[Hereditary hemolytic anemia in newborns: clinical significance of genetic diagnosis].

Ohga, Shouichi; Ishimura, Masataka; Eguchi, Katsuhide; Hasegawa, Ichita; Ogura, Hiromi; Utsugisawa, Taiju; Kanno, Hitoshi

Ohga, Shouichi; Ishimura, Masataka; Eguchi, Katsuhide; Hasegawa, Ichita; Ogura, Hiromi; Utsugisawa, Taiju; Kanno, Hitoshi.

Afiliação

Ohga S; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University.
Ishimura M; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University.
Eguchi K; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University.
Hasegawa I; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University.
Ogura H; Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University.
Utsugisawa T; Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University.
Kanno H; Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University.

Rinsho Ketsueki ; 61(5): 484-490, 2020.

Article em Ja | MEDLINE | ID: mdl-32507813

Assuntos

Anemia Hemolítica Congênita; Membrana Eritrocítica; Eritrócitos; Hemólise; Humanos; Recém-Nascido; Japão

Palavras-chave

Clinical sequence; Hemolysis; Newborn; Syndromic

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anemia Hemolítica Congênita Tipo de estudo: Diagnostic_studies Limite: Humans / Newborn País/Região como assunto: Asia Idioma: Ja Revista: Rinsho Ketsueki Ano de publicação: 2020 Tipo de documento: Article

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