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American Journal of Ophthalmology
|
January 1, 1993
Multiple mitochondrial DNA deletions in myo-neuro-gastrointestinal encephalopathy syndrome
D 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 I
S A Rosen, H Wang, D R Cornblath, et al.
The Biochemical Journal
|
May 1, 1987
Cystine storage in cultured myotubes from patients with nephropathic cystinosis
G S Harper, I Bernardini, O Hurko, et al.
Basic Life Sciences
|
January 1, 1988
Extended laminectomy for spinal stenosis in achondroplasia
E Streeten, S Uematsu, O Hurko, et al.
Genomics
|
July 1, 1994
Yeast kar1 mutants provide an effective method for YAC transfer to new hosts
F 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 carrier
O 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 deletion
M W Becher, M L Wills, W W Noll, et al.
Annals of Neurology
|
March 11, 1999
Abnormal fatty acid metabolism in childhood spinal muscular atrophy
T O Crawford, J T Sladky, O Hurko, et al.
Journal of Spinal Disorders
|
April 26, 2000
Reoperation for spinal restenosis in achondroplasia
M 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 administration
L D Lytle, O Hurko, J A Romero, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 58) with videos related to
Sort By:
Page
of 6
American Journal of Ophthalmology
|
January 1, 1993
Multiple mitochondrial DNA deletions in myo-neuro-gastrointestinal encephalopathy syndrome
D 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 I
S A Rosen, H Wang, D R Cornblath, et al.
The Biochemical Journal
|
May 1, 1987
Cystine storage in cultured myotubes from patients with nephropathic cystinosis
G S Harper, I Bernardini, O Hurko, et al.
Basic Life Sciences
|
January 1, 1988
Extended laminectomy for spinal stenosis in achondroplasia
E Streeten, S Uematsu, O Hurko, et al.
Genomics
|
July 1, 1994
Yeast kar1 mutants provide an effective method for YAC transfer to new hosts
F 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 carrier
O 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 deletion
M W Becher, M L Wills, W W Noll, et al.
Annals of Neurology
|
March 11, 1999
Abnormal fatty acid metabolism in childhood spinal muscular atrophy
T O Crawford, J T Sladky, O Hurko, et al.
Journal of Spinal Disorders
|
April 26, 2000
Reoperation for spinal restenosis in achondroplasia
M 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 administration
L D Lytle, O Hurko, J A Romero, et al.
Page
of 6