Results 281 to 290 of about 192,458 (292)

Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis

International journal of hematology, 2017
Yongwei Wang, Ya-li Du, Gang Liu, Shanshan Guo, B. Hou, Xianyong Jiang, B. Han, Yanzhong Chang, Guangjun Nie   +8 more
semanticscholar   +1 more source

Properties of donated red blood cell components from patients with hereditary hemochromatosis

Transfusion, 2017
C. Sut, H. Hamzeh-Cognasse, S. Laradi, Vincent Bost, Christine Aubrège, S. Acquart, M. Vignal, Nadia Boutahar, C. Arthaud, Marie Ange Eyraud, B. Pozzetto, P. Tiberghien, O. Garraud, F. Cognasse   +13 more
semanticscholar   +1 more source

Hyperferritinemia increases the risk of hyperuricemia in HFE-hereditary hemochromatosis.

Joint, bone, spine : revue du rhumatisme, 2017
J. Flais, E. Bardou-Jacquet, Y. Deugnier, G. Coiffier, A. Perdriger, G. Chalès, M. Ropert, O. Loréal, P. Guggenbuhl   +8 more
semanticscholar   +1 more source

Proton Pump Inhibitors Reduce the Frequency of Phlebotomy in Patients With Hereditary Hemochromatosis.

Clinical Gastroenterology and Hepatology, 2016
René M M van Aerts, C. V. van Deursen, G. Koek   +2 more
semanticscholar   +1 more source

Deferasirox in patients with iron overload secondary to hereditary hemochromatosis: results of a 1‐yr Phase 2 study

European Journal of Haematology, 2015
R. Cançado, M. R. Melo, Roberto Moraes Bastos, P. C. Santos, Elivira M. Guerra‐Shinohara, C. Chiattone, S. Ballas   +6 more
semanticscholar   +1 more source

Successful Treatment of Iron-Overload Cardiomyopathy in Hereditary Hemochromatosis With Deferoxamine and Deferiprone.

Canadian Journal of Cardiology, 2016
Lydie Tauchenová, B. Křížová, M. Kubanek, S. Fraňková, V. Melenovský, J. Tintěra, D. Kautznerová, J. Maluskova, M. Jirsa, J. Kautzner   +9 more
semanticscholar   +1 more source

[Hereditary hemochromatosis].

Sovetskaia meditsina, 1987
Iu N, Tokarev, D A, Settarova
openaire   +2 more sources

Diagnosis and management of hereditary hemochromatosis.

Clinical Liver Disease, 2015
R. Salgia, Kimberly Brown
semanticscholar   +1 more source

Hereditary hemochromatosis type 1 phenotype modifiers in Italian patients. The controversial role of variants in HAMP, BMP2, FTL and SLC40A1 genes.

Blood Cells, Molecules & Diseases, 2015
F. C. Radio, S. Majore, C. Aurizi, F. Sorge, G. Biolcati, S. Bernabini, I. Giotti, F. Torricelli, D. Giannarelli, C. De Bernardo, P. Grammatico   +10 more
semanticscholar   +1 more source

Diagnostic evaluation of hereditary hemochromatosis (HFE and non-HFE).

Hematology/Oncology Clinics of North America, 2014
E. Bardou-Jacquet, P. Brissot
semanticscholar   +1 more source