Zobrazeno 1 - 10 of 26 pro vyhledávání: '"Gur, Mainzer"'
1
Akademický článek
The Compatibility of Children with Obesity to Self-Report Aspects of Physical Activity Domains
Autor: Liraz E. Anavi, Einat Kodesh, Gur Mainzer
Publikováno v: Children, Vol 9, Iss 11, p 1664 (2022)
Questions about the different aspects of physical activity (PA) are commonly asked in the clinical setting, yet their compatibility for use with children, particularly children with obesity (OB) is uncertain. Our aim was to investigate different PA-r
Externí odkaz: https://doaj.org/article/033072ab0228428ea2ecadc9bd6f70f0
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2
Akademický článek
Exercise capacity in patients with cystic fibrosis vs. non-cystic fibrosis bronchiectasis.
Autor: Ronen Bar-Yoseph, Anat Ilivitzki, Dan M Cooper, Michal Gur, Gur Mainzer, Fahed Hakim, Galit Livnat, Zeev Schnapp, George Shalloufeh, Merav Zucker-Toledano, Yael Subar, Lea Bentur
Publikováno v: PLoS ONE, Vol 14, Iss 6, p e0217491 (2019)
BackgroundBronchiectasis is associated with morbidity, low exercise capacity and poor quality of life. There is a paucity of data on exercise capacity using cardiopulmonary exercise test (CPET) in non-cystic fibrosis (CF) bronchiectasis. Our aim was
Externí odkaz: https://doaj.org/article/179047befec04c158426af709188dec5
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4
Cardiopulmonary Exercise Testing in Childhood in Late Preterms: Comparison to Early Preterms and Term-Born Controls
Autor: Ori Hochwald, Lea Bentur, Yara Haddad, Moneera Hanna, Merav Zucker-Toledano, Gur Mainzer, Julie Haddad, Michal Gur, Liron Borenstein-Levin, Amir Kugelman, Ronen Bar-Yoseph
Publikováno v: Journal of Personalized Medicine; Volume 12; Issue 10; Pages: 1547
Background: Late preterm (340–366 weeks gestational age [GA]) infants may have abnormal pulmonary development and possible exercise physiology parameters. We aim to assess the effect of late prematurity on exercise capacity in childhood and to comp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e99f44f5c5f6825363565cfe86d5a483
https://pubmed.ncbi.nlm.nih.gov/36294686
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7
Interventional Correction of Sinus Venosus Atrial Septal Defect and Partial Anomalous Pulmonary Venous Drainage
Autor: Israel Valverde, Tarique Hussain, Antony Hermuzi, Kuberan Pushparajah, Mari Nieves Velasco Forte, Pimpak Prachasilchai, Eric Rosenthal, Nick Byrne, Shakeel A. Qureshi, Markus Henningsson, Gur Mainzer, Gorka Gómez Ciriza
Publikováno v: JACC: Cardiovascular Imaging. 11:275-278
Sinus venosus atrial septal defects (SVASD) with partial anomalous pulmonary venous drainage (PAPVD) are conventionally treated surgically. Cardiac magnetic resonance (CMR) ([Figure 1][1], [Online Video 1][2]), patient-specific 3-dimensional (3D) pri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1a6be5377c8ee3d0936d35ec259a61ef
https://doi.org/10.1016/j.jcmg.2017.07.010
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8
Stenting of the inter-atrial septum in infants and small children: Indications, techniques and outcomes
Autor: Gur Mainzer, Sebastian Góreczny, Jadwiga Moll, Gareth J. Morgan, Paweł Dryżek, Shakeel A. Qureshi, Eric Rosenthal, Thomas Krasemann, Tomasz Moszura
Publikováno v: Catheterization and Cardiovascular Interventions, 91(7), 1294-1300. Wiley-Liss Inc.
Objectives: To evaluate the procedural success and outcome of inter-atrial stenting. Background: Inter-atrial stenting has been shown to be an effective way to maintain inter-atrial blood flow, however it is considered a high risk procedure, usually
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b05863c5ab69543064bb9f968575c69
https://doi.org/10.1002/ccd.27462
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9
Individualized Assessment of Exercise Capacity in Response to Acute and Long-Term Enzyme Replacement Therapy in Pediatric Pompe Disease
Autor: Moneera Hanna, Hanna Mandel, Gur Mainzer, Elena Dumin, Galit Tal, Ronen Bar-Yoseph, Mira Jahshan, George Shallufi, Merav Zucker-Toledano, Lea Bentur
Publikováno v: Journal of Personalized Medicine
Volume 11
Issue 11
Journal of Personalized Medicine, Vol 11, Iss 1105, p 1105 (2021)
Background: Enzyme replacement therapy (ERT) with alglucosidase alfa improves the prospect of patients with infantile-onset Pompe disease (IOPD). However, a progressive decline has been reported. Objective quantification of the response to ERT when a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5aec5b5dbbf1bbcc56ea3be45a455b6
https://doi.org/10.3390/jpm11111105
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10
Exercise capacity in patients with cystic fibrosis vs. non-cystic fibrosis bronchiectasis
Autor: Gur Mainzer, Lea Bentur, Ronen Bar-Yoseph, Fahed Hakim, Yael Subar, Michal Gur, Merav Zucker-Toledano, Dan M. Cooper, George Shalloufeh, Galit Livnat, Zeev Schnapp, Anat Ilivitzki
Publikováno v: PLoS ONE, Vol 14, Iss 6, p e0217491 (2019)
PLoS ONE
PloS one, vol 14, iss 6
Bar-Yoseph, Ronen; Ilivitzki, Anat; Cooper, Dan M; Gur, Michal; Mainzer, Gur; Hakim, Fahed; et al.(2019). Exercise capacity in patients with cystic fibrosis vs. non-cystic fibrosis bronchiectasis.. PloS one, 14(6), e0217491. doi: 10.1371/journal.pone.0217491. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/3fs5s8j0
Author(s): Bar-Yoseph, Ronen; Ilivitzki, Anat; Cooper, Dan M; Gur, Michal; Mainzer, Gur; Hakim, Fahed; Livnat, Galit; Schnapp, Zeev; Shalloufeh, George; Zucker-Toledano, Merav; Subar, Yael; Bentur, Lea | Abstract: BackgroundBronchiectasis is associat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61a44048b97802f6977163767c1446bc
https://doaj.org/article/179047befec04c158426af709188dec5
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