I. Bronsveld

发表

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-Mediated Residual Chloride Secretion Does Not Protect against Early Chronic Pseudomonas aeruginosa Infection in F508del Homozygous Cystic Fibrosis Patients

B. Tümmler, N. Derichs, M. Ballmann, 2004, Pediatric Research.

Categories of ΔF508 homozygous cystic fibrosis twin and sibling pairs with distinct phenotypic characteristics

B. Tümmler, M. Ballmann, J. Bijman, 2000, Twin Research.

Management of Individual Patient Expectations When Starting with Highly Effective CFTR Modulators

H. Heijerman, I. Bronsveld, B. Aalbers, 2021, Journal of personalized medicine.

Potentiator synergy in rectal organoids carrying S1251N, G551D, or F508del CFTR mutations.

H. Janssens, J. Beekman, H. D. de Jonge, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial.

S. Peltz, S. McColley, E. Kerem, 2014, The Lancet. Respiratory medicine.

Diagnostic value of routine chest tube tip culture in surgery for noninfectious lung disease

K. Jenniskens, I. Bronsveld, R. Rentenaar, 2021, Journal of Cardiothoracic Surgery.

Modifying Factors of Cystic Fibrosis Disease: Residual Chloride Secrefion, Genefic Background and Epigenetics

I. Bronsveld, 2000 .

Categor ies of ∆ F 508 homozygous cystic fibrosis twin and sibl ing pai rs wi th distinct phenotypic character istics

B. Tümmler, H. Veeze, F. Mekus, 2007 .

CFTR biomarkers: time for promotion to surrogate end-point

M. Amaral, N. Derichs, M. Proesmans, 2012, European Respiratory Journal.

Assessment of CFTR function in homozygous R117H-7T subjects.

J. Nobel, H. D. de Jonge, H. Arets, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

New clinical diagnostic procedures for cystic fibrosis in Europe.

N. Derichs, F. Vermeulen, I. Fajac, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Residual chloride secretion in intestinal tissue of ΔF508 homozygous twins and siblings with cystic fibrosis

B. Tümmler, M. Ballmann, R. Busche, 2000 .

Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating Ussing chambers.

F. Stanke, B. Tümmler, M. Ballmann, 2004, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Diversity of the basic defect of homozygous CFTR mutation genotypes in humans

H. Blau, T. Dörk, S. Gallati, 2007, Journal of Medical Genetics.

Clinical presentation of exclusive cystic fibrosis lung disease

B. Tümmler, M. Ballmann, J. Bijman, 1999, Thorax.

Females with cystic fibrosis have a larger decrease in sweat chloride in response to lumacaftor/ivacaftor compared to males.

C. K. van der Ent, H. Arets, H. Heijerman, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Cystic-fibrosis-like disease unrelated to the cystic fibrosis transmembrane conductance regulator

T. Dörk, B. Tümmler, M. Ballmann, 1998, Human Genetics.

A randomized placebo-controlled trial of ataluren for the treatment of nonsense mutation cystic fibrosis

S. Peltz, S. McColley, F. Accurso, 2014 .

ECFS standards of care on CFTR-related disorders: Diagnostic criteria of CFTR dysfunction.

F. Vermeulen, I. Sermet-Gaudelus, P. Melotti, 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Fat absorption in cystic fibrosis mice is impeded by defective lipolysis and post-lipolytic events.

H. Verkade, H. D. de Jonge, R. Havinga, 2005, American journal of physiology. Gastrointestinal and liver physiology.

Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium.

B. Tümmler, M. Ballmann, R. Busche, 2000, Gastroenterology.

Effects of long-term tobramycin inhalation solution (TIS) once daily on exacerbation rate in patients with non-cystic fibrosis bronchiectasis

W. Boersma, J. Altenburg, H. Heijerman, 2022, Respiratory Research.

Characterizing responses to CFTR-modulating drugs using rectal organoids derived from subjects with cystic fibrosis

H. Clevers, F. Vleggaar, R. Houwen, 2016, Science Translational Medicine.

Transient correction of the basic defect in sweat glands in an individual with cystic fibrosis carrying the complex CFTR allele F508del-R553Q

F. Stanke, B. Tümmler, M. Ballmann, 2009, Thorax.

A functional CFTR assay using primary cystic fibrosis intestinal organoids

Hans Clevers, H. Clevers, E. Nieuwenhuis, 2013, Nature Medicine.

