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2017
Most cases of adult ITP are chronic form, and the onset of the disease is usually insidious. Signs and symptoms vary widely in each case from no hemorrhagic symptom to severe life-threatening bleeding, such as intracranial hemorrhage. In addition to hemorrhagic symptom, treatment-related complications, such as infection and cardiovascular diseases, may
Hirokazu Kashiwagi, Yoshiaki Tomiyama
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Most cases of adult ITP are chronic form, and the onset of the disease is usually insidious. Signs and symptoms vary widely in each case from no hemorrhagic symptom to severe life-threatening bleeding, such as intracranial hemorrhage. In addition to hemorrhagic symptom, treatment-related complications, such as infection and cardiovascular diseases, may
Hirokazu Kashiwagi, Yoshiaki Tomiyama
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Pediatric Blood & Cancer, 2012
AbstractThe Intercontinental Cooperative ITP Study Group (ICIS) was founded in 1997, when the American practice guidelines demonstrated that there is a substantial lack of clinical data. The aim of the group was to promote basic science and clinical research in the field of ITP.
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AbstractThe Intercontinental Cooperative ITP Study Group (ICIS) was founded in 1997, when the American practice guidelines demonstrated that there is a substantial lack of clinical data. The aim of the group was to promote basic science and clinical research in the field of ITP.
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Targeted ITP strategies: Do they elucidate the biology of ITP and related disorders?
Pediatric Blood & Cancer, 2006An elusive goal in hematology is a detailed understanding of autoimmune blood disorders including idiopathic (immune) thrombocytopenic purpura (ITP), autoimmune hemolytic anemia (AIHA), and Evans Syndrome. While it is clear that these disorders have an autoimmune pathophysiology, the exact mechanisms are not clear.
Ellis J. Neufeld+3 more
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Journal of Pediatric Hematology/Oncology, 2014
Deepak Bansal, Aruna Rajendran
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Deepak Bansal, Aruna Rajendran
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Ascorbate for the treatment of ITP
European Journal of Haematology, 1992J. W. Van Der Beek-Boter+3 more
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