P. Morehart

Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort

Kevin M. Flanigan, Diane M. Dunn, Andrew von Niederhausern et al. · Human Mutation · 2009 · 314 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy

Luca Bello, Kevin M. Flanigan, Robert B. Weiss et al. · The American Journal of Human Genetics · 2016 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Muscle Coenzyme Q: A Potential Test for Mitochondrial Activity and Redox Status

Lili Miles, Michael V. Miles, Peter Tang et al. · Pediatric Neurology · 2005 · 25 citations

Life Sciences, Biochemistry, Physiology +17

Discrepancy between neuroimaging findings and clinical phenotype in Alexander disease.

Argirios Dinopoulos, J. R. Gorospe, John C. Egelhoff et al. · PubMed · 2007 · 21 citations · Full text

Medicine, Neurology, Neuroscience +15

Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations

James J. Collins, Kevin E. Bove, David Dimmock et al. · Neuromuscular Disorders · 2009 · 17 citations

Life Sciences, Genetics, Molecular Biology +17