نتایج جستجو برای: cardiac syndrome x

تعداد نتایج: 1432519  

Journal: :iranian journal of parasitology 0
feidoun sabzi preventive cardiovascular research centre kermanshah, kermanshah university of medical sciences, kermanshah, iran reza faraji preventive cardiovascular research centre kermanshah, kermanshah university of medical sciences, kermanshah, iran

a case of the budd chiary syndrome (bcs) in a 43-yr-old man with hydatid cyst (hc) in the liver is reported from imam ali hospital, kermanshah, western iran in 2016. this case was complicated by inferior vena cava (ivc) thrombosis, right atrial clot and pulmonary emboli. compression of ivc was the likely mechanism. abdominal ultrasonography revealed a huge hc located in segments near ivc and ca...

Journal: :Netherlands Heart Journal 2012

Journal: :Cardiology and Cardiovascular Medicine 2018

حاجی اسماعیلی, محمدرضا, سلیمانی راد, رضا, سیفی, شهرام, صداقت, علیرضا, مرادی مقدم, امید, نیاکان, محمد,

Brugada Syndrome is a rare cause of sudden cardiac arrest and has a unique ECG pattern. In fact, with ST-segment elevation down sloping in the right precordial leads (v1-v3), RBBB pattern in lateral leads and J-point elevation is revealed. We must notice and avoid trigger factors of this syndrome during general anesthesia. Patient is a 39 old man who attended to emergency department with sudden...

2006
WC LEUNG

HKJGOM 2005; 5 (1) 33 Introduction The most frequent foetal chromosomal abnormalities involve the autosomes 21, 18, 13 and sex chromosomes X and Y. Aneuploidy or alterations in copy number of these chromosomes, including Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), Trisomy 13 (Patau syndrome), 45,X (Turner syndrome), 47,XXY (Klinefelter syndrome) and Triploidy (presence of 3 copie...

Journal: :iranian journal of public health 0
m sahebjamee dept. of oral medicine, faculty of dentistry, tehran university of medical sciences, iran ng ameri dept. of oral medicine, faculty of dentistry, tehran university of medical sciences, iran dd farhud genetic clinic, vallie asr sq., 16 keshavarz blvd, tehran, iran.

noonan syndrome is an autosomal dominant disorder that is typically evident at birth. in many affected individuals, this syn­drome is associated with cardiac defects and a distinctive facial appearance. the high frequency of cardiac disorder, oph­thalmic, growth and orthopedic signs, associated with noonan syndrome emphasizes the need for early diagnosis. this re­port aimed to present a 19 year...

Journal: :the journal of tehran university heart center 0
feridoun sabzi imam ali heart center, kermanshah university of medical sciences, kermanshah, iran. abdolrasoul moloudi imam ali heart center, kermanshah university of medical sciences, kermanshah, iran.

severe inflammation after cardiopulmonary bypass with the vasculitis of the acral extremity and vertebro-basilar arterial system leads to the locked-in syndrome and blue toe syndrome. in broad terms, systemic, idiopathic, and environmental factors provoke syndromes that present with digital discoloration or the blue toe syndrome. painful digital discoloration, accompanied by ulceration, suggest...

Journal: :Circulation 2000
G Desideri A Gaspardone M Gentile A Santucci P A Gioffrè C Ferri

BACKGROUND The presence of endothelial dysfunction with increased endothelin-1 plasma concentrations in patients with cardiac syndrome X is still under debate. The aim of the present study was to evaluate the presence of endothelial dysfunction in patients with cardiac syndrome X. METHODS AND RESULTS ++Endothelin-1 levels were evaluated with a sensitive radioimmunoassay with previous purifica...

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