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American Journal of Medical Genetics
|
November 1, 1982
Administration of iduronate sulfatase by plasma exchange to patients with the Hunter syndrome: a clinical study
F R Brown, C W Hall, E F Neufeld, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
Infantile Refsum's disease: biochemical findings suggesting multiple peroxisomal dysfunction
B T Poll-The, J M Saudubray, H Ogier, et al.
Orthopaedic Journal of Sports Medicine
|
July 21, 2022
Outcomes of Biceps Tenotomy Versus Tenodesis During Arthroscopic Rotator Cuff Repair: An Analysis of Patients From a Large Multicenter Database
Ramesh C Srinivasan, Kevin A Hao, Thomas W Wright, et al.
Orthopaedic Journal of Sports Medicine
|
June 26, 2023
Outcomes of Biceps Tenodesis Variations With Concomitant Rotator Cuff Repair: A Multicenter Database Analysis
David P Hagan, Kevin A Hao, Joseph J King, et al.
Lipids in Health and Disease
|
June 18, 2011
Human and great ape red blood cells differ in plasmalogen levels and composition
Ann B Moser, Steven J Steinberg, Paul A Watkins, et al.
Neurology
|
November 1, 1984
Bone marrow transplant in adrenoleukodystrophy
H W Moser, P J Tutschka, F R Brown, et al.
The American Journal of Sports Medicine
|
January 23, 2016
Low- Versus High-Intensity Plyometric Exercise During Rehabilitation After Anterior Cruciate Ligament Reconstruction
Terese L Chmielewski, Steven Z George, Susan M Tillman, et al.
American Journal of Human Genetics
|
January 23, 1999
Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis
E G van Grunsven, E van Berkel, P A Mooijer, et al.
The Johns Hopkins Medical Journal
|
October 1, 1982
Adrenoleukodystrophy: effects of dietary restriction of very long chain fatty acids and of administration of carnitine and clofibrate on clinical status and plasma fatty acids
F R Brown, M A Van Duyn, A B Moser, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
A sibship with a mild variant of Zellweger syndrome
P G Barth, R B Schutgens, R J Wanders, et al.
Page
of 47
Search research articles
Search
Showing results (441-450 of 466) with videos related to
Sort By:
Page
of 47
American Journal of Medical Genetics
|
November 1, 1982
Administration of iduronate sulfatase by plasma exchange to patients with the Hunter syndrome: a clinical study
F R Brown, C W Hall, E F Neufeld, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
Infantile Refsum's disease: biochemical findings suggesting multiple peroxisomal dysfunction
B T Poll-The, J M Saudubray, H Ogier, et al.
Orthopaedic Journal of Sports Medicine
|
July 21, 2022
Outcomes of Biceps Tenotomy Versus Tenodesis During Arthroscopic Rotator Cuff Repair: An Analysis of Patients From a Large Multicenter Database
Ramesh C Srinivasan, Kevin A Hao, Thomas W Wright, et al.
Orthopaedic Journal of Sports Medicine
|
June 26, 2023
Outcomes of Biceps Tenodesis Variations With Concomitant Rotator Cuff Repair: A Multicenter Database Analysis
David P Hagan, Kevin A Hao, Joseph J King, et al.
Lipids in Health and Disease
|
June 18, 2011
Human and great ape red blood cells differ in plasmalogen levels and composition
Ann B Moser, Steven J Steinberg, Paul A Watkins, et al.
Neurology
|
November 1, 1984
Bone marrow transplant in adrenoleukodystrophy
H W Moser, P J Tutschka, F R Brown, et al.
The American Journal of Sports Medicine
|
January 23, 2016
Low- Versus High-Intensity Plyometric Exercise During Rehabilitation After Anterior Cruciate Ligament Reconstruction
Terese L Chmielewski, Steven Z George, Susan M Tillman, et al.
American Journal of Human Genetics
|
January 23, 1999
Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis
E G van Grunsven, E van Berkel, P A Mooijer, et al.
The Johns Hopkins Medical Journal
|
October 1, 1982
Adrenoleukodystrophy: effects of dietary restriction of very long chain fatty acids and of administration of carnitine and clofibrate on clinical status and plasma fatty acids
F R Brown, M A Van Duyn, A B Moser, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
A sibship with a mild variant of Zellweger syndrome
P G Barth, R B Schutgens, R J Wanders, et al.
Page
of 47