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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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ABCA3 -related interstitial lung disease beyond infancyIn: Thorax (2023)ISSN: 0040-6376; 1468-3296Online 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,ISSN: 2312-0541Online 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 - 39ISSN: 1878-3511; 1201-9712Online 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 (2023) in pressISSN: 1432-1076; 0340-6199Online Volltext: dx.doi.org/
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Acute exacerbations in children’s interstitial lung diseaseIn: Thorax Jg. 77 (2022) Nr. 8, S. 799 - 804ISSN: 0040-6376; 1468-3296Online 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,ISSN: 1660-4601; 1661-7827Online 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,ISSN: 1471-2334Online Volltext: dx.doi.org/ (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,ISSN: 1477-7525Online Volltext: dx.doi.org/ (Open Access)
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ERS statement on paediatric long-term noninvasive respiratory supportIn: European Respiratory Journal (ERJ) Jg. 59 (2022) Nr. 6,ISSN: 0903-1936; 1399-3003Online 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 (2022) in pressISSN: 1423-0356; 0025-7931; 0368-9220Online 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,ISSN: 1660-4601; 1661-7827Online 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 - 1369ISSN: 1073-449X; 1535-4970Online 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 - 107ISSN: 1096-9896; 0022-3417; 0368-3494Online 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 - 2052ISSN: 1099-0496; 8755-6863Online 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,ISSN: 1471-2466Online 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,ISSN: 1471-2466Online Volltext: dx.doi.org/ (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,ISSN: 2768-6698; 2768-6701; 1093-4715; 1093-9946Online 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,ISSN: 1471-2466Online Volltext: dx.doi.org/ (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)ISSN: 1664-3224Online 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,ISSN: 1750-1172Online Volltext: dx.doi.org/ (Open Access)
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Von respiratorischer Technologie abhängige KinderIn: Der Pneumologe Jg. 19 (2022) Nr. 3, S. 175 - 185ISSN: 1613-6055; 1613-5636Online 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. 199ISSN: 1873-734X; 1010-7940; 1567-4258; 1878-3309Online Volltext: dx.doi.org/ (Open Access)
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Allergien und schweres AsthmaIn: Der Pneumologe Jg. 18 (2021) Nr. 6, S. 366 - 377ISSN: 1613-6055; 1613-5636Online 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 - 615ISSN: 1520-9512; 1522-1709Online Volltext: dx.doi.org/ (Open Access)
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Bronchoskopische Fremdkörperextraktion - Schritt für SchrittIn: Pneumologie Jg. 75 (2021) Nr. 9, S. 651 - 656ISSN: 0934-8387; 1438-8790Online 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,ISSN: 2052-4439Online 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 - 1275ISSN: 1099-0496; 8755-6863Online 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 - 902ISSN: 1610-0387; 1563-2571; 1610-0379; 0301-0481Online 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 - 2116ISSN: 1558-688X; 0031-5125Online 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 - 415ISSN: 1943-3654; 0020-1324Online 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 - 2633ISSN: 1099-0496; 8755-6863Online 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 - 235ISSN: 0026-9298; 1433-0474Online Volltext: dx.doi.org/
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Mukoviszidose und Transition ins ErwachsenenalterIn: Der Pneumologe Jg. 18 (2021) Nr. 2, S. 97 - 103ISSN: 1613-6055; 1613-5636Online 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 - 91ISSN: 1532-2130; 1090-3798Online 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 - 1229ISSN: 1099-0496; 8755-6863Online Volltext: dx.doi.org/ (Open Access)
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Skin fragility, renal malformation and interstitial lung disease due to compound heterozygous ITGA3 mutationsIn: JDDG - Journal of the German Society of Dermatology (2021) in pressISSN: 1610-0387; 1610-0379Online 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)ISSN: 1664-302XOnline 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) S. 5581812ISSN: 2090-1844; 2090-1836Online 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 - 779ISSN: 0375-4685; 0340-2592; 1433-0563Online 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 - 61ISSN: 0300-8630; 1439-3824Online 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 - 3380ISSN: 1099-0496; 8755-6863Online 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. e79ISSN: 0003-4975; 1552-6259Online 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 - 216ISSN: 1539-3704Online 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 - 18ISSN: 1874-3064Online 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. 132ISSN: 1471-2466Online 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: ERS Monograph Jg. 5 (2019) Nr. 3, S. 00149 - 02018ISSN: 2312-0541; 2312-508XOnline Volltext: dx.doi.org/ Online Volltext (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 - 250ISSN: 1439-3824; 0300-8630Online 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)ISSN: 1664-8021Online 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. S137ISSN: 0960-8966Online 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 - 2053ISSN: 0305-7453; 1460-2091Online Volltext: dx.doi.org/ (Open Access)
