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2017

Journal Article

Antibiotic perturbation of mixed-strain Pseudomonas aeruginosa infection in patients with cystic fibrosis

Tai, Anna S., Sherrard, Laura J., Kidd, Timothy J., Ramsay, Kay A., Buckley, Cameron, Syrmis, Melanie, Grimwood, Keith, Bell, Scott C. and Whiley, David M. (2017). Antibiotic perturbation of mixed-strain Pseudomonas aeruginosa infection in patients with cystic fibrosis. BMC pulmonary medicine, 17 (1) 138, 1-10. doi: 10.1186/s12890-017-0482-7

Antibiotic perturbation of mixed-strain Pseudomonas aeruginosa infection in patients with cystic fibrosis

2017

Journal Article

Early intervention of cystic fibrosis pulmonary exacerbations based on home monitoring eICE through the looking glass

Bell, Scott C. (2017). Early intervention of cystic fibrosis pulmonary exacerbations based on home monitoring eICE through the looking glass. American Journal of Respiratory and Critical Care Medicine, 196 (9), 1090-1092. doi: 10.1164/rccm.201706-1207ED

Early intervention of cystic fibrosis pulmonary exacerbations based on home monitoring eICE through the looking glass

2017

Journal Article

Learning's from the Editors Desk – 2017

Bell, Scott C., Castellani, Carlo and Flume, Patrick A. (2017). Learning's from the Editors Desk – 2017. Journal of Cystic Fibrosis, 16 (6), 645-646. doi: 10.1016/j.jcf.2017.10.001

Learning's from the Editors Desk – 2017

2017

Journal Article

The treatment of the pulmonary and extrapulmonary manifestations of cystic fibrosis

Chin, Melanie, Aaron, Shawn D. and Bell, Scott C. (2017). The treatment of the pulmonary and extrapulmonary manifestations of cystic fibrosis. Presse Medicale, 46 (6), E139-E164. doi: 10.1016/j.lpm.2016.11.030

The treatment of the pulmonary and extrapulmonary manifestations of cystic fibrosis

2017

Journal Article

Tropical Australia is a potential reservoir of non-tuberculous mycobacteria in cystic fibrosis

Sherrard, Laura J., Tay, George T., Butler, Claire A., Wood, Michelle E., Yerkovich, Stephanie, Ramsay, Kay A., Reid, David W., Moore, Vanessa L., Kidd, Timothy J. and Bell, Scott C. (2017). Tropical Australia is a potential reservoir of non-tuberculous mycobacteria in cystic fibrosis. European Respiratory Journal, 49 (5) 1700046, 1700046. doi: 10.1183/13993003.00046-2017

Tropical Australia is a potential reservoir of non-tuberculous mycobacteria in cystic fibrosis

2017

Journal Article

Sources and dynamics of fluorescent particles in hospitals

Pereira, M. L., Knibbs, L. D., He, C., Grzybowski, P., Johnson, G. R., Huffman, J. A., Bell, S. C., Wainwright, C. E., Matte, D. L., Dominski, F. H., Andrade, A. and Morawska, L. (2017). Sources and dynamics of fluorescent particles in hospitals. Indoor Air, 27 (5), 988-1000. doi: 10.1111/ina.12380

Sources and dynamics of fluorescent particles in hospitals

2017

Journal Article

CFTR-dependent defect in alternatively-activated macrophages in cystic fibrosis

Tarique, Abdullah A., Sly, Peter D., Holt, Patrick G., Bosco, Anthony, Ware, Robert S., Logan, Jayden, Bell, Scott C., Wainwright, Claire E. and Fantino, Emmanuelle (2017). CFTR-dependent defect in alternatively-activated macrophages in cystic fibrosis. Journal of Cystic Fibrosis, 16 (4), 475-482. doi: 10.1016/j.jcf.2017.03.011

CFTR-dependent defect in alternatively-activated macrophages in cystic fibrosis

2017

Journal Article

Within-host evolution of Burkholderia pseudomallei during chronic infection of seven Australasian cystic fibrosis patients

Viberg, Linda T., Sarovich, Derek S., Kidd, Timothy J., Geake, James B., Bell, Scott C., Currie, Bart J. and Price, Erin P. (2017). Within-host evolution of Burkholderia pseudomallei during chronic infection of seven Australasian cystic fibrosis patients. mBio, 8 (2) e00356-17, 1-17. doi: 10.1128/mBio.00356-17

Within-host evolution of Burkholderia pseudomallei during chronic infection of seven Australasian cystic fibrosis patients

2017

Journal Article

Treatment decisions for MRSA in patients with cystic fibrosis (CF): When is enough, enough?

