نتایج جستجو برای: von karmans spectrum
تعداد نتایج: 319716 فیلتر نتایج به سال:
The relationships between the Platelet Function Analyzer (PFA)-100 and von Willebrand factor (VWF) levels and bleeding score (BS) were evaluated within a multicentre project on Molecular and Clinical Markers for the Diagnosis and Management of type 1 von Willebrand disease (MCMDM-1VWD). PFA-100 closure time, either with epinephrine (EPI) or adenosine diphosphate (ADP)-cartridges, was measured i...
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objectives: this study compared the effects of individual and group training on general health and stress of parents of children with autism spectrum disorders. methods: a sample of 75 parents of children referring to autistic children foundation (including 50 parents in two experimental groups and 25 parents in control group) was taken into account. sample parents were selected through accessi...
the degree kirchhoff index of a connected graph $g$ is defined as the sum of the terms $d_i,d_j,r_{ij}$ over all pairs of vertices, where $d_i$ is the degree of the $i$-th vertex, and $r_{ij}$ the resistance distance between the $i$-th and $j$-th vertex of $g$. bounds for the degree kirchhoff index of the line and para-line graphs are determined. the special case of regular grap...
Type Vicenza variant of von Willebrand disease (VWD) is characterized by a low plasma von Willebrand factor (VWF) level and supranormal VWF multimers. Two candidate mutations, G2470A and G3864A at exons 17 and 27, respectively, of the VWF gene were recently reported to be present in this disorder. Four additional families, originating from northeast Italy, with both mutations of type Vicenza VW...
Type 1 von Willebrand disease (VWD) is characterized by a partial quantitative deficiency of von Willebrand factor (VWF). Few VWF gene mutations have been identified that cause dominant type 1 VWD. The decreased survival of VWF in plasma has recently been identified as a novel mechanism for type 1 VWD. We report 4 families with moderately severe type 1 VWD characterized by low plasma VWF:Ag and...
Von Willebrand disease type 3 (VWD3) is the most severe form of this bleeding disorder due to the almost complete deficiency of von Willebrand factor (VWF). VWD3 is inherited as an autosomal recessive trait. While heterozygous carriers exhibit mild or no bleeding symptoms, most patients with VWD3, which is characterized by undetectable levels of VWF antigen (VWF:Ag) and reduced concentrations (...
The isomorphism problem in ergodic theory was formulated by von Neumann 1932 his pioneering paper Zur Operatorenmethode der klassischen Mechanik (Ann. of Math. (2), 33(3):587--642, 1932). has been solved for some classes transformations that have special properties, such as the collection with discrete spectrum or Bernoulli shifts. This shows a general classification is impossible (even concret...
به منظور مطالعه فون سخت بالپوشان خانواده carabidae در استان گیلان در تابستان 1390 نمونه های حشرات از مناطق مختلف استان گیلان، با استفاده از روش های مختلف شامل: تله های گودالی، نوری و یا با دست جمع آوری شدند، نمونه ها پس از انتقال به آزمایشگاه و آماده سازی، زیر استریومیکروسکوپ بررسی و با استفاده از منابع علمی مربوطه مورد شناسایی قرار گرفتند. و برای تایید صحت شناسایی نزد دکتر فلیکس در کشور هلند ا...
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