Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Eyup Aslan"'
Publikováno v:
The Journal of Pediatric Academy, Vol 3, Iss 1, Pp 32-34 (2022)
Anatomically corrected malposition of the great arteries is a rare cardiac malformation. In this condition the great arteries are abnormally related to each other and to the ventricles, but arise from the anatomically correct ventricles. In patients
Externí odkaz:
https://doaj.org/article/d11619840564433985a21325aa544f5e
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 43, Iss 2, Pp 192-195 (2015)
Scimitar syndrome is a rare disease associated with a right lung sequestration vascularised by arteries arising from the abdominal aorta and abnormal venous drainage into the inferior vena cava. The infantile form is generally presented with severe h
Externí odkaz:
https://doaj.org/article/cebd62e982af43119abefc8848ec11d4
Autor:
Eyup Aslan, Ahmet Sert, Muammer Buyukinan, Mustafa Ozgur Pirgon, Huseyin Kurku, Hakan Yılmaz, Dursun Odabas
Publikováno v:
Cardiology in the Young. :1-8
Background: The aim of our study was to assess left and right ventricle systolic and diastolic functions in female adolescents with vitamin D deficiency using conventional echocardiography and pulsed-wave tissue Doppler imaging and to investigate car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54deca2ee5e984cbe92068dc381841e4
https://doi.org/10.1017/s1047951123001257
https://doi.org/10.1017/s1047951123001257
Autor:
Yakup Ergul, Fatma Sevinc Sengul, Murat Saygi, Osman Guvenc, Celal Akdeniz, Alper Guzeltas, Eyup Aslan, Volkan Tuzcu, Isa Ozyilmaz
Publikováno v:
Annals of Noninvasive Electrocardiology. 21:500-507
Background In this study, we reported our experience with the use of cardiac event recorders in pediatric patients. Methods We evaluated 583 patients fitted with an event recorder (15–30 days) between March 2010 and November 2014 at our clinic. Exc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a8a41d70954d0059059b21e6dd33f9e
https://doi.org/10.1111/anec.12339
https://doi.org/10.1111/anec.12339
Publikováno v:
Texas Heart Institute Journal. 41:530-532
Cardiac rhabdomyoma, the primary cardiac tumor most often diagnosed in children, is frequently present in patients with tuberous sclerosis. Most pediatric patients with rhabdomyoma are asymptomatic; however, various electrocardiographic abnormalities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7434202aef905e846015fe4758950230
https://doi.org/10.14503/thij-13-3571
https://doi.org/10.14503/thij-13-3571
Publikováno v:
Pediatric Cardiology. 34:1896-1898
Noncompaction of the ventricular myocardium is a rare cardiomyopathy characterized by a pattern of prominent trabecular meshwork and deep intertrabecular recesses. The prevalence of left ventricular noncompaction is 0.01% in adults and 0.14% in pedia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c993a47eb52f760088a4623863a657db
https://doi.org/10.1007/s00246-012-0435-0
https://doi.org/10.1007/s00246-012-0435-0
Publikováno v:
Cardiology in the young. 25(2)
Background:Previous studies have demonstrated structural changes in the heart and cardiac dysfunction in foetuses with intrauterine growth restriction. There are no available data that evaluated left ventricular dimensions and mass in neonates with s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45c5f2b663d39661cc757d3e2762e329
https://pubmed.ncbi.nlm.nih.gov/24355690
https://pubmed.ncbi.nlm.nih.gov/24355690
Publikováno v:
Pediatric cardiology. 34(2)
Pierre-Robin sequence or syndrome (PRS) (OMIM #261800) is characterized by a small mandible (micrognathia), posterior displacement/retraction of the tongue (glossoptosis), and upper airway obstruction. It has an incidence varying from 1 in 8,500 to 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19a9fc5e2e0b3b127d896de2465b49bb
https://pubmed.ncbi.nlm.nih.gov/22447382
https://pubmed.ncbi.nlm.nih.gov/22447382
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 49, Iss 8, Pp 696-697 (2021)
Externí odkaz:
https://doaj.org/article/46b56a94f54041dbae369fd0f9323fc2
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 44, Iss 6, Pp 503-506 (2016)
Summary– Jeune syndrome (Asphyxiating thoracic dysplasia) is a rare dystrophy of the skeleton, inherited as an autosomal recessive condition. Patients develop a narrowed thorax, rhizomelic dwarfism, and hepatic, renal, and pancreatic abnormalities.
Externí odkaz:
https://doaj.org/article/f30c1c6e3f5f490d9c76d726f66e70c1