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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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ALPINE2: Efficacy and safety of 14-day vs 28-day inhaled aztreonam for Pa eradication in children with cystic fibrosisIn: Journal of Cystic Fibrosis Jg. 23 (2024) Nr. 1, S. 80 - 86Online Volltext: dx.doi.org/ (Open Access)
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Clinical recommendations for the inpatient management of lower respiratory tract infections in children and adolescents with severe neurological impairment in GermanyIn: European Journal of Pediatrics Jg. 183 (2024) Nr. 3, S. 987 - 999Online Volltext: dx.doi.org/ (Open Access)
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Heimbeatmung von Kindern und JugendlichenIn: Monatsschrift Kinderheilkunde Jg. 172 (2024) Nr. 2, S. 138 - 147Online Volltext: dx.doi.org/
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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 - 963Online Volltext: dx.doi.org/
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Kinderpneumologische Aspekte bei der Betreuung von Kindern mit neuromuskulären Erkrankungen am Beispiel der Muskeldystrophie Typ DuchenneIn: Klinische Pädiatrie (2024) in pressOnline Volltext: dx.doi.org/
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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 - 812Online Volltext: dx.doi.org/
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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) 1284878Online Volltext: dx.doi.org/ (Open Access)
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Neutrophilia in the bronchoalveolar lavage fluid increases coughing during flexible fiberoptic bronchoscopy in a pediatric cohortIn: Frontiers in Pediatrics Jg. 12 (2024) 1347983Online Volltext: dx.doi.org/ (Open Access)
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Notfallpläne zum Management von Notfällen bei Kindern mit außerklinischer BeatmungIn: Klinische Pädiatrie Jg. 236 (2024) Nr. 02, S. 57 - 63Online Volltext: dx.doi.org/ (Open Access)
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Opportunistic Screening for Low Bone Mineral Density in Adults with Cystic Fibrosis Using Low-Dose Computed Tomography of the Chest with Artificial IntelligenceIn: Journal of Clinical Medicine (JCM) Jg. 13 (2024) Nr. 19, 5961Online Volltext: dx.doi.org/ (Open Access)
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Targeted PCR of Mucorales in pediatric bronchoalveolar lavage samples indicates low prevalence of airway colonization and sample contaminationIn: Infectious Diseases Jg. 56 (2024) Nr. 3, S. 255 - 258Online Volltext: dx.doi.org/
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ABCA3 -related interstitial lung disease beyond infancyIn: Thorax Jg. 78 (2023) Nr. 6, S. 587 - 595Online Volltext: dx.doi.org/ (Open Access)
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Diffuse alveolar haemorrhage in children : An international multicentre studyIn: ERJ Open Research Jg. 9 (2023) Nr. 2, 00733-2022Online Volltext: dx.doi.org/ (Open Access)
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Epidemiological trends in nontuberculous mycobacterial infection among people with cystic fibrosis in GermanyIn: International Journal of Infectious Diseases Jg. 129 (2023) S. 32 - 39Online Volltext: dx.doi.org/ (Open Access)
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How personality influences health outcomes and quality of life in adult patients with cystic fibrosisIn: BMC Pulmonary Medicine Jg. 23 (2023) Nr. 1, 190Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Impact of elexacaftor/tezacaftor/ivacaftor on lung function, nutritional status, pulmonary exacerbation frequency and sweat chloride in people with cystic fibrosis : real-world evidence from the German CF RegistryIn: The Lancet Regional Health - Europe Jg. 32 (2023) 100690Online Volltext: dx.doi.org/ (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, 2873Online Volltext: dx.doi.org/ (Open Access)
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Pediatric multi-drug-resistant tuberculosis in Germany : Diagnostic and therapeutic challenges of an “orphan disease”In: European Journal of Pediatrics Jg. 182 (2023) Nr. 11, S. 5167 - 5179Online Volltext: dx.doi.org/ (Open Access)
