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Haematologica
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July 10, 2012
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients
Sara Pelucchi, Raffaella Mariani, Stefano Calza, et al.
Parkinsonism & Related Disorders
|
April 13, 2015
Movement disorders and brain iron overload in a new subtype of aceruloplasminemia
Jean-Marc Melgari, Massimo Marano, Carlo Cosimo Quattrocchi, et al.
British Journal of Haematology
|
November 22, 2023
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group
Paola Corti, Giulia Maria Ferrari, Martha Caterina Faraguna, et al.
Medicine and Science in Sports and Exercise
|
March 31, 2011
Index measured at an intermediate altitude to predict impending acute mountain sickness
Pietro Amedeo Modesti, Stefano Rapi, Rita Paniccia, et al.
Blood
|
February 26, 2004
Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis
Carmela Lanzara, Antonella Roetto, Filomena Daraio, et al.
European Journal of Heart Failure
|
July 22, 2022
Intravenous iron therapy improves the hypercapnic ventilatory response and sleep disordered breathing in chronic heart failure
Sergio Caravita, Andrea Faini, Carlo Vignati, et al.
Blood
|
December 15, 2010
Modulation of hepcidin production during hypoxia-induced erythropoiesis in humans in vivo: data from the HIGHCARE project
Alberto Piperno, Stefania Galimberti, Raffaella Mariani, et al.
Journal of Hepatology
|
December 3, 2014
Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis
Marie de Tayrac, Marie-Paule Roth, Anne-Marie Jouanolle, et al.
Journal of Gastroenterology
|
June 10, 2010
Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders
Yoshibumi Kaneko, Hiroaki Miyajima, Alberto Piperno, et al.
Med (New York, N.Y.)
|
December 19, 2024
Hb Monza: A novel extensive HBB duplication with preserved α-β subunit interaction and unstable hemoglobin phenotype
Ivan Civettini, Arianna Zappaterra, Paola Corti, et al.
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Search research articles
Search
Showing results (71-80 of 91) with videos related to
Sort By:
Page
of 10
Haematologica
|
July 10, 2012
CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients
Sara Pelucchi, Raffaella Mariani, Stefano Calza, et al.
Parkinsonism & Related Disorders
|
April 13, 2015
Movement disorders and brain iron overload in a new subtype of aceruloplasminemia
Jean-Marc Melgari, Massimo Marano, Carlo Cosimo Quattrocchi, et al.
British Journal of Haematology
|
November 22, 2023
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group
Paola Corti, Giulia Maria Ferrari, Martha Caterina Faraguna, et al.
Medicine and Science in Sports and Exercise
|
March 31, 2011
Index measured at an intermediate altitude to predict impending acute mountain sickness
Pietro Amedeo Modesti, Stefano Rapi, Rita Paniccia, et al.
Blood
|
February 26, 2004
Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis
Carmela Lanzara, Antonella Roetto, Filomena Daraio, et al.
European Journal of Heart Failure
|
July 22, 2022
Intravenous iron therapy improves the hypercapnic ventilatory response and sleep disordered breathing in chronic heart failure
Sergio Caravita, Andrea Faini, Carlo Vignati, et al.
Blood
|
December 15, 2010
Modulation of hepcidin production during hypoxia-induced erythropoiesis in humans in vivo: data from the HIGHCARE project
Alberto Piperno, Stefania Galimberti, Raffaella Mariani, et al.
Journal of Hepatology
|
December 3, 2014
Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis
Marie de Tayrac, Marie-Paule Roth, Anne-Marie Jouanolle, et al.
Journal of Gastroenterology
|
June 10, 2010
Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders
Yoshibumi Kaneko, Hiroaki Miyajima, Alberto Piperno, et al.
Med (New York, N.Y.)
|
December 19, 2024
Hb Monza: A novel extensive HBB duplication with preserved α-β subunit interaction and unstable hemoglobin phenotype
Ivan Civettini, Arianna Zappaterra, Paola Corti, et al.
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of 10