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Treatment of profound thrombocytopenia in a patient with Gaucher disease type 1: Is there a role for substrate reduction therapy.
Ha, Christine I; DeArmey, Stephanie; Cope, Heidi; Rairikar, Mugdha; Kishnani, Priya S.
Afiliação
  • Ha CI; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • DeArmey S; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • Cope H; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • Rairikar M; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • Kishnani PS; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
Mol Genet Metab Rep ; 12: 82-84, 2017 Sep.
Article em En | MEDLINE | ID: mdl-28702360
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Mol Genet Metab Rep Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Mol Genet Metab Rep Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos