Atıf İçin Kopyala
Tekgunduz E., YILMAZ M., ERKURT M. A., KİKİ İ., Kaya A. H., KAYNAR L., ...Daha Fazla
TRANSFUSION AND APHERESIS SCIENCE, cilt.57, sa.1, ss.27-30, 2018 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
57
Sayı:
1
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Basım Tarihi:
2018
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Doi Numarası:
10.1016/j.transci.2018.02.012
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Dergi Adı:
TRANSFUSION AND APHERESIS SCIENCE
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.27-30
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Anahtar Kelimeler:
Thrombotic microangiopathy, Thrombotic thrombocytopenic purpura, Hemolytic-uremic syndrome, TTP, HUS, HEMOLYTIC-UREMIC SYNDROME, THROMBOCYTOPENIC PURPURA, ADULT PATIENTS, DIAGNOSIS, MANAGEMENT, REGISTRY, AHUS, TTP, ECULIZUMAB, CONSENSUS
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Dokuz Eylül Üniversitesi Adresli:
Evet
Özet
Thrombotic microangiopathies (TMAs) are rare, but life-threatening disorders characterized by microangiopathic hemolytic anemia and thrombocytopenia (MAHAT) associated with multiorgan dysfunction as a result of microvascular thrombosis and tissue ischemia. The differentiation of the etiology is of utmost importance as the pathophysiological basis will dictate the choice of appropriate treatment.