N. Derichs

发表

Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data

Antonia Zapf, Burkhard Tümmler, Javier Sanz, 2010, Thorax.

Recommendations for the classification of diseases as CFTR-related disorders.

B. Kerem, J. Zieleński, P. Pignatti, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Local and Systemic Alterations of the L-Arginine/Nitric Oxide Pathway in Sputum, Blood, and Urine of Pediatric Cystic Fibrosis Patients and Effects of Antibiotic Treatment

D. Tsikas, N. Derichs, M. Ballmann, 2020, Journal of clinical medicine.

Activated L-Arginine/Nitric Oxide Pathway in Pediatric Cystic Fibrosis and Its Association with Pancreatic Insufficiency, Liver Involvement and Nourishment: An Overview and New Results

D. Tsikas, N. Derichs, M. Ballmann, 2020, Journal of clinical medicine.

Hyperviscous airway periciliary and mucous liquid layers in cystic fibrosis measured by confocal fluorescence photobleaching

A. Verkman, N. Derichs, W. Finkbeiner, 2011, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Functional analysis of F508del CFTR in native human colon.

F. Stanke, B. Tümmler, N. Derichs, 2010, Biochimica et biophysica acta.

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.

CFTR functional measurements in human models for diagnosis, prognosis and personalized therapy: Report on the pre-conference meeting to the 11th ECFS Basic Science Conference, Malta, 26-29 March 2014.

M. Drumm, A. Mehta, M. Amaral, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Evaluation of portal venous gas detected by ultrasound examination for diagnosis of necrotising enterocolitis

G. Rau, B. Bohnhorst, N. Derichs, 2008, Archives of Disease in Childhood Fetal and Neonatal Edition.

Diagnostik von Bronchiektasen

N. Derichs, 2014, Der Pneumologe.

CFTR biomarkers: time for promotion to surrogate end-point

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

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.

Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

P. Lebecque, N. Derichs, K. De Boeck, 2009, Thorax.

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

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

Homozygosity for L997F in a child with normal clinical and chloride secretory phenotype provides evidence that this Cystic Fibrosis Transmembrane Conductance Regulator mutation does not cause cystic fibrosis

S. Gallati, N. Derichs, C. Stolpe, 2005, Clinical genetics.

Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID): A new designation and management recommendations for infants with an inconclusive diagnosis following newborn screening.

N. Derichs, R. Parad, A. Munck, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Riociguat for the treatment of Phe508del homozygous adults with cystic fibrosis.

N. Derichs, F. Vermeulen, J. Davies, 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Airway surface liquid depth imaged by surface laser reflectance microscopy

A. Verkman, N. Derichs, J. Thiagarajah, 2010, The Journal of general physiology.

Immunochemical Analysis of Mutant CFTR in Lung Explants

B. Tümmler, N. Derichs, M. Ballmann, 2012, Cellular Physiology and Biochemistry.

Local and Systemic Alterations of the L-Arginine / Nitric Oxide Pathway in Sputum, Blood, and Urine of Pediatric Cystic Fibrosis Patients and E ﬀ ects of Antibiotic Treatment

D. Tsikas, N. Derichs, M. Ballmann, 2020 .

Diagnosis of Cystic Fibrosis: Consensus Guidelines from the Cystic Fibrosis Foundation

Margaret Rosenfeld, Frank Accurso, Philip M. Farrell, 2017, The Journal of pediatrics.

Appendicitis in a Preterm Infant with Incarcerated Inguinal Hernia

N. Derichs, C. Dammann, S. Glüer, 2006 .

Targeting a genetic defect: cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis

N. Derichs, 2013, European Respiratory Review.

Diagnosis of Cystic Fibrosis in Nonscreened Populations

J. Nick, P. Sosnay, N. Derichs, 2017, The Journal of pediatrics.

Real life practice of sweat testing in Europe.

N. Derichs, K. De Boeck, M. Wilschanski, 2017, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Measurement of ion transport function in rectal biopsies.

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

Cystic Fibrosis: Lessons from the Sweat Gland

George Havenith, Yawei Yu, Simon Hodder, 2015 .

GLPG1837, a CFTR potentiator, in p.Gly551Asp (G551D)-CF patients: An open-label, single-arm, phase 2a study (SAPHIRA1).

N. Derichs, P. Dřevínek, J. Davies, 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Nasal potential difference measurements in diagnosis of cystic fibrosis: an international survey.

B. Tümmler, N. Derichs, M. Ballmann, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Cystic Fibrosis Diagnostic Challenges over 4 Decades: Historical Perspectives and Lessons Learned

C. Castellani, N. Derichs, P. Farrell, 2017, The Journal of pediatrics.

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.

Functional fluorescently labeled bithiazole ΔF508-CFTR corrector imaged in whole body slices in mice.

A. Verkman, N. Derichs, J. Sutcliffe, 2011, Bioconjugate chemistry.

Recommendations for the classification of diseases as CFTR-related disorders.

B. Kerem, J. Zieleński, P. Pignatti, 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, P. Melotti, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis

P. Lebecque, N. Derichs, I. Sermet, 2009, Thorax.

The European Cystic Fibrosis Society–Clinical Trials Network: an international network to optimize clinical research for a rare disease

C. Castellani, N. Derichs, P. Dřevínek, 2013 .

P028 Riociguat for the treatment of adult Phe508del homozygous cystic fibrosis: efficacy data from the Phase II Rio-CF study

N. Derichs, F. Vermeulen, J. Davies, 2018, Journal of Cystic Fibrosis.