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Journal of Pediatrics | 32 |
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Koenig, Harold M.; And Others – Journal of Pediatrics, 1975
Measured were the free erthrocyte protoporphyrin levels (a blood component) in 29 Ss with alpha thalassemia (a hereditary anemis), 19 Ss with iron deficiency anemia, and 24 normal control Ss. (DB)
Descriptors: Anemia, Biochemistry, Exceptional Child Research, Medical Evaluation

Voorhess, Mary L.; And Others – Journal of Pediatrics, 1975
Urinanalysis was performed on 24-hour samples of 11 iron deficient children (1 to 13 years of age) to determine levels of monoamine oxidase (an enzyme). (DB)
Descriptors: Anemia, Biochemistry, Exceptional Child Research, Medical Evaluation

Jowsey, Jenifer; Johnson, Kenneth A. – Journal of Pediatrics, 1972
Descriptors: Anatomy, Diseases, Exceptional Child Research, Medical Evaluation

Lovric, V. Albert; And Others – Journal of Pediatrics, 1975
Descriptors: Anemia, Biochemistry, Exceptional Child Research, Medical Evaluation

Geller, Gary; And Others – Journal of Pediatrics, 1975
Serum of five children ages 1 to 19 months with congenital pure red cell aplasia (incomplete or defective development of red blood cells) was injected in normal mice to determine possible inhibition of red blood cell formulating stimulants. (CL)
Descriptors: Biochemistry, Exceptional Child Research, Medical Evaluation, Medical Research

Feinberg, S. B.; Fisch, R. O. – Journal of Pediatrics, 1972
Descriptors: Diseases, Exceptional Child Research, Medical Evaluation, Physical Development

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

Booth, Carol W.; And Others – Journal of Pediatrics, 1975
Prenatal monitoring for metachromatic leukodystrophy (a fatal inherited metabolic disorder) suggested that the determination of levels of cerebroside sulfatase in the amniotic fluid helped in the prenatal detection of this disorder. (DB)
Descriptors: Biochemistry, Exceptional Child Research, Medical Evaluation, Medical Research

Gatti, Richard A.; And Others – Journal of Pediatrics, 1972
Descriptors: Diseases, Exceptional Child Research, Infants, Medical Evaluation

Moss, Arthur J.; And Others – Journal of Pediatrics, 1975
Investigated in 16 persons ages 3 to 23 years with severe cystic fibrosis was the absorption level of digoxin (a lipid soluble medication). (CL)
Descriptors: Biochemistry, Cystic Fibrosis, Exceptional Child Research, Medical Evaluation

Neal, William A.; And Others – Journal of Pediatrics, 1975
Nineteen of thirty-three children (5-to 18-years-old) whose arterial septal heart defects were surgically repaired did not undergo pre-operative cardiac catheterization. (CL)
Descriptors: Adolescents, Children, Exceptional Child Research, Heart Disorders

McIntosh, Sue – Journal of Pediatrics, 1975
Sequential urinalysis of four premature infants with marked physiologic anemia demonstrated no erythropoietin (substances which may stimulate red blood cell formulation). (CL)
Descriptors: Biochemistry, Exceptional Child Research, Infants, Medical Evaluation

Dobson, Velma; And Others – Journal of Pediatrics, 1975
Evaluated was retinal functioning of 15 4-year-old children who had received phototherapy for neonatal hyperbilirubinemia (jaundice). (DB)
Descriptors: Exceptional Child Research, Followup Studies, Infants, Medical Evaluation

Strauss, Milton E.; And Others – Journal of Pediatrics, 1976
Studied were the behavioral characteristics of 60 methadone addicted infants and 53 nonaddicted infants during the first year of life (neonatal period, and at 3, 6, and 12 months of age). (PT)
Descriptors: Behavior Patterns, Cognitive Development, Drug Abuse, Infants

Schaller, Jane – Journal of Pediatrics, 1972
Descriptors: Diseases, Exceptional Child Research, Medical Case Histories, Medical Evaluation