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Phase 3 Open-Label Clinical Trial of Elexacaftor/Tezacaftor/Ivacaftor in Children Aged 2–5 Years with Cystic Fibrosis and at Least One F508del AlleleIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 208 (2023) Nr. 1, S. 59 - 67Online Volltext: dx.doi.org/ (Open Access)
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Real-life impact of highly effective CFTR modulator therapy in children with cystic fibrosisIn: Frontiers in Pharmacology Jg. 14 (2023) 1176815Online Volltext: dx.doi.org/ (Open Access)
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Tracheostomy decannulation in children : A proposal for a structured approach on behalf of the working group chronic respiratory insufficiency within the German-speaking society of pediatric pulmonologyIn: European Journal of Pediatrics Jg. 182 (2023) Nr. 7, S. 2999 - 3006Online Volltext: dx.doi.org/
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Acute exacerbations in children’s interstitial lung diseaseIn: Thorax Jg. 77 (2022) Nr. 8, S. 799 - 804Online Volltext: dx.doi.org/ (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, 13150Online Volltext: dx.doi.org/ (Open Access)
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Biofilm infection of a central venous port-catheter caused by Mycobacterium avium complex in an immunocompetent child with cystic fibrosisIn: BMC Infectious Diseases Jg. 22 (2022) Nr. 1, 921Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Cough suppression and HRQoL in adult people with cystic fibrosis : an unexplored correlationIn: Health and Quality of Life Outcomes Jg. 20 (2022) Nr. 1, 141Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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ERS statement on paediatric long-term noninvasive respiratory supportIn: European Respiratory Journal (ERJ) Jg. 59 (2022) Nr. 6, 2101404Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Effect of Triple Combination CFTR Modulator Therapy on Sleep in Adult Patients with Cystic FibrosisIn: Respiration: International Journal of Thoracic Medicine Jg. 101 (2022) Nr. 8, S. 766 - 774Online Volltext: dx.doi.org/
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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, 7923Online Volltext: dx.doi.org/ (Open Access)
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Efficacy and Safety of Elexacaftor/Tezacaftor/Ivacaftor in Children 6 Through 11 Years of Age with Cystic Fibrosis Heterozygous for F508del and a Minimal Function Mutation : A Phase 3b, Randomized, Placebo-controlled StudyIn: American Journal of Respiratory and Critical Care Medicine (AJRCCM) Jg. 206 (2022) Nr. 11, S. 1361 - 1369Online Volltext: dx.doi.org/ (Open Access)
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Healthcare resource utilisation and medical costs for children with interstitial lung diseases (chILD) in EuropeIn: Thorax Jg. 77 (2022) Nr. 8, S. 781 - 789Online Volltext: dx.doi.org/ (Open Access)
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Homozygous WASHC4 variant in two sisters causes a syndromic phenotype defined by dysmorphisms, intellectual disability, profound developmental disorder, and skeletal muscle involvementIn: The Journal of Pathology Jg. 256 (2022) Nr. 1, S. 93 - 107Online Volltext: dx.doi.org/ (Open Access)
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Indications and outcome of home high-flow nasal therapy in children, a single-center experienceIn: Pediatric Pulmonology Jg. 57 (2022) Nr. 9, S. 2048 - 2052Online Volltext: dx.doi.org/ (Open Access)
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Investigation of respiratory rate in patients with cystic fibrosis using a minimal-impact biomotion systemIn: BMC Pulmonary Medicine Jg. 22 (2022) Nr. 1, 59Online Volltext: dx.doi.org/ (Open Access)
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Multiple breath washout lung function reveals ventilation inhomogeneity unresponsive to mechanical assisted cough in patients with neuromuscular diseaseIn: BMC Pulmonary Medicine Jg. 22 (2022) Nr. 1, 217Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Next Generation Sequencing of Free Microbial DNA for Rapid Identification of Pathogens in Critically Ill Children with Systemic Inflammatory Response Syndrome (SIRS)In: Frontiers in Bioscience (FBS): Landmark Jg. 27 (2022) Nr. 11, 302Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Obstructive sleep apnea and nocturnal hypoxemia in adult patients with cystic fibrosisIn: BMC Pulmonary Medicine Jg. 22 (2022) Nr. 1, 446Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Phenotypic spectrum in recessive STING-associated vasculopathy with onset in infancy: Four novel cases and analysis of previously reported casesIn: Frontiers in Immunology Jg. 13 (2022) 1029423Online Volltext: dx.doi.org/ (Open Access)
