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O Hurko

Showing results (31-40 of 58) with videos related to

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American Journal of Ophthalmology|January 1, 1993
Multiple mitochondrial DNA deletions in myo-neuro-gastrointestinal encephalopathy syndromeD R Johns, A B Threlkeld, N R Miller, 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.
Basic Life Sciences|January 1, 1988
Extended laminectomy for spinal stenosis in achondroplasiaE Streeten, S Uematsu, O Hurko, et al.
Genomics|July 1, 1994
Yeast kar1 mutants provide an effective method for YAC transfer to new hostsF Spencer, Y Hugerat, G Simchen, et al.
American Journal of Human Genetics|June 1, 1989
Dystrophin analysis in clonal myoblasts derived from a Duchenne muscular dystrophy carrierO Hurko, E P Hoffman, L McKee, et al.
Human Pathology|May 20, 1999
Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletionM W Becher, M L Wills, W W Noll, et al.
Annals of Neurology|March 11, 1999
Abnormal fatty acid metabolism in childhood spinal muscular atrophyT O Crawford, J T Sladky, O Hurko, et al.
Journal of Spinal Disorders|April 26, 2000
Reoperation for spinal restenosis in achondroplasiaM C Ain, I Elmaci, O Hurko, et al.
Journal of Neural Transmission|January 1, 1972
The effects of 6-hydroxydopamine pretreatment on the accumulation of dopa and dopamine in brain and peripheral organs following L-dopa administrationL D Lytle, O Hurko, J A Romero, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Ophthalmology|January 1, 1993
Multiple mitochondrial DNA deletions in myo-neuro-gastrointestinal encephalopathy syndromeD R Johns, A B Threlkeld, N R Miller, 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.
Basic Life Sciences|January 1, 1988
Extended laminectomy for spinal stenosis in achondroplasiaE Streeten, S Uematsu, O Hurko, et al.
Genomics|July 1, 1994
Yeast kar1 mutants provide an effective method for YAC transfer to new hostsF Spencer, Y Hugerat, G Simchen, et al.
American Journal of Human Genetics|June 1, 1989
Dystrophin analysis in clonal myoblasts derived from a Duchenne muscular dystrophy carrierO Hurko, E P Hoffman, L McKee, et al.
Human Pathology|May 20, 1999
Kearns-Sayre syndrome with features of Pearson's marrow-pancreas syndrome and a novel 2905-base pair mitochondrial DNA deletionM W Becher, M L Wills, W W Noll, et al.
Annals of Neurology|March 11, 1999
Abnormal fatty acid metabolism in childhood spinal muscular atrophyT O Crawford, J T Sladky, O Hurko, et al.
Journal of Spinal Disorders|April 26, 2000
Reoperation for spinal restenosis in achondroplasiaM C Ain, I Elmaci, O Hurko, et al.
Journal of Neural Transmission|January 1, 1972
The effects of 6-hydroxydopamine pretreatment on the accumulation of dopa and dopamine in brain and peripheral organs following L-dopa administrationL D Lytle, O Hurko, J A Romero, et al.
Pageof 6