Your browser doesn't support javascript.
loading
A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene.
Noris, Patrizia; Marconi, Caterina; De Rocco, Daniela; Melazzini, Federica; Pippucci, Tommaso; Loffredo, Giuseppe; Giangregorio, Tania; Pecci, Alessandro; Seri, Marco; Savoia, Anna.
Afiliação
  • Noris P; Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Marconi C; Department of Medical and Surgical Science, Policlinico Sant'Orsola Malpighi and University of Bologna, Bologna, Italy.
  • De Rocco D; Institute for Maternal and Child Health, IRCCS Burlo Garofolo, Trieste, Italy.
  • Melazzini F; Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Pippucci T; Department of Medical and Surgical Science, Policlinico Sant'Orsola Malpighi and University of Bologna, Bologna, Italy.
  • Loffredo G; Department of Oncology, Azienda Ospedaliera "Santobono-Pausilipon", Pausilipon Hospital, Naples, Italy.
  • Giangregorio T; Institute for Maternal and Child Health, IRCCS Burlo Garofolo, Trieste, Italy.
  • Pecci A; Department of Internal Medicine, IRCCS Policlinico San Matteo Foundation and University of Pavia, Pavia, Italy.
  • Seri M; Department of Medical and Surgical Science, Policlinico Sant'Orsola Malpighi and University of Bologna, Bologna, Italy.
  • Savoia A; Institute for Maternal and Child Health, IRCCS Burlo Garofolo, Trieste, Italy.
Br J Haematol ; 181(5): 698-701, 2018 06.
Article em En | MEDLINE | ID: mdl-28466964
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trombocitopenia / Trombopoetina / Alelos / Doenças Genéticas Inatas / Mutação Limite: Female / Humans / Male Idioma: En Revista: Br J Haematol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trombocitopenia / Trombopoetina / Alelos / Doenças Genéticas Inatas / Mutação Limite: Female / Humans / Male Idioma: En Revista: Br J Haematol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália