Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Fahrettin, Uysal"'
Publikováno v:
Turkish Archives of Pediatrics, Vol 59, Iss 5, Pp 480-487 (2024)
Objective: Coarctation of the aorta (CoA) accounts for 3.5% of all congenital heart diseases in children. The clinical manifestations range from heart failure to asymptomatic hypertension. Treatment options include surgical repair, balloon angioplast
Externí odkaz:
https://doaj.org/article/feb50e5436fd4a5bbe2ee89cf6f1ca3d
Publikováno v:
Clinical and Experimental Ocular Trauma and Infection, Vol 3, Iss 2, Pp 19-19 (2021)
The first edition of the book "ALGORITHMS FROM SYMPTOMS TO DIAGNOSIS IN CHILDREN" attracted great interest despite all adverse conditions such as the pandemic, and the "EXTENDED AND UPDATED 2nd EDITION" was published immediately
Externí odkaz:
https://doaj.org/article/bcc51b5d55f84db9bccbdf3233ce2f83
Autor:
Fahrettin Uysal, Burcu Turkgenc, Guven Toksoy, Ozlem M. Bostan, Elif Evke, Oya Uyguner, Cengiz Yakicier, Hulya Kayserili, Ergun Cil, Sehime G. Temel
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-8 (2017)
Abstract Background Jervell and Lange-Nielsen syndrome (JLNS) isa recessive model of long QT syndrome which might also be related to possible hearing loss. Although the syndrome has been demonstrated to be originated from homozygous or compound heter
Externí odkaz:
https://doaj.org/article/547b936f1a3f48028b40b8469462b7d9
Autor:
Fahrettin, Uysal, Tuğberk, Akça, Abdüsselam, Genç, Zehra, Avcı Küpeli, Erencan, Özfırat, Uygur, Canatan, Berfin, Uysal, Işık, Şenkaya Sığnak
Publikováno v:
Turkish Journal of Thoracic and Cardiovascular Surgery. 30:327-333
Background: The aim of this study was to evaluate the efficacy and feasibility of a novel method of narrowing pulmonary arteries with catheter angiography using radiofrequency energy in rabbits. Methods: A total of nine New Zealand white rabbits weig
Publikováno v:
Clinical Pediatrics. 61:453-460
Coronavirus disease 2019 (COVID-19) is the greatest pandemic in a century. In this study, children with mild COVID-19 infections were evaluated at least 8 weeks after the polymerase chain reaction (PCR) test positivity, and the frequency of hypertens
Publikováno v:
Cardiology in the young.
Danon disease is a rare and fatal disease caused by a mutation in the lysosome-associated membrane protein 2 gene. Impaired intracellular autophagy causes lysosomal vacuoles to accumulate mainly in myocardial and skeletal muscle cells, leading to hyp
Publikováno v:
Pediatric Cardiology. 43:147-154
In this study, we report our experience with the use of external loop recorders (ELRs), in terms of diagnostic efficiency according to symptoms and symptom-rhythm correlation in pediatric patients. We evaluated ELRs applied to 178 patients between Ap
Autor:
Fahrettin Uysal, Ozlem Mehtap Bostan, Muhammed Hamza Halil Toprak, Isik Senkaya Signak, Ergun Cil
Publikováno v:
Annals of Pediatric Cardiology, Vol 9, Iss 2, Pp 195-196 (2016)
Congenital ventricular diverticulum is a rare cardiac anomaly defined as a localized protrusion of the ventricular free wall. Although, it is usually asymptomatic, complications such as embolism, infective endocarditis, and arrhythmias can occur. The
Externí odkaz:
https://doaj.org/article/5fd951ccbb9c41aab8fa77cffb7fa538
Publikováno v:
Cardiology in the Young. 29:119-122
IntroductionDiagnostic and interventional catheter angiography of the heart is frequently used in paediatric cardiology. It is also possible to detect urinary system anomalies with cineurography images that may be obtained during angiocardiography. I
Autor:
Burcu Turkgenc, Güven Toksoy, Cengiz Yakicier, Oya Uyguner, Sehime Gulsun Temel, Elif Evke, Hülya Kayserili, Fahrettin Uysal, Ergun Cil, Özlem M. Bostan
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-8 (2017)
BMC Medical Genetics
BMC Medical Genetics
Background: Jervell and Lange-Nielsen syndrome (JLNS) isa recessive model of long QT syndrome which might also be related to possible hearing loss. Although the syndrome has been demonstrated to be originated from homozygous or compound heterozygous