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Thorax|October 18, 2013
Is chest CT useful in newborn screened infants with cystic fibrosis at 1 year of age?Lena P Thia, Alistair Calder, Janet Stocks, et al.
Pediatric Dermatology|July 15, 2020
Keratinocytic epidermal nevi associated with localized fibro-osseous lesions without hypophosphatemiaLien Mestach, Satyamaanasa Polubothu, Alistair Calder, et al.
Orphanet Journal of Rare Diseases|February 9, 2017
An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypesPolona Le Quesne Stabej, Chela James, Louise Ocaka, et al.
Canadian Respiratory Journal|February 21, 2020
Postinfectious Bronchiolitis Obliterans in Children: Diagnostic Workup and Therapeutic Options: A Workshop ReportSilvija-Pera Jerkic, Folke Brinkmann, Alistair Calder, et al.
Journal of Medical Genetics|August 31, 2021
Expanding the phenotype of <i>SPARC</i>-related osteogenesis imperfecta: clinical findings in two patients with pathogenic variants in <i>SPARC</i> and literature reviewAnna Durkin, Catherine DeVile, Paul Arundel, et al.
American Journal of Human Genetics|December 3, 2013
SAMS, a syndrome of short stature, auditory-canal atresia, mandibular hypoplasia, and skeletal abnormalities is a unique neurocristopathy caused by mutations in GoosecoidDavid A Parry, Clare V Logan, Alexander P A Stegmann, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 12, 2020
Minimal change in structural, functional and inflammatory markers of lung disease in newborn screened infants with cystic fibrosis at one yearGwyneth Davies, Lena P Thia, Janet Stocks, et al.
Nature|August 27, 2025
The evolution of hominin bipedalism in two stepsGayani Senevirathne, Serena C Fernandopulle, Daniel Richard, et al.
ERJ Open Research|August 2, 2019
Evaluation of inter-observer variation for computed tomography identification of childhood interstitial lung diseaseJoseph Jacob, Catherine M Owens, Alan S Brody, et al.
Thorax|November 22, 2019
One-year outcomes in a multicentre cohort study of incident rare diffuse parenchymal lung disease in children (ChILD)Steve Cunningham, Catriona Graham, Morag MacLean, et al.
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