نتایج جستجو برای: noninvasive diagnosis

تعداد نتایج: 494451  

Journal: :JDDG: Journal der Deutschen Dermatologischen Gesellschaft 2017

Journal: :hepatitis monthly 0
yi xiang zheng viral hepatitis key laboratory of hunan province, department of infectious disease, xiangya hospital, central south university, changsha, china shu juan ma department of epidemiology and health statistics, school of public health, central south university, changsha, china meng hou lu viral hepatitis key laboratory of hunan province, department of infectious disease, xiangya hospital, central south university, changsha, china; viral hepatitis key laboratory of hunan province, department of infectious disease, xiangya hospital, central south university, changsha, china

conclusions fib-4 confirmed the best value for diagnosis of significant fibrosis. apri had a sub-optimal diagnosis accuracy for significant fibrosis. lsm showed the most balance diagnosis value for cirrhosis with the highest sensitivity and moderate specificity. patients and methods a total of 544 patients with chb were assessed for fibrosis stage by four noninvasive tests containing liver stif...

Journal: :Journal of Vascular Surgery 2001

Journal: :Clinical and Molecular Hepatology 2012

Journal: :PLOS Neglected Tropical Diseases 2016

Journal: :international journal of molecular and cellular medicine 0
mohammad kazemi department of genetics and molecular biology, school of medicine, isfahan university of medical sciences, isfahan, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی اصفهان (isfahan university of medical sciences)سازمان های دیگر: pediatric inherited diseases research center, re search institute for primordial prevention of non- pediatric inherited diseases research center, re search institute for primordial prevention of non-communicable disease, isfahan university of medical sciences, isfahan, iran. mansoor salehi medical genetic center of genome, isfahan, iran.سازمان های دیگر: pediatric inherited diseases research center, re

down syndrome (ds) is a birth defect with huge medical and social costs, caused by trisomy of whole or part of chromosome 21. it is the most prevalent genetic disease worldwide and the common genetic cause of intellectual disabilities appearing in about 1 in 400-1500 newborns. although the syndrome had been described thousands of years before, it was named after john langdon down who described ...

Journal: :Analytical chemistry 2003
Arjan W Simonetti Willem J Melssen Marinette van der Graaf Geert J Postma Arend Heerschap Lutgarde M C Buydens

A new classification approach was developed to improve the noninvasive diagnosis of brain tumors. Within this approach, information is extracted from magnetic resonance imaging and spectroscopy data, from which the relative location and distribution of selected tumor classes in feature space can be calculated. This relative location and distribution is used to select the best information extrac...

2010
H. Christina Fan Stephen R. Quake

We recently demonstrated noninvasive detection of fetal aneuploidy by shotgun sequencing cell-free DNA in maternal plasma using next-generation high throughput sequencer. However, GC bias introduced by the sequencer placed a practical limit on the sensitivity of aneuploidy detection. In this study, we describe a method to computationally remove GC bias in short read sequencing data by applying ...

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