Results 231 to 240 of about 44,640 (263)
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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
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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
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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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Annals of Internal Medicine, 1968
Abstract The unique occurrence of severe pancytopenia and splenomegaly in a young woman with brucellosis is reported.
E C, Lynch, J C, McKechnie, C P, Alfrey
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Abstract The unique occurrence of severe pancytopenia and splenomegaly in a young woman with brucellosis is reported.
E C, Lynch, J C, McKechnie, C P, Alfrey
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2018
Abstract This chapter guides the reader on the diagnosis and management of pancytopenia in hospitalized patients.
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Abstract This chapter guides the reader on the diagnosis and management of pancytopenia in hospitalized patients.
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Posttransplantation and pancytopenia
Blood, 2012![Figure][1] A 33-year-old female with a history of a live related renal transplant on azathioprine and prednisolone and tacrolimus was asymptomatic until 3 years later when she developed low-grade fever, epigastric discomfort, and headache. She had hepatosplenomegaly but no lymphadenopathy.
Vikram, Narang, Updesh Singh, Sachdeva
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American Journal of Medical Genetics, 2000
We report on a Mexican girl who developed cerebellar ataxia at age 3 years and pancytopenia at age 13 years. Cerebral computed tomography scan and magnetic resonance imaging showed evidence of severe cerebellar atrophy. Telangiectasias were not present; immunoglobulins and alpha-fetoprotein levels were normal.
A, González-del Angel +6 more
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We report on a Mexican girl who developed cerebellar ataxia at age 3 years and pancytopenia at age 13 years. Cerebral computed tomography scan and magnetic resonance imaging showed evidence of severe cerebellar atrophy. Telangiectasias were not present; immunoglobulins and alpha-fetoprotein levels were normal.
A, González-del Angel +6 more
openaire +2 more sources