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Randomized controlled phase 2 trial of hydroxychloroquine in childhood interstitial lung diseaseIn: Orphanet Journal of Rare Diseases Jg. 17 (2022) Nr. 1, 289Online Volltext: dx.doi.org/ (Open Access)
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Von respiratorischer Technologie abhängige KinderIn: Der Pneumologe Jg. 19 (2022) Nr. 3, S. 175 - 185Online Volltext: dx.doi.org/
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A waterlily sign in an 8-year-old boyIn: European Journal of Cardio-Thoracic Surgery Jg. 60 (2021) Nr. 1, S. 199Online Volltext: dx.doi.org/ (Open Access)
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Allergien und schweres AsthmaIn: Der Pneumologe Jg. 18 (2021) Nr. 6, S. 366 - 377Online Volltext: dx.doi.org/
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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 - 615Online Volltext: dx.doi.org/ (Open Access)
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Bronchoskopische Fremdkörperextraktion - Schritt für SchrittIn: Pneumologie Jg. 75 (2021) Nr. 9, S. 651 - 656Online Volltext: dx.doi.org/
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Coil embolisation for massive haemoptysis in cystic fibrosisIn: BMJ Open Respiratory Research Jg. 8 (2021) Nr. 1, e000985Online Volltext: dx.doi.org/ (Open Access)
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EVALI (E-cigarette or vaping product use associated lung injury) : First case report of an adolescent in EuropeIn: Pediatric Pulmonology Jg. 56 (2021) Nr. 5, S. 1274 - 1275Online Volltext: dx.doi.org/
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Hautfragilität, Nierenfehlbildungen und interstitielle Lungenerkrankung aufgrund von compound-heterozygoten ITGA3-MutationenIn: Journal der Deutschen Dermatologischen Gesellschaft (JDDG) Jg. 19 (2021) Nr. 6, S. 899 - 902Online Volltext: dx.doi.org/ (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 - 2116Online Volltext: dx.doi.org/ 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 - 415Online Volltext: dx.doi.org/ (Open Access)
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Hypersensitivity pneumonitis : Lessons from a randomized controlled trial in childrenIn: Pediatric Pulmonology Jg. 56 (2021) Nr. 8, S. 2627 - 2633Online Volltext: dx.doi.org/ (Open Access)
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Langzeitbeatmung bei Kindern und Jugendlichen : ein Fall für die Rehabilitation?In: Monatsschrift Kinderheilkunde Jg. 169 (2021) Nr. 3, S. 226 - 235Online Volltext: dx.doi.org/
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Mukoviszidose und Transition ins ErwachsenenalterIn: Der Pneumologe Jg. 18 (2021) Nr. 2, S. 97 - 103Online Volltext: dx.doi.org/
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Nusinersen does not improve lung function in a cohort of children with spinal muscular atrophy : A single-center retrospective studyIn: European Journal of Paediatric Neurology Jg. 31 (2021) S. 88 - 91Online Volltext: dx.doi.org/
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Sedation for bronchoscopy in children : A prospective randomized double-blinded trialIn: Pediatric Pulmonology Jg. 56 (2021) Nr. 5, S. 1221 - 1229Online Volltext: dx.doi.org/ (Open Access)
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Skin fragility, renal malformation and interstitial lung disease due to compound heterozygous ITGA3 mutationsIn: Journal der Deutschen Dermatologischen Gesellschaft (JDDG) Jg. 19 (2021) Nr. 6, S. 899 - 901Online Volltext: dx.doi.org/ (Open Access)
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Species-Specific Interferon-Gamma Release Assay for the Diagnosis of Mycobacterium abscessus Complex InfectionIn: Frontiers in Microbiology Jg. 12 (2021) 692395Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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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) 5581812Online Volltext: dx.doi.org/ (Open Access)
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Zystisches Nephrom bei einem 15 Monate alten Patienten mit DICER1-MutationIn: Der Urologe Jg. 60 (2021) Nr. 6, S. 776 - 779Online Volltext: dx.doi.org/
