Presentation, diagnosis and clinical course of the spectrum of progressive-fibrosing interstitial lung diseases

…, HK Poonyagariyagorn, W Wuyts… - European …, 2018 - Eur Respiratory Soc
… Conflict of interest: W. Wuyts reports receiving the following, outside the submitted work:
grants paid to his university from Boehringer Ingelheim and Hoffmann La Roche; and travel fees …

The pathogenesis of pulmonary fibrosis: a moving target

WA Wuyts, C Agostini, KM Antoniou… - European …, 2013 - Eur Respiratory Soc
… In a comprehensive review on mechanisms of fibrosis, Wynn and Ramalingam [76] suggest
Wuyts: Laboratory of Pneumology, Dept of Respiratory Medicine, Katholieke Universiteit …

Molecular basis of multiple exostoses: mutations in the EXT1 and EXT2 genes

W Wuyts, W Van Hul - Human mutation, 2000 - Wiley Online Library
Hereditary multiple exostoses (EXT) is an autosomal dominant disorder characterized by the
formation of exostoses, which are cartilage‐capped bony protuberances mainly located on …

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)

…, P Olson, M Dioszegi, C Lacza, W Wuyts… - Human molecular …, 2001 - academic.oup.com
Sclerosteosis is a progressive sclerosing bone dysplasia with an autosomal recessive
mode of inheritance. Radiologically, it is characterized by a generalized hyperostosis and …

Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease

…, N Patel, M Ebeling, E Van Hul, W Wuyts… - Journal of medical …, 2002 - jmg.bmj.com
Van Buchem disease is an autosomal recessive skeletal dysplasia characterised by
generalised bone overgrowth, predominantly in the skull and mandible. Clinical complications …

Diagnosis of hypersensitivity pneumonitis in adults: an official ATS/JRS/ALAT clinical practice guideline

…, M Selman, SLF Walsh, WA Wuyts… - American journal of …, 2020 - atsjournals.org
Background: This guideline addresses the diagnosis of hypersensitivity pneumonitis (HP). It
represents a collaborative effort among the American Thoracic Society, Japanese …

ERS clinical practice guidelines on treatment of sarcoidosis

…, P Korsten, AG Mathioudakis, WA Wuyts… - European …, 2021 - Eur Respiratory Soc
Background The major reasons to treat sarcoidosis are to lower the morbidity and mortality
risk or to improve quality of life (QoL). The indication for treatment varies depending on which …

Nintedanib in patients with progressive fibrosing interstitial lung diseases—subgroup analyses by interstitial lung disease diagnosis in the INBUILD trial: a randomised …

…, L Richeldi, T Moua, B Crestani, WA Wuyts… - The lancet Respiratory …, 2020 - thelancet.com
Background The INBUILD trial investigated the efficacy and safety of nintedanib versus
placebo in patients with progressive fibrosing interstitial lung diseases (ILDs) other than …

A novel deletion involving the connexin-30 gene, del (GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non …

…, H Shahin, KR Siemering, D Weil, W Wuyts… - Journal of medical …, 2005 - jmg.bmj.com
METHODS This study was done on probands with ARNSHI and their relatives from Spain,
Italy, France, Belgium, the United Kingdom, Israel, the Palestinian Authority, the USA, Brazil, …

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

…, ST Bennett, W Wuyts, W Van Hul… - Human molecular …, 2002 - academic.oup.com
Paget's disease of bone (PDB) is a common disorder characterized by focal abnormalities
of increased and disorganized bone turnover. Genetic factors are important in the …