CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs AC Merveille, EE Davis, A Becker-Heck, M Legendre, I Amirav, G Bataille, ... Nature genetics 43 (1), 72-78, 2011 | 395 | 2011 |
MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia M Boon, J Wallmeier, L Ma, NT Loges, M Jaspers, H Olbrich, ... Nature communications 5 (1), 4418, 2014 | 280 | 2014 |
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6 MA Zariwala, HY Gee, M Kurkowiak, DA Al-Mutairi, MW Leigh, TW Hurd, ... The American Journal of Human Genetics 93 (2), 336-345, 2013 | 224 | 2013 |
Assessment of methacholine-induced airway constriction by ultrafast high-resolution computed tomography I Amirav, SS Kramer, MM Grunstein, EA Hoffman Journal of applied physiology 75 (5), 2239-2250, 1993 | 213 | 1993 |
Hypertonic saline or high volume normal saline for viral bronchiolitis: mechanisms and rationale A Mandelberg, I Amirav Pediatric pulmonology 45 (1), 36-40, 2010 | 198 | 2010 |
Aerosol therapy with valved holding chambers in young children: importance of the facemask seal I Amirav, MT Newhouse Pediatrics 108 (2), 389-394, 2001 | 152 | 2001 |
CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia A Horani, SL Brody, TW Ferkol, D Shoseyov, MG Wasserman, A Ta-shma, ... PloS one 8 (8), e72299, 2013 | 151 | 2013 |
Immunofluorescence analysis and diagnosis of primary ciliary dyskinesia with radial spoke defects A Frommer, R Hjeij, NT Loges, C Edelbusch, C Jahnke, J Raidt, C Werner, ... American journal of respiratory cell and molecular biology 53 (4), 563-573, 2015 | 141 | 2015 |
DNAH11 localization in the proximal region of respiratory cilia defines distinct outer dynein arm complexes GW Dougherty, NT Loges, JA Klinkenbusch, H Olbrich, P Pennekamp, ... American journal of respiratory cell and molecular biology 55 (2), 213-224, 2016 | 137 | 2016 |
Metered-dose inhaler accessory devices in acute asthma: efficacy and comparison with nebulizers: a literature review I Amirav, MT Newhouse Archives of pediatrics & adolescent medicine 151 (9), 876-882, 1997 | 134 | 1997 |
Sole pathogen in acute bronchiolitis: is there a role for other organisms apart from respiratory syncytial virus? D Miron, I Srugo, Z Kra-Oz, Y Keness, D Wolf, I Amirav, I Kassis The Pediatric infectious disease journal 29 (1), e7-e10, 2010 | 126 | 2010 |
LRRC6 mutation causes primary ciliary dyskinesia with dynein arm defects A Horani, TW Ferkol, D Shoseyov, MG Wasserman, YS Oren, B Kerem, ... PloS one 8 (3), e59436, 2013 | 120 | 2013 |
A double-blind, placebo-controlled, randomized trial of montelukast for acute bronchiolitis I Amirav, AS Luder, N Kruger, Y Borovitch, I Babai, D Miron, M Zuker, ... Pediatrics 122 (6), e1249-e1255, 2008 | 113 | 2008 |
Transmission of coronavirus by nebulizer: a serious, underappreciated risk I Amirav, MT Newhouse Cmaj 192 (13), E346-E346, 2020 | 103 | 2020 |
Nebuliser hood compared to mask in wheezy infants: aerosol therapy without tears! I Amirav, I Balanov, M Gorenberg, D Groshar, AS Luder Archives of disease in childhood 88 (8), 719-723, 2003 | 103 | 2003 |
The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results M Goutaki, E Maurer, FS Halbeisen, I Amirav, A Barbato, L Behan, ... European respiratory journal 49 (1), 2017 | 92 | 2017 |
Lung function in patients with primary ciliary dyskinesia: an iPCD Cohort study FS Halbeisen, M Goutaki, BD Spycher, I Amirav, L Behan, M Boon, ... European respiratory journal 52 (2), 2018 | 90 | 2018 |
Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis I Amirav, J Wallmeier, NT Loges, T Menchen, P Pennekamp, H Mussaffi, ... Human mutation 37 (4), 396-405, 2016 | 90 | 2016 |
Measurement of peak inspiratory flow with in‐check dial device to simulate low‐resistance (Diskus) and high‐resistance (Turbohaler) dry powder inhalers in children with asthma I Amirav, MT Newhouse, Y Mansour Pediatric pulmonology 39 (5), 447-451, 2005 | 80 | 2005 |
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defect C Edelbusch, S Cindrić, GW Dougherty, NT Loges, H Olbrich, J Rivlin, ... Human mutation 38 (8), 964-969, 2017 | 78 | 2017 |