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Wim Wuyts

Showing results (41-50 of 135) with videos related to

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Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|June 2, 2020
Predominant dendriform pulmonary ossification in a usual interstitial pneumonia-like distribution: to be distinguished from idiopathic pulmonary fibrosisHans Slabbynck, Tom de Beukelaar, Didier De Surgeloose, et al.
American Journal of Medical Genetics|November 29, 2002
Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletionWim Wuyts, Dominique Roland, Hermann-Josef Lüdecke, et al.
Clinical Chemistry|May 8, 2004
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmiasAlessia Bagattin, Caterina Veronese, Barbara Bauce, et al.
Plos One|November 21, 2022
Physical activity pattern of patients with interstitial lung disease compared to patients with COPD: A propensity-matched studySofie Breuls, Cintia Pereira de Araujo, Astrid Blondeel, et al.
Genes|January 21, 2023
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?Thomas Clabout, Laurence Maes, Frederic Acke, et al.
Audiology & Neuro-Otology|September 3, 2020
A New Pathogenic Variant in the TRIOBP Associated with Profound Deafness Is Remediable with Cochlear ImplantationAhmet M Tekin, Geert de Ceulaer, Paul Govaerts, et al.
Respiratory Medicine|May 5, 2018
Sildenafil added to pirfenidone in patients with advanced idiopathic pulmonary fibrosis and risk of pulmonary hypertension: A Phase IIb, randomised, double-blind, placebo-controlled study - Rationale and study designJürgen Behr, Steven D Nathan, Sergio Harari, et al.
Acta Clinica Belgica|March 7, 2025
Interleukin 6 inhibition in refractory antisynthetase syndrome: case-based literature reviewAnna Driesen, Jean-Baptiste Vulsteke, Luk Corluy, et al.
Clinical Dysmorphology|September 6, 2007
A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and reviewWinnie Courtens, Jan Wauters, Marek Wojciechowski, et al.
European Journal of Medical Genetics|February 21, 2006
A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and reviewWinnie Courtens, Wim Wuyts, Stefaan Scheers, et al.
Pageof 14

Showing results (41-50 of 135) with videos related to

Sort By:
Pageof 14
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG|June 2, 2020
Predominant dendriform pulmonary ossification in a usual interstitial pneumonia-like distribution: to be distinguished from idiopathic pulmonary fibrosisHans Slabbynck, Tom de Beukelaar, Didier De Surgeloose, et al.
American Journal of Medical Genetics|November 29, 2002
Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletionWim Wuyts, Dominique Roland, Hermann-Josef Lüdecke, et al.
Clinical Chemistry|May 8, 2004
Denaturing HPLC-based approach for detecting RYR2 mutations involved in malignant arrhythmiasAlessia Bagattin, Caterina Veronese, Barbara Bauce, et al.
Plos One|November 21, 2022
Physical activity pattern of patients with interstitial lung disease compared to patients with COPD: A propensity-matched studySofie Breuls, Cintia Pereira de Araujo, Astrid Blondeel, et al.
Genes|January 21, 2023
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?Thomas Clabout, Laurence Maes, Frederic Acke, et al.
Audiology & Neuro-Otology|September 3, 2020
A New Pathogenic Variant in the TRIOBP Associated with Profound Deafness Is Remediable with Cochlear ImplantationAhmet M Tekin, Geert de Ceulaer, Paul Govaerts, et al.
Respiratory Medicine|May 5, 2018
Sildenafil added to pirfenidone in patients with advanced idiopathic pulmonary fibrosis and risk of pulmonary hypertension: A Phase IIb, randomised, double-blind, placebo-controlled study - Rationale and study designJürgen Behr, Steven D Nathan, Sergio Harari, et al.
Acta Clinica Belgica|March 7, 2025
Interleukin 6 inhibition in refractory antisynthetase syndrome: case-based literature reviewAnna Driesen, Jean-Baptiste Vulsteke, Luk Corluy, et al.
Clinical Dysmorphology|September 6, 2007
A de novo subtelomeric monosomy 11q (11q24.2-qter) and trisomy 20q (20q13.3-qter) in a girl with findings compatible with Jacobsen syndrome: case report and reviewWinnie Courtens, Jan Wauters, Marek Wojciechowski, et al.
European Journal of Medical Genetics|February 21, 2006
A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and reviewWinnie Courtens, Wim Wuyts, Stefaan Scheers, et al.
Pageof 14