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A three-miRNA-based expression signature at diagnosis can predict occurrence of relapse in children with t(8;21) RUNX1-RUNX1T1 acute myeloid leukaemia.
Zampini, Matteo; Bisio, Valeria; Leszl, Anna; Putti, Maria C; Menna, Giuseppe; Rizzari, Carmelo; Pession, Andrea; Locatelli, Franco; Basso, Giuseppe; Tregnago, Claudia; Pigazzi, Martina.
Afiliação
  • Zampini M; Haematology-Oncology Laboratory, Istituto di Ricerca Pediatrica (IRP) - Fondazione Città della Speranza, Padova, Italy.
  • Bisio V; Women and Child Health Department, Haematology-Oncology Clinic and Laboratory, University of Padova, Padova, Italy.
  • Leszl A; Department of Women's and Children's Health, Padova University Hospital, Padua, Italy.
  • Putti MC; Department of Women's and Children's Health, Padova University Hospital, Padua, Italy.
  • Menna G; Department of Paediatric Haemato-Oncology, Santobono-Pausilipon Hospital, Napoli, Italy.
  • Rizzari C; Department of Paediatrics, Centro Ricerca Tettamanti, Università di Milano-Bicocca, Monza, Italy.
  • Pession A; Department of Paediatrics, Sant'Orsola Hospital, University of Bologna, Bologna, Italy.
  • Locatelli F; Department of Paediatric Oncohaematology, Bambino Gesù Children's Hospital IRCCS, Rome, Italy.
  • Basso G; Department of Paediatric Science, University of Pavia, Pavia, Italy.
  • Tregnago C; Women and Child Health Department, Haematology-Oncology Clinic and Laboratory, University of Padova, Padova, Italy.
  • Pigazzi M; Women and Child Health Department, Haematology-Oncology Clinic and Laboratory, University of Padova, Padova, Italy.
Br J Haematol ; 183(2): 298-301, 2018 10.
Article em En | MEDLINE | ID: mdl-28961307
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 8 / Cromossomos Humanos Par 21 / Leucemia Mieloide Aguda / Proteína 1 Parceira de Translocação de RUNX1 Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Br J Haematol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 8 / Cromossomos Humanos Par 21 / Leucemia Mieloide Aguda / Proteína 1 Parceira de Translocação de RUNX1 Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Br J Haematol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália