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Toplam kayıt 67, listelenen: 31-40
Severe Arterial Thrombophilia Associated with a Homozygous Mthfr Gene Mutation (A1298C) in a Young Man with Klinefelter Syndrome
(Sage Publications Inc, 2008)
Klinefelter syndrome (KS) is the most common sex chromosome disorder in men. It may be associated with an increased risk for venous thrombosis and thromboembolism, which is partially explained by hypofibrinolysis due to ...
Update On The Safety And Efficacy Of Retroviral Gene Therapy For Immunodeficiency Due To Adenosine Deaminase Deficiency
(Amer Soc Hematology, 2016)
Adenosine deaminase (ADA) deficiency is a rare, autosomal-recessive systemic metabolic disease characterized by severe combined immunodeficiency (SCID). The treatment of choice for ADA-deficient SCID (ADA-SCID) is hematopoietic ...
Human Bone Marrow Megakaryocytes And Platelets Express Ppar Gamma, And Ppar Gamma Agonists Blunt Platelet Release Of Cd40 Ligand And Thromboxanes
(Amer Soc Hematology, 2004)
Peroxisome proliferator-activated receptor gamma (PPARgamma) is a ligand-activated transcription factor important in lipid metabolism, diabetes, and inflammation. We evaluated whether human platelets and megakaryocytes ...
Splenic Artery Embolization: An Alternative Approach In A Critically Ill Patient With Autoimmune Hemolytic Anemia
(Aves Yayincilik, 2011)
Assessment of general health status and hematological parameters usually precedes the use of invasive diagnostic and therapeutic procedures in critically ill patients. Angiography can be effective and safe as a substitute ...
Atraumatic Osteonecrosis After Estrogen Replacement Therapy Associated with Low Protein S Level in a Patient with Turner Syndrome
(Sage Publications Inc, 2010)
Atraumatic osteonecrosis has been associated with a variety of clinical conditions including corticosteroid usage, alcoholism, infections, hyperbaric events, storage disorders, marrow-infiltrating diseases, coagulation ...
Beta-Globin Haplotype And Xmni Polymorphism At Position G-Gamma-158 And Hbf Production In Fanconis Anemia
(Ferrata Storti Foundation, 1992)
Background. Patients with aplastic anemia show to a variable degree an increase of the red blood cell volume and percentage of HbF. The extent of HbF reactivation in sickle cell anemia and thalassemia major is related to ...
Myocardial Infarction And Deep Venous Thrombosis In A Young Patient With Behcet Disease
(Sage Publications Inc, 2006)
Behcet disease (BD) is a chronic relapsing systemic vasculitic disorder affecting the arteries, veins, and vessels of any size. Vascular lesions in BD usually represent an occlusive nature suggesting a hypercoagulable/ ...
Thrombopoietin As A Drug: Biologic Expectations, Clinical Realities, And Future Directions
(Westminster Publ Inc, 2002)
After the cloning of thrombopoietin (c-mpl ligand, Tpo) in 1994, 2 recombinant thrombopoietic growth factors, full-length glycosylated recombinant human Tpo (reHuTPO) and polyethylene glycol conjugated megakaryocyte growth ...
Clinical Investigation Of Oral Findings In Inherited Disorders Of Platelet Function
(Aves Yayincilik, 2011)
Objective: Bleeding disorders are a very important health problem due to the associated high risk of hemorrhage during dental procedures. The present study aimed to investigate oral manifestations of inherited disorders ...
European Guidelines For Empirical Antibacterial Therapy For Febrile Neutropenic Patients In The Era Of Growing Resistance: Summary Of The 2011 4Th European Conference On Infections In Leukemia
(Ferrata Storti Foundation, 2013)
Owing to increasing resistance and the limited arsenal of new antibiotics, especially against Gram-negative pathogens, carefully designed antibiotic regimens are obligatory for febrile neutropenic patients, along with ...