Orak hücreli anemi hastalarında T helper, T sitotoksik ve doğal öldürücü hücre profili ve klinik prognozla ilişkisi

Author:

Atmış Bahriye,Kılınç Yurdanur,Yılmaz Mustafa,Atmış Anıl,Karagün Barbaros Şahin,Şaşmaz Hatice İlgen

Publisher

Cukurova Medical Journal

Subject

General Earth and Planetary Sciences,General Environmental Science

Reference30 articles.

1. 1. Herrick JB. Peculiar elongated and sickle-shaped red blood corpuscles in a case of severe anemia. Arch Intern Med 1910; 6:517

2. 2. Dover G, Platt O. Sickle cell disease. In: Nathan D, Orkin SH, Ginsburg D, Look AT (eds). Hematology of Infancy and Childhood. 6th ed, Philadelphia: WB Saunders Company, 2003: 790-841.

3. 3. Wang WC, Lukens JN. Sickle cell anemia and other sickling syndromes. In: Richard Lee G, Foerster J, Lukens J, Paraskevas F, Greer JP, Rodgers GM (eds), Wintrobe’s Clinical Hematology Volume 1,10th Ed. Baltimore: Williams & Wilkins, 1999: 1346-1397.

4. 4. Hernández P, Cruz C, Santos MN, Ballester JM. Immunologic dysfunction in sickle cell anaemia. Acta Haematol 1980; 63(3):156-61.

5. 5. Musa BO, Onyemelukwe GC, Hambolu JO, Mamman AI, Isa AH. Pattern of serum cytokine expression and T-cell subsets in sickle cell disease patients in vaso-occlusive crisis. Clin Vaccine Immunol. 2010;17(4):602-8.

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