Last Updated: 09/26/2026
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Found 8 publications
Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy.
Journal: Annals of neurology
Published: February 26, 2018
Fine Needle Aspiration of Thyroid Nodules Using the Bethesda System for Reporting Thyroid Cytopathology: An Institutional Experience in a Rural Setting.
Journal: International journal of endocrinology
Published: October 03, 2016
The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development.
Journal: Neuromuscular disorders : NMD
Published: March 26, 2015
Dystrophin quantification: Biological and translational research implications.
Journal: Neurology
Published: October 31, 2014
Clinical phenotypes as predictors of the outcome of skipping around DMD exon 45.
Journal: Annals of neurology
Published: May 07, 2014
The ZZ domain of dystrophin in DMD: making sense of missense mutations.
Journal: Human mutation
Published: August 15, 2013
LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophy.
Journal: Annals of neurology
Published: August 27, 2012
Quantification of dystrophin immunofluorescence in dystrophinopathy muscle specimens.
Journal: Neuropathology and applied neurobiology
Published: January 17, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026