Results 181 to 190 of about 42,497 (216)

Hemophagocytic lymphohistiocytosis in the context of hepatitis-associated severe aplastic anemia: A case report. [PDF]

Medicine (Baltimore)
Xu J, Yuan H, Chen G, Qu J, Wang H, Chen R, Jiang M.   +6 more
europepmc   +1 more source

A Case of Hepatosplenic Gamma Delta T Cell Lymphoma With Concomitant Bone Marrow Aplasia Following Azathioprine Therapy, Treatment Course and Review of the Literature. [PDF]

Cancer Rep (Hoboken)
Younis R, Hauspurg H, Voss A.
europepmc   +1 more source

A rare case of dyskeratosis congenita with DKC1 mutation presenting initially as thrombocytopenia: Case report. [PDF]

Medicine (Baltimore)
Wen R, Tian J.
europepmc   +1 more source

Correction to "Successful Haploidentical Hematopoietic Stem Cell Transplantation for Paroxysmal Nocturnal Hemoglobinuria With Severe Pancytopenia Developed After Long-Term Aplastic Anemia Treatment". [PDF]

Clin Case Rep
europepmc   +1 more source

Correction: Analysis of the efficacy of avatrombopag for the delayed platelet engraftment after allogeneic hematopoietic stem cell transplantation for aplastic anemia. [PDF]

Front Med (Lausanne)
Zhang X, Feng J, Tan Z, Zhang H, Hu H, Zhao Y, Wu D, Zhang Y, Wu L, Hu T, Yan Z, Ye B, Liu W.   +12 more
europepmc   +1 more source

A meta-analysis of immunosuppressive and Pharmacological therapies in aplastic anaemia with and without Indigenous equine antithymocyte globulin (eATG). [PDF]

Ann Hematol
George B, Ross CR, Damodar S, Seth T, Dolai TK, Banerjee S, Manguesh R, Malhotra P.   +7 more
europepmc   +1 more source

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Aplastic anemia: Pathophysiology

Seminars in Hematology, 2022
Bone marrow failure (BMF) syndromes are a heterogeneous group of benign hematological conditions characterized by uni- or multi-lineage marrow and/or peripheral blood cytopenia(s), and can be classified in constitutional or acquired syndromes based on pathophysiology.
Giudice V., Selleri C.
openaire   +3 more sources