نتایج جستجو برای: encyclopaedia of islam leiden

تعداد نتایج: 21182079  

Journal: :The Classical World 1971

Journal: :Stridon 2023

This article presents a study of publicly available Svenskt översättarlexikon ‘The Swedish Encyclopaedia Translators’ (SwET 2009), most probably the first digital encyclopaedia translators. The is situated in fields sociology translators, (literary) translator studies, and translation history, focuses on how female translators are described, characterized evaluated version SwET from 2022. Three...

2002
Peter Roach

This book is aimed at first-year students of Phonetics. It is based on a book I wrote which was published in 1992. The book, which had the title Introducing Phonetics, has now been deleted from the publisher's list. The title was misleading: this is not an introduction to Phonetics but a series of short explanations of technical terms used in the subject. I have, in fact, written what I hope is...

Background & Aims:Thromboembolism is an acute cardiovascular disease that ranges from clinically unimportant to massive embolism. Both acquired and hereditary risk factors contribute to the disease.
We aimed to determine the prevalence of two hereditary predisposing factor of the disease, prothrombin G20210A and factor V Leiden (G1691A) polymorphisms, in Kerman population.<br /...

Journal: :Journal of Complexity 2003

Journal: :international journal of reproductive biomedicine 0
majid teremmahi ardestani hossein hadi nodushan abbas aflatoonian nasrin ghasemi mohammad hasan sheikhha

background: recurrent pregnancy loss (rpl) caused by various genetic and non-genetic factors. after chromosome abnormality, thrombophilia is one of the most important genetic factors that could cause rpl. factor v leiden and factor ii g20210a mutation were the most common mutations cause thrombophilia in the world. objective: the purpose of this study was to determine the frequency of factor v ...

Journal: :journal of research in medical sciences 0
mohammad saadatnia mansour salehi ahmad movahedian sz samsam shariat mehri salari marzieh tajmirriahi

background: factor v g1691a (fv leiden), fii ga20210, and methylenetetrahydrofolate reductase (mthfr) c677t mutations are the most common genetic risk factors for thromboembolism in the western countries. however, there is rare data in iran about cerebral venous and sinus thrombosis (cvst) patients. the aim of this study was to evaluate the frequency of common genetic thrombophilic factors in c...

2005
Simon Baron-Cohen

Acknowledgments: The author was supported by the MRC during the period of this work. Portions of this article also appeared in Encarta (2004). 2 2 Introduction Autism, a condition of neurodevelopment, is more common in males, with onset typically in infancy. It is diagnosed when a child or adult has abnormalities in a 'triad' of behavioral domains: social development, communication, and repetit...

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