نتایج جستجو برای: luise von flotow

تعداد نتایج: 96742  

Adhinav Jaimini Anupam Mondal Dinesh Singh Madhavi Tripathi Maria D'Souza Rajnish Sharma

  We report an unusual case of a young male with cerebellar hemangioblastoma treated previously for medullary carcinoma of thyroid, whose PET/CT scans revealed a constellation of findings that suggested the rare Von Hippel Lindau syndrome. The diagnosis was clinched by confirming the findings on whole body contrast enhanced computed tomography (CECT) and contrast enha...

Journal: :British journal of haematology 2010
Giancarlo Castaman Alberto Tosetto Anne Goodeve Augusto B Federici Stefan Lethagen Ulrich Budde Javier Batlle Dominique Meyer Claudine Mazurier Jenny Goudemand Jeroen Eikenboom Reinhard Schneppenheim Jorgen Ingerslev David Habart Frank Hill Ian Peake Francesco Rodeghiero

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...

2006

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Journal: :Blood 2002
Alessandra Casonato Elena Pontara Francesca Sartorello Maria Grazia Cattini Maria Teresa Sartori Roberto Padrini Antonio Girolami

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...

Journal: :Blood 2006
Sandra L Haberichter Michael Balistreri Pamela Christopherson Patricia Morateck Stefana Gavazova Daniel B Bellissimo Marilyn J Manco-Johnson Joan Cox Gill Robert R Montgomery

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...

Journal: :Acta haematologica 2012
Augusto B Federici Paula James

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 (...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه گیلان - دانشکده کشاورزی 1391

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...

Journal: :نشریه دانشکده فنی 0
ناصر توحیدی

es wird gezeigt, dass bei der standiger zunahme der production von roheisen ,die fast ausschliesslich in hochofen erfolgt, der gestelldurchmesser und die ofeneinheit zunimmt demgegenuber der spezifische brennstoffverbrauch abnimmt. weiterhin wird die entwicklungsrichtung der stahlerzeungsverfanren wegen der wirtschaftlichen und technischen hinsicht untersucht und festgestellt, dass nuter versch...

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