Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Fabiola Dell'Acqua"'
Autor:
Francesco Pegoraro, Aurora Chinnici, Linda Beneforti, Michele Tanturli, Irene Trambusti, Carmela De Fusco, Concetta Micalizzi, Veronica Barat, Simone Cesaro, Stefania Gaspari, Fabiola Dell’Acqua, Alessandra Todesco, Fabio Timeus, Maurizio Aricò, Claudio Favre, Annalisa Tondo, Maria Luisa Coniglio, Elena Sieni, AIEOP Histiocytosis Working Group
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Primary hemophagocytic lymphohistiocytosis (pHLH) is a severe, life-threatening hyperinflammatory syndrome caused by defects in genes of the granule-dependent cytotoxic pathway. Here we investigated the clinical presentation and outcome in a large
Externí odkaz:
https://doaj.org/article/a8dd69a4db024b2788b7c5b238c97b72
Autor:
Francesco Pegoraro, Aurora Chinnici, Linda Beneforti, Michele Tantuli, Irene Trambusti, Carmen De Fusco, Concetta Micalizzi, Alessandra Todesco, Fabiola Dell’acqua, Stefania Gaspari, Maria Luisa Coniglio, Elena Sieni
Publikováno v:
HemaSphere, Vol 7, p e62871f1 (2023)
Externí odkaz:
https://doaj.org/article/67f5d3e0d3f9442fa533351249d9fc2e
Autor:
Fabiola Guerra, Vincenzo L’Imperio, Sonia Bonanomi, Marco Spinelli, Tiziana Angela Coliva, Fabiola Dell’Acqua, Giulia Maria Ferrari, Paola Corti, Adriana Balduzzi, Andrea Biondi, Fabio Pagni, Francesco Saettini
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Myelofibrosis is a rare myeloproliferative disorder. The detailed descriptions of myelofibrosis in children and adolescents is limited to a few case series and case reports describing fewer than 100 patients, thus suggesting the extreme rarity of thi
Externí odkaz:
https://doaj.org/article/7ca332c4736d403eb287546d77247977
Autor:
Francesco Ceppi, Giacomo Gotti, Anja Möricke, Daniela Silvestri, Fiona Poyer, Jana Lentes, Anke Bergmann, Jan Trka, Julia Alten, Sara Elitzur, Draga Barbaric, Barbara Buldini, Fabiola Dell'Acqua, Fabian Schumacher, Gabriella Casazza, Joelle Tchinda, Karin Nebral, Valentino Conter, Andishe Attarbaschi, Martin Schrappe
Publikováno v:
European Journal of Cancer. 175:120-124
Near-tetraploidy-defined by DNA index 1.79-2.28 or 81-103 chromosomes-is a rare cytogenetic abnormality observed both in children and adults with T-cell acute lymphoblastic leukaemia (T-ALL) and its prognostic value is not yet determined.We report a
Autor:
Claudia Brusadelli, Francesca Vendemini, Paola Corti, Giulia Maria Ferrari, Fabiola Dell’Acqua
Publikováno v:
Medico e Bambino pagine elettroniche. 24:197-200
The paper reports the case of a three-month-old girl presenting with maculopapular lesions all over her scalp, trunk, axilla region and groin. One month earlier she had been diagnosed with LCH through skin biopsy for persisting maculopapular rash. No
Autor:
Adriana Balduzzi, M L Coniglio, Maria Iascone, Manuel Quadri, F Vendemini, Grazia Fazio, E Sieni, Massimo Provenzi, Carmelo Rizzari, Francesco Saettini, Laura Pezzoli, Simona Sala, Giovanni Cazzaniga, Sonia Bonanomi, Fabiola Dell’Acqua, Ilaria Castelli, Andrea Biondi
Publikováno v:
Pediatric Hematology and Oncology. 38:174-178
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory multisystemic disease. Familial hemophagocytic lymphohistiocytosis (FHL) represents a group of rare autosomal recess...
Autor:
Cristina Matteo, Antonella Colombini, Laura Rachele Bettini, Luca Porcu, Silvia Barzaghi, Tommaso Ceruti, Daniela Silvestri, Angela Amoroso, Fabiola Dell'Acqua, Giacomo Gotti, Claudia Nastasi, Massimo Zucchetti, Carmelo Rizzari
Background: l-Asparaginase (ASP) plays a crucial role in the treatment of childhood acute lymphoblastic leukemia (ALL). Currently, different ASP products are available in the market, including both native and pegylated drugs. Several biogeneric Esche
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abb68f59a32fd0de93ce67f88e44d718
https://hdl.handle.net/10281/427805
https://hdl.handle.net/10281/427805
Autor:
Martha Caterina Faraguna, Francesca Musto, Viola Crescitelli, Maria Iascone, Luigina Spaccini, Davide Tonduti, Tiziana Fedeli, Gaia Kullmann, Francesco Canonico, Alessandro Cattoni, Fabiola Dell’Acqua, Carmelo Rizzari, Serena Gasperini
Publikováno v:
Genes. 13:442
Mucopolysaccharidosis-plus syndrome (MPS-PS) is a novel autosomal recessive disorder caused by a mutation in the VPS33A gene. This syndrome presents with typical symptoms of mucopolysaccharidosis, as well as congenital heart defects, renal, and hemat
Autor:
Marta Galbiati, Grazia Fazio, Valentina Decimi, Carmelo Rizzari, Angelo Selicorni, Andrea Biondi, Silvia Maitz, Fabiola Dell'Acqua, Giovanni Cazzaniga
Publikováno v:
European Journal of Medical Genetics. 59:634-640
Williams syndrome (WBS) is a rare neurodevelopmental disorder with specific phenotypic characteristics and cardiac abnormalities, but is not considered as a cancer predisposing condition. However, in rare cases, malignancies have been described in pa