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Michael Wilschanski

Hadassah Hebrew University Medical Center, Jerusalem

BIOGRAPHY

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PUBLICATIONS

Combination of Helicobacter pylori strain and tumor necrosis factor-alpha polymorphism of the host increases the risk of peptic ulcer disease in children.

Journal of pediatric gastroenterology and nutrition Aug, 2007 | Pubmed ID: 17667716

Patterns of gastrointestinal disease associated with mutations of CFTR.

Current gastroenterology reports Jun, 2008 | Pubmed ID: 18625144

Small molecules to treat cystic fibrosis.

Proceedings of the American Thoracic Society Nov, 2010 | Pubmed ID: 21030520

Chronic ataluren (PTC124) treatment of nonsense mutation cystic fibrosis.

The European respiratory journal Jul, 2011 | Pubmed ID: 21233271

New drugs for cystic fibrosis.

Expert opinion on investigational drugs Sep, 2011 | Pubmed ID: 21745147

Novel therapeutic approaches for cystic fibrosis.

Discovery medicine Feb, 2013 | Pubmed ID: 23449115

Nutritional Status Improved in Cystic Fibrosis Patients with the G551D Mutation After Treatment with Ivacaftor.

Digestive diseases and sciences Jan, 2016 | Pubmed ID: 26250833

ESPEN-ESPGHAN-ECFS guidelines on nutrition care for infants, children, and adults with cystic fibrosis.

Clinical nutrition (Edinburgh, Scotland) 06, 2016 | Pubmed ID: 27068495

Introduction.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society Nov, 2017 | Pubmed ID: 28986025

Advancing the GI frontier for patients with CF.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society Jan, 2018 | Pubmed ID: 29208346

Cystic fibrosis: a gastrointestinal cancer syndrome.

The Lancet. Oncology Jun, 2018 | Pubmed ID: 29706381

Primary sclerosing cholangitis is associated with abnormalities in CFTR.

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society Sep, 2018 | Pubmed ID: 29807875

INSTITUTIONS

Hadassah Hebrew University Medical Center, Jerusalem

JOVE ARTICLES

Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD)

George M. Solomon¹,

Inez Bronsveld²,

Kathryn Hayes³,

Michael Wilschanski⁴,

Paola Melotti⁵,

Steven M. Rowe¹,

Isabelle Sermet-Gaudelus^6,7

¹Department of Medicine and the Gregory Fleming James Cystic Fibrosis Center, University of Alabama at Birmingham,

²Department of Pulmonology and Tuberculosis, University Medical Center Utrecht,

³Center for Experimental Medicine, Queens University, Northern Ireland,

⁴, Hadassah Hebrew University Medical Center, Jerusalem,

⁵Centro Fibrosi Cistica, Azienda Ospedaliera Universitaria Integrata,

⁶Service de Pneumologie et Allergologie Pédiatriques and Center de Ressources et de Compétence de la Mucoviscidose, Hôpital Necker Enfants Malades,

⁷INSERM U 1151, Institut Necker Enfants Malades

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