Bell, Scott C. and Flume, Patrick A. (2017). Treatment decisions for MRSA in patients with cystic fibrosis (CF): When is enough, enough?. Thorax, 72 (4), 297-299. doi: 10.1136/thoraxjnl-2016-209605

Treatment decisions for MRSA in patients with cystic fibrosis (CF): When is enough, enough?

2017

Journal Article

Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis

Sherrard, Laura J., Tai, Anna S., Wee, Bryan A., Ramsay, Kay A., Kidd, Timothy J., Ben Zakour, Nouri L., Whiley, David M., Beatson, Scott A. and Bell, Scott C. (2017). Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis. PLoS One, 12 (3) e0172179, e0172179.1-e0172179.15. doi: 10.1371/journal.pone.0172179

Within-host whole genome analysis of an antibiotic resistant Pseudomonas aeruginosa strain sub-type in cystic fibrosis

2017

Journal Article

A rapid pipeline to model rare neurodevelopmental disorders with simultaneous CRISPR/Cas9 gene editing

Bell, Scott, Peng, Huashan, Crapper, Liam, Kolobova, Ilaria, Maussion, Gilles, Vasuta, Cristina, Yerko, Volodymyr, Pan Wong, Tak and Ernst, Carl (2017). A rapid pipeline to model rare neurodevelopmental disorders with simultaneous CRISPR/Cas9 gene editing. Stem Cells Translational Medicine, 6 (3), 886-896. doi: 10.1002/sctm.16-0158

A rapid pipeline to model rare neurodevelopmental disorders with simultaneous CRISPR/Cas9 gene editing

2017

Journal Article

Lumacaftor/ivacaftor treatment of patients with cystic fibrosis heterozygous for F508del-CFTR

Rowe, Steven M., McColley, Susanna A., Rietschel, Ernst, Li, Xiaolei, Bell, Scott C., Konstan, Michael W., Marigowda, Gautham, Waltz, David and Boyle, Michael P. (2017). Lumacaftor/ivacaftor treatment of patients with cystic fibrosis heterozygous for F508del-CFTR. Annals of the American Thoracic Society, 14 (2), 213-219. doi: 10.1513/AnnalsATS.201609-689OC

Lumacaftor/ivacaftor treatment of patients with cystic fibrosis heterozygous for F508del-CFTR

2017

Journal Article

Implication of LRRC4C and DPP6 in neurodevelopmental disorders

Maussion, Gilles, Cruceanu, Cristiana, Rosenfeld, Jill A., Bell, Scott C., Jollant, Fabrice, Szatkiewicz, Jin, Collins, Ryan L., Hanscom, Carrie, Kolobova, Ilaria, de Champfleur, Nicolas Menjot, Blumenthal, Ian, Chiang, Colby, Ota, Vanessa, Hultman, Christina, O'Dushlaine, Colm, McCarroll, Steve, Alda, Martin, Jacquemont, Sebastien, Ordulu, Zehra, Marshall, Christian R., Carter, Melissa T., Shaffer, Lisa G., Sklar, Pamela, Girirajan, Santhosh, Morton, Cynthia C., Gusella, James F., Turecki, Gustavo, Stavropoulos, Dimitri J., Sullivan, Patrick F. ... Ernst, Carl (2017). Implication of LRRC4C and DPP6 in neurodevelopmental disorders. American Journal of Medical Genetics, Part A, 173 (2), 395-406. doi: 10.1002/ajmg.a.38021

Implication of LRRC4C and DPP6 in neurodevelopmental disorders

2017

Journal Article

Effect of Nerve Stimulation Use on the Success Rate of Ultrasound-Guided Subsartorial Saphenous Nerve Block A Randomized Controlled Trial

