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Plos One|March 31, 2023
Mapping EQ5D utilities from forced vital capacity and diffusing capacity in fibrotic interstitial lung diseaseAlyson W Wong, Huiying Sun, Ingrid A Cox, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|November 29, 2019
Donation after circulatory death in lung transplantation-five-year follow-up from ISHLT RegistryDirk Van Raemdonck, Shaf Keshavjee, Bronwyn Levvey, et al.
The Medical Journal of Australia|February 2, 2018
Diagnosis and management of idiopathic pulmonary fibrosis: Thoracic Society of Australia and New Zealand and Lung Foundation Australia position statements summaryHelen E Jo, Jyotika D Prasad, Lauren K Troy, et al.
ERJ Open Research|August 26, 2021
Mortality in combined pulmonary fibrosis and emphysema patients is determined by the sum of pulmonary fibrosis and emphysemaAn Zhao, Eyjolfur Gudmundsson, Nesrin Mogulkoc, et al.
Internal Medicine Journal|June 4, 2026
Idiopathic Pulmonary Fibrosis update, comparing the Australasian Interstitial Lung Disease Registry to the Australian Idiopathic Pulmonary Fibrosis RegistryMichelle Chee, Yet Hong Khor, Dan Jackson, et al.
Respirology (Carlton, Vic.)|November 24, 2020
Diagnosis and management of connective tissue disease-associated interstitial lung disease in Australia and New Zealand: A position statement from the Thoracic Society of Australia and New ZealandAdelle S Jee, Robert Sheehy, Peter Hopkins, et al.
Nature Communications|December 3, 2024
Compassionate access to virus-specific T cells for adoptive immunotherapy over 15 yearsMichelle A Neller, George R Ambalathingal, Nada Hamad, et al.
The European Respiratory Journal|November 16, 2023
Mortality surrogates in combined pulmonary fibrosis and emphysemaAn Zhao, Eyjolfur Gudmundsson, Nesrin Mogulkoc, et al.
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