Zobrazeno 1 - 5
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pro vyhledávání: '"B. Bouslama"'
Publikováno v:
Transfusion Clinique et Biologique. 22:291-298
Autoimmune hemolytic anemia is a rare condition in children which differs from the adult form. It is defined by immune-mediated destruction of red blood cells caused by autoantibodies. Characteristics of the autoantibodies are responsible for the var
Publikováno v:
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 22(5-6)
Autoimmune hemolytic anemia is a rare condition in children which differs from the adult form. It is defined by immune-mediated destruction of red blood cells caused by autoantibodies. Characteristics of the autoantibodies are responsible for the var
Akademický článek
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Akademický článek
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Autor:
Liu C; Sorbonne University, AP-HP, Paediatric Haematology and Oncology Department Armand-Trousseau Hospital Paris France., Ballerini P; Sorbonne University, AP-HP, Laboratory of Haematology Armand-Trousseau Hospital Paris France.; Sorbonne University, AP-HP, French Reference Centre for Inherited Platelet Disorders Armand-Trousseau Hospital Paris France., Nguyen G; Sorbonne University, AP-HP, Laboratory of Haematology Armand-Trousseau Hospital Paris France.; Sorbonne University, AP-HP, French Reference Centre for Inherited Platelet Disorders Armand-Trousseau Hospital Paris France., Mincheva Z; Sorbonne University, AP-HP, Laboratory of Haematology Armand-Trousseau Hospital Paris France.; Sorbonne University, AP-HP, French Reference Centre for Inherited Platelet Disorders Armand-Trousseau Hospital Paris France., Copin B; Sorbonne University, AP-HP, Service de Génétique et Embryologie Médicales Armand-Trousseau Hospital Paris France., Bouslama B; Sorbonne University, AP-HP, Laboratory of Haematology Armand-Trousseau Hospital Paris France.; Sorbonne University, AP-HP, French Reference Centre for Inherited Platelet Disorders Armand-Trousseau Hospital Paris France., Leverger G; Sorbonne University, AP-HP, Paediatric Haematology and Oncology Department Armand-Trousseau Hospital Paris France.; Sorbonne University, AP-HP, French Reference Centre for Inherited Platelet Disorders Armand-Trousseau Hospital Paris France., Petit A; Sorbonne University, AP-HP, Paediatric Haematology and Oncology Department Armand-Trousseau Hospital Paris France.; Sorbonne University, AP-HP, French Reference Centre for Inherited Platelet Disorders Armand-Trousseau Hospital Paris France., Favier R; Sorbonne University, AP-HP, Laboratory of Haematology Armand-Trousseau Hospital Paris France.; Sorbonne University, AP-HP, French Reference Centre for Inherited Platelet Disorders Armand-Trousseau Hospital Paris France., Lapillonne H; Sorbonne University, AP-HP, Laboratory of Haematology Armand-Trousseau Hospital Paris France.; Sorbonne University, AP-HP, French Reference Centre for Inherited Platelet Disorders Armand-Trousseau Hospital Paris France., Boutroux H; Sorbonne University, AP-HP, Paediatric Haematology and Oncology Department Armand-Trousseau Hospital Paris France.; Sorbonne University, AP-HP, French Reference Centre for Inherited Platelet Disorders Armand-Trousseau Hospital Paris France.
Publikováno v:
EJHaem [EJHaem] 2022 Nov 06; Vol. 4 (1), pp. 145-152. Date of Electronic Publication: 2022 Nov 06 (Print Publication: 2023).