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Diagnostics (Basel, Switzerland)|February 22, 2020
Long-Term Outcomes of Early Enzyme Replacement Therapy for Mucopolysaccharidosis IV: Clinical Case Studies of Two SiblingsSharon Barak, Yair Anikster, Ifat Sarouk, et al.
The Clinical Respiratory Journal|May 17, 2021
Spontaneous pneumothorax-When do we need to intervene?Moshe Ashkenazi, Alon Bak, Ifat Sarouk, et al.
Respiratory Medicine|June 3, 2015
FVC deterioration, airway obstruction determination, and life span in Ataxia telangiectasiaDaphna Vilozni, Moran Lavie, Ifat Sarouk, et al.
Journal of Asthma and Allergy|June 29, 2018
Omalizumab in allergic bronchopulmonary aspergillosis in patients with cystic fibrosisMoshe Ashkenazi, Saray Sity, Ifat Sarouk, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 14, 2018
Secondary enuresis and urological manifestations in children with ataxia telangiectasiaAndreea Nissenkorn, Tomer Erlich, Dorit E Zilberman, et al.
Diabetes Research and Clinical Practice|October 29, 2015
Glucose intolerance in cystic fibrosis as a determinant of pulmonary function and clinical statusMoran Lavie, Dor Fisher, Daphna Vilozni, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 24, 2015
Liver Disease in Pediatric Patients With Ataxia Telangiectasia: A Novel ReportBatia Weiss, Alexander Krauthammer, Michalle Soudack, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|July 1, 2015
Nocardia Colonization: A Risk Factor for Lung Deterioration in Cystic Fibrosis Patients?Adi Dagan, Nathan Keller, Daphna Vilozni, et al.
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