HEMOCROMATOSIS HEREDITARIA PDF

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Hemocromatosis hereditaria. Powell L.W., Isselbacher omatosis Pardo A., Salido E., Quintero omatosis hereditaria: implicaciones. Abstract. TAPIAS M, Mónica and IDROVO C, Victor. Hereditay hemochromatosis. Rev Col Gastroenterol [online]. , vol, n.4, pp ISSN Hemocromatosis hereditaria: Presentación de 2 casos y revisión de la literatura. Rev Col Gastroenterol [online]. , vol, n.2, pp ISSN

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Am J Med,pp. Iron; hemochromatosis; iron homeostasis; iron overload; HFE; genetic disease. Med Clin Barc, pp.

Hemocromatosis hereditaria

Hereditary hemochromatosis is a disorder related to iron metabolism. How to cite this article.

Nat Genet, 25pp. Prevalencia de la mutacion CysTyr del gen de la hemocromatosis en pacientes diagnosticados de hemocromatosis hereditaria de Cantabria.

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Blood Cells Mol Dis, 27pp. Rev Col Gastroenterol [online]. HFE mutations in patients with hereditary haemochromatosis in Sweden.

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No significant differences in phenotypic expression or in the frequency of CY homozygosity were observed between patients born in the North and South of Spain. Long-term survival in patients with hereditary hemochromatosis.

Hemocromatosis hereditaria – Bibliografía

Prevalence of the CY mutation for haemochromatosis on the Island of Majorca. J Hepatol, 34heredotaria. Continuing navigation will be considered as acceptance of this use. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q Gastroenterology,pp. Clinical features of genetic hemochromatosis in women compared with men.

The diseas has traditionally been described in groups of celtic origin of northern Europe for more than years. Autosomal dominant reticuloendothelial iron overload associated with a 3-base pair deletion in the ferroportin 1 gene SLC11A3. J Clin Invest,pp.

J Hepatol, 38pp. A total of The UK Hemochromatosis Consortium. Spanish pdf Article in xml format Article references How to cite this article Automatic translation Send this article by e-mail. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.

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Hemocromatosis hereditaria: Presentación de 2 casos y revisión de la literatura

Si continua navegando, consideramos que acepta su uso. Chelation therapy has limited use in this disorder, and is not recommended.

Blood Cells Mol Dis, 26pp. Blood, 97pp. Clin Genet, 58pp.

Am J Gastroenterol, 92pp. J Hepatol, 33pp.

Eur J Hum Genet, 9pp. In Spain, the available data are contradictory and limited to small series in specific regions. January Pages Gastreonterology,pp. The genotypic hsreditaria phenotypic expression of HH in Spain is very similar to that reported in Northern Europe.