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Wim Wuyts

Showing results (81-90 of 135) with videos related to

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Respiratory Medicine|April 10, 2019
Serious adverse events in patients with idiopathic pulmonary fibrosis in the placebo arms of 6 clinical trialsWim Wuyts, Danielle Antin-Ozerkis, J Terrill Huggins, et al.
Genes, Chromosomes & Cancer|February 16, 2007
A combined analytical approach reveals novel EXT1/2 gene mutations in a large cohort of Italian multiple osteochondromas patientsEmanuela Signori, Emanuela Massi, Maria Giovanna Matera, et al.
Journal of Inherited Metabolic Disease|April 19, 2011
Clinical and molecular studies of EXT1/EXT2 in BulgariaMalina Kirilova Stancheva-Ivanova, Wim Wuyts, Els van Hul, et al.
Respiration; International Review of Thoracic Diseases|December 14, 2018
Nintedanib in Idiopathic Pulmonary Fibrosis: Practical Management Recommendations for Potential Adverse EventsElisabeth Bendstrup, Wim Wuyts, Tiago Alfaro, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society|December 23, 2018
Presentation, diagnosis and clinical course of the spectrum of progressive-fibrosing interstitial lung diseasesVincent Cottin, Nikhil A Hirani, David L Hotchkin, et al.
Human Mutation|January 16, 2007
GM1 gangliosidosis: molecular analysis of nine patients and development of an RT-PCR assay for GLB1 gene expression profilingAnna Caciotti, Maria Alice Donati, Elena Procopio, et al.
European Journal of Cancer (Oxford, England : 1990)|August 19, 2008
Microsatellite instability in sporadic colon carcinomas has no independent prognostic value in a Belgian study populationVanessa Deschoolmeester, Nancy Van Damme, Marc Baay, et al.
The Lancet. Respiratory Medicine|May 11, 2016
Safety and tolerability of acetylcysteine and pirfenidone combination therapy in idiopathic pulmonary fibrosis: a randomised, double-blind, placebo-controlled, phase 2 trialJürgen Behr, Elisabeth Bendstrup, Bruno Crestani, et al.
Human Molecular Genetics|October 11, 2002
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's diseaseLynne J Hocking, Gavin J A Lucas, Anna Daroszewska, et al.
The Journal of Molecular Diagnostics : JMD|March 26, 2017
Targeted Next-Generation Sequencing of 51 Genes Involved in Primary Electrical DiseaseDorien Proost, Johan Saenen, Geert Vandeweyer, et al.
Pageof 14

Showing results (81-90 of 135) with videos related to

Sort By:
Pageof 14
Respiratory Medicine|April 10, 2019
Serious adverse events in patients with idiopathic pulmonary fibrosis in the placebo arms of 6 clinical trialsWim Wuyts, Danielle Antin-Ozerkis, J Terrill Huggins, et al.
Genes, Chromosomes & Cancer|February 16, 2007
A combined analytical approach reveals novel EXT1/2 gene mutations in a large cohort of Italian multiple osteochondromas patientsEmanuela Signori, Emanuela Massi, Maria Giovanna Matera, et al.
Journal of Inherited Metabolic Disease|April 19, 2011
Clinical and molecular studies of EXT1/EXT2 in BulgariaMalina Kirilova Stancheva-Ivanova, Wim Wuyts, Els van Hul, et al.
Respiration; International Review of Thoracic Diseases|December 14, 2018
Nintedanib in Idiopathic Pulmonary Fibrosis: Practical Management Recommendations for Potential Adverse EventsElisabeth Bendstrup, Wim Wuyts, Tiago Alfaro, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society|December 23, 2018
Presentation, diagnosis and clinical course of the spectrum of progressive-fibrosing interstitial lung diseasesVincent Cottin, Nikhil A Hirani, David L Hotchkin, et al.
Human Mutation|January 16, 2007
GM1 gangliosidosis: molecular analysis of nine patients and development of an RT-PCR assay for GLB1 gene expression profilingAnna Caciotti, Maria Alice Donati, Elena Procopio, et al.
European Journal of Cancer (Oxford, England : 1990)|August 19, 2008
Microsatellite instability in sporadic colon carcinomas has no independent prognostic value in a Belgian study populationVanessa Deschoolmeester, Nancy Van Damme, Marc Baay, et al.
The Lancet. Respiratory Medicine|May 11, 2016
Safety and tolerability of acetylcysteine and pirfenidone combination therapy in idiopathic pulmonary fibrosis: a randomised, double-blind, placebo-controlled, phase 2 trialJürgen Behr, Elisabeth Bendstrup, Bruno Crestani, et al.
Human Molecular Genetics|October 11, 2002
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's diseaseLynne J Hocking, Gavin J A Lucas, Anna Daroszewska, et al.
The Journal of Molecular Diagnostics : JMD|March 26, 2017
Targeted Next-Generation Sequencing of 51 Genes Involved in Primary Electrical DiseaseDorien Proost, Johan Saenen, Geert Vandeweyer, et al.
Pageof 14