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Journal of Pediatric Gastroenterology and Nutrition|June 1, 2010
Evidence of intestinal inflammation in patients with cystic fibrosisSteven L Werlin, Ishay Benuri-Silbiger, Eitan Kerem, et al.
Respiratory Medicine Case Reports|February 21, 2025
Non-classical pulmonary exacerbation in cystic fibrosis revealing ALK-Translocated lung cancer: A case reportMohamad Hadhud, Johnathan Arnon, Anat Hershko-Moshe, et al.
Clinical Nutrition (Edinburgh, Scotland)|January 3, 2024
ESPEN-ESPGHAN-ECFS guideline on nutrition care for cystic fibrosisMichael Wilschanski, Anne Munck, Estefania Carrion, et al.
Annals of the American Thoracic Society|October 23, 2020
Ivacaftor in People with Cystic Fibrosis and a 3849+10kb C→T or D1152H Residual Function MutationEitan Kerem, Malena Cohen-Cymberknoh, Reuven Tsabari, et al.
Pancreas|December 19, 2025
Genetic and Electrophysiological Characterization of Acute Recurrent Pancreatitis in Israeli PatientsMaayan Tiosano, Liron Birimberg-Schwartz, Michael Wilschanski, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 23, 2016
An international consensus report on a new algorithm for the management of infant diarrhoeaAndrea Lo Vecchio, Yvan Vandenplas, Marc Benninga, et al.
Chest|May 18, 2010
An international randomized multicenter comparison of nasal potential difference techniquesGeorge M Solomon, Michael W Konstan, Michael Wilschanski, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 7, 2025
Fecal microbiota changes in people with cystic fibrosis after 6 months of elexacaftor/tezacaftor/ivacaftor: Findings from the promise studyJennifer T Duong, Hillary S Hayden, Adrian J Verster, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 21, 2015
The impact of a national population carrier screening program on cystic fibrosis birth rate and age at diagnosis: Implications for newborn screeningPatrick Stafler, Meir Mei-Zahav, Michael Wilschanski, et al.
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