Über die Rolle der Blutzellen in der Diagnostik erblicher Stoffwechselkrankheiten
- 1 October 1963
- journal article
- Published by Springer Nature in Klinische Wochenschrift
- Vol. 41 (19), 937-941
- https://doi.org/10.1007/bf01478534
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- HEREDITARY ENZYMATIC EFFECTS AS ILLUSTRATED BY HYPOPHOSPHATASIA*Annals of the New York Academy of Sciences, 2006
- LEUKOCYTE DEBRANCHING ENZYME IN GLYCOGEN STORAGE DISEASEJournal of Clinical Investigation, 1963
- A nanomole adaption of the automatic amino acid analysis according to Spackman, Stein, and Moore (1985)Biochemical and Biophysical Research Communications, 1962
- PHOSPHORYLASE ACTIVITY IN LEUCOCYTES FROM PATIENTS WITH GLYCOGEN-STORAGE DISEASEThe Lancet, 1961
- PYRIMIDINE METABOLISM IN MAN. IV. THE ENZYMATIC DEFECT OF OROTIC ACIDURIA*Journal of Clinical Investigation, 1961
- Metabolism of the white blood cells in maple-syrup-urine diseaseBiochimica et Biophysica Acta, 1960
- A STUDY OF SUBJECTS WITH ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY. II. INVESTIGATION OF LEUKOCYTE ENZYMES*Journal of Clinical Investigation, 1959
- A STUDY OF SUBJECTS WITH ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY: INVESTIGATION OF PLATELET ENZYMES*Journal of Clinical Investigation, 1959
- The enzymic defect of hereditary methemoglobinemia: diaphoraseBiochimica et Biophysica Acta, 1959
- Uridyl Transferases and the Formation of Uridine Triphosphate : Uridyl Transferases and the Formation of Uridine DiphosphogalactoseNature, 1953