نتایج جستجو برای: mareks disease

تعداد نتایج: 1490097  

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 ...

Journal: :iranian journal of diabetes and obesity 0
sied kazem razavi ratki md, department of radiology, faculty of medicine, shahid sadoughi university of medical sciences yazd, iran. amirpasha amelshahbaz md, department of radiology, faculty of medicine, shahid sadoughi university of medical sciences yazd, iran. reza nafisi-moghadam md, department of radiology, faculty of medicine, shahid sadoughi university of medical sciences yazd, iran. naser hossein sartipzadeh md, department of cardiology, afshar hospital, shahid sadoughi university of medical sciences, yazd, iran

cardiovascular disease (cad) screening in asymptomatic patients with diabetes mellitus is controversial. an exercise stress test is a safe and effective initial testing for ischemic heart disease (ihd) screening. treadmill stress test is not the best screening method for a particular patient who is not able to exercise, abnormal electrocardiogram (ecg) or positive exercise treadmill test (ett) ...

2010
David Pearce

When the new research area of logic programming and non-monotonic reasoning emerged at the end of the 1980s, it focused notably on the study of mathematical relations between different non-monotonic formalisms, especially between the semantics of stable models and various non-monotonic modal logics. Given the many and varied embeddings of stable models into systems of modal logic, the modal int...

Journal: :international journal of endocrinology and metabolism 0
silvia santos palacios department of endocrinology and nutrition, university clinic of navarra, uoov}{{mt{6of3qvyrra, spain +94-8255400, [email protected] eider pascual-corrales department of endocrinology and nutrition, university clinic of navarra, uoov}{{mt{6of3qvyrra, spain +94-8255400, [email protected] juan carlos galofre department of endocrinology and nutrition, university clinic of navarra, uoov}{{mt{6of3qvyrra, spain +94-8255400, [email protected]; department of endocrinology and nutrition, university clinic of navarra, uoov}{{mt{6of3qvyrra, spain +94-8255400, [email protected]

the ideal approach for adequate management of subclinical hyperthyroidism (low levels of thyroid-stimulating hormone [tsh] and normal thyroid hormone level) is a matter of intense debate among endocrinologists. the prevalence of low serum tsh levels ranges between 0.5% in children and 15% in the elderly population. mild subclinical hyperthyroidism is more common than severe subclinical hyperthy...

Journal: :gastroenterology and hepatology from bed to bench 0
iraj shahramian fellow of pediatric gastroentrology ,assistant professor of pediatric, department of pediatric, zabol university of medical sciences, zabol iran seyed mohsen dehghani professor of pediatric gastroentrology, department of pediatric gastroentrology, shiraz university of medical sciences, shiraz iran mahmood haghighat professor of pediatric gastroentrology , department of pediatric gastroentrology, shiraz university of medical sciences, shiraz iran noormohamad noori professor of pediatric cardiology , children and adolescents health research center ,zahedan medical university ,iran alireza teymoori assistant professor of demography , children and adolescents health research center ,zahedan medical university ,iran elham sharafi resident of ophtalmology ,zahedan medical university ,zahedan ,iran

abstract introduction : celiac disease (cd) is an autoimmune disorder triggered by ingestion of gluten in genetically predisposed individuals.  this study reports evaluated prevalence of cd in patients with beta-thalassemia major. materials and methods: in this case-control study in a period of 3 years  which was performed on 620 children in two groups of  beta-thalassemia major  patients (n=20...

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