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1. Full Text Short and long-term effects of pulmonary rehabilitation in interstitial lung diseases: A randomised controlled trial
by Perez-Bogerd, Silvia and Wuyts, Wim and Barbier, Veronica and Demeyer, Heleen and Van Muylem, Alain and Janssens, Wim and Troosters, Thierry
Respiratory research, ISSN 1465-9921, 09/2018, Volume 19, Issue 1, pp. 182 - 182
Life Sciences & Biomedicine | Respiratory System | Science & Technology | Humans | Middle Aged | Male | Treatment Outcome | Lung Diseases, Interstitial - diagnosis | Time Factors | Lung Diseases, Interstitial - rehabilitation | Outpatient Clinics, Hospital - trends | Exercise Tolerance - physiology | Female | Aged | Exercise - physiology | Lung Diseases, Interstitial - physiopathology | Usage | Lung diseases, Interstitial | Care and treatment | Exercise | Research | Health aspects | Index Medicus
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2. Full Text Multiplex protein profiling of bronchoalveolar lavage in idiopathic pulmonary fibrosis and hypersensitivity pneumonitis
by Stijn, Willems and Verleden Stijn, E and Vanaudenaerde Bart, M and Marijke, Wynants and Christophe, Dooms and Jonas, Yserbyt and Jana, Somers and Verbeken Eric, K and Verleden Geert, M and Wuyts Wim, A
Annals of thoracic medicine, ISSN 1817-1737, 01/2013, Volume 8, Issue 1, pp. 38 - 45
idiopathic pulmonary fibrosis | Bronchoalveolar lavage | hypersensitivity pneumonitis | interstitial lung disease | enzyme-linked immunosorbent assay | Cardiac & Cardiovascular Systems | Respiratory System | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Bronchoscopy | Care and treatment | Usage | Pulmonary fibrosis | Hypersensitivity pneumonitis | Diagnosis | Research | Health aspects | Risk factors | Proteins | Angiogenesis | Lungs | Disease | Rodents | Family medical history | Patients | Alveoli | Original
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3. Full Text Erratum to: “Differential diagnosis of usual interstitial pneumonia: when is it truly idiopathic?” Wim A. Wuyts, Alberto Cavazza, Giulio Rossi, Francesco Bonella, Nicola Sverzellati and Paolo Spagnolo. Eur Respir Rev 2014; 23: 308–319
European respiratory review, ISSN 0905-9180, 12/2014, Volume 23, Issue 134, p. 537
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4. Gastro-oesophageal reflux and idiopathic pulmonary fibrosis: In search of evidence
by Wuyts, Wim and Crestani, Bruno
The European respiratory journal, ISSN 0903-1936, 09/2016, Volume 48, Issue 3, pp. 623 - 625
Life Sciences & Biomedicine | Respiratory System | Science & Technology
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5. Full Text Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease
by Hocking, LJ and Lucas, GJA and Daroszewska, A and Mangion, J and Olavesen, M and Cundy, T and Nicholson, GC and Ward, L and Bennett, ST and Wuyts, W and Van Hul, W and Ralston, SH
Human molecular genetics, ISSN 0964-6906, 10/2002, Volume 11, Issue 22, pp. 2735 - 2739
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Osteoporosis. Osteomalacia. Paget disease | General aspects. Genetic counseling | Biological and medical sciences | Medical sciences | Diseases of the osteoarticular system | Medical genetics | Protein Structure, Tertiary | Sequestosome-1 Protein | Humans | Middle Aged | Ubiquitin - metabolism | Osteitis Deformans - metabolism | Male | Binding Sites - genetics | Case-Control Studies | Osteitis Deformans - genetics | DNA - genetics | Proteins | Carrier Proteins - genetics | Adaptor Proteins, Signal Transducing | Carrier Proteins - metabolism | DNA Mutational Analysis | Base Sequence | Carrier Proteins - chemistry | Female | Aged | Mutation | Index Medicus
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6. Insights into idiopathic pulmonary fibrosis in the real world
by Cottin, Vincent and Wuyts, Wim
The European respiratory journal, ISSN 0903-1936, 07/2015, Volume 46, Issue 1, pp. 16 - 18
Life Sciences & Biomedicine | Respiratory System | Science & Technology | Idiopathic Pulmonary Fibrosis - therapy | Female | Male | Idiopathic Pulmonary Fibrosis - physiopathology | Humans
