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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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Diagnostic Evaluation and Clinical Findings in Children With Persistent Tachypnea of Infancy/Neuroendocrine Cell Hyperplasia of Infancy : A European Multicenter Retrospective StudyIn: Chest, Jg. 168, 2025, Nr. 1, S. 171 – 182
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Elexacaftor/tezacaftor/ivacaftor in children aged ≥6 years with cystic fibrosis heterozygous for F508del and a minimal function mutation : Results from a 96-week open-label extension studyIn: European Respiratory Journal (ERJ), Jg. 66, 2025, Nr. 1, 2402435DOI (Open Access)
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Kinderpneumologische Aspekte bei der Betreuung von Kindern mit neuromuskulären Erkrankungen am Beispiel der Muskeldystrophie Typ DuchenneIn: Klinische Pädiatrie, Jg. 237, 2025, Nr. 2, S. 59 – 65
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Predictors of Physical Activity Enjoyment in Adults with Cystic Fibrosis : The Role of Quality of Life and Motivation ; A Single-Center StudyIn: Healthcare, Jg. 13, 2025, Nr. 17, 2194DOI (Open Access)
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Trigger issues with a life support device in childrenIn: Sleep Medicine, Jg. 131, 2025, 106534DOI (Open Access)
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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 – 86DOI (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 – 999DOI (Open Access)
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Heimbeatmung von Kindern und JugendlichenIn: Monatsschrift Kinderheilkunde, Jg. 172, 2024, Nr. 2, S. 138 – 147
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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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Neutrophilia in the bronchoalveolar lavage fluid increases coughing during flexible fiberoptic bronchoscopy in a pediatric cohortIn: Frontiers in Pediatrics, Jg. 12, 2024, 1347983DOI (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 – 63DOI (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, 5961DOI (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 – 258
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ABCA3 -related interstitial lung disease beyond infancyIn: Thorax, Jg. 78, 2023, Nr. 6, S. 587 – 595DOI (Open Access)
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Diffuse alveolar haemorrhage in children : An international multicentre studyIn: ERJ Open Research, Jg. 9, 2023, Nr. 2, 00733-2022DOI (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 – 39DOI (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, 190DOI, 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, 100690DOI (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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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 – 5179DOI (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 – 67DOI (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, 1176815DOI (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 – 3006
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Acute exacerbations in children’s interstitial lung diseaseIn: Thorax, Jg. 77, 2022, Nr. 8, S. 799 – 804DOI (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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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, 921DOI, 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, 141DOI, 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, 2101404DOI, 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 – 774
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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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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 – 1369DOI (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 – 789DOI (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 – 107DOI (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 – 2052DOI (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, 59DOI (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, 217DOI, 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, 302DOI, 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, 446DOI, 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, 1029423DOI (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, 289DOI (Open Access)
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Von respiratorischer Technologie abhängige KinderIn: Der Pneumologe, Jg. 19, 2022, Nr. 3, S. 175 – 185
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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. 199DOI (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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Bronchoskopische Fremdkörperextraktion - Schritt für SchrittIn: Pneumologie, Jg. 75, 2021, Nr. 9, S. 651 – 656
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Coil embolisation for massive haemoptysis in cystic fibrosisIn: BMJ Open Respiratory Research, Jg. 8, 2021, Nr. 1, e000985DOI (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 – 1275
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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 – 902DOI (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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Hypersensitivity pneumonitis : Lessons from a randomized controlled trial in childrenIn: Pediatric Pulmonology, Jg. 56, 2021, Nr. 8, S. 2627 – 2633DOI (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 – 235
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Mukoviszidose und Transition ins ErwachsenenalterIn: Der Pneumologe, Jg. 18, 2021, Nr. 2, S. 97 – 103
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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 – 91
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Sedation for bronchoscopy in children : A prospective randomized double-blinded trialIn: Pediatric Pulmonology, Jg. 56, 2021, Nr. 5, S. 1221 – 1229DOI (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 – 901DOI (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, 692395DOI, 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, 5581812DOI (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 – 779
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Diagnosis and Care of Infants and Children with Pompe DiseaseIn: Klinische Pädiatrie, Jg. 232, 2020, Nr. 02, S. 55 – 61
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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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Pleuropulmonary Blastoma Misinterpreted as Spontaneous Pneumothorax in an InfantIn: The Annals of Thoracic Surgery, Jg. 110, 2020, Nr. 1, S. e79DOI (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 – 216DOI, 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 – 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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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 – 02018DOI (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 – 250
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Genetic Diagnostic Elucidation of a Patient With Multiorgan Granulomas, Facial Peculiarities, and Psychomotor RetardationIn: Frontiers in Genetics, Jg. 9, 2018, 355DOI (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. S137