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Diagnosis and Care of Infants and Children with Pompe DiseaseIn: Klinische Pädiatrie Jg. 232 (2020) Nr. 02, S. 55 - 61Online Volltext: dx.doi.org/
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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 - 3380Online Volltext: dx.doi.org/
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Pleuropulmonary Blastoma Misinterpreted as Spontaneous Pneumothorax in an InfantIn: The Annals of Thoracic Surgery Jg. 110 (2020) Nr. 1, S. e79Online Volltext: dx.doi.org/ (Open Access)
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Ventilation Techniques and Risk for Transmission of Coronavirus Disease, Including COVID-19 : A Living Systematic Review of Multiple Streams of EvidenceIn: Annals of Internal Medicine Jg. 173 (2020) Nr. 3, S. 204 - 216Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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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 - 18Online Volltext: dx.doi.org/ (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. 132Online Volltext: dx.doi.org/ (Open Access)
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Reducing the frequency of respiratory tract infections in severe neurological disorders by inhaled antibiotics : A retrospective data analysisIn: ERJ Open Research Jg. 5 (2019) Nr. 3, S. 00149 - 02018Online Volltext: dx.doi.org/ (Open Access)
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Differences of Medical Care for Acute Severe Viral Bronchiolitis in Two Urban Areas in EuropeIn: Klinische Pädiatrie Jg. 230 (2018) Nr. 5, S. 245 - 250Online Volltext: dx.doi.org/
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Genetic Diagnostic Elucidation of a Patient With Multiorgan Granulomas, Facial Peculiarities, and Psychomotor RetardationIn: Frontiers in Genetics Jg. 9 (2018) 355Online Volltext: dx.doi.org/ (Open Access)
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Metabolic Myopathies II : P.355Glycogen storage disease type IV: a wide clinical range of neuromuscular phenotypesIn: Neuromuscular Disorders Jg. 28 (2018) Nr. SUPPL. 2, S. S137Online Volltext: dx.doi.org/
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Prevalence and characterization of azole-resistant Aspergillus fumigatus in patients with cystic fibrosis : a prospective multicentre study in GermanyIn: Journal of Antimicrobial Chemotherapy Jg. 73 (2018) Nr. 8, S. 2047 - 2053Online Volltext: dx.doi.org/ (Open Access)
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Pulmonary interstitial Glycogenosis – a systematic analysis of new casesIn: European Respiratory Journal (ERJ) Jg. 52 (2018) Nr. Suppl. 62, S. OA3787Online Volltext: dx.doi.org/
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Pulmonary interstitial glycogenosis – A systematic analysis of new casesIn: Respiratory Medicine Jg. 140 (2018) S. 11 - 20Online Volltext: dx.doi.org/ (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. 96Online Volltext: dx.doi.org/ (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 - 631Online Volltext: dx.doi.org/
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Glomerular and Tubular Renal Function after Repeated Once-Daily Tobramycin Courses in Cystic Fibrosis PatientsIn: Pulmonary Medicine (2017) 2602653Online Volltext: dx.doi.org/ (Open Access)
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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. 1036Online Volltext: dx.doi.org/
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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 - 18Online Volltext: dx.doi.org/
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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 - 379Online Volltext: dx.doi.org/
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Upper airway microbial colonization in patients with neuromuscular disordersIn: Respirology Jg. 21 (2016) Nr. 7, S. 1285 - 1291Online Volltext: dx.doi.org/
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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 - 1263Online Volltext: dx.doi.org/ (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 - 35Online Volltext: dx.doi.org/ (Open Access)
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Normal values for inspiratory muscle function in childrenIn: Physiological Measurement Jg. 35 (2014) Nr. 10, S. 1975 - 1981Online Volltext: dx.doi.org/ (Open Access)
