Diet and Inborn Errors of Metabolism

This publication has 20 references indexed in Scilit:

• The reduction of methaemoglobin in red blood cells and studies on the cause of idiopathic methaemoglobinaemia
  Biochemical Journal, 1948
• QUANTITATIVE CLINICAL CHEMISTRY. INTERPRETATIONS
  The Lancet Healthy Longevity, 1947
• Studies in alcaptonuria
  Biochemical Journal, 1947
• PHENYLPYRUVIC OLIGOPHRENIA. REPORT OF A CASE IN AN INFANT WITH QUANTITATIVE CHEMICAL STUDIES OF THE URINE
  Journal of Clinical Investigation, 1943
• The Pharmacology of Sodium Hydroxyacetate with Observations on the Toxicity of Glycine*†
  Journal of the American Pharmaceutical Association (Scientific ed.), 1942
• PHENYLPYRUVIC OLIGOPHRENIA
  Archives of Neurology & Psychiatry, 1937
• INHERITANCE OF PHENYLPYRUVIC AMENTIA (PHENYLKETONURIA)
  The Lancet, 1935
• Über Ausscheidung von Phenylbrenztraubensäure in den Harn als Stoffwechselanomalie in Verbindung mit Imbezillität.
  Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1934
• A new error of tyrosine metabolism: tyrosinosis. The intermediary metabolism of tyrosine and phenylalanine
  Biochemical Journal, 1932
• Familiäre Cystindiathese.
  Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1903