [Abstract][Full Text] [Related]
25. Paraquat-induced Fanconi syndrome. Gil HW; Yang JO; Lee EY; Hong SY Nephrology (Carlton); 2005 Oct; 10(5):430-2. PubMed ID: 16221089 [TBL] [Abstract][Full Text] [Related]
26. 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 [TBL] [Abstract][Full Text] [Related]
27. Acute metabolic acidosis in a GLUT2-deficient patient with Fanconi-Bickel syndrome: new pathophysiology insights. Mihout F; Devuyst O; Bensman A; Brocheriou I; Ridel C; Wagner CA; Mohebbi N; Boffa JJ; Plaisier E; Ronco P Nephrol Dial Transplant; 2014 Sep; 29 Suppl 4():iv113-6. PubMed ID: 25165176 [TBL] [Abstract][Full Text] [Related]
28. [Glycogenosis of the liver with galactose utilization disorder and a severe Fanconi syndrome]. Lampert F; Mayer H Z Kinderheilkd; 1967; 98(2):133-45. PubMed ID: 5230448 [No Abstract] [Full Text] [Related]
29. Identification of a novel mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome presenting with neonatal diabetes mellitus and galactosaemia. Yoo HW; Shin YL; Seo EJ; Kim GH Eur J Pediatr; 2002 Jun; 161(6):351-3. PubMed ID: 12029458 [TBL] [Abstract][Full Text] [Related]
30. 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]
31. [Fanconi syndrome with hepatic cirrhosis. Presentation of a case]. Ortiz Méndez VM; Bonilla Aguirre R; Farfán Boldo J; Velázquez A; Olvera Hidalgo C Bol Med Hosp Infant Mex; 1981; 38(1):169-75. PubMed ID: 7284065 [TBL] [Abstract][Full Text] [Related]
32. The Fanconi syndrome associated with hepatic glycogenosis and abnormal metabolism of galactose. Garty R; Cooper M; Tabachnik E J Pediatr; 1974 Dec; 85(6):821-3. PubMed ID: 4529611 [No Abstract] [Full Text] [Related]
33. Renal cortical tubular glycogen localization in glycogenosis type II (Pompe's disease). Witzleben CL Lab Invest; 1969 May; 20(5):424-9. PubMed ID: 4305720 [No Abstract] [Full Text] [Related]
34. [A case of glycogenosis with recurrent hypoglycemia without enzymatic deficiency on liver biopsy]. Grenet P; Badoual J; Lestradet H; Martinetti J; Sanna N; Voyer J Ann Pediatr (Paris); 1972; 19(6):499-506. PubMed ID: 4341583 [No Abstract] [Full Text] [Related]