(Q40779698)

23 September 2017

1 reference

title

Inborn errors of metabolism: clues to understanding human behavioral disorders (English)

1 reference

PubMed ID

823933

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A823933

31 July 2022

1

1 reference

PubMed ID

823933

23 September 2017

language of work or name

English

0 references

publication date

1 July 1976

1 reference

23 September 2017

1 reference

23 September 2017

6

1 reference

23 September 2017

3

1 reference

23 September 2017

263-284

1 reference

https://scigraph.springernature.com/pub.10.1007/bf01065723

23 September 2017

0 references

cites work

Serum Dopamine-Beta-Hydroxylase Activity

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF01065723

Maple syrup urine disease metabolites studies in cerebellum cultures.

21 January 2018

1 reference

12 December 2020

Reduced monoamine oxidase activity in blood platelets from bipolar depressed patients

1 reference

12 December 2020

Metachromatic leukodystrophy (MLD). 8. MLD in adults; diagnosis and pathogenesis

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12 December 2020

Intelligence quotients and intelligence loss in patients with phenylketonuria and some variant states

1 reference

12 December 2020

Congenital adrenal hyperplasia. II. Cognitive and behavioral studies

1 reference

12 December 2020

Two functional X chromosomes in human fetal oocytes.

1 reference

12 December 2020

Dopamine-β-Hydroxylase Deficits in the Brains of Schizophrenic Patients

1 reference

12 December 2020

Folate-responsive homocystinuria and "schizophrenia". A defect in methylation due to deficient 5,10-methylenetetrahydrofolate reductase activity

1 reference

12 December 2020

The genetics of galactose-1-phosphate uridyl transferase deficiency

1 reference

12 December 2020

Restricted variation in the glycolytic enzymes of human brain and erythrocytes.

1 reference

12 December 2020

Psychiatric illness in the families of hyperactive children.

1 reference

12 December 2020

1 reference

12 December 2020

New variant of phenylketonuria with progressive neurological illness unresponsive to phenylalanine restriction

1 reference

12 December 2020

Correlation of erythrocyte catechol-O-methyltransferase activity between siblings

1 reference

12 December 2020

Cytogenetic and psychosexual incongruities with a note on space-form blindness

1 reference

12 December 2020

Congenital adrenal hyperplasia. I. Family studies of IQ

1 reference

12 December 2020

Heme biosynthesis in intermittent acute prophyria: decreased hepatic conversion of porphobilinogen to porphyrins and increased delta aminolevulinic acid synthetase activity

1 reference

12 December 2020

Amino acid metabolism and its disorders.

1 reference

12 December 2020

Further evidence of sex-linked major-gene influence on human spatial visualizing ability

1 reference

12 December 2020

The Psychiatric Status of the Legal Families of Adopted Hyperactive Children

1 reference

12 December 2020

A phenylethylamine oxidising defect in migraine

1 reference

12 December 2020

Behavioral phenotypes in organic genetic disease. Presidential address to the Society for Pediatric Research, May 1, 1971.

1 reference

12 December 2020

Cystinuria: increased prevalence in patients with mental disease.

1 reference

12 December 2020

Nonketotic hyperglycinemia. Glycine accumulation due to absence of glycerine cleavage in brain

1 reference

12 December 2020

Editorial: Metabolic hypotheses in schizophrenia

1 reference

12 December 2020

The variability in manifestations of untreated patients with phenylketonuria (phenylpyruvic aciduria).

1 reference

12 December 2020

Phenylketonuria and its variations. A review of recent developments

1 reference

12 December 2020

A family study of the hyperactive child syndrome

1 reference

12 December 2020

Reduced Catechol- O -Methyltransferase Activity in Red Blood Cells of Women with Primary Affective Disorder

1 reference

12 December 2020

Alcohol Problems in Adoptees Raised Apart From Alcoholic Biological Parents

1 reference

12 December 2020

Inheritance of very low serum dopamine-beta-hydroxylase activity

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01065723

1 reference

23 September 2017

1 reference

PubMed ID

823933