Literature DB >> 823933

Inborn errors of metabolism: clues to understanding human behavioral disorders.

G S Omenn.   

Abstract

Detailed behavioral and biochemical investigation of patients with inborn errors of metabolism, especially those intrinsic to the nervous system, may provide many clues to the genetic predisposition underlying human behavioral traits. Relatives of such patients and other individuals with homologous enzymatic lesions due to alleles specifying intermediate activity need to be studied as well. Among the metabolic disorders discussed selectively here, some masquerade as schizophrenia, manic-depressive illness, or hyperactivity syndrome of childhood, providing examples of the striking heterogeneity to be found for these common behavioral disorders.

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Year:  1976        PMID: 823933     DOI: 10.1007/BF01065723

Source DB:  PubMed          Journal:  Behav Genet        ISSN: 0001-8244            Impact factor:   2.805


  32 in total

1.  Congenital adrenal hyperplasia. II. Cognitive and behavioral studies.

Authors:  L S McGuire; K O Ryan; G S Omenn
Journal:  Behav Genet       Date:  1975-04       Impact factor: 2.805

2.  Serum dopamine-beta-hydroxylase activity.

Authors:  R Weinshilboum; J Axelrod
Journal:  Circ Res       Date:  1971-03       Impact factor: 17.367

3.  Two functional X chromosomes in human fetal oocytes.

Authors:  S M Gartler; R M Liskay; N Gant
Journal:  Exp Cell Res       Date:  1973-12       Impact factor: 3.905

4.  Reduced monoamine oxidase activity in blood platelets from bipolar depressed patients.

Authors:  D L Murphy; R Weiss
Journal:  Am J Psychiatry       Date:  1972-05       Impact factor: 18.112

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

Authors:  J L Berman; R Ford
Journal:  J Pediatr       Date:  1970-11       Impact factor: 4.406

6.  Maple syrup urine disease metabolites studies in cerebellum cultures.

Authors:  D H Silberberg
Journal:  J Neurochem       Date:  1969-07       Impact factor: 5.372

7.  The genetics of galactose-1-phosphate uridyl transferase deficiency.

Authors:  E Beutler; M C Baluda; P Sturgeon; R W Day
Journal:  J Lab Clin Med       Date:  1966-10

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

Authors:  J M Freeman; J D Finkelstein; S H Mudd
Journal:  N Engl J Med       Date:  1975-03-06       Impact factor: 91.245

9.  Dopamine-beta-hydroxylase deficits in the brains of schizophrenic patients.

Authors:  C D Wise; L Stein
Journal:  Science       Date:  1973-07-27       Impact factor: 47.728

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

Authors:  J Austin; D Armstrong; S Fouch; C Mitchell; D Stumpf; L Shearer; O Briner
Journal:  Arch Neurol       Date:  1968-03
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  4 in total

Review 1.  Neurochemistry and behavior in man.

Authors:  G S Omenn
Journal:  West J Med       Date:  1976-12

Review 2.  Genetics and schizophrenic behavior.

Authors:  E Kahn
Journal:  Psychiatr Q       Date:  1980

3.  Phenylketonuria (PKU) and the single gene: an old story retold.

Authors:  R M Murphey
Journal:  Behav Genet       Date:  1983-03       Impact factor: 2.805

Review 4.  Genetic disorders presenting as "schizophrenia". Karl Bonhoeffer's early view of the psychoses in the light of medical genetics.

Authors:  P Propping
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

  4 in total

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