Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Giulia Camarda"'
Autor:
Federica Plano, Anna Maria Corsale, Emilia Gigliotta, Giulia Camarda, Candida Vullo, Marta Di Simone, Mojtaba Shekarkar Azgomi, Maria Speciale, Melania Carlisi, Nadia Caccamo, Francesco Dieli, Serena Meraviglia, Sergio Siragusa, Cirino Botta
Publikováno v:
Hematology Reports, Vol 15, Iss 1, Pp 23-49 (2023)
Multiple myeloma (MM) is an incurable hematologic malignancy characterized by a multistep evolutionary pathway, with an initial phase called monoclonal gammopathy of undetermined significance (MGUS), potentially evolving into the symptomatic disease,
Externí odkaz:
https://doaj.org/article/7740141384cd44b4a8428f1cc65be042
Autor:
Vincenzo Accurso, Marco Santoro, Salvatrice Mancuso, Giorgia Vajana, Riccardo Tomasello, Cristina Rotolo, Giulia Camarda, Marta Mattana, Sergio Siragusa
Publikováno v:
Clinical Case Reports, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Rarely essential thrombocythemia (ET) is diagnosed in more than one person within a family. Familial myeloproliferative neoplasms are underdiagnosed. In this report, we describe 6 couples of familial ET, evaluating the heterogeneity of the m
Externí odkaz:
https://doaj.org/article/07b61b9c2e81440897f57997f09c341e
Autor:
Anna Maria Corsale, Mojtaba Shekarkar Azgomi, Federica Plano, Marta Di Simone, Cristina Perez, Carmela Picone, Emilia Gigliotta, Candida Vullo, Giulia Camarda, Cristina Rotolo, Maria Speciale, Marco Santoro, Nadia Caccamo, Francesco Dieli, Bruno Paiva, Serena Meraviglia, Sergio Siragusa, Cirino Botta
Publikováno v:
Blood. 140:9943-9944
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c885e9477ffc6b603370bf83f3b27b0b
https://doi.org/10.1182/blood-2022-167131
https://doi.org/10.1182/blood-2022-167131
Autor:
Marco Santoro, Vincenzo Accurso, Cristina Rotolo, Marta Mattana, Sergio Siragusa, Giorgia Vajana, Giulia Camarda, Riccardo Tomasello, Salvatrice Mancuso
Essential thrombocythemia is chronic myeloproliferative neoplasia, as defined by WHO in 2016, with the best prognosis. A small percentage of ET cases can be considered Familial ET. In this report we describe 6 cases of Familial ET, evaluating the het
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9639e8f31a1aa2dcac03a034b5636b86
https://doi.org/10.22541/au.162696960.02615189/v1
https://doi.org/10.22541/au.162696960.02615189/v1