Chloride conductance and genetic background modulate the cystic fibrosis phenotype of Delta F508 homozygous twins and siblings.

B. Tümmler, M. Ballmann, D. Halley, 2001, The Journal of clinical investigation.

CHAPTER 7 Increased fecal bile salt excretion is independent of the presence of dietary fat malabsorption in two mouse models for cystic fibrosis

F. Kuipers, B. Scholte, H. Verkade, 1998 .

Measurement of ion transport function in rectal biopsies.

J. Clancy, N. Derichs, M. Hug, 2011, Methods in molecular biology.

Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation

J. Clancy, M. Ballmann, F. Accurso, 2011, Thorax.

Inhibition of Heat-Stable Toxin-Induced Intestinal Salt and Water Secretion by a Novel Class of Guanylyl Cyclase C Inhibitors.

J. Schuurkes, E. Cox, H. D. de Jonge, 2015, The Journal of infectious diseases.

β2-Adrenergic receptor agonists activate CFTR in intestinal organoids and subjects with cystic fibrosis

J. Hanrahan, C. Majoor, H. Janssens, 2016, European Respiratory Journal.

The effect of maintenance azithromycin on radiological features in patients with bronchiectasis - Analysis from the BAT randomized controlled trial.

W. Boersma, P. D. de Jong, J. Altenburg, 2021, Respiratory medicine.

Emphysema Is Common in Lungs of Cystic Fibrosis Lung Transplantation Patients: A Histopathological and Computed Tomography Study

P. D. de Jong, A. Vink, O. Mets, 2015, PloS one.

Is sweat chloride predictive of severity of cystic fibrosis lung disease assessed by chest computed tomography?

H. Tiddens, D. Caudri, I. Bronsveld, 2017, Pediatric pulmonology.

Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD).

I. Sermet-Gaudelus, S. Rowe, P. Melotti, 2018, Journal of visualized experiments : JoVE.

Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism.

N. Derichs, P. Melotti, K. De Boeck, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

The BATTLE study: Effects of long-term tobramycin inhalation solution (TIS) once daily on exacerbation rate in patients with non-cystic fibrosis bronchiectasis. Study protocol of a double blind, randomized, placebo-controlled trial: study protocol

W. Boersma, J. Altenburg, H. Heijerman, 2022, Contemporary clinical trials communications.

Treatment with inhaled antibiotics in bronchiectasis, side effects, and evaluation of the tolerance test; analysis from the BATTLE randomized controlled trial

W. Boersma, H. Heijerman, I. Bronsveld, 2023, The clinical respiratory journal.

Exocrine Pancreatic Alterations in Long-Lived Surviving Cystic Fibrosis Mice

M. Corey, P. Durie, W. Ip, 1996, Pediatric Research.

Results of a phase IIa study of VX-809, an investigational CFTR corrector compound, in subjects with cystic fibrosis homozygous for the F508del-CFTR mutation

F. Accurso, M. Ashlock, M. Konstan, 2012 .

Radiological and long‐term clinical response to elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with advanced lung disease

F. M. Mohamed Hoesein, H. Heijerman, I. Bronsveld, 2023, Pediatric pulmonology.

New clinical diagnostic procedures for cystic fibrosis in Europe.

N. Derichs, F. Vermeulen, P. Melotti, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Influence of perfusate temperature on nasal potential difference

F. Vermeulen, P. Melotti, K. De Boeck, 2012, European Respiratory Journal.

Standardized Measurement of Nasal Membrane Transepithelial Potential Difference (NPD).

I. Sermet-Gaudelus, S. Rowe, P. Melotti, 2018, Journal of visualized experiments : JoVE.