User profiles for Israel Amirav

Israel Amirav

Professor Pediatrics, University of Alberta, Tel Aviv University
Verified email at ualberta.ca
Cited by 5186

CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs

…, EE Davis, A Becker-Heck, M Legendre, I Amirav… - Nature …, 2011 - nature.com
Primary ciliary dyskinesia (PCD) is an inherited disorder characterized by recurrent infections
of the upper and lower respiratory tract, reduced fertility in males and situs inversus in …

[HTML][HTML] MCIDAS mutations result in a mucociliary clearance disorder with reduced generation of multiple motile cilia

…, GW Dougherty, J Raidt, C Werner, I Amirav… - Nature …, 2014 - nature.com
Reduced generation of multiple motile cilia (RGMC) is a rare mucociliary clearance disorder.
Affected persons suffer from recurrent infections of upper and lower airways because of …

[PDF][PDF] ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6

…, W Zhou, R Airik, S Natarajan, SJ Allen, I Amirav… - The American Journal of …, 2013 - cell.com
Defects of motile cilia cause primary ciliary dyskinesia (PCD), characterized by recurrent
respiratory infections and male infertility. Using whole-exome resequencing and high-…

[PDF][PDF] Hypertonic saline or high volume normal saline for viral bronchiolitis: mechanisms and rationale

A Mandelberg, I Amirav - Pediatric pulmonology, 2010 - researchgate.net
In recent years and particularly in the last 5 years, there have been substantial advances in
our understanding of the mechanisms governing mucus clearance (MC) in health and …

[HTML][HTML] CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia

…, A Ta-shma, KS Wilson, PV Bayly, I Amirav… - PloS one, 2013 - journals.plos.org
Background Primary ciliary dyskinesia (PCD) is a genetic disorder characterized by impaired
ciliary function, leading to chronic sinopulmonary disease. The genetic causes of PCD are …

Immunofluorescence analysis and diagnosis of primary ciliary dyskinesia with radial spoke defects

…, S Sauer, JK Marthin, KG Nielsen, I Amirav… - American journal of …, 2015 - atsjournals.org
Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder caused
by several distinct defects in genes responsible for ciliary beating, leading to defective …

DNAH11 localization in the proximal region of respiratory cilia defines distinct outer dynein arm complexes

…, G Baktai, M Aviram, L Bentur, I Amirav… - American journal of …, 2016 - atsjournals.org
Primary ciliary dyskinesia (PCD) is a recessively inherited disease that leads to chronic
respiratory disorders owing to impaired mucociliary clearance. Conventional transmission …

Assessment of methacholine-induced airway constriction by ultrafast high-resolution computed tomography

I Amirav, SS Kramer, MM Grunstein… - Journal of applied …, 1993 - journals.physiology.org
Assessment of changes in airway dimensions during bronchoconstriction is conventionally
based on measurements of respiratory mechanics. We evaluated the efficacy of ultrafast high-…

[HTML][HTML] LRRC6 Mutation Causes Primary Ciliary Dyskinesia with Dynein Arm Defects

…, MG Wasserman, YS Oren, B Kerem, I Amirav… - PloS one, 2013 - journals.plos.org
Despite recent progress in defining the ciliome, the genetic basis for many cases of primary
ciliary dyskinesia (PCD) remains elusive. We evaluated five children from two unrelated, …

Aerosol therapy with valved holding chambers in young children: importance of the facemask seal

I Amirav, MT Newhouse - Pediatrics, 2001 - publications.aap.org
Objective. Masks are an essential interface between valved holding chambers (VHCs), or
spacers, and a small child's face for providing aerosol therapy. Clinical experience suggests …