Zobrazeno 1 - 10 of 41 pro vyhledávání: '"Özlem M. Bostan"'
1
The Role of External Loop Recorders in Arrhythmia-Related Symptoms in Children: A Single Center Experience
Autor: Tugberk Akca, Abdusselam Genc, Fahrettin Uysal, Hasan Turkmen, Özlem M. Bostan
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55447a3d137495cc0c091215408d79c1
https://doi.org/10.1007/s00246-021-02705-y
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2
The frequency of asymptomatic urinary system abnormalities in children detected with cineurography imaging during angiocardiography
Autor: Ergün Çil, Fahrettin Uysal, Orcun Oral, Özlem M. Bostan, Muhammet Hamza Halil Toprak
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0493c24b505a25116967fd1e7ba00128
https://doi.org/10.1017/s1047951118001828
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3
'Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports'
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
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
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab7ed426b031af7c41aff9f40885bdd5
http://link.springer.com/article/10.1186/s12881-017-0474-8
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4
Syncope in Children: Is Rhythm Holter Monitoring Necessary?
Autor: Ergün Çil, Tuba Deniz, Özlem M. Bostan, Fatma Çetinkaya, Fahrettin Uysal
Publikováno v: Güncel Pediatri. 14:124-128
Giris: Senkop geciren hastalarda anamnez, fizik muayene ve elektrokardiyografi EKG ile etiyoloji aciklanamiyorsa genellikle Holter monitorizasyonu HM yapilir. Bu calismada senkoplu cocuklarda HM’nin tanisal degerinin belirlenmesi amaclanmistir.Gere
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f451c12d9993e233d3631d6a1907a23f
https://doi.org/10.4274/jcp.32932
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5
Congenital arteriovenous fistula between descending aorta and the left innominate vein
Autor: Mete Han Kızılkaya, Sedat Giray Kandemirli, Özlem M. Bostan, Basak Erdemli Gursel, Tugberk Akca
Publikováno v: Surgical and radiologic anatomy : SRA. 42(4)
Thoracic aortocaval fistulae are rare entities where a direct shunt between thoracic arteries and systemic veins is seen. They can be traumatic or congenital in origin. Congenital thoracic aortocaval fistulae usually involve descending aorta and azyg
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::601bdd926e692883dd0122c5e59c149e
https://pubmed.ncbi.nlm.nih.gov/31292677
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6
Correction: Arterial tortuosity syndrome: 40 new families and literature review
Autor: Damien Bonnet, Paul Coucke, David R. Deyle, Mohammed Z. Haider, Fahrettin Uysal, Eudice E. Fontenot, Inge De Wandele, Margot A. Cousin, Waheed Al-Manea, Sehime Gulsun Temel, Massimiliano Rossi, Fabienne Giuliano, Sofie De Schepper, Joshua S. Hardin, Mazen Al-Essa, Ergun Cil, N Canham, Majed Dasouki, Harry C. Dietz, Juliette Albuisson, Pamela Moceri, Sophie Dupuis-Girod, Koenraad Devriendt, David Warner, Bart Loeys, Özlem M. Bostan, Andrea Taylor, Neus Baena, Elise Schaefer, Sheela Nampoothiri, Eric W. Klee, Karin Pichler, Elaine C. Davis, Andy Willaert, Odile Boute, Tiffany Busa, Björn Fischer-Zirnsak, Alper Gezdirici, Jamal Ghoumid, Manuel F. Landecho, Shehla Mohammed, Yuri A. Zarate, Maria Ramos-Arroyo, Tom R. Collins, Aude Beyens, Stanislas Lyonnet, Laura Muiño-Mosquera, Uwe Kornak, Marine Vanhomwegen, Helen Michael, Anna Rajeb, Mohammed Zain Seidahmed, Anne De Paepe, Deepthi De Silva, Bert Callewaert, Elisabeth Steichen-Gersdorf, Lut Van Laer, Annekatrien Boel, Anne Legrand, Xavier Jeunemaitre, Lionel Van Maldergem, Katrina Prescott, Mustafa A. Salih, Julie De Backer
Publikováno v: Genetics in Medicine
In the published version of this paper the author Neus Baena's name was incorrectly given as Neus Baena Diez. This has now been corrected in both the HTML and PDF versions of the paper.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dabb6bb8991e9be6fc030af1fe1474c3
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9
Arterial tortuosity syndrome: 40 new families and literature review
Autor: Uwe Kornak, Fabienne Giuliano, Aude Beyens, Mustafa A. Salih, Massimiliano Rossi, Marine Vanhomwegen, Lut Van Laer, Fahrettin Uysal, Koenraad Devriendt, David R. Deyle, Mohammed Z. Haider, Elise Schaefer, Tom R. Collins, Annekatrien Boel, Mazen Al-Essa, Elaine C. Davis, Elisabeth Steichen-Gersdorf, Ergun Cil, Eudice E. Fontenot, Andy Willaert, Bart Loeys, Eric W. Klee, Björn Fischer-Zirnsak, Joshua S. Hardin, Sophie Dupuis-Girod, N Canham, Majed Dasouki, Harry C. Dietz, Laura Muiño-Mosquera, Yuri A. Zarate, Karin Pichler, Xavier Jeunemaitre, Neus Baena Diez, Maria Ramos-Arroyo, Damien Bonnet, Paul Coucke, Waheed Al-Manea, Anne De Paepe, Tiffany Busa, Anna Rajeb, Shehla Mohammed, Odile Boute, Sofie De Schepper, Mohammed Zain Seidahmed, Juliette Albuisson, Andrea Taylor, Deepthi De Silva, Inge De Wandele, Helen Michael, Margot A. Cousin, Sehime Gulsun Temel, Pamela Moceri, Julie De Backer, Lionel Van Maldergem, Stanislas Lyonnet, Özlem M. Bostan, Katrina Prescott, Bert Callewaert, Anne Legrand, David Warner, Sheela Nampoothiri, Alper Gezdirici, Jamal Ghoumid, Manuel F. Landecho
Publikováno v: Genetics in Medicine
Genetics in medicine
PurposeWe delineate the clinical spectrum and describe the histology in arterial tortuosity syndrome (ATS), a rare connective tissue disorder characterized by tortuosity of the large and medium-sized arteries, caused by mutations in SLC2A10.MethodsWe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43678bceae2d29bcdcd1efbb1ec1895a
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10
Two Cases Diagnosed with Tuberosclerosis in Neonatal Period
Autor: Onur Bagci, Fahrettin Uysal, Pelin Dogan, Zeynep Yazici, Nilgün Köksal, Hilal Özkan, Ipek Guney Varal, Özlem M. Bostan
Publikováno v: The Journal of Pediatric Research. 1:229-232
Ya z›fl ma Ad re si/Ad dress for Cor res pon den ce Dr. Ipek Guney Varal, Uludag Universitesi Tip Fakultesi, Cocuk Sagligi ve Hastaliklari Anabilim Dali, Neonatoloji Bilim Dali, Bursa, Turkiye Tel.: +90 532 341 33 89 E-posta: ibettyg@yahoo.com Ge l
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5d3f73d1f04b3a567480bf2bfe706144
https://doi.org/10.4274/jpr.36855
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