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Mitglied/er, Klinik für Allgemeine Pädiatrie mit Schwerpunkt Neuropädiatrie
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Die folgenden Publikationen sind in der Online-Universitätsbibliographie der Universität Duisburg-Essen verzeichnet. Weitere Informationen finden Sie gegebenenfalls auch auf den persönlichen Webseiten der Person.
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Impact of habitual physical activity and exercise capacity on quality of life in adolescents and adults with cystic fibrosisIn: Pediatric Pulmonology, Jg. 59, 2024, Nr. 4, S. 949 – 963
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Longitudinal Evaluation of Physical Fitness in Adults with Cystic Fibrosis in the Era of CFTR-Modulating-TherapiesIn: Research Quarterly for Exercise and Sport, Jg. 95, 2024, Nr. 4, S. 804 – 812
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Longitudinal changes in habitual physical activity in adult people with cystic fibrosis in the presence or absence of treatment with elexacaftor/tezacaftor/ivacaftorIn: Frontiers in Sports and Active Living, Jg. 6, 2024, 1284878DOI (Open Access)
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Long-Term Follow-Up of Health-Related Quality of Life and Short-Term Intervention with CFTR Modulator Therapy in Adults with Cystic Fibrosis : Evaluation of Changes over Several Years with or without 33 Weeks of CFTR Modulator TherapyIn: Healthcare, Jg. 11, 2023, Nr. 21, 2873DOI (Open Access)
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Barriers for Sports and Exercise Participation and Corresponding Barrier Management in Cystic FibrosisIn: International Journal of Environmental Research and Public Health = IJERPH, Jg. 19, 2022, Nr. 20, 13150DOI (Open Access)
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Effects of a Long-Term Monitored Exercise Program on Aerobic Fitness in a Small Group of Children with Cystic FibrosisIn: International Journal of Environmental Research and Public Health = IJERPH, Jg. 19, 2022, Nr. 13, 7923DOI (Open Access)
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Aerosolized lancovutide in adolescents (≥12 years) and adults with cystic fibrosis – a randomized trialIn: Journal of Cystic Fibrosis, Jg. 20, 2021, Nr. 1, S. 61 – 67DOI (Open Access)
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Association between habitual physical activity (HPA) and sleep quality in patients with cystic fibrosisIn: Sleep and Breathing, Jg. 25, 2021, Nr. 2, S. 609 – 615DOI (Open Access)
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Health-Related and Motor Performance-Related Fitness and Physical Activity Among Youth With Cystic FibrosisIn: Perceptual and Motor Skills, Jg. 128, 2021, Nr. 5, S. 2097 – 2116DOI, Online Volltext (Open Access)
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Home Noninvasive Ventilation in Pediatric Subjects With Neuromuscular Diseases : One Size Fits AllIn: Respiratory Care, Jg. 66, 2021, Nr. 3, S. 410 – 415
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Trainability of Health-Related and Motor Performance Fitness in Adults with Cystic Fibrosis within a 12-Month Partially Supervised Exercise ProgramIn: Pulmonary Medicine, 2021, 5581812DOI (Open Access)
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An 8 week open-label interventional multicenter study to explore the lung clearance index as endpoint for clinical trials in cystic fibrosis patients ≥8 years of age, chronically infected with Pseudomonas aeruginosaIn: BMC Pulmonary Medicine, Jg. 20, 2020, Nr. 1, S. 167DOI (Open Access)
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Effects of a long-term exercise program on motor performance in children and adolescents with CFIn: Pediatric Pulmonology, Jg. 55, 2020, Nr. 12, S. 3371 – 3380
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Changes in clinical markers during a short-term transfer program of adult cystic fibrosis patients from pediatric to adult careIn: Open Respiratory Medicine Journal, Jg. 13, 2019, Nr. 1, S. 11 – 18DOI (Open Access)
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Multiplex PCR of bronchoalveolar lavage fluid in children enhances the rate of pathogen detectionIn: BMC Pulmonary Medicine, Jg. 19, 2019, Nr. 1, S. 132DOI (Open Access)
