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Molecular Therapy : the Journal of the American Society of Gene Therapy|October 29, 2013
AAV1.NT-3 gene therapy for charcot-marie-tooth neuropathyZarife Sahenk, Gloria Galloway, Kelly Reed Clark, et al.
The New England Journal of Medicine|September 28, 1995
Myoblast transfer in the treatment of Duchenne's muscular dystrophyJ R Mendell, J T Kissel, A A Amato, et al.
Neurology|April 1, 1989
Duchenne muscular dystrophy: patterns of clinical progression and effects of supportive therapyM H Brooke, G M Fenichel, R C Griggs, et al.
Travel Medicine and Infectious Disease|November 14, 2025
Probable scrub typhus-like infection in Colombia: seroconversion and serological reactivity to Orientia spp. among patients with acute undifferentiated febrile illness in Villeta municipalityCarlos Ramiro Silva-Ramos, Nicole L Mendell, Patricia A Crocquet-Valdes, et al.
Muscle & Nerve|June 15, 2010
Novel diagnostic features of dysferlinopathiesXiomara Q Rosales, Julie M Gastier-Foster, Sarah Lewis, et al.
Gene Therapy|February 5, 2021
AAV1.NT-3 gene therapy for X-linked Charcot-Marie-Tooth neuropathy type 1Burcak Ozes, Morgan Myers, Kyle Moss, et al.
The European Journal of Neuroscience|October 15, 2011
Combined delivery of Nogo-A antibody, neurotrophin-3 and the NMDA-NR2d subunit establishes a functional 'detour' in the hemisected spinal cordLisa Schnell, Arsen S Hunanyan, William J Bowers, et al.
Plos One|May 16, 2024
Validity of remote live stream video evaluation of the North Star Ambulatory Assessment in patients with Duchenne muscular dystrophyLinda P Lowes, Lindsay N Alfano, Megan A Iammarino, et al.
Psychoneuroendocrinology|May 25, 2019
Dissociable involvement of estrogen receptors in perirhinal cortex-mediated object-place memory in male ratsKrista A Mitchnick, Ari L Mendell, Cassidy E Wideman, et al.
Annals of Neurology|March 1, 1993
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysisL J Ptacek, L Gouw, H Kwieciński, et al.
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