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Hereditary red blood cell membrane defects. Detection of PIEZO1 mutations associated with SPTA1 mutations. An unusual clinical case of hereditary xerocytosis.
Fortugno, Carmelo; Galea, Eulalia; Cantaffa, Renato; Gigliotti, Francesco; Fabiano, Rachele Lucia; Talarico, Valentina; Raiola, Giuseppe; Galati, Maria Concetta.
Afiliação
  • Fortugno C; Department of Pediatric Onco-Hematology, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Galea E; Department of Pediatric Onco-Hematology, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Cantaffa R; Department of Pediatric Onco-Hematology, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Gigliotti F; Department of Pediatric Onco-Hematology, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Fabiano RL; Department of Pediatric Onco-Hematology, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Talarico V; Department of Pediatrics, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Raiola G; Department of Pediatrics, Pugliese Ciaccio Hospital, Catanzaro, Italy.
  • Galati MC; Department of Pediatric Onco-Hematology, Pugliese Ciaccio Hospital, Catanzaro, Italy.
Pediatr Hematol Oncol ; 38(2): 184-190, 2021 Mar.
Article em En | MEDLINE | ID: mdl-33136529
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esferocitose Hereditária / Hidropisia Fetal / Membrana Celular / Eritrócitos / Anemia Hemolítica Congênita Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Child, preschool / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esferocitose Hereditária / Hidropisia Fetal / Membrana Celular / Eritrócitos / Anemia Hemolítica Congênita Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Child, preschool / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article