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Wim Wuyts

University of Antwerp

127

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5872

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A New Pathogenic Variant in the TRIOBP Associated with Profound Deafness Is Remediable with Cochlear Implantation.

2020 Audiology and Neuro-otology
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Adams–Oliver syndrome caused by mutations of the EOGT gene

2019 American Journal of Medical Genetics Part A
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Nationwide survey of physicians' attitude and approach to the clinical evaluation of interstitial lung disease in Singapore

2018 European Respiratory Journal
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Elucidating the genetic architecture of Adams–Oliver syndrome in a large European cohort

2018 Human Mutation
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BAL cell transcriptome predicts survival in IPF and can be used to gauge and model treatment effects interfering with the TGF-beta pathway

2018 European Respiratory Journal
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Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment

2018 European Journal of Human Genetics
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Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children

2018 Otology & Neurotology
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EFFECT OF PIRFENIDONE ON EXERCISE CAPACITY AND DYSPNEA IN PATIENTS WITH IDIOPATHIC PULMONARY FIBROSIS (IPF) AND MORE ADVANCED LUNG FUNCTION IMPAIRMENT

2018 Chest
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Multiple Solid Organ Transplantation in Telomeropathy: Case Series and Literature Review

2018 Transplantation
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Reply to Rajchgot et al.: Combination Nintedanib and Pirfenidone for Treatment of Idiopathic Pulmonary Fibrosis

2018 American Journal of Respiratory and Critical Care Medicine
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