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Airway clearance techniques in neuromuscular disorders: A state of the art reviewIn: Respiratory Medicine, Jg. 136, 2018, S. 98 – 110DOI (Open Access)
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Bacteraemia and fungaemia in cystic fibrosis patients with febrile pulmonary exacerbation : a prospective observational studyIn: BMC Pulmonary Medicine, Jg. 17, 2017, Nr. 1, S. 96DOI (Open Access)
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Chest physiotherapy can affect the lung clearance index in cystic fibrosis patientsIn: Pediatric Pulmonology, Jg. 52, 2017, Nr. 5, S. 625 – 631
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Glomerular and Tubular Renal Function after Repeated Once-Daily Tobramycin Courses in Cystic Fibrosis PatientsIn: Pulmonary Medicine, 2017, 2602653DOI (Open Access)
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S2k-Leitlinie : Nichtinvasive und invasive Beatmung als Therapie der chronischen respiratorischen Insuffizienz – Revision 2017In: Pneumologie, Jg. 71, 2017, Nr. 11, S. 722 – 795
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The microbiome and secondary lung disease in neuromuscular patients : Is it time to change our clinical practice? - ReplyIn: Respirology, Jg. 22, 2017, Nr. 5, S. 1036
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Validation of the screening tool ApneaLink® in comparison to polysomnography for the diagnosis of sleep-disordered breathing in children and adolescents.In: Sleep Medicine, Jg. 37, 2017, S. 13 – 18
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Practical Recommendations for Diagnosis and Management of Respiratory Muscle Weakness in Late-Onset Pompe DiseaseIn: International Journal of Molecular Sciences (IJMS), Jg. 17, 2016, Nr. 10, S. 1735DOI (Open Access)
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Respiratory Muscle Weakness and Respiratory Failure in Pediatric Neuromuscular Disorders : The Value of Noninvasive Determined Tension-Time IndexIn: Neuropediatrics, Jg. 47, 2016, Nr. 6, S. 374 – 379
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Sequential Inhalational Tobramycin-Colistin-Combination in CF-Patients with Chronic P. Aeruginosa Colonization - an Observational StudyIn: Cellular Physiology and Biochemistry, Jg. 39, 2016, Nr. 3, S. 1141 – 1151DOI (Open Access)
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Upper airway microbial colonization in patients with neuromuscular disordersIn: Respirology, Jg. 21, 2016, Nr. 7, S. 1285 – 1291
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Decline in lung volume with Duchenne muscular dystrophy is associated with ventilation inhomogeneityIn: Respiratory Care, Jg. 60, 2015, Nr. 9, S. 1257 – 1263DOI (Open Access)
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Mechanical insufflation/exsufflation improves vital capacity in neuromuscular disordersIn: Chronic Respiratory Disease, Jg. 12, 2015, Nr. 1, S. 31 – 35DOI (Open Access)
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Empfehlungen der Deutschen Atemwegsliga zur Messung der AtemmuskelfunktionIn: Pneumologie, Jg. 68, 2014, Nr. 5, S. 307 – 314
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Normal values for inspiratory muscle function in childrenIn: Physiological Measurement, Jg. 35, 2014, Nr. 10, S. 1975 – 1981DOI (Open Access)
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Open randomised prospective comparative multi-centre intervention study of patients with Cystic fibrosis and early diagnosed diabetes mellitusIn: BMC Pediatrics, Jg. 14, 2014, Nr. 1, S. 70DOI (Open Access)
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Optimum insufflation capacity and peak cough flow in neuromuscular disordersIn: Annals of the American Thoracic Society, Jg. 11, 2014, Nr. 10, S. 1560 – 1568
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Pathophysiologische Bedeutung des Schlafs bei Zwerchfelllähmung und anderen neuromuskulären ErkrankungenIn: Der Pneumologe, Jg. 11, 2014, Nr. 5, S. 402 – 412
