Sotelo N, García R, Tostado R, Dhanakotti N

Idioma: Ingles.
Referencias bibliográficas: 10
Paginas: 163-167
Archivo PDF: 183.07 Kb.

RESUMEN

Sin resumen

REFERENCIAS (EN ESTE ARTÍCULO)

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2. Pascual JM. Hereditary syndrome of glucose transport. Med Clin (Barc.) 2006; 127(18): 709-714.

3. Garty R, Cooper M, Taibachnik E. The Fanconi syndrome associated with hepatic glycogenosis and abnormal metabolism of galactose. J Pediatr 1974; 85: 821-823.

4. Velasquez JL. Síndrome de Fanconi. Bol Med Hosp Infant Mex 1987; 44: 509-510.

5. Santer R, Schneppenheim R, Suter D, Schanb J, Steinman B. Fanconi-Bickel syndrome- the original patient and his natural history, historical steps leading to the primary defect, and a review of the literature. Eur J Pediatr 1998; 157: 783-797.

6. Velasquez-Jones L, Portillo HV, Sanjines R, Gamboa-Marrufo A, Feria-Kaiser K, Valencia-Mayoral P. Síndrome de Fanconi-Bickel. Bol Med Hosp Infant Mex 1991; 48: 255-259.

7. Santer R, Steinmann B, Schaub J. Fanconi-Bickel syndrome a congenital defect of facilitative glucose transport. Curr Mol Med 2002; 2: 213-227.

8. De Vivo D, Lackie M, Ferrendelli J, McDougal D. Chronic ketosis and cerebral metabolism. Ann Neurol 1987; 3: 331-337.

9. Sakamoto O, Ogawa E, Ohura T, Igarashi Y, Matsubara Y, Narisawa K, et al. Mutation analysis of the GLUT 2 gene in patients with fanconi-Bickel syndrome. Pediatr Res 2000; 48: 586-589.

10. Karande S, Kumbhare N, Kulkarni M. Fanconi-Bickel syndrome. Indian Pediatrics 2007; 44: 223-225.