Results 251 to 260 of about 45,095 (307)
A Rare Case of Waldenström Macroglobulinemia Presenting as Bilateral Bloody Pleural Effusion and Pancytopenia. [PDF]
Chen YQ, Wang H, Feng Q.
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A case of marginal zone lymphoma presenting with paraneoplastic vasculitis and pulmonary infiltration. [PDF]
Uslu NZ, Yilmaz U, Bilir E, Balci MK.
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COVID-19-Associated Severe Aplastic Anemia in an 18-Month-Old Child: A Case Report. [PDF]
Hamidoglu H +2 more
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British Journal of Haematology, 1979
Summary. Circulating T‐lymphocytes from a 13‐year‐old boy with autoimmune anaemia, severe neutropenia and thrombocytopenia inhibited autologous and normal homologous bone marrow myeloid colony formation in vitro. This inhibition was abolished when the patient's antithymocyte globulin and complement‐treated T‐lymphocytes were used.
G, Daneshbod-Skibba +3 more
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Summary. Circulating T‐lymphocytes from a 13‐year‐old boy with autoimmune anaemia, severe neutropenia and thrombocytopenia inhibited autologous and normal homologous bone marrow myeloid colony formation in vitro. This inhibition was abolished when the patient's antithymocyte globulin and complement‐treated T‐lymphocytes were used.
G, Daneshbod-Skibba +3 more
openaire +2 more sources
Journal of the American Veterinary Medical Association, 1970
SUMMARY Tropical canine pancytopenia (tcp) is a newly recognized disease of dogs in diverse tropical and subtropical areas. The disease has been responsible for the death of large numbers of military dogs in Southeast Asia. Unilateral or bilateral epistaxis is the most dramatic clinical sign of the disease.
D L, Huxsoll +3 more
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SUMMARY Tropical canine pancytopenia (tcp) is a newly recognized disease of dogs in diverse tropical and subtropical areas. The disease has been responsible for the death of large numbers of military dogs in Southeast Asia. Unilateral or bilateral epistaxis is the most dramatic clinical sign of the disease.
D L, Huxsoll +3 more
openaire +2 more sources
The American Journal of the Medical Sciences, 1999
There has been little systematic study of the clinical spectrum of pancytopenia, and the optimal diagnostic approach to pancytopenia remains undefined.The authors studied 134 hospitalized pancytopenic patients in Zimbabwe in both consecutive and nonconsecutive fashion.The most common cause of pancytopenia was megaloblastic anemia, followed by aplastic ...
D G, Savage +10 more
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There has been little systematic study of the clinical spectrum of pancytopenia, and the optimal diagnostic approach to pancytopenia remains undefined.The authors studied 134 hospitalized pancytopenic patients in Zimbabwe in both consecutive and nonconsecutive fashion.The most common cause of pancytopenia was megaloblastic anemia, followed by aplastic ...
D G, Savage +10 more
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Procainamide‐associated pancytopenia
American Journal of Hematology, 1988AbstractA 42‐year‐old male developed thrombocytopenia and anemia along with agranulocytosis during treatment with procainamide. Bone marrow hypoplasia was evident on biopsy, and the patient was without evidence of systemic lupus erythematosis. He had prompt marrow recovery on drug withdrawal. While procainamide‐induced agranulocytosis has been reported
A F, Shields, J A, Berenson
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