Montgomery, Shaylyn H., Shamji, Colleen M., Yi, Grace S., Yarnold, Cynthia H., Head, Stephen J., Bell, Scott C. and Schwarz, Stephan K. W. (2017). Effect of Nerve Stimulation Use on the Success Rate of Ultrasound-Guided Subsartorial Saphenous Nerve Block A Randomized Controlled Trial. Regional Anesthesia and Pain Medicine, 42 (1), 25-31. doi: 10.1097/AAP.0000000000000522

Effect of Nerve Stimulation Use on the Success Rate of Ultrasound-Guided Subsartorial Saphenous Nerve Block A Randomized Controlled Trial

2017

Journal Article

JCF - 2016

Bell, Scott C., Castellani, Carlo and Flume, Patrick A. (2017). JCF - 2016. Journal of Cystic Fibrosis, 16 (1), 6-6. doi: 10.1016/j.jcf.2016.12.014

JCF - 2016

2017

Journal Article

Clostridium difficile infection in cystic fibrosis: an uncommon but life-threatening complication

Piccolo, Francesco, Tai, Anna Sze, Ee, Hooi, Mulrennan, Siobhain, Bell, Scott and Ryan, Gerard (2017). Clostridium difficile infection in cystic fibrosis: an uncommon but life-threatening complication. Respirology Case Reports, 5 (1) e00204, e00204. doi: 10.1002/rcr2.204

Clostridium difficile infection in cystic fibrosis: an uncommon but life-threatening complication

2017

Journal Article

Limitations to providing adult cystic fibrosis care in Europe: results of a care centre survey

Madge, Susan, Bell, Scott C., Burgel, Pierre- Régis, De Rijcke, Karleen, Blasi, Francesco and Elborn, J. Stuart (2017). Limitations to providing adult cystic fibrosis care in Europe: results of a care centre survey. Journal of Cystic Fibrosis, 16 (1), 85-88. doi: 10.1016/j.jcf.2016.07.001

Limitations to providing adult cystic fibrosis care in Europe: results of a care centre survey

2016

Journal Article

Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium

Bryant, Josephine M., Grogono, Dorothy M., Rodriguez-Rincon, Daniela, Everall, Isobel, Brown, Karen P., Moreno, Pablo, Verma, Deepshikha, Hill, Emily, Drijkoningen, Judith, Gilligan, Peter, Esther, Charles R., Noone, Peadar G., Giddings, Olivia, Bell, Scott C., Thomson, Rachel, Wainwright, Claire E., Coulter, Chris, Pandey, Sushil, Wood, Michelle E., Stockwell, Rebecca E., Ramsay, Kay A., Sherrard, Laura J., Kidd, Timothy J., Jabbour, Nassib, Johnson, Graham R., Knibbs, Luke D., Morawska, Lidia, Sly, Peter D., Jones, Andrew ... Floto, R. Andres (2016). Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium. Science, 354 (6313), 751-757. doi: 10.1126/science.aaf8156

Emergence and spread of a human-transmissible multidrug-resistant nontuberculous mycobacterium

2016

Journal Article

Lesch-Nyhan syndrome: Models, theories, and therapies

Bell, Scott, Kolobova, Ilaria, Crapper, Liam and Ernst, Carl (2016). Lesch-Nyhan syndrome: Models, theories, and therapies. Molecular Syndromology, 7 (6), 302-311. doi: 10.1159/000449296

Lesch-Nyhan syndrome: Models, theories, and therapies

2016

Journal Article

Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki

Smyth, Alan R., Bell, Scott C., Bojcin, Snezana, Bryon, Mandy, Duff, Alistair, Flume, Patrick, Kashirskaya, Nataliya, Munck, Anne, Ratjen, Felix, Schwarzenberg, Sarah Jane, Sermet-Gaudelus, Isabelle, Southern, Kevin W., Taccetti, Giovanni, Ullrich, Gerald and Wolfe, Sue (2016). Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki. Pediatria Polska, 91 (Supp.1), S30-S53. doi: 10.1016/j.pepo.2016.08.014

Standardy opieki Europejskiego Towarzystwa Mukowiscydozy: wytyczne i najlepsze praktyki