Որոնման արդյունքները - Wim Wuyts
- Ցուցադրվում են 1 - 20 արդյունքները 92
- Գնացեք Հաջորդ էջ
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Positional cloning of a gene involved in hereditary multiple exostoses Wim Wuyts
Հրապարակվել է 1996Artigo -
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Management of Fibrosing Interstitial Lung Diseases Toby M. Maher, Wim Wuyts
Հրապարակվել է 2019Revisão -
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First Data on Efficacy and Safety of Nintedanib in Patients with Idiopathic Pulmonary Fibrosis and Forced Vital Capacity of ≤50 % of Predicted Value Wim Wuyts, Martin Kolb, Susanne Stowasser, Wibke Stansen, John T. Huggins, Ganesh Raghu
Հրապարակվել է 2016Artigo -
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Short and long-term effects of pulmonary rehabilitation in interstitial lung diseases: a randomised controlled trial Silvia Perez‐Bogerd, Wim Wuyts, Veronica Barbier, Heleen Demeyer, Alain Van Muylem, Wim Janssens, Thierry Troosters
Հրապարակվել է 2018Artigo -
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Effects of Corticosteroid Treatment and Antigen Avoidance in a Large Hypersensitivity Pneumonitis Cohort: A Single-Centre Cohort Study Laurens De Sadeleer, Frederik Hermans, Els De Dycker, Jonas Yserbyt, Johny Verschakelen, Eric Verbeken, Geert M. Verleden, Wim Wuyts
Հրապարակվել է 2018Artigo -
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Physical activity pattern of patients with interstitial lung disease compared to patients with COPD: A propensity-matched study Sofie Breuls, Cintia Laura Pereira de Araújo, Astrid Blondeel, Jonas Yserbyt, Wim Janssens, Wim Wuyts, Thierry Troosters, Heleen Demeyer
Հրապարակվել է 2022Artigo -
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Tiling resolution array-CGH shows that somatic mosaic deletion of the EXT gene is causative in EXT gene mutation negative multiple osteochondromas patients Károly Szuhai, Ivy Jennes, Daniëlle de Jong, Judith V.M.G. Bovée, Małgorzata Wiweger, Wim Wuyts, Pancras C.W. Hogendoorn
Հրապարակվել է 2010Artigo -
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Multiple osteochondromas: mutation update and description of the multiple osteochondromas mutation database (MOdb) Ivy Jennes, Elena Pedrini, Monia Zuntini, Marina Mordenti, Sahila Balkassmi, Carla Asteggiano, Brett Casey, Egbert Bakker, Luca Sangiorgi, Wim Wuyts
Հրապարակվել է 2009Revisão -
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Two-color multiplex ligation-dependent probe amplification: Detecting genomic rearrangements in hereditary multiple exostoses Stefan J. White, Geraldine R. Vink, Marjolein Kriek, Wim Wuyts, Jan Schouten, Egbert Bakker, Martijn H. Breuning, Johan T. den Dunnen
Հրապարակվել է 2004Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Medicine
Internal medicine
Lung
Biology
Pathology
Idiopathic pulmonary fibrosis
Genetics
Gene
Pulmonary fibrosis
Intensive care medicine
Fibrosis
Mutation
Disease
Interstitial lung disease
Lung function
Diffusing capacity
Nintedanib
Phenotype
Physical therapy
Vital capacity
Alternative medicine
Immunology
Nursing
Placebo
Pulmonary function testing
Quality of life (healthcare)
Clinical trial
Hereditary multiple exostoses
Biochemistry
Cell biology