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Annals of Neurology|February 7, 2017
Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsyTracy A Glauser, Katherine Holland, Valerie P O'Brien, et al.
Neuromuscular Disorders : NMD|October 20, 2018
Longitudinal pulmonary function testing outcome measures in Duchenne muscular dystrophy: Long-term natural history with and without glucocorticoidsCraig M McDonald, Heather Gordish-Dressman, Erik K Henricson, et al.
Neurology|July 21, 2017
Pretreatment seizure semiology in childhood absence epilepsySudha Kilaru Kessler, Shlomo Shinnar, Avital Cnaan, et al.
Anesthesia and Analgesia|May 29, 2002
An evaluation of the efficacy and tolerability of oral tramadol hydrochloride tablets for the treatment of postsurgical pain in childrenJulia C Finkel, John B Rose, Michael L Schmitz, et al.
Muscle & Nerve|May 17, 2013
The cooperative international neuromuscular research group Duchenne natural history study--a longitudinal investigation in the era of glucocorticoid therapy: design of protocol and the methods usedCraig M McDonald, Erik K Henricson, R Ted Abresch, et al.
Blood|December 24, 2005
Cardiac morbidity and mortality in deferoxamine- or deferiprone-treated patients with thalassemia majorCaterina Borgna-Pignatti, Maria Domenica Cappellini, Piero De Stefano, et al.
Clinical Pharmacology and Therapeutics|June 14, 2023
Model-Informed Precision Dosing Guidance of Ethosuximide Developed from a Randomized Controlled Clinical Trial of Childhood Absence EpilepsyKana Mizuno, Edmund V Capparelli, Tsuyoshi Fukuda, et al.
Neurology|May 31, 2013
Pretreatment EEG in childhood absence epilepsy: associations with attention and treatment outcomeDennis Dlugos, Shlomo Shinnar, Avital Cnaan, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 21, 2006
Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysisRachel A Ruotolo, Nestor A Veitia, Aaron Corbin, et al.
Muscle & Nerve|May 8, 2013
The cooperative international neuromuscular research group Duchenne natural history study: glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measuresErik K Henricson, R Ted Abresch, Avital Cnaan, et al.
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