Marianna De Muro Selected Research

Autosomal Dominant Iron Overload

2/2018

Characterization of three novel pathogenic SLC40A1 mutations and genotype/phenotype correlations in 7 Italian families with type 4 hereditary hemochromatosis.

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Marianna De Muro Research Topics

Disease

4	Neoplasms (Cancer) 01/2021 - 01/2012
2	Polycythemia Vera 01/2021 - 01/2020
2	Multiple Myeloma 07/2011 - 07/2009
1	Iron Overload 01/2019
1	Autosomal Dominant Iron Overload 02/2018
1	Hemochromatosis (Bronze Diabetes) 02/2018
1	Splenomegaly 03/2016
1	Thrombosis (Thrombus) 03/2016
1	Philadelphia Chromosome 01/2012
1	Paraproteinemias (Monoclonal Gammopathy) 07/2009
1	Proteinuria 07/2009
1	Disease Progression 07/2009
1	Plasmacytoma 06/2003

Drug/Important Bio-Agent (IBA)

2	givinostatIBA 01/2021 - 01/2020
2	Deferasirox FDA Link 01/2019 - 06/2016
1	Janus Kinase 2IBA 01/2021
1	Ferritins (Ferritin)IBA 01/2019
1	metal transporting protein 1 (ferroportin)IBA 02/2018
1	IronIBA 02/2018
1	HepcidinsIBA 02/2018
1	Pharmaceutical PreparationsIBA 01/2012
1	Hydroxyurea (Hydrea)FDA LinkGeneric 01/2012
1	Dexamethasone (Maxidex)FDA LinkGeneric 07/2011
1	Lenalidomide (CC 5013)FDA Link 07/2011
1	Immunoglobulins (Immunoglobulin)IBA 07/2009
1	Immunoglobulin A (IgA)IBA 07/2009
1	Immunoglobulin G (IgG)IBA 07/2009
1	Prednisone (Sone)FDA LinkGeneric 06/2003
1	Melphalan (Alkeran)FDA LinkGeneric 06/2003

Therapy/Procedure

2	Therapeutics 03/2016 - 07/2011
1	Drug Therapy (Chemotherapy) 07/2011