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Birth Defects Original Article Series
|
January 1, 1976
The neuronal ceroid lipofuscinoses in British Columbia: a clinical epidemiologic and ultrastructural study
P M MacLeod, C L Dolman, E Chang, et al.
The Medical Journal of Australia
|
October 29, 1983
Non-specific senile dementia mimicking Huntington's disease in two siblings
V J Ojeda, W Knezevic, D J Willsher, et al.
Neurology
|
June 1, 1977
Progressive cerebellar ataxia, spasticity, psychomotor retardation, and hexosaminidase deficiency in a 10-year-old child: juvenile Sandhoff disease
P M MacLeod, S Wood, J E Jan, et al.
The New England Journal of Medicine
|
March 1, 1984
Prenatal diagnosis of neuronal ceroid lipofuscinosis
P M MacLeod, C L Dolman, R E Nickel, et al.
Archives of Neurology
|
February 1, 1975
Hereditary mental depression and Parkinsonism with taurine deficiency
T L Perry, P J Bratty, S Hansen, et al.
Neurology
|
November 1, 1976
Krabbe's leukodystrophy without globoid cells
H G Dunn, C L Dolman, D F Farrell, et al.
Developmental Medicine and Child Neurology
|
October 1, 1979
Progressive rubella panencephalitis: clinical course and response to 'isoprinosine'
J E Jan, A J Tingle, G Donald, et al.
American Journal of Diseases of Children (1960)
|
February 1, 1975
Optic nerve hypoplasia with hypopituitarism. Septo-optic dysplasia with hypopituitarism
H Patel, W J Tze, J U Crichton, et al.
American Journal of Medical Genetics
|
December 1, 1985
Prenatal diagnosis of neuronal ceroid-lipofuscinoses
P M MacLeod, C L Dolman, R E Nickel, et al.
The Journal of Bone and Joint Surgery. British Volume
|
January 1, 1982
A review of the morphology of Perthes' disease
A Catterall, J Pringle, P D Byers, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 50 results.
Birth Defects Original Article Series
|
January 1, 1976
The neuronal ceroid lipofuscinoses in British Columbia: a clinical epidemiologic and ultrastructural study
P M MacLeod, C L Dolman, E Chang, et al.
The Medical Journal of Australia
|
October 29, 1983
Non-specific senile dementia mimicking Huntington's disease in two siblings
V J Ojeda, W Knezevic, D J Willsher, et al.
Neurology
|
June 1, 1977
Progressive cerebellar ataxia, spasticity, psychomotor retardation, and hexosaminidase deficiency in a 10-year-old child: juvenile Sandhoff disease
P M MacLeod, S Wood, J E Jan, et al.
The New England Journal of Medicine
|
March 1, 1984
Prenatal diagnosis of neuronal ceroid lipofuscinosis
P M MacLeod, C L Dolman, R E Nickel, et al.
Archives of Neurology
|
February 1, 1975
Hereditary mental depression and Parkinsonism with taurine deficiency
T L Perry, P J Bratty, S Hansen, et al.
Neurology
|
November 1, 1976
Krabbe's leukodystrophy without globoid cells
H G Dunn, C L Dolman, D F Farrell, et al.
Developmental Medicine and Child Neurology
|
October 1, 1979
Progressive rubella panencephalitis: clinical course and response to 'isoprinosine'
J E Jan, A J Tingle, G Donald, et al.
American Journal of Diseases of Children (1960)
|
February 1, 1975
Optic nerve hypoplasia with hypopituitarism. Septo-optic dysplasia with hypopituitarism
H Patel, W J Tze, J U Crichton, et al.
American Journal of Medical Genetics
|
December 1, 1985
Prenatal diagnosis of neuronal ceroid-lipofuscinoses
P M MacLeod, C L Dolman, R E Nickel, et al.
The Journal of Bone and Joint Surgery. British Volume
|
January 1, 1982
A review of the morphology of Perthes' disease
A Catterall, J Pringle, P D Byers, et al.
Page
of 5