Harold Tabori

Adherence to therapies in cystic fibrosis: a targeted literature review

J. Mainz, D. Grossoehme, S. Gala, 2017, Expert review of respiratory medicine.

Elevated Levels of Toxic Bile Acids in Serum of Cystic Fibrosis Patients with CFTR Mutations Causing Pancreatic Insufficiency

J. Mainz, T. Lehmann, S. Lüth, 2022, International journal of molecular sciences.

Clinical approach to the diagnosis and treatment of cystic fibrosis and CFTR-related disorders

J. Mainz, R. Michl, J. Hentschel, 2016, Expert review of respiratory medicine.

Validity and Reliability of a Novel Multimodal Questionnaire for the Assessment of Abdominal Symptoms in People with Cystic Fibrosis (CFAbd-Score)

J. Mainz, M. Lorenz, R. Michl, 2019, The Patient - Patient-Centered Outcomes Research.

Pseudomonas aeruginosa colonization in the upper and lower airways of a child with cystic fibrosis: a father’s meticulous approach to successful eradication

J. Mainz, M. Lorenz, J. Ribeiro, 2019, Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia.

Effects of Ivacaftor in Three Pediatric Siblings With Cystic Fibrosis Carrying the Mutations G551D And F508del.

J. Mainz, J. Hentschel, C. Arnold, 2017, Archivos de bronconeumologia.

Relation of Ultrasound Findings and Abdominal Symptoms obtained with the CFAbd-Score in Cystic Fibrosis Patients

J. Mainz, M. Lorenz, R. Michl, 2017, Scientific Reports.

Abdominal symptoms in cystic fibrosis and their relation to genotype, history, clinical and laboratory findings

J. Mainz, A. Gerber, M. Lorenz, 2017, PloS one.