Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Lorenza, Torti"'
Autor:
Marianna De Muro, Annelot Julia Janssen, Sergio Amadori, Paolo de Fabritiis, Dante Sabatino, Pasquale Niscola, Lorenza Torti, Malgorzata Monika Trawinska, Cristiano Tesei, Felice Bombaci, Mario Tarricone, Monica Bocchia, Carmen Fava, Sara Galimberti, Alessandra Iurlo, Luigia Luciano, Elisabetta Abruzzese
Publikováno v:
Therapeutic Advances in Hematology, Vol 14 (2023)
Background: Hematological patients are a highly vulnerable population with an increased risk of developing severe COVID-19 symptoms due to their immunocompromised status. COVID-19 has proven to cause serious mental health issues, such as stress, anxi
Externí odkaz:
https://doaj.org/article/af627156801d40d49d02c8981f132558
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 15, Iss 1 (2023)
Background: Although the association between comorbidities and the severity of COVID-19 infection has been extensively discussed, data on COVID-19 and hemoglobinopathies are still limited. SARS-Cov2 reinfections with severe acute respiratory syndrome
Externí odkaz:
https://doaj.org/article/26d436a182064c89936dc293d7e60d3f
Autor:
Peter Hokland, Shahina Daar, Wael Khair, Sujit Sheth, Ali T. Taher, Lorenza Torti, Chattree Hantaweepant, Deborah Rund
Publikováno v:
Hokland, P, Daar, S, Khair, W, Sheth, S, Taher, A T, Torti, L, Hantaweepant, C & Rund, D 2023, ' Thalassaemia-A global view ', British Journal of Haematology, vol. 201, no. 2, pp. 199-214 . https://doi.org/10.1111/bjh.18671
The thalassaemias are a group of genetic disorders of haemoglobin which are endemic in the tropics but are now found worldwide due to migration. Basic standard of care therapy includes regular transfusions to maintain a haemoglobin level of around 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a73d65c2dc0203fb029a21b5674f381c
https://doi.org/10.1111/bjh.18671
https://doi.org/10.1111/bjh.18671
Autor:
Lorenza Torti, Laura Maffei, Francesco Sorrentino, Paolo De Fabritiis, Rossella Miceli, Elisabetta Abruzzese
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 12, Iss 1 (2020)
Not required for Letters
Externí odkaz:
https://doaj.org/article/89a98939e05b4c0db8d935c4a636ad99
Autor:
Lorenza Torti
Publikováno v:
British Journal of Haematology. 199:11-13
In the not so distant past, pregnancy in thalassaemia patients was considered a very high risk and often not recommended. The results regarding alpha-thalassaemia and in particular haemoglobin H disease by Srimeuniwai and colleagues are very encourag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a4a0e67047029e53e4b59de26e554de
https://doi.org/10.1111/bjh.18362
https://doi.org/10.1111/bjh.18362
Autor:
Luciana Teofili, Immacolata Izzi, Eugenia Rosa Nuzzolo, Giancarlo Scoppettuolo, Katleen de Gaetano Donati, Lorenza Torti, Marianna Rossi
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 4, Iss 1, Pp e2012062-e2012062 (2012)
We retrospectively compared the incidence of neutropenia in two groups of HIV patients with lymphoma, who underwent chemotherapy supported by once-per-cycle administration of pegfilgrastim or by daily subcutaneous injection of filgrastim, respectivel
Externí odkaz:
https://doaj.org/article/40aeb99b649240cfa78f2ca19414b84f
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 4, Iss 1, Pp e2012008-e2012008 (2012)
We describe the case of a 17- year old female who developed fatal haemophagocytic syndrome (HPS) one month following acute infection caused by Epstein-Barr virus (EBV). Despite initiation of treatment and reduction of EBV load, laboratory signs of HP
Externí odkaz:
https://doaj.org/article/2f45ba85b0fb4aabb82ca12bdc704255
Autor:
Luciana Teofili, Fiorina Giona, Lorenza Torti, Tonia Cenci, Bianca Maria Ricerca, Carlo Rumi, Vittorio Nunes, Robin Foà, Giuseppe Leone, Maurizio Martini, Luigi Maria Larocca
Publikováno v:
Haematologica, Vol 95, Iss 1 (2010)
Background The MPLSer505Asn mutation has been reported to be a cause of hereditary thrombocythemia. Recently, we detected this mutation in a large proportion of children with familial thrombocythemia, suggesting that in Italy the incidence of MPLSer5
Externí odkaz:
https://doaj.org/article/cfd573153e074a31a18f768547655b28
Autor:
Maurizio Martini, Luciana Teofili, Tonia Cenci, Fiorina Giona, Lorenza Torti, Massimiliano Rea, Robin Foà, Giuseppe Leone, Luigi Maria Larocca
Publikováno v:
Haematologica, Vol 93, Iss 7 (2008)
HIF2A transcription factor plays a central role in the regulation of the hypoxia responding pathway in mammalian cells, by modulating erythropoiesis and angiogenesis. Molecular alterations of oxygen sensing pathway constituents are implicated in here
Externí odkaz:
https://doaj.org/article/a0f1933d30294085bf69323cd7f5b64f
Autor:
Francesco Sorrentino, Rocco Rago, Maurizio Poggi, Laura Maffei, Elisabetta Abruzzese, Donatella Dell'Anna, Lorenza Torti, Stefano Aureli, Giovanni Loyola, Paolo de Fabritiis
Publikováno v:
Blood. 136:22-23
Introduction Major thalassemia (TM) and sickle cell disease (SCD), two common genetic hemoglobinopathies, were often fatal 50 years ago. Novel therapeutic and diagnostic methods are increasing lifespan and quality of life. Recent advances in iron che
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea90020c88c35845fd1eff24d9d0fe6e
https://doi.org/10.1182/blood-2020-134563
https://doi.org/10.1182/blood-2020-134563