Descriptor
Exceptional Child Research | 5 |
Medical Evaluation | 5 |
Mental Retardation | 5 |
Medical Research | 3 |
Diseases | 2 |
Infants | 2 |
Special Health Problems | 2 |
Adolescents | 1 |
Biochemistry | 1 |
Congenital Impairments | 1 |
Downs Syndrome | 1 |
More ▼ |
Source
Journal of Pediatrics | 5 |
Author
Aase, Jon M. | 1 |
Anand, Sudhir K. | 1 |
Elsas, Louis J. | 1 |
Gong, Bradley T. | 1 |
Griffin, Robert F. | 1 |
Smith, David W. | 1 |
Zee, David S. | 1 |
Publication Type
Education Level
Audience
Location
Laws, Policies, & Programs
Assessments and Surveys
What Works Clearinghouse Rating

Griffin, Robert F.; Elsas, Louis J. – Journal of Pediatrics, 1975
In an attempt to improve the identification of the asymptomatic carrier of classic phenylketonuria (PKU) 59 male and female normal control Ss were differentiated from 18 males and females heterozgous for PKU. (DB)
Descriptors: Biochemistry, Exceptional Child Research, Genetics, Identification

Zee, David S.; And Others – Journal of Pediatrics, 1974
Reported is the case of a female infant whose early symptom of ophthalmoplegia (paralysis of one or more motor nerves in the eye) led to eventual diagnosis and treatment for maple syrup urine disease, a condition in which early dietary restrictions can prevent severe mental retardation and neurologic disability. (DB)
Descriptors: Diseases, Exceptional Child Research, Eye Movements, Infants

Aase, Jon M.; And Others – Journal of Pediatrics, 1973
Descriptors: Downs Syndrome, Drafting, Ears, Exceptional Child Research

Anand, Sudhir K.; And Others – Journal of Pediatrics, 1972
Descriptors: Adolescents, Diseases, Exceptional Child Research, Medical Case Histories

Smith, David W.; Gong, Bradley T. – Journal of Pediatrics, 1973
Descriptors: Congenital Impairments, Exceptional Child Research, Growth Patterns, Infants