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Comparison of PCR and culture based detection of pathogens in bronchoalveolar fluid in neutropenic childrenIn: European Respiratory Journal (ERJ), Jg. 42, 2013, Nr. Suppl. 57, S. 4473
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Development of a quantitative immunofluorescence assay for detection of Stenotrophomonas maltophilia antibodies in patients with cystic fibrosisIn: Journal of Cystic Fibrosis, Jg. 12, 2013, Nr. 6, S. 651 – 654DOI (Open Access)
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Inhalation treatment with glutathione in patients with cystic fibrosis: A randomized clinical trialIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM), Jg. 188, 2013, Nr. 1, S. 83 – 89
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Long-term follow-up of pediatric patients receiving total body irradiation before hematopoietic stem cell transplantation and post-transplant survival of >2 yearsIn: Pediatric Blood and Cancer, Jg. 60, 2013, Nr. 11, S. 1792 – 1797
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M.Pompe im Kindesalter : Aktueller Stand der Diagnostik und TherapieIn: Monatsschrift Kinderheilkunde, Jg. 160, 2012, Nr. 12, S. 1243 – 1248
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Total body irradiation (TBI) in the conditioning regimens prior to hematopoietic stem cell transplantation (HSCT) : Long-term follow-up of 98 pediatric patientsIn: Strahlentherapie und Onkologie: Journal of Radiation Oncology, Biology, Physics, Jg. 188, 2012, Nr. Suppl. 1, S. 108
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Molecular Analysis of Staphylococcus Aureus Isolates from an Ongoing Prospective Observational Longitudinal Multicenter Study Determining Staphylococcus Aureus Airway Colonization or Infection in Cystic Fibrosis PatientsIn: Pediatric Pulmonology, Jg. 34, 2011, S. 323 – 323
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Non-invasive ventilation on a pediatric intensive care unit : feasibility, efficacy, and predictors of successIn: Pediatric Pulmonology, Jg. 46, 2011, Nr. 11, S. 1114 – 1120
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Stenotrophomonas maltophilia in cystic fibrosis : improved detection by the use of selective agar and evaluation of antimicrobial resistanceIn: Journal of Cystic Fibrosis, Jg. 10, 2011, Nr. 6, S. 422 – 427DOI (Open Access)
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Nicht-Invasive Beatmung auf einer pädiatrischen Intensivstation: Evaluation von Machbarkeit, Effektivität und Prädiktoren für den Erfolg der Therapie
36. Jahrestagung der Gesellschaft für Neonatologie und Pädiatrische Intensivmedizin und 18. Jahrestagung der Gesellschaft für Pädiatrische Infektiologie gemeinsam mit Société Luxembourgoise de Pédiatrie Saarbrücken, 17.–19. Juni 2010,In: Klinische Pädiatrie, Jg. 222, 2010, S. 7 – S7 -
Nichtinvasive und invasive Beatmung als Therapie der chronischen respiratorischen InsuffizienzIn: Pneumologie, Jg. 64, 2010, Nr. 4, S. 207 – 240
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Non-invasive ventilation reduces respiratory tract infections in children with neuromuscular disordersIn: Pediatric Pulmonology, Jg. 43, 2008, Nr. 1, S. 67 – 71
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Schwache Atmung – schwaches Herz : Atemmuskelversagen und Kardiomyopathie bei neuromuskulären ErkrankungenIn: Nervenheilkunde, Jg. 27, 2008, Nr. 4, S. 284 – 291
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Nasal Staphylococcus aureus carriage is not a risk factor for lower-airway infection in young cystic fibrosis patientsIn: Journal of Clinical Microbiology, Jg. 45, 2007, Nr. 9, S. 2979 – 2984
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Chest infections in young neuromuscular patients : The critical importance of preserving Vital Capacity - ReplyIn: Neuromuscular Disorders, Jg. 16, 2006, Nr. 9-10, S. 614 – 615
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IPPB-assisted coughing in neuromuscular disordersIn: Pediatric Pulmonology, Jg. 41, 2006, Nr. 6, S. 551 – 557
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Predictors of severe chest infections in pediatric neuromuscular disordersIn: Neuromuscular Disorders, Jg. 16, 2006, Nr. 5, S. 325 – 328