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7. Full Text Management of Fibrosing Interstitial Lung Diseases
by Maher, Toby M and Wuyts, Wim
Advances in therapy, ISSN 0741-238X, 07/2019, Volume 36, Issue 7, pp. 1518 - 1531
Pharmacology & Pharmacy | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Autoimmune Diseases - physiopathology | Lung Diseases, Interstitial - immunology | Lung Diseases, Interstitial - therapy | Humans | Autoimmune Diseases - complications | Pulmonary Fibrosis - prevention & control | Autoimmune Diseases - therapy | Respiratory Function Tests | Lung Diseases, Interstitial - complications | Immunosuppressive Agents - pharmacology | Disease Progression | Pulmonary Fibrosis - etiology | Medical research | Hospitals | Systemic scleroderma | Collagen | Lung diseases | Immunotherapy | Mortality | Scleroderma (Disease) | Medicine, Experimental | Drug approval | Immunosuppressive agents | Health technology assessment | Immunosuppression | Treatment | Collagen diseases | Rheumatic diseases | Respiratory | Review | Interstitial lung disease
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8. Full Text Nintedanib with add-on pirfenidone in idiopathic pulmonary fibrosis: Results of the INJOURNEY trial
by Vancheri, Carlo and Kreuter, Michael and Richeldi, Luca and Ryerson, Christopher J and Valeyre, Dominique and Grutters, Jan C and Wiebe, Sabrina and Stansen, Wibke and Quaresma, Manuel and Stowasser, Susanne and Wuyts, Wim A and INJOURNEY Trial Investigators
American journal of respiratory and critical care medicine, ISSN 1073-449X, 02/2018, Volume 197, Issue 3, pp. 356 - 363
Clinical trial | The destruction of the lung architecture | Myofibroblasts | Drug therapy | Interstitial lung diseases | Resulting in excessive deposition of extracellular matrix | Respiratory System | Life Sciences & Biomedicine | Critical Care Medicine | General & Internal Medicine | Science & Technology | Severity of Illness Index | Drug Administration Schedule | Follow-Up Studies | Risk Assessment | Humans | Middle Aged | Male | Survival Rate | Treatment Outcome | Disease Progression | Dose-Response Relationship, Drug | Idiopathic Pulmonary Fibrosis - diagnosis | Idiopathic Pulmonary Fibrosis - mortality | Patient Safety | Female | Indoles - therapeutic use | Aged | Pyridones - therapeutic use | Drug Therapy, Combination | Idiopathic Pulmonary Fibrosis - drug therapy | Studies | Pulmonary fibrosis | Disease | Clinical trials | Fibroblasts | Clinical medicine | Drug dosages | Index Medicus | Abridged Index Medicus
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9. Full Text Effect of pirfenidone in patients with more advanced idiopathic pulmonary fibrosis
by Costabel, Ulrich and Albera, Carlo and Glassberg, Marilyn K and Lancaster, Lisa H and Wuyts, Wim A and Petzinger, Ute and Gilberg, Frank and Kirchgaessler, Klaus-Uwe and Noble, Paul W
Respiratory research, ISSN 1465-9921, 03/2019, Volume 20, Issue 1, pp. 55 - 55
Antifibrotic | Advanced disease | Lung function | Pirfenidone | Idiopathic pulmonary fibrosis | Life Sciences & Biomedicine | Respiratory System | Science & Technology | Drug therapy | Patient outcomes | Pulmonary fibrosis | Medical research | Respiratory function | Medical treatment | Lung diseases | Clinical trials | Patients | Subgroups | Quality of life | Medicine | Medical prognosis | Fibrosis | Clinical medicine | Safety | Index Medicus | Letter to the Editor
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10. Full Text First Data on Efficacy and Safety of Nintedanib in Patients with Idiopathic Pulmonary Fibrosis and Forced Vital Capacity of ≤50 % of Predicted Value
by Wuyts, Wim A and Kolb, Martin and Stowasser, Susanne and Stansen, Wibke and Huggins, John T and Raghu, Ganesh
Lung, ISSN 0341-2040, 10/2016, Volume 194, Issue 5, pp. 739 - 743
