نتایج جستجو برای: fh

تعداد نتایج: 3804  

Journal: :American heart journal 2014
Joshua W Knowles Emily C O'Brien Karen Greendale Katherine Wilemon Jacques Genest Laurence S Sperling William A Neal Daniel J Rader Muin J Khoury

Familial hypercholesterolemia (FH) is a genetic disease characterized by substantial elevations of low-density lipoprotein cholesterol, unrelated to diet or lifestyle. Untreated FH patients have 20 times the risk of developing coronary artery disease, compared with the general population. Estimates indicate that as many as 1 in 500 people of all ethnicities and 1 in 250 people of Northern Europ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شیراز 1388

در سال های اخیر، با بهره گیری از ویژگی های قابل توجه سیستم های دسترسی چندگانه با استفاده از تقسیم کد و امکان استفاده ی همزمان چند کاربر با نرخ انتقال داده ی بالا از یک کانال توسط مدولاسیون چند حامله، روش های متعددی تحت نام کلی mc-cdma پیشنهاد و مورد بررسی قرار گرفته است. در این پایان نامه یکی از این تکنیک ها به نامfh-th-mc-wcdma ، که از پرش فرکانسی وزمانی بهره می برد را مورد مطالعه قرار می دهیم...

Journal: :The Journal of the American Osteopathic Association 2014
Thomas B Repas J Ross Tanner

Familial hypercholesterolemia (FH) is an autosomal dominant disorder resulting in severe elevation of total and low-density lipoprotein cholesterol levels. There are more than 600,000 individuals in the United States with FH. Individuals with FH tend to experience premature cardiovascular disease and often die from sudden cardiac death at a young age. Statins alone or in combination with other ...

2017
Mahtab Sharifi Marta Futema Devaki Nair Steve E. Humphries

PURPOSE OF REVIEW Familial hypercholesterolaemia (FH) is an inherited disorder of low-density lipoprotein cholesterol (LDL-C) which is characterised by a raised cholesterol level from birth and a high risk of premature coronary heart disease. In this paper, we review the genetic basis of FH and its impact on the clinical presentation. RECENT FINDINGS Mutations in any of three genes (LDLR, APO...

Journal: :Biomedicines 2021

A family history (FH+) of Alzheimer’s disease (AD) and ɛ4 allele the ApoE gene are main genetic risk factors for developing AD, whereas plays a protective role in age-related macular degeneration. Ocular vascular changes have been reported both pathologies. We analyzed choroidal thickness using optical coherence tomography (OCT) foveal avascular zone (FAZ) OCT-angiography compared results with ...

2011
Sheikh Tasnim Jahan Md. Saifur Rahman Khan Md. Moniruzzaman Md. Rezowanur Rahman Sams Mohammad Anowar Sadat Reza-ul Jalil

The objective of present work is to investigate the enhancement of dissolution profile for oral delivery of Fexofenadine Hydrochloride (FH) through solid dispersion (SD) technique by the method of solvent evaporation. The SD was prepared by using ethanol as a solvent. Tablets were formulated containing solid dispersion of FH and compared with tablets of same formula without solid dispersion of ...

2014
M M Ruseva M Takahashi T Fujita M C Pickering

Uncontrolled activation of the complement alternative pathway is associated with complement-mediated renal disease. Factor B and factor D are essential components of this pathway, while factor H (FH) is its major regulator. In complete FH deficiency, uncontrolled C3 activation through the alternative pathway results in plasma C3 depletion and complement-mediated renal disease. These are depende...

Journal: :CoRR 2010
Fang Liu Daiyuan Peng Zhengchun Zhou Xiaohu Tang

Frequency hopping (FH) sequences play a key role in frequency hopping spread spectrum communication systems. It is important to find FH sequences which have simultaneously good Hamming correlation,large family size and large period. In this paper, a new set of FH sequences with large period is proposed, and the Hamming correlation distribution of the new set is investigated. The construction of...

Journal: :Archives of endocrinology and metabolism 2015
Maria de Fátima Borges Priscila de Melo Franciscon Thamy Contursi Cambraia Débora Matias Oliveira Beatriz Pires Ferreira Elisabete Aparecida Mantovani Rodrigues de Resende Heloísa Marcelina Cunha Palhares

OBJECTIVE To report our experience of treating central precocious puberty (CPP) with a GnRH analogue with respect to the final heights (FH) attained in patients who completed treatment. SUBJECTS AND METHODS Among 105 records of children diagnosed with precocious puberty, 62 cases (54 girls and 8 boys), who were treated with leuprolide acetate/3.75 mg/monthly, were selected, and divided into 4...

2016
Leopoldo Pérez de Isla Rodrigo Alonso Nelva Mata Adriana Saltijeral Ovidio Muñiz Patricia Rubio - Marin José L. Diaz - Diaz Raimundo de Andrés Daniel Zambón Jesús Galiana Mar Piedecausa Rocio Aguado Daniel Mosquera José I Vidal Enrique Ruiz Laura Manjón Marta Mauri Teresa Padró José P. Miramontes Pedro Mata

Arterioscler Thromb Vasc Biol is available at http://atvb.ahajournals.org DOI: 10.1161/ATVBAHA.116.307514 Objective—Heterozygous familial hypercholesterolemia (FH) is the most common premature atherosclerotic cardiovascular disease (ASCVD)–related monogenic disorder, and it is associated with ischemic heart disease. There is limited information whether FH increases the risk of peripheral arteri...

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