Browsing by Publisher "Wiley-Liss"
Now showing items 1-8 of 8
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An Artificial Intelligent Diagnostic System on Differential Recognition of Hematopoietic Cells From Microscopic Images
(Wiley-Liss, 1997)Despite their advantages, none of the automated white blood cell differential counters have replaced the conventional microscopic evaluations of blood and bone marrow slides by hematologists, We have analyzed the smears ... -
Cerebral Infarct Associated With Factor V Leiden Mutation In A Boy With Hemophilia A
(Wiley-Liss, 1997)An 11-year-old boy with mild hemophilia A was admitted to our hospital because of focal convulsions, Magnetic resonance imaging showed an old occipital infarct. Protein C, S, antithrombin ill, anticardiolipin antibodies ... -
Dysplastic Changes in Idiopathic Thrombocytopenic Purpura and The Effect of Corticosteroids to Increase Dysplasia and Cause Hyperdiploid Macropolycytes
(Wiley-Liss, 2000)This study evaluates the dysplastic hematological changes in nine patients with idiopathic thrombocytopenic purpura (ITP) in 11 attacks, before and after corticosteroid treatment. The pretreatment blood smears of patients ... -
Effects Of Oral Cyclophosphamide And Prednisolone Therapy On The Endothelial Functions And Clinical Findings In Patients With Early Diffuse Systemic Sclerosis
(Wiley-Liss, 2003)Objective. The endothelial damage of microvascular structures in systemic sclerosis (SSc; scleroderma) is associated with increased levels of endothelial adhesion molecules and endothelium-associated cytokines, including ... -
Evaluation Of Prenatal-Onset Osteochondrodysplasias By Ultrasonography: A Retrospective And Prospective Analysis
(Wiley-Liss, 2008)The osteochondrodysplasia or skeletal dysplasias are a heterogenous group of over 350 distinct disorders of skeletogenesis. Many manifest in the prenatal diagnosis. A retrospective analysis evaluated 1,500 cases referred ... -
Factor V Q 506 Mutation In Children With Thrombosis
(Wiley-Liss, 1996)The factor V Leiden mutation in 12-children with thrombosis and in 20 controls was investigated, Five heterozygous individuals and 1 homozygous individual among the cases with thrombosis and 1 heterozygous individual among ... -
Loss of Maternal Allele in a Child with Myelodysplastic Syndrome and Monosomy 7
(Wiley-Liss, 1999)Monosomy 7 or partial deletion of the long arm of chromosome 7 is frequently described in children with myelodysplastic syndrome and acute myeloblastic leukemia, Parental origin of chromosome 7 in children with sporadic ... -
The Significance Of The Bone Marrow Biopsy Pattern In Chronic Lymphocytic Leukemia: A Prognostic Dilemma
(Wiley-Liss, 1999)Although bone marrow biopsy pattern (BMBP) has long been suggested to be an independent prognostic factor in chronic lymphocytic leukemia (CLL), conflicting reports continue to appear in the literature. To investigate this ...