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Inherited Metabolic Disorders

Exhibiting 14 entries found in the GMN corpus.

YearTitle & TagsAuthor(s)
1963 CEA simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants.
1822 CE​–1823 CEAccount of a singular variety of urine, which turned black soon after being discharged; with some particulars respecting its chemical properties.
1882 CEDe l’epithélioma primitif de la rate; hypertrophie idiopathique de la rate sans leucémie.
1926 CEDer Morbus Gaucher und die ihm ähnlichen Erkrankungen. (Die lipoidzellige Splenohepatomegalie Typus Niemann und die diabetische Lipoidzellenhyperplasie der Milz.)
1914 CEEin unbekanntes Krankheitsbild.
1909 CEInborn errors of metabolism.
1861 CEKlinik der Leberkrankheiten. Bd. 2.
1859 CELieber das Alcapton; ein neuer Beitrag zur Frage: welche Stoffe des Harns können Kupferreduction bewirken?
1887 CEOn arrested cerebral development, with special reference to its cortical pathology.
1810 CEOn cystic oxide, a new species of urinary calculus.
1846 CE​–1848 CESeveral specimens of cystine exhibited, with the particulars of two cases in which this deposit occurred in the urine.
1880 CE​–1881 CESymmetrical changes in the region of the yellow spot in each eye of an infant.
1895 CEUeber die Pentosurie, eine neue Anomalie des Stoffwechsels.
1934 CEUtskillelse av fenylpyrodruesyre i urinen som stoffskifteanomali i forbindelse med imbecilletet.