Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Simone K Visser"'
Autor:
Aditi Aiyer, Simone K. Visser, Peter Bye, Warwick J. Britton, Gregory S. Whiteley, Trevor Glasbey, Frederik H. Kriel, Jessica Farrell, Theerthankar Das, Jim Manos
Publikováno v:
Antibiotics, Vol 10, Iss 10, p 1176 (2021)
Cystic fibrosis (CF) is a genetic disorder causing dysfunctional ion transport resulting in accumulation of viscous mucus that fosters chronic bacterial biofilm-associated infection in the airways. Achromobacter xylosoxidans and Stenotrophomonas malt
Externí odkaz:
https://doaj.org/article/22e2235e12b7425f853ff2c60469d213
Autor:
Amelia Lin, Keith Wong, Simone K Visser, Helen Jo, Yasmeen Al‐Hindawi, Katrin Kosbab‐Jackson, Molly Cocks, Anastasia Volovets, Paul Haber, Kirsten Hammond, Nicole Taylor, Veronica Yozghatlian, Edmund MT Lau, Nathaniel S Marshall, Tara Aquino‐Salomon, Sheila Sivam
Publikováno v:
The Medical journal of Australia.
Autor:
Koliarne Tong, Claire E. Wainwright, Peter G. Middleton, Hugh Greville, Douglas J. Dorahy, Daniel Barker, Peter A. B. Wark, Lucy D. Burr, Simone K. Visser
Publikováno v:
Journal of Cystic Fibrosis. 19:415-420
Lumacaftor/ivacaftor (LUM/IVA) improves outcomes in cystic fibrosis (CF) patients homozygous for Phe508del with ppFEV140%. There is limited safety or efficacy data in patients with ppFEV140%. We determined whether LUM/IVA in patients with ppFEV140 wo
Autor:
Hyun Lee, Yeon-Mok Oh, Simone K. Visser, Raja Dhar, James D. Chalmers, Hayoung Choi, Tu Q. Nguyen, Lucy Morgan
Publikováno v:
Respirology. 26:619-621
Autor:
Trevor Glasbey, Warwick J. Britton, Gregory Stuart Whiteley, Theerthankar Das, Peter T. P. Bye, Jessica A. Farrell, Frederik H. Kriel, Jim Manos, Simone K. Visser, Aditi Aiyer
Publikováno v:
Antibiotics, Vol 10, Iss 1176, p 1176 (2021)
Antibiotics
Volume 10
Issue 10
Antibiotics
Volume 10
Issue 10
Cystic fibrosis (CF) is a genetic disorder causing dysfunctional ion transport resulting in accumulation of viscous mucus that fosters chronic bacterial biofilm-associated infection in the airways. Achromobacter xylosoxidans and Stenotrophomonas malt
Autor:
Samantha A Nolan, Edmund M.T. Lau, Keith Kh Wong, Sheila Sivam, Tiffany Dwyer, Jody M Bell, Phillip A. Munoz, Veronica Yozghatlian, Nicole Taylor, Ruth Dentice, Helen E. Jo, Simone K. Visser
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 21(1)
Spirometry is usually performed under the supervision of a trained respiratory scientist to ensure acceptability and repeatability of results. To evaluate the quality of spirometry performance by adult cystic fibrosis (CF) patients with and without o
Autor:
T. Aquino-Salomon, Simone K. Visser, N. Marshall, A. Lin, Veronica Yozghatlian, Y. Al-Hindawi, Edmund M.T. Lau, Sheila Sivam, Helen E. Jo
Publikováno v:
Journal of Cystic Fibrosis. 20:S24-S25
Autor:
Surya Kant Tripathi, Daniel J. Smith, B Archana, Shubham Sharma, Suresh Anantharaj, Srinivas Rajagopala, Antoni Torres, Arjun Khanna, AT Hill, Stuart Elborn, Rajesh Swarnakar, Murali Mohan, Sonali Trivedi, Rachel C. Thomson, Francesco Blasi, Robert Wilson, Katerina Dimakou, Tobias Welte, George D'Souza, Aleemuddin Naveed M, Aditya Jindal, Arjun Padmanabhan, Paul T. King, Honney Sawhney, Rajendra Prasad, Grant W. Waterer, Simon Finch, Girija Nair, Samir Gami, Simone K. Visser, Stefano Aliberti, Anne B. Chang, Gayathri Devi H. Jayadevappa, Sunil Vyas, Babaji Ghewade, Naveen Dutt, Deepak Talwar, Raja Dhar, Charles Haworth, Chien-Li Holmes-Liew, Felix Ringhausen, Megan Crichton, Lata Jayaram, Sundeep Salvi, Amelia Shoemark, Anthony De Soyza, Kripesh R. Sarmah, James D. Chalmers, Kummannoor Venugopal, Lucy Morgan, Eva Polverino, Montse Vendrell, Pieter Goeminne, Sheetu Singh, Padukudru Anand Mahesh, Pierre-Régis Burgel, Kaushik Saha, Lucy D. Burr, Himanshu Garg, Arpan Shah, Enna Salama, Michael Loebinger, Peter G. Middleton, Saurabh Karmakar, Justin Waring, Arti Shah, Conroy Wong
Publikováno v:
Respiratory infections.
Bronchiectasis is reported to be more frequent in females. There have been no large studies examining the impact of biological sex on disease characteristics, aetiology, severity, quality of life or management. Patients were prospectively enrolled fr
Publikováno v:
Medical Journal of Australia. 209:177-183
Once neglected in research and underappreciated in practice, there is renewed interest in bronchiectasis unrelated to cystic fibrosis. Bronchiectasis is a chronic lung disease characterised by chronic cough, sputum production and recurrent pulmonary
Autor:
Chien Li Holmes-Liew, Peter G. Middleton, Warwick J. Britton, Greg J. Fox, Enna Stroil-Salama, Rachel Thomson, Lucy Morgan, Simone K. Visser, Graeme P. Maguire, Peter T. P. Bye, Paul T. King, Anne B. Chang, Lucy D. Burr, Daniel J. Smith
Publikováno v:
Lung. 197(6)
Australian data regarding the management of patients with bronchiectasis is scarce. We sought to compare the management of adults with bronchiectasis attending tertiary Australian centres with recent national and international guidelines. The Austral