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Revista de Gastroenterología del Perú
© Sociedad de Gastroenterología del Perú
ISSN
versión electrónica 1609-722X

Rev. Gastroenterol. Perú    2003; 23 (4): 303-306


HEMOCROMATOSIS HEREDITARIA

Lidia Landa Garrido *, José Huamán Muñante **, Víctor Valencia Caballero **, 
Zenaida Lozano Miranda ***, Augusto Nago Nago ****


 

BIBLIOGRAFÍA

  1. DANTAS W. Hemocromatose Hereditária. Rev Gastroenterol Perú 2001;21:42-55

  1. DE CASO A, LÓPEZ-HUERTA M, TERRAZO M y cols. Gen de la Hemocromatosis primaria: implicaciones diagnósticas y terapéuticas. Medicina General 2000;29:970-975

  2. BACON B AND BRITTON R. Hereditary Hemochro-matosis. Gastrointestinal and Liver disease. 6th Edition, 1998;2:1097-1103

  3. ANDREWS N. Disorders of Iron Metabolism. N Engl J Med 1999;341:1986-1995 (book review)

  4. PIETRANGELO A, MONTOSI G, TOTARO A, et al. Hereditary Hemochromatosis in Adults without Pathogenic Mutations in the Hemochromatosis Gene. N Engl J Med 1999;341:725-732

  5. PIETRANGELO A. Hemochromatosis: Genetics, pathophysiology, diagnosis and treatment. N Engl J Med 2000;343:516-517

  6. BURKE W, IMPERATORE G, MCDONNELL SM, et al. Contribution of different HFE genotypes to iron overload disease: a pooled analysis. Genetics in Medicine 2000;2:271-277

  7. WAHEED A, PARKKILA S, ZHOU XY, et al. Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with 2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells. Proc Natl Acad Sci 1997;94:12384-89

  8. BULAJ Z, AJIOKA R, PHILLIPS J, et al. Disease-Related Conditions in Relatives of Patients with Hemochromatosis N Engl J Med 2000;343:1529-1535

  9. WAHEED A, PARKKILA S, SAARNIO J. Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum. Proc Natl Acad Sci 1999;96:1579-84

  10. SCULLY R, MARK E, MCNEELY W, et al. Case Records of the Massachusetts General Hospital N Engl J Med 

  11. ADAMS PC. Population screening for haemochro-matosis. Gut 2000; 46: 301-303

  12. EDWARDS CQ, GRIFFEN LM, GOLDGAR D, et al. Prevalence of hemochromatosis among 11,065 presumably healthy blood donors. N Engl J Med 1988;318:1355-62

  13. GORE J AND FALLON J. Case 31-1994 A 25-Year-Old Man with the Recent Onset of Diabetes Mellitus and Congestive Heart Failure. N Engl J Med 1994; 331: 460-466

  14. WILLIS G, WIMPERIS JZ, LONSDALE R, et al. Incidence of liver disease in people with HFE mutations. Gut 2000;46:401-404

  15. TUOMAINEN TP, KONTULA K, NYYSSÖNEN K, et al. Increased Risk of Acute Myocardial Infarction in Carriers of the Hemochromatosis Gene Cys282Tyr Mutation.Circulation 1999;100:1274-1279

  16. CIFUENTES P, DOWLING P AND OZAKI R. ¿Should all patients with diabetes mellitus be screened for hemochromatosis?. West J Med 2002;176:110-114

  17. FORD ES AND COGSWELL ME. Diabetes and serum ferritin concentration among U.S. adults. Diabetes Care 1999;22:1978-1983

  18. PÉREZ DE NANCLARES G, CASTAÑO L, GAZTAMBIDE S, et al. Excess Iron Storage in Patients with Type 2 Diabetes Unrelated to Primary Hemochromatosis. N Engl J Med 2000;343:891

  19. EDWARDS C, KUSHNER J. Screening for Hemochromatosis. N Engl J Med 1993;328:1616-1620

  20. POWELL L, GEORGE K, MCDONNELL, S, et al. Diagnosis of Hemochromatosis. Ann Intern Med 1998; 129:925-931

  21. BACON B, OLYNYK J, BRUNT E, et al. HFE Genotype in patients with Hemochromatosis and other Liver diseases. Ann Intern Med 1999;130:953-962

  22. BRAVO A, SHETH S AND CHOPRA S. LIVER BIOPSY. N Engl J Med 2001;344:495-500

  23. BARTON J, MCDONELL S, ADAMS P, et al. Management of Hemochromatosis. Ann Intern Med 1998;129:932-939

 

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