Urinary Alanine Excretor in a Huntington's Chorea Family

Author:

Cowie Valerie,Seakins J. W. T.

Abstract

In the course of urine-testing with Phenistix in a survey∗ of the inmates of remand homes, classifying schools and approved schools, only one positive result has been obtained from 2,300 boys and 541 girls tested so far in the London area. This was obtained with the urine of a boy who proved not to be Phenylketonuric, and further investigations were carried out in his case and with members of his family.

Publisher

Royal College of Psychiatrists

Subject

General Medicine

Reference6 articles.

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3. Mayer-Gross W. , Slater E. , and Roth M. , Clinical Psychiatry, 1960. London.

4. An inborn defect in the metabolism of tyrosine in infants on a normal diet

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1. Hypothalamic Dysfunction and Neuroendocrine and Metabolic Alterations in Huntington Disease: Clinical Consequences and Therapeutic Implications;Reviews in the Neurosciences;2007-01

2. Literaturverzeichnis;Über methodische Vorarbeiten zu Stoffwechselanalysen an isolierten und kultivierten Zellen von Patienten mit erblichen Alterungsprozessen;1977

3. Der Einflu� der Verabreichung von Aminos�uren, speziell von l-DOPA und ?-Methyldopa, auf die Zusammensetzung des Liquor cerebrospinalis bei extrapyramidalen Syndromen;Zeitschrift f�r Neurologie;1973

4. SERUM LEVELS OF PHENYLALANINE AND TYROSINE IN HUNTINGTON'S CHOREA;Acta Psychiatrica Scandinavica;1971-03

5. FERRIC CHLORIDE REACTION IN HUNTINGTON'S CHOREA;Acta Psychiatrica Scandinavica;1971-03

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