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Valeria Maria Pinto
Valeria Maria Pinto
Ente Ospedaliero Ospedali Galliera Genova
Adresă de e-mail confirmată pe galliera.it
Titlu
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The prognosis of clinical monoclonal B cell lymphocytosis differs from prognosis of Rai 0 chronic lymphocytic leukaemia and is recapitulated by biological risk factors
D Rossi, E Sozzi, A Puma, L De Paoli, S Rasi, V Spina, A Gozzetti, ...
British journal of haematology 146 (1), 64-75, 2009
1922009
Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias
R Russo, I Andolfo, F Manna, A Gambale, R Marra, BE Rosato, P Caforio, ...
American journal of hematology 93 (5), 672-682, 2018
1522018
Prevalence and risk factors for pulmonary arterial hypertension in a large group of β-thalassemia patients using right heart catheterization: a Webthal study
G Derchi, R Galanello, P Bina, MD Cappellini, A Piga, ME Lai, A Quarta, ...
Circulation 129 (3), 338-345, 2014
1242014
Sickle cell disease: a review for the internist
VM Pinto, M Balocco, S Quintino, GL Forni
Internal and emergency medicine 14 (7), 1051-1064, 2019
1222019
Management of iron overload in beta-thalassemia patients: clinical practice update based on case series
VM Pinto, GL Forni
International Journal of Molecular Sciences 21 (22), 8771, 2020
962020
SARS-CoV-2 infection in beta thalassemia: preliminary data from the Italian experience
I Motta, MM De Amicis, VM Pinto, M Balocco, F Longo, F Bonetti, ...
American journal of hematology, 2020
842020
Beta‐2‐microglobulin is an independent predictor of progression in asymptomatic multiple myeloma
D Rossi, M Fangazio, L De Paoli, A Puma, P Riccomagno, V Pinto, ...
Cancer 116 (9), 2188-2200, 2010
822010
Management of the aging beta-thalassemia transfusion-dependent population–The Italian experience
VM Pinto, M Poggi, R Russo, A Giusti, GL Forni
Blood reviews, 100594, 2019
662019
Current challenges in the management of patients with sickle cell disease–A report of the Italian experience
G Russo, L De Franceschi, R Colombatti, P Rigano, S Perrotta, V Voi, ...
Orphanet journal of rare diseases 14 (1), 120, 2019
632019
Adverse events after infusions of cryopreserved hematopoietic stem cells depend on non-mononuclear cells in the infused suspension and patient age
G Milone, S Mercurio, A Strano, S Leotta, V Pinto, K Battiato, S Coppoletta, ...
Cytotherapy 9 (4), 348-355, 2007
622007
Pre-emptive treatment of acute GVHD: a randomized multicenter trial of rabbit anti-thymocyte globulin, given on day+ 7 after alternative donor transplants
A Bacigalupo, T Lamparelli, G Milone, MP Sormani, F Ciceri, J Peccatori, ...
Bone marrow transplantation 45 (2), 385, 2010
592010
Red blood cell alloimmunisation in transfusion-dependent thalassaemia: a systematic review
M Franchini, GL Forni, G Marano, M Cruciani, C Mengoli, V Pinto, ...
Blood Transfusion 17 (1), 4, 2019
482019
Treatment of hepatitis C virus infection with direct‐acting antiviral drugs is safe and effective in patients with hemoglobinopathies
R Origa, ML Ponti, A Filosa, A Galeota Lanza, A Piga, GM Saracco, ...
American journal of hematology 92 (12), 1349-1355, 2017
472017
Luspatercept for the treatment of anaemia in non-transfusion-dependent β-thalassaemia (BEYOND): a phase 2, randomised, double-blind, multicentre, placebo-controlled trial
AT Taher, MD Cappellini, A Kattamis, E Voskaridou, S Perrotta, AG Piga, ...
The Lancet Haematology 9 (10), e733-e744, 2022
462022
Management of beta‐thalassemia–associated osteoporosis
A Giusti, V Pinto, GL Forni, A Pilotto
Annals of the New York Academy of Sciences 1368 (1), 73-81, 2016
462016
Daily alternating deferasirox and deferiprone therapy for ‘hard-to-chelate'β-thalassemia major patients
M Balocco, P Carrara, V Pinto, GL Forni
462010
Neridronate improves bone mineral density and reduces back pain in β‐thalassaemia patients with osteoporosis: results from a phase 2, randomized, parallel‐arm, open‐label study
GL Forni, S Perrotta, A Giusti, G Quarta, L Pitrolo, MD Cappellini, ...
British journal of haematology 158 (2), 274-282, 2012
452012
Acute promyelocytic leukemia during pregnancy: report of 3 cases
U Consoli, A Figuera, G Milone, CR Meli, G Guido, F Indelicato, ...
International journal of hematology 79 (1), 31-36, 2004
402004
Overall and complication‐free survival in a large cohort of patients with β‐thalassemia major followed over 50 years
GL Forni, B Gianesin, KM Musallam, F Longo, R Rosso, R Lisi, ...
American Journal of Hematology 98 (3), 381-387, 2023
362023
Complex modes of inheritance in hereditary red blood cell disorders: a case series study of 155 patients
I Andolfo, S Martone, BE Rosato, R Marra, A Gambale, GL Forni, V Pinto, ...
Genes 12 (7), 958, 2021
362021
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