نتایج جستجو برای: genetic diagnosis

تعداد نتایج: 1054612  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه پیام نور - دانشگاه پیام نور استان تهران - دانشکده مهندسی برق و کامپیوتر 1392

با وجود حجم بالای اطلاعات متنی، نیازمند سیستمی کارا جهت دسته بندی خودکار متون داریم. بنابراین، باید دسته بندی را طوری انجام داد که ضمن افزایش دقت، سبب کاهش زمان و هزینه شود. فرایند دسته بندی متون دارای گام‎های پیش پردازش، وزن دهی، کاهش ویژگی و دسته بندی است که برای هر گام روش‎های مختلفی تا کنون ارائه شده است. یکی از گام‎های تعیین کننده در دسته بندی، کاهش ویژگی‎ها است. این موضوع در زبان فارسی به...

Journal: :journal of biomedical physics and engineering 0
a javadpour neuroscience research center, baqiyatallah university of medical sciences, tehran, iran. a mohammadi neuroscience research center, baqiyatallah university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی بقیه الله (baqiyatallah university of medical sciences)

normal 0 false false false en-us x-none fa background:  regarding the importance of right diagnosis in medical applications, various methods have been exploited for processing medical images solar. the method of segmentation is used to analyze anal to miscall structures in medical imaging. objective:  this study describes a new method for brain magnetic resonance image (mri) segmentation via a ...

Journal: :Hong Kong medical journal = Xianggang yi xue za zhi 2015
Judy F C Chow William S B Yeung Vivian C Y Lee Estella Y L Lau P C Ho Ernest H Y Ng

OBJECTIVE To report the outcomes of more than 100 cycles of preimplantation genetic diagnosis for monogenetic diseases. DESIGN Case series. SETTING Tertiary assisted reproductive centre in Hong Kong, where patients needed to pay for the cost of preimplantation genetic diagnosis on top of standard in-vitro fertilisation charges. PATIENTS Patients undergoing preimplantation genetic diagnosi...

Background: Sexual reproduction affords the stands for conserving genetic characteristics and sequentially, genetic inconsistency may influence the capability to imitate. Materials and Methods: Research was conducted by subject in PubMed and other databases. Results: A significant number of genotypes have been related with infertility phenotypes and evaluation of precise genes in humans and mod...

Journal: :genetics in the 3rd millennium 0
مازیار سیدیان maziar seyedian tehran university of medical sciences, tehran, iranاستاد یار نورولوژی، دانشگاه علوم پزشکی تهران، تهران، ایران

alzheimers disease (ad) is by far the most common cause of dementia. definite diagnosis of ad is based on pathological findings. nincds-adrda criteria, published more than 25 years ago, are commonly used for the clinical diagnosis of ad. however, considering serious shortcomings of these criteria, new criteria have been proposed. according to these new criteria, ad can be diagnosed in predement...

Journal: :iranian journal of public health 0
farideh razi ensieh nasli esfahani bagher larijani parvin pasalar

the aim of the clinical laboratory in endocrine disease diagnosis and management is detecting either the hormones or their downstream reaction metabolites or some other related substances. in the case of hormone measurement almost all the routine methods are based on immunoassay with different labels (radioimmunoassay, enzyme linked immunosorbant assay, chemiluminescence assays …) and different...

Journal: :iranian journal of child neurology 0
joseph g. gleeson

abstract objective the last two decades have seen major advancements in our understanding of some of the most common neurodevelopmental disorders in the field of child neurology. however, in the majority of individual patients, it is still not possible to arrive at a molecular diagnosis, due in part to lack of knowledge of molecular causes of these tremendously complex conditions. common geneti...

2001
C. Cadrin

Objective: To provide family practitioners, obstetricians, and geneticists with guidelines and recommendations for prenatal diagnosis. Options: These guidelines apply to non-invasive screening techniques (including maternal serum screening and ultrasound) and to invasive techniques (including amniocentesis and chorionic villus sampling). Outcomes: Improved prenatal diagnosis of congenital abnor...

Journal: :Human reproduction 2003
John A Robertson

The use of preimplantation genetic diagnosis (PGD) to screen embryos for aneuploidy and genetic disease is growing. New uses of PGD have been reported in the past year for screening embryos for susceptibility to cancer, for late-onset diseases, for HLA-matching for existing children, and for gender. These extensions have raised questions about their ethical acceptability and the adequacy of reg...

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