Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Alan S, Brody"'
Autor:
Joseph Jacob, Catherine M. Owens, Alan S. Brody, Thomas Semple, Tom A. Watson, Alistair Calder, Pilar Garcia-Peña, Paolo Toma, Anand Devaraj, Henry Walton, Antonio Moreno-Galdó, Paul Aurora, Alexandra Rice, Timothy J. Vece, Steve Cunningham, Andre Altmann, Athol U. Wells, Andrew G. Nicholson, Andrew Bush
Publikováno v:
ERJ Open Research, Vol 5, Iss 3 (2019)
Externí odkaz:
https://doaj.org/article/295346478a9d48bab055b75889eacd68
Autor:
Vivianne Calheiros Chaves Gomes, Mara Cristina Coelho Silva, Jose Holanda Maia Filho, Pedro Daltro, Simone Gusmao Ramos, Alan S. Brody, Edson Marchiori
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 39, Iss 5, Pp 569-578 (2013)
OBJECTIVE: Neuroendocrine cell hyperplasia of infancy (NEHI) is a form of childhood interstitial lung disease characterized by tachypnea, retractions, crackles, and hypoxia. The aim of this study was to report and discuss the clinical, imaging, and h
Externí odkaz:
https://doaj.org/article/30c7f9ca83074efaa810b94321503ce0
Autor:
Alan S. Brody, Scott K. Nagle, Marcel van Straten, Caroline Ernst, R. Paul Guillerman, Harm A.W.M. Tiddens
Publikováno v:
Journal of Cystic Fibrosis, 19(2), 176-183. Elsevier
Numerous issues must be addressed when developing standard operating procedures for clinical research studies involving chest computed tomography of lung disease in patients with cystic fibrosis (CF). Study success depends on the provision of adequat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6648561d66a6dee8f489aa25cbc8c8d9
https://doi.org/10.1016/j.jcf.2019.09.001
https://doi.org/10.1016/j.jcf.2019.09.001
Autor:
John P. Clancy, Nara S. Higano, Laura L. Walkup, Zackary I. Cleveland, Robert P. Thomen, Jason C. Woods, David J. Roach, Alan S. Brody, Andrew H. Schapiro
Publikováno v:
Am J Respir Crit Care Med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05835d7635b33d80b42797e060d6cc04
https://doi.org/10.1164/rccm.202001-0031le
https://doi.org/10.1164/rccm.202001-0031le
Publikováno v:
Pediatric Pulmonology. 54:822-827
BACKGROUND Neuroendocrine cell hyperplasia of infancy (NEHI) is a rare pediatric interstitial lung disease (ILD). Distinct chest computed tomography (CT) define its radiographic appearance-specifically, ground-glass (GG) opacities most prominent in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53db60193234634e5e9fc2aa32d8285d
https://doi.org/10.1002/ppul.24301
https://doi.org/10.1002/ppul.24301
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 21(2)
This study was performed to describe the natural history of CF lung disease in young children over an 18 month period to assess the use of CT scanning as an outcome measure for intervention trials.Chest CT scans were obtained at baseline and after 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d23deadbd269f3f0548c316f0cbe7ac
https://pubmed.ncbi.nlm.nih.gov/34961706
https://pubmed.ncbi.nlm.nih.gov/34961706
Autor:
R. Paul Guillerman, Alan S. Brody
Publikováno v:
Pediatric pulmonology. 56(7)
These "rules" are suggestions for clinicians who order chest computed tomography (CTs). The first three address CT scanning technique and the ordering details that we find cause the most confusion. The next three are on patient preparation, and speci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da29b8e40f8864b5cb06835262aab85a
https://pubmed.ncbi.nlm.nih.gov/33852774
https://pubmed.ncbi.nlm.nih.gov/33852774
Autor:
Andre Altmann, Alan S. Brody, Antonio Moreno-Galdó, Catherine M. Owens, Andrew G. Nicholson, Andrew Bush, Paolo Tomà, Anand Devaraj, Tom A. Watson, Timothy J. Vece, Pilar Garcia-Peña, Joseph Jacob, Paul Aurora, Alexandra Rice, Athol U. Wells, Thomas Semple, Henry Walton, Alistair Calder, Steve Cunningham
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Scientia
ERJ Open Research, Vol 5, Iss 3 (2019)
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Jacob, J, Owens, C M, Brody, A S, Semple, T, Watson, T A, Calder, A, Garcia-peña, P, Toma, P, Devaraj, A, Walton, H, Moreno-galdó, A, Aurora, P, Rice, A, Vece, T J, Cunningham, S, Altmann, A, Wells, A U, Nicholson, A G & Bush, A 2019, ' Evaluation of inter-observer variation for computed tomography identification of childhood interstitial lung disease ', ERJ Open Research, vol. 5, no. 3, pp. 00100-2019 . https://doi.org/10.1183/23120541.00100-2019
ERJ Open Research
instname
Scientia
ERJ Open Research, Vol 5, Iss 3 (2019)
Recercat: Dipósit de la Recerca de Catalunya
Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Jacob, J, Owens, C M, Brody, A S, Semple, T, Watson, T A, Calder, A, Garcia-peña, P, Toma, P, Devaraj, A, Walton, H, Moreno-galdó, A, Aurora, P, Rice, A, Vece, T J, Cunningham, S, Altmann, A, Wells, A U, Nicholson, A G & Bush, A 2019, ' Evaluation of inter-observer variation for computed tomography identification of childhood interstitial lung disease ', ERJ Open Research, vol. 5, no. 3, pp. 00100-2019 . https://doi.org/10.1183/23120541.00100-2019
ERJ Open Research
Interstitial lung diseases (ILDs) that present in childhood (chILD) are seen far less frequently than ILDs presenting in adults which themselves constitute rare disorders [1]. Histopathological [2, 3] and imaging [4] characterisation of chILD disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db4ac2dcb0a4998ba8796aa45600c61c
http://hdl.handle.net/2072/444787
http://hdl.handle.net/2072/444787
Publikováno v:
Pediatric Pulmonology. 53:1369-1377
Background Chest computerized tomography (CT) scores are associated with the frequency of future pulmonary exacerbations in people with cystic fibrosis (CF). However, cut-off values to identify children with mild lung disease with different risks for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f4b6c3f6a698942922d94f4e4142c47
https://doi.org/10.1002/ppul.24144
https://doi.org/10.1002/ppul.24144
Autor:
John P. Clancy, David J. Roach, Francesca Pennati, Alan S. Brody, Andrea Aliverti, Robert J. Fleck, Jason C. Woods
Publikováno v:
Journal of Magnetic Resonance Imaging. 48:531-542
Background: Lung disease is the most frequent cause of morbidity and mortality in patients with cystic fibrosis (CF), and there is a shortage of sensitive biomarkers able to regionally monitor disease progression and to assess early responses to ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77adc0e227ea7e133cc6c7bd01959b4e
https://doi.org/10.1002/jmri.25978
https://doi.org/10.1002/jmri.25978