Histidinemia and infantile autism

Journal of Autism and Developmental Disorders

Volumn 9, Issue 1, 1979, Pages 55-60

  Kotsopoulos, S ^a,b   Kutty, K M ^b  

^a MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

^b Dr C A Janeway Child Health Centre ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID;

AUTISM; BLOOD AND HEMOPOIETIC SYSTEM; CASE REPORT; CENTRAL NERVOUS SYSTEM; ENZYME DEFICIENCY; HISTIDINEMIA; INFANTILE AUTISM; SCHOOL CHILD;

AMINO ACID METABOLISM, INBORN ERRORS; AUTISTIC DISORDER; CHILD; CHILD DEVELOPMENT; FAMILY CHARACTERISTICS; HISTIDINE; HUMAN; MALE; PARENT-CHILD RELATIONS; SPEECH DISORDERS;

EID: 0018755170     PISSN: 01623257     EISSN: 15733432     Source Type: Journal    
DOI: 10.1007/BF01531292     Document Type: Article

References (9)

1. The “autistic syndrome” and phenylketonuria
2. Histidinemia
3. Malabsorption and cerebral dysfunction: A multivariate and comparative study of autistic children
4. Delayed speech and histidinemia
5. Routine newborn screening for histidinemia
6. Biochemical studies of children with the syndrome of autism, childhood schizophrenia and related developmental disabilities: A review
7. Infantile autism and other child psychoses
8. Causes of infantile autism: Some considerations from recent research