B. Wiedemann

发表

Rationale and study design of ViPS – variable pressure support for weaning from mechanical ventilation: study protocol for an international multicenter randomized controlled open trial

P. Pelosi, S. Jaber, R. Beale, 2013, Trials.

Correlation of heart-type fatty acid-binding protein with mortality and echocardiographic data in patients with pulmonary embolism at intermediate risk.

R. Strasser, M. Langer, B. Wiedemann, 2010, American heart journal.

Microcurrent transcutaneous electric nerve stimulation in painful diabetic neuropathy: a randomized placebo-controlled study.

H. Reichmann, R. Sabatowski, G. Gossrau, 2011, Pain medicine.

Benchmarking improves quality in cystic fibrosis care: a pilot project involving 12 centres.

M. Stern, P. Wenzlaff, B. Wiedemann, 2011, International journal for quality in health care : journal of the International Society for Quality in Health Care.

Reliability of brain CT evaluation by stroke neurologists in telemedicine

H. Reichmann, A. Kunz, I. Dzialowski, 2013, Neurology.

Regional lung aeration and ventilation during pressure support and biphasic positive airway pressure ventilation in experimental lung injury

P. Pelosi, C. Stroszczynski, A. Carvalho, 2010, Critical care.

Acute effects of NPPV in interstitial lung disease with chronic hypercapnic respiratory failure.

G. Höffken, B. Wiedemann, D. Koschel, 2010, Respiratory medicine.

Gastroenteropancreatic Neuroendocrine Tumors: Standardizing Therapy Monitoring with 68Ga-DOTATOC PET/CT Using the Example of Somatostatin Receptor Radionuclide Therapy

W. Luboldt, K. Zöphel, B. Wiedemann, 2010, Molecular imaging.

Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project.

B. Wiedemann, G. Steinkamp, 2002, Thorax.

Prospective evaluation of emerging bacteria in cystic fibrosis.

E. Rietschel, F. Ratjen, B. Wiedemann, 2005, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

The German cystic fibrosis quality assurance project: clinical features in children and adults.

M. Stern, B. Wiedemann, G. Steinkamp, 2001, The European respiratory journal.

Distribution of regional lung aeration and perfusion during conventional and noisy pressure support ventilation in experimental lung injury.

P. Pelosi, A. Carvalho, P. Spieth, 2011, Journal of applied physiology.

The effects of salbutamol on epithelial ion channels depend on the etiology of acute respiratory distress syndrome but not the route of administration

P. Pelosi, M. Kasper, P. Spieth, 2014, Respiratory Research.

Factors Associated with Worse Lung Function in Cystic Fibrosis Patients with Persistent Staphylococcus aureus

J. Mainz, B. Tümmler, M. Ballmann, 2016, PloS one.

From registry to quality management: the German Cystic Fibrosis Quality Assessment project 1995–2006

M. Stern, P. Wenzlaff, B. Wiedemann, 2008, European Respiratory Journal.

Sino nasal inhalation of isotonic versus hypertonic saline (6.0%) in CF patients with chronic rhinosinusitis - Results of a multicenter, prospective, randomized, double-blind, controlled trial.

J. Mainz, J. Hentschel, J. Beck, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Effects of Intravascular Volume Replacement on Lung and Kidney Function and Damage in Nonseptic Experimental Lung Injury

P. Pelosi, M. Kasper, P. Spieth, 2013, Anesthesiology.

Diabetes and Neurodegeneration in Wolfram Syndrome

G. Salzano, O. Kordonouri, A. Huebner, 2011, Diabetes Care.

Higher Levels of Spontaneous Breathing Reduce Lung Injury in Experimental Moderate Acute Respiratory Distress Syndrome*

P. Pelosi, M. Kasper, P. Spieth, 2014, Critical care medicine.

Objectives: To assess the effects of different levels of spontaneous breathing during biphasic positive airway pressure/airway pressure release ventilation on lung function and injury in an experimental model of moderate acute respiratory distress syndrome. Design: Multiple-arm randomized experiment

P. Pelosi, M. Kasper, P. Spieth, 2014 .

Evaluation of body mass index percentiles for assessment of malnutrition in children with cystic fibrosis

M. Stern, T. Hirche, B. Wiedemann, 2007, European Journal of Clinical Nutrition.

3D-Imaging of alveoli during mechanical ventilation

A. Popp, J. Roeseler, M. Kasper, 2009 .

Effects of vaporized perfluorohexane and partial liquid ventilation on regional distribution of alveolar damage in experimental lung injury

M. Kasper, P. Spieth, M. Gama de Abreu, 2007, Intensive Care Medicine.

Effects of vaporized perfluorohexane and partial liquid ventilation on regional distribution of alveolar damage in experimental lung injury

M. Kasper, P. Spieth, M. Gama de Abreu, 2006, Intensive Care Medicine.

Higher Levels of Spontaneous Breathing Induce Lung Recruitment and Reduce Global Stress/Strain in Experimental Lung Injury

M. Andreeff, P. Pelosi, J. Kotzerke, 2014, Anesthesiology.

Antigen‐specific IgG antibodies in feather duvet lung

G. Höffken, B. Wiedemann, D. Koschel, 2010, European journal of clinical investigation.

Concordant genotype of upper and lower airways P aeruginosa and S aureus isolates in cystic fibrosis

J. Mainz, J. Beck, B. Tümmler, 2009, Thorax.

Sinu-nasal inhalation of Dornase alfa in CF. Results of a double-blind placebo-controlled pilot trial

J. Mainz, J. Beck, H. Mentzel, 2008 .

Sinonasal inhalation of dornase alfa administered by vibrating aerosol to cystic fibrosis patients: a double-blind placebo-controlled cross-over trial.

J. Mainz, J. Beck, A. Koitschev, 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Pulmonary Hypertension in Chronic Hypersensitivity Pneumonitis

G. Höffken, M. Halank, B. Wiedemann, 2012, Lung.

Detection of relevant colonic neoplasms with PET/CT: promising accuracy with minimal CT dose and a standardised PET cut-off

D. Aust, W. Luboldt, T. Vogl, 2010, European radiology.

83* Sinonasal inhalation of tobramycin in cystic fibrosis patients with P. aeruginosa colonization of the upper airways – results of a multicentric placebo-controlled pilot study

J. Mainz, J. Beck, P. Schelhorn-Neise, 2011 .

Forceps biopsy and suction catheter for sampling in pulmonary nodules and infiltrates

G. Höffken, B. Wiedemann, D. Koschel, 2011, European Respiratory Journal.

Prevalence of CF-related chronic rhinosinusitis – results from a multicentre interdisciplinary study

J. Mainz, J. Beck, B. Wiedemann, 2010 .

Statistical limitations of percent ideal body weight as measure for nutritional failure in patients with cystic fibrosis.

M. Stern, H. Hirche, B. Wiedemann, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.