H H Morris|M J Bennett - JoVE Visualize

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Archives of Neurology|July 1, 1987

Electrophysiologic pathologic correlations in patients with complex partial seizuresH H Morris, M L Estes, H Lüders, et al.

The Journal of Laboratory and Clinical Medicine|April 1, 1977

Studies in neuronal ceroid-lipofuscinosis: leukocyte peroxidase deficiency in a patient with neuronal ceroid-lipofuscinosis (Jansky-Bielschowsky type)Y C Awasthi, H H Morris, S S Schochet, et al.

Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 1, 1987

Extraoperative cortical functional localization in patients with epilepsyR P Lesser, H Lüders, G Klem, et al.

Electroencephalography and Clinical Neurophysiology|July 1, 1995

Generator locations of movement-related potentials with tongue protrusions and vocalizations: subdural recording in humanA Ikeda, H O Lüders, R C Burgess, et al.

Electroencephalography and Clinical Neurophysiology|November 1, 1995

Movement-related potentials associated with bilateral simultaneous and unilateral movements recorded from human supplementary motor areaA Ikeda, H O Lüders, H Shibasaki, et al.

International Journal of Radiation Oncology, Biology, Physics|February 1, 1991

Marrow antioxidant enzyme activity in tumor-bearing and non-tumor-bearing mice following vincristine treatmentR M Johnke, D P Loven, R S Abernathy, et al.

Journal of Inherited Metabolic Disease|January 1, 1991

Familial combined hyperlipidaemia: use of stable isotopes to demonstrate overproduction of very low-density lipoprotein apolipoprotein B by the liverJ A Cortner, P M Coates, M J Bennett, et al.

Pediatric Pathology|November 1, 1991

Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected siblingM J Bennett, P Rinaldo, D S Millington, et al.

Archives of Pathology & Laboratory Medicine|July 1, 1997

Clinical, biochemical, and morphologic investigations of a case of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyR H Amirkhan, C F Timmons, K O Brown, et al.

Neuropediatrics|November 1, 1990

Decreased erythrocyte and platelet phospholipids and fatty acids in juvenile neuronal ceroid-lipofuscinosis (Batten disease)M J Bennett, J H Galloway, I J Cartwright, et al.

Pageof 35

Showing results (221-230 of 346) with videos related to

Sort By:

Pageof 35

Archives of Neurology|July 1, 1987

Electrophysiologic pathologic correlations in patients with complex partial seizuresH H Morris, M L Estes, H Lüders, et al.

The Journal of Laboratory and Clinical Medicine|April 1, 1977

Studies in neuronal ceroid-lipofuscinosis: leukocyte peroxidase deficiency in a patient with neuronal ceroid-lipofuscinosis (Jansky-Bielschowsky type)Y C Awasthi, H H Morris, S S Schochet, et al.

Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 1, 1987

Extraoperative cortical functional localization in patients with epilepsyR P Lesser, H Lüders, G Klem, et al.

Electroencephalography and Clinical Neurophysiology|July 1, 1995

Generator locations of movement-related potentials with tongue protrusions and vocalizations: subdural recording in humanA Ikeda, H O Lüders, R C Burgess, et al.

Electroencephalography and Clinical Neurophysiology|November 1, 1995

Movement-related potentials associated with bilateral simultaneous and unilateral movements recorded from human supplementary motor areaA Ikeda, H O Lüders, H Shibasaki, et al.

International Journal of Radiation Oncology, Biology, Physics|February 1, 1991

Marrow antioxidant enzyme activity in tumor-bearing and non-tumor-bearing mice following vincristine treatmentR M Johnke, D P Loven, R S Abernathy, et al.

Journal of Inherited Metabolic Disease|January 1, 1991

Familial combined hyperlipidaemia: use of stable isotopes to demonstrate overproduction of very low-density lipoprotein apolipoprotein B by the liverJ A Cortner, P M Coates, M J Bennett, et al.

Pediatric Pathology|November 1, 1991

Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected siblingM J Bennett, P Rinaldo, D S Millington, et al.

Archives of Pathology & Laboratory Medicine|July 1, 1997

Clinical, biochemical, and morphologic investigations of a case of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyR H Amirkhan, C F Timmons, K O Brown, et al.

Neuropediatrics|November 1, 1990

Decreased erythrocyte and platelet phospholipids and fatty acids in juvenile neuronal ceroid-lipofuscinosis (Batten disease)M J Bennett, J H Galloway, I J Cartwright, et al.

Pageof 35