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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 – 2053DOI (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. OA3787
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Pulmonary interstitial glycogenosis – A systematic analysis of new casesIn: Respiratory Medicine, Jg. 140, 2018, S. 11 – 20DOI (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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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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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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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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Normal values for inspiratory muscle function in childrenIn: Physiological Measurement, Jg. 35, 2014, Nr. 10, S. 1975 – 1981DOI (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.e2
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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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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 – 52
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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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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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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 -
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 – 1059
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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 – 43
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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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Inhalation of Moli1901 in patients with cystic fibrosisIn: Chest, Jg. 131, 2007, Nr. 5, S. 1461 – 1466
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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. F233
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Novel nuclear encoded autosomal recessive mitochondriopathyIn: Neuromuscular disorders, Jg. 16, 2006, Nr. 9-10, S. 660
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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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Sleep disordered breathing in spinal muscular atrophyIn: Neuromuscular Disorders, Jg. 14, 2004, Nr. 12, S. 797 – 803
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Chiari-Malformation Typ 1 mit Kompression des zervikalen Myelons als Ursache für Laryngomalazie
46. Jahrestagung der Gesellschaft für Pädiatrische Pneumologie, 12.–15.03.2025, Leipzig, Germany,In: Klinische Pädiatrie. Stuttgart: Thieme, Jg. 237, 2025, Nr. 02, S. S7 – S7 -
Notfallmanagement bei Patienten mit chronisch respiratorischer Insuffizienz
34. Jahrestagung der Arbeitsgemeinschaft für Pädiatrische Pneumologie und Allergologie (APPA) e. V.; 23. – 24. Mai 2025, Jena,In: Allergologie. München-Deisenhofen: Dustri, Jg. 48, 2025, Nr. 05, S. 288 – 288 -
Long-term safety and efficacy of Elexacaftor/ tezacaftor/ivacaftor in children aged=2 years with cystic fibrosisIn: Respirology. Hoboken: Wiley-Blackwell - STM, Jg. 29, 2024, Nr. Suppl. 2, S. 16
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Beschreibung von Versorgungsstandards, Inanspruchnahme von Gesundheitsressourcen und Therapieentscheidungen bei LUM/IVA-behandelten Patienten mit Mukoviszidose in Deutschland und Österreich : Zwischenanalyseergebnisse der nicht-interventionellen Studie DECIDE
44. Jahrestagung der Gesellschaft für Pädiatrische Pneumologie, 16.–18.03.2023 , Frankfurt, Germany,In: Klinische Pädiatrie. Stuttgart: Thieme, Jg. 235, 2023, Nr. 02, S. 119 – 120 -
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). Sheffield: European Respiratory Society, Jg. 62, 2023, Nr. Supplement 67: ERS International Congress 2023 abstracts, PA2164 -
Epidemiologische Trends bei Infektionen mit nichttuberkulösen Mykobakterien bei Patienten mit Mukoviszidose in DeutschlandIn: Klinische Pädiatrie. Stuttgart: Thieme, Jg. 235, 2023, Nr. 02, S. 118
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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. Stuttgart: Thieme, Jg. 77, 2023, Nr. S 01, S. S20 -
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). Sheffield: European Respiratory Society, Jg. 62, 2023, Nr. Supplement 67: ERS International Congress 2023 abstracts, OA2507DOI, Online Volltext (Open Access) -
Fate or missed opportunities - challenges in diagnosing paediatric drug resistant tuberculosis in GermanyIn: European Respiratory Journal (ERJ). Sheffield: European Respiratory Society, Jg. 58, 2021, Nr. Suppl. 65, PA3149DOI (Open Access)
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Species-specific Interferon-Gamma Release Assay for the diagnosis of Mycobacterium abscessus complex infection in Cystic Fibrosis patientsIn: European Respiratory Journal (ERJ). Sheffield: European Respiratory Society, Jg. 58, 2021, Nr. Suppl. 65, PA1017DOI (Open Access)
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Assessment of fibrosis in lung biopsies from the European childhood interstitial lung disease (chILD) registryIn: European Respiratory Journal (ERJ). Sheffield: European Respiratory Society, Jg. 56, 2020, Nr. Suppl. 64DOI (Open Access)
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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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Psychossocial and spiritual needs in Cystic Fibrosis patientsIn: European Respiratory Journal (ERJ). Sheffield: European Respiratory Society, Jg. 54, 2019, Nr. Suppl. 63, S. PA4524DOI (Open Access)
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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. Hoboken: Wiley, Jg. 53, 2018, Nr. Supplement 2, S. 344DOI (Open Access) -
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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Percent predicted forced vital capacity is a viable outcome measure in Laminin alpha 2 – Deficient congenital muscular dystrophyIn: Neuromuscular Disorders. Amsterdam; Oxford; Frankfurt, M. [u.a.]: Elsevier, Jg. 22, 2012, Nr. 9-10, S. 893 – 894
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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 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 -
Cystic fibrosis and non-CF bronchiectasis : Cystic fibrosisIn: Bronchoalveolar Lavage in Basic Research and Clinical Medicine / Schildgen, Oliver; Schildgen, Verena; Brockmann, Michael (Hrsg.). Boca Raton: CRC Press, 2023, S. 112 – 117
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Eine kumulative Habilitationsschrift über Untersuchungen zum chronischen Atemversagen bei Kindern mit neuromuskolären ErkrankungenDuisburg ; Essen, 2017
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Auswirkungen der rt-PA-Therapie beim experimentellen Schlaganfall der Ratte auf das Gerinnungs- und Fibrinolysesystem sowie intrazerebrale BlutungenDuisburg-Essen, 2004
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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. Stuttgart: Thieme, Jg. 234, 2022, Nr. 5, S. 338 -
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, Virtual,In: Neuromuscular Disorders. Amsterdam; Oxford; Frankfurt, M. [u.a.]: Elsevier, Jg. 31, 2021, Nr. Supplement 1: 26th International Congress of the World Muscle Society; 20th– 24th September 2021, S. S143