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Pulse Oximetry Is Insufficient for Timely Diagnosis of Hepatopulmonary Syndrome in Children with Liver CirrhosisIn: The Journal of Pediatrics Jg. 164 (2014) Nr. 3, S. 546 - 552.e2Online Volltext: dx.doi.org/
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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 - 654Online Volltext: dx.doi.org/ (Open Access)
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Pulse Oximetry Is Insufficient for Timely Diagnosis of Hepatopulmonary Syndrome in Children with Liver CirrhosisIn: Transplant International Jg. 26 (2013) Nr. Suppl. 1, S. 52 - 52Online Volltext: dx.doi.org/
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M.Pompe im Kindesalter : Aktueller Stand der Diagnostik und TherapieIn: Monatsschrift Kinderheilkunde Jg. 160 (2012) Nr. 12, S. 1243 - 1248Online Volltext: dx.doi.org/
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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 - 1120Online Volltext: dx.doi.org/
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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 - S7Online Volltext: dx.doi.org/ -
Treatment of Duchenne muscular dystrophy with ciclosporin A : a randomised, double-blind, placebo-controlled multicentre trialIn: The Lancet Neurology Jg. 9 (2010) Nr. 11, S. 1053 - 1059Online Volltext: dx.doi.org/
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Acute changes of coagulation and fibrinolysis parameters after experimental thromboembolic stroke and thrombolytic therapyIn: Neuroscience letters Jg. 441 (2008) Nr. 1, S. 39 - 43Online Volltext: dx.doi.org/
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Schwache Atmung – schwaches Herz : Atemmuskelversagen und Kardiomyopathie bei neuromuskulären ErkrankungenIn: Nervenheilkunde Jg. 27 (2008) Nr. 4, S. 284 - 291Online Volltext: dx.doi.org/
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Inhalation of Moli1901 in patients with cystic fibrosisIn: Chest Jg. 131 (2007) Nr. 5, S. 1461 - 1466Online Volltext: dx.doi.org/
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Nasal nitric oxide to diagnose primary ciliary dyskinesia in newbornsIn: Archives of disease in childhood/ Fetal and Neonatal Jg. 91 (2006) Nr. 3, S. F233Online Volltext: dx.doi.org/
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Novel nuclear encoded autosomal recessive mitochondriopathyIn: Neuromuscular disorders Jg. 16 (2006) Nr. 9-10, S. 660Online Volltext: dx.doi.org/
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Respiratory failure in Pompe disease : treatment with noninvasive ventilationIn: Neurology Jg. 64 (2005) Nr. 8, S. 1465 - 1467Online Volltext: dx.doi.org/
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Sleep disordered breathing in spinal muscular atrophyIn: Neuromuscular Disorders Jg. 14 (2004) Nr. 12, S. 797 - 803Online Volltext: dx.doi.org/
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Long-term safety and efficacy of Elexacaftor/ tezacaftor/ivacaftor in children aged=2 years with cystic fibrosisIn: Respirology Jg. 29 (2024) Nr. Suppl. 2, S. 16
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Epidemiological Trends in Nontuberculous Mycobacterial Infection among People with Cystic Fibrosis in Germany
International Congress of the European Respiratory Society (ERS) 2023 ; 9 - 13 September 2023, Milan, Italy,In: European Respiratory Journal (ERJ) Jg. 62 (2023) Nr. Supplement 67: ERS International Congress 2023 abstracts, PA2164Online Volltext: dx.doi.org/ -
Epidemiologische Trends bei Infektionen mit nichttuberkulösen Mykobakterien bei Patienten mit Mukoviszidose in DeutschlandIn: Klinische Pädiatrie Jg. 235 (2023) Nr. 02, S. 118Online Volltext: dx.doi.org/
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Hydroxychloroquin bei kindlichen interstitiellen Lungenerkrankungen – Ergebnisse einer randomisierten Phase 2 Studie
63. Kongress der Deutschen Gesellschaft für Pneumologie und Beatmungsmedizin e. V.,In: Pneumologie Jg. 77 (2023) Nr. S 01, S. S20Online Volltext: dx.doi.org/ -
The effect of nutritional parameters on the prognosis of childhood interstitial lung diseases
International Congress of the European Respiratory Society (ERS) 2023 ; 9 - 13 September 2023, Milan, Italy,In: European Respiratory Journal (ERJ) Jg. 62 (2023) Nr. Supplement 67: ERS International Congress 2023 abstracts, OA2507Online Volltext: dx.doi.org/ Online Volltext (Open Access) -
