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pro vyhledávání: '"Hamisa Iddy"'
Autor:
Clara Chamba, Hamisa Iddy, Erius Tebuka, Furahini Tluway, Elisha Osati, Neema Budodi, Collins Meda, Mbonea Yonazi, Anna Schuh, Lucio Luzzatto, Julie Makani
Publikováno v:
Case Reports in Hematology, Vol 2018 (2018)
Acute chest syndrome (ACS) is a life-threatening complication of sickle cell disease (SCD) with blood transfusion an integral part in its management. Red cell exchange (RCE) transfusion is usually regarded as preferable to top-up transfusion, because
Externí odkaz:
https://doaj.org/article/75ca3b5ce4964342bf852bd9c45a6a55
Publikováno v:
Therapeutic Advances in Rare Disease. 2:263300402110099
Wiskott–Aldrich syndrome (WAS) is a rare immunodeficiency X-linked genetic disorder. It is often featured with a clinical triad of thrombocytopenia with low mean platelet volume, eczematoid dermatitis and recurrent infections. The clinical manifest
Autor:
Furahini Tluway, Lucio Luzzatto, Collins Meda, Julie Makani, Mbonea Yonazi, Elisha Osati, Anna Schuh, Clara Chamba, Neema Budodi, Hamisa Iddy, Erius Tebuka
Publikováno v:
Case Reports in Hematology, Vol 2018 (2018)
Case Reports in Hematology
Case Reports in Hematology
Acute chest syndrome (ACS) is a life-threatening complication of sickle cell disease (SCD) with blood transfusion an integral part in its management. Red cell exchange (RCE) transfusion is usually regarded as preferable to top-up transfusion, because