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AJNR. American Journal of Neuroradiology|September 1, 1995
Seizure-induced transient hippocampal abnormalities on MR: correlation with positron emission tomography and electroencephalographyJ E Cox, V P Mathews, C C Santos, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 25, 2022
Antipseudomonal treatment decisions during CF exacerbation managementD R VanDevanter, N E West, D B Sanders, et al.
Neurology|November 26, 2003
Mycophenolate mofetil for myasthenia gravis: an analysis of efficacy, safety, and tolerabilityM N Meriggioli, E Ciafaloni, K A Al-Hayk, et al.
Physical Therapy|December 20, 2014
Further Development and Validation of the Affordances in the Home Environment for Motor Development-Infant Scale (AHEMD-IS)Priscila M Caçola, Carl Gabbard, Maria I L Montebelo, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 22, 2021
C-reactive protein (CRP) as a biomarker of pulmonary exacerbation presentation and treatment responseD R VanDevanter, S L Heltshe, M Skalland, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 18, 2020
Changes in symptom scores as a potential clinical endpoint for studies of cystic fibrosis pulmonary exacerbation treatmentD R VanDevanter, S L Heltshe, D B Sanders, et al.
Brazilian Journal of Physical Therapy|December 10, 2015
The new affordances in the home environment for motor development - infant scale (AHEMD-IS): Versions in English and Portuguese languagesPriscila M Caçola, Carl Gabbard, Maria I L Montebelo, et al.
Pediatric Pulmonology|July 12, 2024
Treatment of small as well as large declines in lung function enhances recovery to baseline in people with CFMichael S Schechter, Joshua S Ostrenga, Elizabeth A Cromwell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 8, 2017
Longitudinal development of initial, chronic and mucoid Pseudomonas aeruginosa infection in young children with cystic fibrosisS L Heltshe, U Khan, V Beckett, et al.
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