Fate or missed opportunities - challenges in diagnosing paediatric drug resistant tuberculosis in GermanyIn: European Respiratory Journal (ERJ) Jg. 58 (2021) Nr. Suppl. 65, PA3149Online Volltext: dx.doi.org/
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Homozygous WASHC4 variant in two sisters causes a syndromic phenotype with skeletal muscle involvement
26th International Congress of the World Muscle Society; 20th– 24th September 2021,In: Neuromuscular Disorders Jg. 31 (2021) Nr. Supplement 1, S. S143Online Volltext: dx.doi.org/ -
Species-specific Interferon-Gamma Release Assay for the diagnosis of Mycobacterium abscessus complex infection in Cystic Fibrosis patientsIn: European Respiratory Journal (ERJ) Jg. 58 (2021) Nr. Suppl. 65, PA1017Online Volltext: dx.doi.org/
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Assessment of fibrosis in lung biopsies from the European childhood interstitial lung disease (chILD) registryIn: European Respiratory Journal (ERJ) Jg. 56 (2020) Nr. Suppl. 64,Online Volltext: dx.doi.org/
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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) Jg. 54 (2019) Nr. Suppl. 63, S. PA4045Online Volltext: dx.doi.org/
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Psychossocial and spiritual needs in Cystic Fibrosis patientsIn: European Respiratory Journal (ERJ) Jg. 54 (2019) Nr. Suppl. 63, S. PA4524Online Volltext: dx.doi.org/
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Changes In Actigraphy-Measured Habitual Activity And Sleep Parameters During A Partially Supervised Exercise Program For Adult CF Patients
32nd Annual North American Cystic Fibrosis Conference, 18-20 October 2018, Denver, USA,In: Pediatric Pulmonology Jg. 53 (2018) Nr. Supplement 2, S. 344Online Volltext: dx.doi.org/ (Open Access) -
Myasthenic symptoms : From initial presentation to diagnosisIn: Neuromuscular Disorders / 17th International Congress of The World Muscle Society Jg. 22 (2012) Nr. 9-10, S. 856Online Volltext: dx.doi.org/
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Percent predicted forced vital capacity is a viable outcome measure in Laminin alpha 2 – Deficient congenital muscular dystrophyIn: Neuromuscular Disorders / 17th International Congress of The World Muscle Society Jg. 22 (2012) Nr. 9-10, S. 893 - 894Online Volltext: dx.doi.org/
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Novel nuclear encoded autosomal recessive mitochondriopathyIn: Neuromuscular Disorders Jg. 16 (2006) Nr. 9-10, S. 660 - 660
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Intermittent positive pressure breathing (IPPB) improves peak cough flow in pediatric neuromuscular disordersIn: Neuromuscular Disorders Jg. 14 (2004) Nr. 8-9, S. 598 - 598
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Cystic fibrosis and non-CF bronchiectasis : Cystic fibrosisIn: Bronchoalveolar Lavage in Basic Research and Clinical Medicine / Schildgen, Oliver; Schildgen, Verena; Brockmann, Michael (Hrsg.) 2023, S. 112 - 117Online Volltext: dx.doi.org/
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Eine kumulative Habilitationsschrift über Untersuchungen zum chronischen Atemversagen bei Kindern mit neuromuskolären ErkrankungenDuisburg ; Essen (2017) 1 CD-ROM
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Auswirkungen der rt-PA-Therapie beim experimentellen Schlaganfall der Ratte auf das Gerinnungs- und Fibrinolysesystem sowie intrazerebrale BlutungenDuisburg-Essen (2004) 114 Bl. : Ill., graph. Darst.
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Description of Care Standards, Health Resource Utilization and Treatment Decisions in LUM/IVA-treated Patients with Cystic Fibrosis in Germany and Austria : Interim Analysis Results of the DECIDE non-interventional Study
44. Jahrestagung der Gesellschaft für Pädiatrische Pneumologie, 16.–18.03.2023 , Frankfurt, Germany,In: Klinische Pädiatrie Jg. 235 (2023) Nr. 02, S. 119 - 120Online Volltext: dx.doi.org/ Online Volltext -
Körperliche Aktivität und motorische Leistungsfähigkeit bei Kindern mit Cystischer Fibrose : verbessern sie sich unter der Therapie mit Elexacaftor-Tezacaftor-Ivacaftor
43. Jahrestagung der Gesellschaft für Pädiatrische Pneumologie ; 28.–30. September 2022, Bern, Switzerland,In: Klinische Pädiatrie Jg. 234 (2022) Nr. 5, S. 338Online Volltext: dx.doi.org/