Tyrosine kinase | Clinical trial | Pneumology/Respiratory System | Medicine & Public Health | Interstitial lung diseases | Disease progression | Enzyme Inhibitors - adverse effects | Dyspnea - chemically induced | Humans | Middle Aged | Male | Diarrhea - chemically induced | Enzyme Inhibitors - therapeutic use | Disease Progression | Vital Capacity - drug effects | Indoles - adverse effects | Female | Indoles - therapeutic use | Aged | Idiopathic Pulmonary Fibrosis - physiopathology | Idiopathic Pulmonary Fibrosis - drug therapy | Pulmonary fibrosis | Research | Drug therapy | Patient outcomes | Vital signs | Product safety | Index Medicus
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11. Full Text The aging lung : tissue telomere shortening in health and disease
by Everaerts, Stephanie and Lammertyn, Elise J and Martens, es S and De Sadeleer, Laurens J and Maes, Karen and van Batenburg, Aernoud A and Goldschmeding, Roel and van Moorsel, Coline H M and Dupont, Lieven J and Wuyts, Wim A and Vos, Robin and Gayan-Ramirez, Ghislaine and Kaminski, Naftali and Hogg, James C and Janssens, Wim and Verleden, Geert M and Nawrot, Tim S and Verleden, Stijn E and McDonough, John E and Vanaudenaerde, Bart M
Respiratory research, ISSN 1465-9921, 05/2018, Volume 19, Issue 1, pp. 95 - 95
Chronic hypersensitivity pneumonitis | RAS | Middle Aged | BOS | Cellular senescence | Cystic fibrosis | Male | Chronic lungallograft dysfunction | Telomere length | Lung Diseases/genetics | Journal Article | Telomere Shortening/physiology | Young Adult | Research Support, Non-U.S. Gov't | Chronic obstructive pulmonary disease | Chronic lung allograft dysfunction | Life Sciences & Biomedicine | Respiratory System | Science & Technology | Aging | Telomeres | Research | Lungs | Health aspects | Index Medicus
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12. Full Text Efficacy and safety of nintedanib in patients with advanced idiopathic pulmonary fibrosis
by Richeldi, Luca and Kolb, Martin and Jouneau, Stéphane and Wuyts, Wim A and Schinzel, Birgit and Stowasser, Susanne and Quaresma, Manuel and Raghu, Ganesh
BMC pulmonary medicine, ISSN 1471-2466, 01/2020, Volume 20, Issue 1, pp. 3 - 3
Clinical trial | Vital capacity | Interstitial lung diseases | Tyrosine kinase inhibitor | Life Sciences & Biomedicine | Respiratory System | Science & Technology | Index Medicus | Life Sciences | Medication | Human health and pathology | Pulmonology and respiratory tract | Pharmaceutical sciences
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13. Idiopathic pulmonary fibrosis: Time for greater expectations?
by Wuyts, Wim and Cottin, Vincent
The European respiratory journal, ISSN 0903-1936, 08/2018, Volume 52, Issue 2
Life Sciences & Biomedicine | Respiratory System | Science & Technology
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14. Full Text Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)
by Balemans, W and Ebeling, M and Patel, N and Van Hul, E and Olson, P and Dioszegi, M and Lacza, C and Wuyts, W and Van den Ende, J and Willems, P and Paes-Alves, AF and Hill, S and Bueno, M and Ramos, FJ and Tacconi, P and Dikkers, FG and Stratakis, C and Lindpaintner, K and Vickery, B and Foernzler, D and Van Hul, W
Human molecular genetics, ISSN 0964-6906, 03/2001, Volume 10, Issue 5, pp. 537 - 543
LOCALIZATION | TISSUE GROWTH-FACTOR | GENE | CHROMOSOME 17Q12-Q21 | DISEASE | SEQUENCE | BRCA1 | PHYSICAL MAP | UMCG Approved | REGION | FAMILY | Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Miscellaneous. Osteoarticular involvement in other diseases | Biological and medical sciences | Medical sciences | Diseases of the osteoarticular system | Amino Acid Sequence | Bone Density | Humans | RNA, Messenger - genetics | Molecular Sequence Data | Chromosome Mapping | Genetic Markers | Proteins - genetics | Sequence Homology, Amino Acid | Osteochondrodysplasias - physiopathology | Osteochondrodysplasias - genetics | Chromosomes, Human, Pair 17 | DNA Mutational Analysis | Base Sequence | Protein Conformation | Bone Morphogenetic Proteins | DNA, Complementary | Genetic Linkage | SOST gene | van Buchem disease | sclerosteosis | Index Medicus
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