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Toplam kayıt 6, listelenen: 1-6
Comparison Of Primary Human Cytotoxic T-Cell And Natural Killer Cell Responses Reveal Similar Molecular Requirements For Lytic Granule Exocytosis But Differences In Cytokine Production
(Amer Soc Hematology, 2013)
Cytotoxic lymphocytes, encompassing cytotoxic T lymphocytes (CTLs) and natural killer (NK) cells, kill pathogen-infected, neoplastic, or certain hematopoietic cells through the release of perforin-containing lytic granules. ...
Chronic Myeloid Leukemia Presenting With Visual And Auditory Impairment In An Adolescent: An Insight To Management Strategies
(Springer India, 2010)
A 15-year-old girl presented with progressive deterioration in vision and hearing over 1 week. A huge spleen was palpated below the left costal margin laying down to inguinal region. Blood count showed hyperleukocytosis ...
An Unusual Presentation of Pediatric Acute Lymphoblastic Leukemia with Parotid Gland Involvement and Dactylitis
(Aves Yayincilik, 2010)
Mumps infection during the course of childhood acute lymphoblastic leukemia (ALL) treatment has been reported to have a mild course and this was related to the intrinsic low cytopathological effect of the virus, contrasting ...
The European Hematology Association Roadmap for European Hematology Research: A Consensus Document
(Ferrata Storti Foundation, 2016)
The European Hematology Association (EHA) Roadmap for European Hematology Research highlights major achievements in diagnosis and treatment of blood disorders and identifies the greatest unmet clinical and scientific needs ...
The Glycocalyx and Trauma: A Review
(Lippincott Williams & Wilkins, 2016)
In the United States trauma is the leading cause of mortality among those under the age of 45, claiming approximately 192,000 lives each year. Significant personal disability, lost productivity, and long-term healthcare ...
The Frequency of A91V in the Perforin Gene and the Effect of Tumor Necrosis Factor-Alpha Promoter Polymorphism on Acquired Hemophagocytic Lympholmstiocytosis
(Galenos Yayıncılık, 2011)
Objective: Numerous acquired etiological factors, such as infections, malignancies, and collagen tissue disorders, are involved in the development of acquired hemophagocytic lymphohistiocytosis (AHLH). Not everyone with ...