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Ifosfamide, Idarubicin, And Etoposide In Relapsed/Refractory Hodgkin Disease Or Non-Hodgkin Lymphoma: A Salvage Regimen With High Response Rates Before Autologous Stem Cell Transplantation
(Elsevier Science Inc, 2005)
To achieve long-term disease-free survival, high-dose therapy and autologous stem cell transplantation (ASCT) is the current standard approach in patients with relapsed or refractory Hodgkin disease (HD) or non-Hodgkin ...
Impact Of Obesity On The Risk For Polycystic Ovary Syndrome
(Endocrine Soc, 2008)
Context: Although it is we I I established that adiposity increases the severity of the clinical features of polycystic ovary syndrome (PCOS), the data regarding the prevalence of PCOS in obese women and the change in body ...
Is Visual Loss Due to Giant Cell Arteritis Reversible?
(Yonsei Univ Coll Medicine, 2003)
Giant cell arteritis (GCA) is a common systemic vasculitis with an unknown etiology. It mainly affects people older than 50 years of age and often presents with symptoms such as headache, jaw claudication, visual loss, ...
Six2 and Bmp4 Mutations Associate with Anomalous Kidney Development
(Amer Soc Nephrology, 2008)
Renal hypodysplasia (RHD) is characterized by reduced kidney size and/or maldevelopment of the renal tissue following abnormal organogenesis. Mutations in renal developmental genes have been identified in a subset of ...
Significance of Factor V, Prothrombin, Mthfr, and Pai-1 Genotypes in Childhood Cerebral Thrombosis
(Sage Publications Inc, 2007)
The aim of this study was to evaluate the significance of factor V (FV) G1691A, prothrombin G20210A, methylenetetrahydrofolate reductase (MTHFR) C677T, and plasminogen activator inhibitor-1 (PAI-1) 4G/5G genotypes in ...
Skewed X Chromosome Inactivation in Blood Cells of Women with Scleroderma
(Wiley, 2005)
Objective. Scleroderma (SSc) is an autoimmune disease of unknown etiology. The disease is 3-8 times more frequent in women than in men. The role of X chromosome inactivation (XCI) in the predisposition of women to autoinimunity ...
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 ...