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Case 4-2018: A Newborn with Thrombocytopenia, Cataracts, and Hepatosplenomegaly
New England Journal of Medicine, 2018Virginia M Pierce
exaly +2 more sources
Syndrome of iron deficiency anemia, hepatosplenomegaly, hypogonadism, dwarfism and geophagia
American Journal of Medicine, 1961Ananda S Prasad
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Prevalence of hepatosplenomegaly in beta thalassemia minor subjects in Iran
European Journal of Radiology, 2009Mehran Karimi +2 more
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Systemic Ehrlichiosis Presenting as Progressive Hepatosplenomegaly
Southern Medical Journal, 1997A 42-year-old white man had headache, fever, chills, abdominal pain, nausea and vomiting, night sweats, and dark urine for 3 days before admission; he had history of a tick bite 6 weeks earlier. Progressive systemic deterioration, heralded by progressive hepatosplenomegaly and pancytopenia, occurred despite doxycycline therapy.
A D, Friedman, G K, Daniel, W A, Qureshi
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Waldenström Macroglobulinemia: 2025 Update on Diagnosis, Risk Stratification, and Management
American journal of hematology/oncologyWaldenström macroglobulinemia (WM) is a lymphoplasmacytic lymphoma with immunoglobulin M (IgM) monoclonal protein. Clinical features include anemia, thrombocytopenia, hepatosplenomegaly, lymphadenopathy, and rarely hyperviscosity.
M. Gertz
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