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Pulmonary interstitial Glycogenosis – a systematic analysis of new casesIn: European Respiratory Journal Jg. 52 (2018) Nr. Suppl. 62, S. OA3787ISSN: 0903-1936; 1399-3003Online Volltext: dx.doi.org/
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Pulmonary interstitial glycogenosis – A systematic analysis of new casesIn: Respiratory Medicine Jg. 140 (2018) S. 11 - 20ISSN: 1532-3064; 0954-6111Online 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. 96ISSN: 1471-2466Online 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 - 631ISSN: 1099-0496; 8755-6863Online 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) S. 2602653ISSN: 2090-1844; 2090-1836Online 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. 1036ISSN: 1440-1843; 1323-7799Online 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 - 18ISSN: 1389-9457; 1878-5506Online 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 - 379ISSN: 0174-304X; 0077-7811; 0028-3797; 1439-1899Online 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 - 1291ISSN: 1440-1843; 1323-7799Online 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 - 1263ISSN: 1943-3654; 0098-9142Online 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 - 35ISSN: 1479-9723; 1479-9731Online 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 - 1981ISSN: 0967-3334; 0143-0815; 1361-6579Online 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.e2ISSN: 1097-6833; 0022-3476Online 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 Jg. 42 (2013) Nr. Suppl. 57, S. 4473ISSN: 0903-1936; 1399-3003
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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 - 654ISSN: 1873-5010; 1569-1993Online 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 - 52ISSN: 0934-0874; 1432-2277Online 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 - 1248ISSN: 0026-9298; 1433-0474Online 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 - 1120ISSN: 1099-0496; 8755-6863Online 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 - S7ISSN: 0300-8630Online 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 - 1059ISSN: 1474-4422Online 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 - 43ISSN: 0304-3940; 1872-7972Online 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 - 291ISSN: 0722-1541; 2567-5788Online Volltext: dx.doi.org/
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Inhalation of Moli1901 in patients with cystic fibrosisIn: Chest Jg. 131 (2007) Nr. 5, S. 1461 - 1466ISSN: 1931-3543; 0012-3692Online 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. F233ISSN: 1359-2998; 1468-2052Online Volltext: dx.doi.org/
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Novel nuclear encoded autosomal recessive mitochondriopathyIn: Neuromuscular disorders Jg. 16 (2006) Nr. 9-10, S. 660ISSN: 0960-8966; 1873-2364Online 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 - 1467ISSN: 0028-3878; 1526-632XOnline Volltext: dx.doi.org/
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Sleep disordered breathing in spinal muscular atrophyIn: Neuromuscular Disorders Jg. 14 (2004) Nr. 12, S. 797 - 803ISSN: 0960-8966; 1873-2364Online Volltext: dx.doi.org/
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EP.305 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) S. S143ISSN: 0960-8966; 1873-2364Online Volltext: dx.doi.org/ -
Fate or missed opportunities - challenges in diagnosing paediatric drug resistant tuberculosis in GermanyIn: European Respiratory Journal (ERJ) Jg. 58 (2021) Nr. Suppl. 65,ISSN: 0903-1936; 1399-3003Online Volltext: dx.doi.org/
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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) Jg. 58 (2021) Nr. Suppl. 65,ISSN: 0903-1936; 1399-3003Online 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 Jg. 56 (2020) Nr. Suppl. 64,ISSN: 1399-3003; 0903-1936Online 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 Jg. 54 (2019) Nr. Suppl. 63, S. PA4045ISSN: 0903-1936; 1399-3003Online Volltext: dx.doi.org/
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Psychossocial and spiritual needs in Cystic Fibrosis patientsIn: European Respiratory Journal Jg. 54 (2019) Nr. Suppl. 63, S. PA4524ISSN: 0903-1936; 1399-3003Online 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. 344ISSN: 1099-0496; 8755-6863Online 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. 856ISSN: 0960-8966Online 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 - 894ISSN: 0960-8966Online Volltext: dx.doi.org/
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Novel nuclear encoded autosomal recessive mitochondriopathyIn: Neuromuscular Disorders Jg. 16 (2006) Nr. 9-10, S. 660 - 660ISSN: 0960-8966
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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 - 598ISSN: 0960-8966
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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.