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Neurology|April 1, 1987
Comparison of Duchenne and normal myoblasts from a heterozygoteO Hurko, L McKee, J Zuurveld, et al.The Journal of Biological Chemistry|August 5, 1992
The multiple ADP/ATP translocase genes are differentially expressed during human muscle developmentJ Lunardi, O Hurko, W K Engel, et al.Neurosurgery|August 1, 1994
Total craniospinal decompression in achondroplastic stenosisS Uematsu, H Wang, S E Kopits, et al.Journal of Neurosurgery|September 1, 1990
Craniocervical decompression for cervicomedullary compression in pediatric patients with achondroplasiaJ Aryanpur, O Hurko, C Francomano, et al.Proceedings of the National Academy of Sciences of the United States of America|December 1, 1992
Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathyM Yoneda, A Chomyn, A Martinuzzi, et al.The Journal of Biological Chemistry|May 31, 1996
Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathyG Hofhaus, D R Johns, O Hurko, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Directly repeated sequences associated with pathogenic mitochondrial DNA deletionsD R Johns, S L Rutledge, O C Stine, et al.Journal of Pediatric Orthopedics|July 27, 2000
Motor milestones in children with diastrophic dysplasiaM M Crockett, M F Carten, O Hurko, et al.Neurology|September 1, 1989
Compression syndromes due to hypertrophic nerve roots in hereditary motor sensory neuropathy type IS A Rosen, H Wang, D R Cornblath, et al.The Biochemical Journal|May 1, 1987
Cystine storage in cultured myotubes from patients with nephropathic cystinosisG S Harper, I Bernardini, O Hurko, et al.Pageof 22