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Respiratory failure in Pompe disease : treatment with noninvasive ventilationIn: Neurology, Jg. 64, 2005, Nr. 8, S. 1465 – 1467
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Respiratory function assessment and intervention in neuromuscular disordersIn: Current Opinion in Neurology, Jg. 18, 2005, Nr. 5, S. 543 – 547
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Respiratory function in congenital muscular dystrophy and limb girdle muscular dystrophy 2IIn: Neurology, Jg. 62, 2004, Nr. 3, S. 513 – 514
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Sleep disordered breathing in spinal muscular atrophyIn: Neuromuscular Disorders, Jg. 14, 2004, Nr. 12, S. 797 – 803
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Daytime predictors of sleep disordered breathing in children and adolescents with neuromuscular disordersIn: Neuromuscular Disorders, Jg. 13, 2003, Nr. 2, S. 123 – 128
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Hyperinsufflationsassistiertes Hustenmanöver bei neuromuskulären ErkrankungenIn: Monatsschrift Kinderheilkunde, Jg. 151, 2003, Nr. 3, S. 269 – 273
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Long-term noninvasive ventilation in children and adolescents with neuromuscular disordersIn: European Respiratory Journal (ERJ), Jg. 22, 2003, Nr. 4, S. 631 – 636
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Nichtinvasive Beatmung bei neuromuskulären ErkrankungenIn: Monatsschrift Kinderheilkunde, Jg. 151, 2003, Nr. 3, S. 262 – 268
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Nächtliche nichtinvasive Beatmung bei Kindern und Jugendlichen mit neuromuskulären Erkrankungen : Einfluss auf Schlaf und SymptomeIn: Wiener Klinische Wochenschrift, Jg. 115, 2003, Nr. 24, S. 855 – 859
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Progrediente neuromuskuläre Erkrankungen : Chronisches Atemmuskelversagen und schlafbezogene AtmungsstörungenIn: Monatsschrift Kinderheilkunde, Jg. 151, 2003, Nr. 3, S. 256 – 261
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Patterns and predictors of sleep disordered breathing in primary myopathiesIn: Thorax, Jg. 57, 2002, Nr. 8, S. 724 – 728
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Home non-invasive ventilation in paediatric patients with respiratory insufficiency due to neuromuscular disease – One size fits all?In: European Respiratory Journal (ERJ). Sheffield: European Respiratory Society, Jg. 54, 2019, Nr. Suppl. 63, S. PA4045DOI (Open Access)
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Myasthenic symptoms : From initial presentation to diagnosisIn: Neuromuscular Disorders. Amsterdam; Oxford; Frankfurt, M. [u.a.]: Elsevier, Jg. 22, 2012, Nr. 9-10, S. 856
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Long-term follow-up of pediatric patients receiving total body irradiation before bone marrow transplantation
43rd Congress of the International Society of Paediatric Oncology (SIOP) 2011 ; 28th–30th October, 2011, Auckland, New Zealand,In: Pediatric Blood and Cancer. Hoboken: Wiley-Blackwell - STM, Jg. 57, 2011, Nr. 5, S. 827 -
Intermittent positive pressure breathing (IPPB) improves peak cough flow in pediatric neuromuscular disorders
9th International Congress of the World-Muscle-Society, September 01-04, 2004, Göteborg, Sweden,In: Neuromuscular Disorders. Amsterdam; Oxford; Frankfurt, M. [u.a.]: Elsevier, Jg. 14, 2004, Nr. 8-9, S. 598 – 598 -
Comparison of respiratory function in different subgroups of congenital muscular dystrophy
8th International Congress of the World-Muscle-Society, September 03-06, 2003, Szeged, Hungary,In: Neuromuscular Disorders. Amsterdam; Oxford; Frankfurt, M. [u.a.]: Elsevier, Jg. 13, 2003, Nr. 7-8, S. 656 – 656 -
Long-term effects of noninvasive ventilation in children with neuromuscular diseases
10th International Congress on Neuromuscular Diseases, July 07-12, 2002, Vancouver, Canada,In: Journal of the Neurological Sciences. Amsterdam: Elsevier, Jg. 199, 2002, Nr. Suppl. 1, S. S6 -
Daytime predictors of nocturnal hypoventilation in children with progressive neuromuscular diseases
10th International Congress on Neuromuscular Diseases, July 07-12, 2002, Vancouver, Canada,In: Journal of the Neurological Sciences. Amsterdam: Elsevier, Jg. 199, 2002, Nr. Suppl. 1, S. S32