H G Dunn|P M MacLeod - JoVE Visualize

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Neurology|June 1, 1977

Progressive cerebellar ataxia, spasticity, psychomotor retardation, and hexosaminidase deficiency in a 10-year-old child: juvenile Sandhoff diseaseP M MacLeod, S Wood, J E Jan, et al.

Clinical Genetics|July 16, 2003

Syndromes of disordered chromatin remodelingJ Ausió, D B Levin, G V De Amorim, et al.

Developmental Medicine and Child Neurology|July 1, 1994

Acute encephalopathy and status epilepticus associated with human herpes virus 6 infectionC M Jones, H G Dunn, E E Thomas, et al.

Human Genetics|January 1, 1981

Further delineation of X-linked mental retardationD S Herbst, H G Dunn, F J Dill, et al.

Neurobehavioral Toxicology and Teratology|January 1, 1981

Intrinsic defects in the fetal alcohol syndrome: studies on 76 cases from British Columbia and the Yukon TerritoryD F Smith, G G Sandor, P M MacLeod, et al.

Neurology|November 1, 1976

Krabbe's leukodystrophy without globoid cellsH G Dunn, C L Dolman, D F Farrell, et al.

Neurology|July 1, 1980

Failure of aminooxyacetic acid therapy in Huntington diseaseT L Perry, J M Wright, S Hansen, et al.

Human Genetics|January 1, 1984

Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase with reduced affinity for PP-ribose-P in four related males with goutF F Snyder, A E Chudley, P M MacLeod, et al.

American Journal of Medical Genetics|December 1, 1985

Prenatal diagnosis of neuronal ceroid-lipofuscinosesP M MacLeod, C L Dolman, R E Nickel, et al.

Neurology|June 1, 1982

Long-term follow-up after cerebral hemispherectomy: neurophysiologic, radiologic, and psychological findingsC M Verity, E H Strauss, P D Moyes, et al.

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Showing results (51-60 of 72) with videos related to

Sort By:

Pageof 8

Neurology|June 1, 1977

Progressive cerebellar ataxia, spasticity, psychomotor retardation, and hexosaminidase deficiency in a 10-year-old child: juvenile Sandhoff diseaseP M MacLeod, S Wood, J E Jan, et al.

Clinical Genetics|July 16, 2003

Syndromes of disordered chromatin remodelingJ Ausió, D B Levin, G V De Amorim, et al.

Developmental Medicine and Child Neurology|July 1, 1994

Acute encephalopathy and status epilepticus associated with human herpes virus 6 infectionC M Jones, H G Dunn, E E Thomas, et al.

Human Genetics|January 1, 1981

Further delineation of X-linked mental retardationD S Herbst, H G Dunn, F J Dill, et al.

Neurobehavioral Toxicology and Teratology|January 1, 1981

Intrinsic defects in the fetal alcohol syndrome: studies on 76 cases from British Columbia and the Yukon TerritoryD F Smith, G G Sandor, P M MacLeod, et al.

Neurology|November 1, 1976

Krabbe's leukodystrophy without globoid cellsH G Dunn, C L Dolman, D F Farrell, et al.

Neurology|July 1, 1980

Failure of aminooxyacetic acid therapy in Huntington diseaseT L Perry, J M Wright, S Hansen, et al.

Human Genetics|January 1, 1984

Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase with reduced affinity for PP-ribose-P in four related males with goutF F Snyder, A E Chudley, P M MacLeod, et al.

American Journal of Medical Genetics|December 1, 1985

Prenatal diagnosis of neuronal ceroid-lipofuscinosesP M MacLeod, C L Dolman, R E Nickel, et al.

Neurology|June 1, 1982

Long-term follow-up after cerebral hemispherectomy: neurophysiologic, radiologic, and psychological findingsC M Verity, E H Strauss, P D Moyes, et al.

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