نتایج جستجو برای: gilberts disease

تعداد نتایج: 1490103  

Journal: :international journal of endocrinology and metabolism 0
malgorzata anna basinska kazimierz wielki university in bydgoszcz, poland +31-523708400, [email protected]; kazimierz wielki university in bydgoszcz, poland +31-523708400, [email protected] anna andruszkiewicz nicolaus copernicus university in torun, poland

conclusions beliefs in health locus of control and type of illness in female patient group are predictors of illness acceptance (p = 0,0009). patients and methods three methods were applied: multidimensional health locus of control scale by k.a. wallston, b.s. wallston and r. devellis; the acceptance of illness scale by b.j. felton, t.a. revenson, and g.a. hinrichsena; and a personal questionna...

Journal: :فصلنامه علمی پژوهشی گیاهان دارویی 0
a milajerdi school of nutritional sciences and dietetics, tehran university of medical sciences, tehran, iran v bitarafan school of nutritional sciences and dietetics, tehran university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences) m mahmoudi department of cellular molecular nutrition, school of nutritional sciences and dietetics, tehran university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی تهران (tehran university of medical sciences)

background: saffron (crocus satious l.) provides a variety of promising preventive and therapeutic effects with non-considerable side effects. objective: based on our knowledge, this is the first study that simultaneously has reviewed the effect of saffron extract and its constituents on the factors associated with neuropsychological, cardiovascular, and gastrointestinal tract diseases. methods...

Journal: :iranian journal of child neurology 0
mohammad ghofrani 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2.pediatric neurology center of excellence & pediatric neurology department sciences, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: ghofrani m. lysosomal storage disease (lsds). iran j child neurol. 2015 autumn;9:4(suppl.1): 1. pls see pdf.

Journal: :middle east journal of digestive diseases 0
kourosh masnadishirazi mohammad hossein somi yoosef bafandeh firooz saremi nooshin mylanchy parisa rezaeifar

background there are few reports from iran about the epidemiology and clinical features of inflammatory bowel disease (ibd). this study aims to determine the epide­miologic profile and clinical features of ibd in northwest iran referral centers. methods in a cross-sectional setting, we evaluated 200 patients with definitive diagno­ses of ibd who referred to tabriz educational hospitals during t...

Journal: :iranian red crescent medical journal 0
meltem erol department of pediatrics, bagcilar training and research hospital, istanbul, turkey; corresponding author: meltem erol, department of pediatrics, bagcilar training and research hospital, istanbul, turkey. tel: +90-5324578397, fax: +90-2124404242, e-mail: ozlem bostan gayret department of pediatrics, bagcilar training and research hospital, istanbul, turkey ozgul yigit department of pediatrics, bagcilar training and research hospital, istanbul, turkey kubra serefoglu cabuk department of ophtalmology, bagcilar training and research hospital, istanbul, turkey mehmet toksoz department of radiology, bagcilar training and research hospital, istanbul, turkey mahir tiras department of pediatrics, bagcilar training and research hospital, istanbul, turkey

conclusions in cases of unusual vascular lesions, metabolic diseases must be considered. in homocystinuria, early diagnosis and treatment are important. blood homocysteine levels can be returned to normal, and some complications can be prevented. introduction homocystinuria is a hereditary disease caused by a defect in the enzymes involved in metabolizing methionine. homocystinuria can influenc...

Journal: :مجله علوم اعصاب شفای خاتم 0
safieh ebrahimi department of medical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, iran mohammad jalili-nik department of medical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, iran hossein abde-ahad department of medical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, iran mahdi hassanian department of medical biochemistry, school of medicine, mashhad university of medical sciences, mashhad, iran

thrombin is a multifunctional enzyme which has key roles in coagulation cascade and inflammatory events. the pro-inflammatory functions of thrombin occur by different mechanisms including increasing mast cell degranulation, up-regulating the expression of cell adhesion molecules (cams) and promoting the secretion of inflammatory chemokines and cytokines. dysregulated signaling functions of thro...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان فارس - دانشکده دندانپزشکی 1387

چکیده ندارد.

Journal: :iranian journal of child neurology 0
parvaneh karimzadeh 1. pediatric neurology research center, shahid behesti university of medical sciences, tehran, iran 2. department of pediatric neurology, pediatric neurology center of excellence, faculty of medicine, mofid children hospital, shahid behesti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p. pelizaeus-merzbacher- disease (pmd) and pelizaeus-merzbacher-like disease (pmld). iran j child neurol autumn 2014;8:4 (suppl.1):9-10.   pls see pdf.

Journal: :acta medica iranica 0
f. asgarani m. keyhani r. a. sharifian g. r. toogeh r. aghanouri h. jalaeekhoo

castleman’s disease (angiofollicular lymphoid hyperplasia) includes a heterogeneous group of lymphoproliferative disorders. the cause of this disease remains uncertain. there are two types of localized castleman’s disease: the more common hyaline vascular and the plasma cell types. mixed variant is an uncommon localized lesion in general population. the lesions can occur in any part of the body...

Journal: :iranian journal of radiology 0
parvaneh karimzadeh pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran; pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran. tel: +98-2122909559, fax: +98-2122909559 farzad ahmadabadi ardabil university of medical sciences, ardabil, iran omid aryani special medical center, tehran, iran massoud houshmand department of human genetics, national institute for genetic engineering and biotechnology, tehran, iran alireza khatami pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran

pelizaeus­-merzbacher-like disease (pmld) is a hypomyelinating leukoencephalopathy disorder with a genetically heterogeneous pattern. mutations in the gja12/gjc2 gene cause one form of autosomal recessive pelizaeus­-merzbacher-like disease. here, we report a new mutation in a ­10-month-old girl with nystagmus, psychomotor delay, hypotonicity, head nodding and dysmyelination from healthy second ...

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