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Bianca Maria Ricerca

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Mediterranean Journal of Hematology and Infectious Diseases|March 19, 2011
Infections in thalassemia and hemoglobinopathies: focus on therapy-related complicationsBianca Maria Ricerca, Arturo Di Girolamo, Deborah Rund
International Journal of Molecular Sciences|July 14, 2023
Total Antioxidant Capacity: Biochemical Aspects and Clinical SignificanceAndrea Silvestrini, Elisabetta Meucci, Bianca Maria Ricerca, et al.
Haematologica|February 12, 2002
Absence of hepcidin gene mutations in 10 Italian patients with primary iron overloadSilvia Majore, Francesco Binni, Bianca Maria Ricerca, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|February 11, 2017
The role of molecular typing and perfect match transfusion in sickle cell disease and thalassaemia: An innovative transfusion strategyRossana Putzulu, Nicola Piccirillo, Nicoletta Orlando, et al.
Clinical Biochemistry|August 9, 2011
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacementAngelo Minucci, Bianca Maria Ricerca, Domenico Tripodi, et al.
Blood Cells, Molecules & Diseases|September 24, 2013
TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern ItalyFrancesca Clementina Radio, Silvia Majore, Francesco Binni, et al.
Haematologica|August 29, 2009
Hereditary thrombocytosis caused by MPLSer505Asn is associated with a high thrombotic risk, splenomegaly and progression to bone marrow fibrosisLuciana Teofili, Fiorina Giona, Lorenza Torti, et al.
The Journal of Infection|June 21, 2011
Common occurrence of anaemia at the end of pregnancy following exposure to zidovudine-free regimensCarmela Pinnetti, Silvia Baroncelli, Atim Molinari, et al.
Leukemia & Lymphoma|May 8, 2013
Anemia in diffuse large B-cell non-Hodgkin lymphoma: the role of interleukin-6, hepcidin and erythropoietinMaria Chiara Tisi, Valentina Bozzoli, Manuela Giachelia, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 11, 2019
Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivoBartholomew P Roland, Kristen R Richards, Stacy L Hrizo, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Mediterranean Journal of Hematology and Infectious Diseases|March 19, 2011
Infections in thalassemia and hemoglobinopathies: focus on therapy-related complicationsBianca Maria Ricerca, Arturo Di Girolamo, Deborah Rund
International Journal of Molecular Sciences|July 14, 2023
Total Antioxidant Capacity: Biochemical Aspects and Clinical SignificanceAndrea Silvestrini, Elisabetta Meucci, Bianca Maria Ricerca, et al.
Haematologica|February 12, 2002
Absence of hepcidin gene mutations in 10 Italian patients with primary iron overloadSilvia Majore, Francesco Binni, Bianca Maria Ricerca, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|February 11, 2017
The role of molecular typing and perfect match transfusion in sickle cell disease and thalassaemia: An innovative transfusion strategyRossana Putzulu, Nicola Piccirillo, Nicoletta Orlando, et al.
Clinical Biochemistry|August 9, 2011
Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacementAngelo Minucci, Bianca Maria Ricerca, Domenico Tripodi, et al.
Blood Cells, Molecules & Diseases|September 24, 2013
TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern ItalyFrancesca Clementina Radio, Silvia Majore, Francesco Binni, et al.
Haematologica|August 29, 2009
Hereditary thrombocytosis caused by MPLSer505Asn is associated with a high thrombotic risk, splenomegaly and progression to bone marrow fibrosisLuciana Teofili, Fiorina Giona, Lorenza Torti, et al.
The Journal of Infection|June 21, 2011
Common occurrence of anaemia at the end of pregnancy following exposure to zidovudine-free regimensCarmela Pinnetti, Silvia Baroncelli, Atim Molinari, et al.
Leukemia & Lymphoma|May 8, 2013
Anemia in diffuse large B-cell non-Hodgkin lymphoma: the role of interleukin-6, hepcidin and erythropoietinMaria Chiara Tisi, Valentina Bozzoli, Manuela Giachelia, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 11, 2019
Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivoBartholomew P Roland, Kristen R Richards, Stacy L Hrizo, et al.
Pageof 1