Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Selman Vefa Yildirim"'
Publikováno v:
Cardiology in the Young. 17:275-282
Introduction: The first step in diagnosing congenital cardiac malformations is to assess the arrangement of the atrial appendages. In patients with abnormal lateralization of the organs of the body, the arrangement of atrial appendages is neither nor
Publikováno v:
Acta Paediatrica. 94:1055-1059
Aim: To evaluate left ventricular (LV) diastolic function in children with end-stage renal disease (ESRD) using conventional pulsed-Doppler echocardiography and Doppler tissue imaging (DTI), and to compare the findings with these two modalities. Meth
Publikováno v:
Advances in Therapy. 23:719-724
Movement and anxiety during echocardiographic study may reduce the reliability and affect the quality of echocardiographic images. Thus, sedation is an essential component when it is performed in infants. This randomized, single-blinded, placebo-cont
Publikováno v:
The International Journal of Cardiovascular Imaging. 22:399-402
Sinus valsalva aneurysm is a rare condition. Most aneurysms usually originate from the right or non-coronary sinus. A few series were reported about the sinus valsalva aneurysm describing its origin, diagnostic tools and prognosis. We describe a case
Autor:
Selman Vefa Yildirim
Publikováno v:
Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology. 39:147-149
Stent implantation into a ductus arteriosus or systemic-pulmonary shunt is a relatively new but infrequent approach for palliation. A 22-month-old boy with a modified Blalock-Taussig shunt for tetralogy of Fallot was admitted with severe cyanosis. Ec
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 61:179-182
Proboscis lateralis is a rare facial anomaly resulting in incomplete formation of one side of the nose. We report a left-sided proboscis lateralis case of a 9 months old male with left-sided heminasal aplasia, microphthalmi, coloboma iris and retina
Publikováno v:
Rheumatology International
Kawasaki disease (KD) is an acute, febrile, and multisystem vasculitis of early childhood with a striking predilection for the coronary arteries. The most significant complication is coronary artery abnormalities, including coronary aneurysms. The et
Publikováno v:
Journal of Child Neurology. 22:787-789
Cerebral venous angioma is a congenital anomaly of the medullary vein, the vessel that drains into the transparenchymal venous stem. This lesion is also referred to as a developmental venous anomaly. A few reports in the literature have documented de
Autor:
Selman Vefa Yildirim, Serife Ulusan, F Bolat, Osman Kizilkilic, Tulin Yildirim, E.A. Niron, Nebil Bal
Publikováno v:
The British Journal of Radiology. 78:441-443
Solid-pseudopapillary tumour of the pancreas is a rare benign or low-grade malignant epithelial tumour; its association with pancreatic dorsal agenesis has been reported only once before. We present the radiological and histological findings of a cas
Autor:
Ayten, Gümüş, Selman Vefa, Yildirim
Publikováno v:
The Turkish journal of pediatrics. 54(5)
Persistent left and absent right superior vena cava is a rare congenital anomaly, which is usually asymptomatic. Persistent left superior vena cava (PLSVC) is generally coexistent with right superior vena cava (RSVC), but rarely associated with absen