نتایج جستجو برای: double aortic arch

تعداد نتایج: 365024  

Journal: :European heart journal 2013
Andreas M E Koch Martin Glöckler Robert Cesnjevar

Antzelevitch C. Ionic and cellular mechanisms underlying the development of acquired Brugada syndrome in patients treated with antidepressants. J Cardiovasc Electrophysiol 2012;23:423–432. 32. Casini S, Tan HL, Bhuiyan ZA, Bezzina CR, Barnett P, Cerbai E, Mugelli A, Wilde AA, Veldkamp MW. Characterization of a novel SCN5A mutation associated with Brugada syndrome reveals involvement of DIIIS4-S...

2010
Muzaffer Sariaydin Serhat Findik Atilla Guven Atici Sevket Ozkaya Aziz Uluisik

A 51-year-old male patient with a past history of lung tuberculosis was referred to our clinic for routine control. The patient reported no complaints and chest X-ray was normal. Three-dimensional thoracic computed tomography revealed a balanced-type double aortic arch with no compression of trachea or esophagus.

Journal: :Internal medicine 2005
Yutaka Kajikawa Shunji Takemoto Yuu Suganami Masafumi Inoue

chest X-ray film (Fig. 1). Clinical examination was normal. Computed tomographic angiography of the chest (Figs. 2, 3) showed a balanced type of double aortic arch, both of which arose from the ascending aorta anterior to the tracheae. Each arch gave origin to the common carotid and subclavian artery, and joined right posterior ward to form the descending aorta. The patient had neither respirat...

Journal: :Chirurgia 1973
V Marinescu I Pavelescu T Stefănescu M Roşca-Sichitiu

Journal: :Wiener klinische Wochenschrift 2008

Journal: :International Medical Case Reports Journal 2010

Journal: :International Journal of Gerontology 2018

Journal: :Indian Journal of Vascular and Endovascular Surgery 2015

Journal: :Journal of the American College of Cardiology 2001
D B McElhinney B J Clark P M Weinberg M L Kenton D McDonald-McGinn D A Driscoll E H Zackai E Goldmuntz

OBJECTIVES The purpose of this study was to determine the frequency of chromosome 22q11 deletions in patients with isolated anomalies of the aortic arch and its branches. BACKGROUND Chromosome 22q11 deletions are often present in patients with certain forms of congenital cardiovascular disease, including tetralogy of Fallot, truncus arteriosus and interruption of the aortic arch. Among patien...

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