The Clinical Evaluation of Cobalamin Deficiency by Determination of Methylmalonic Acid in Serum or Urine is not Invalidated by the Presence of Heterozygous Methylmalonic-Acidaemia

Articles in the same Issue

1. Sonstiges
2. Titelei
3. Honours
4. Cholecystokinin and Glucose-Induced Insulinaemia in Dogs With and Without Pancreatic Acinar Atrophy
5. Magnitude and Kinetics of Alterations in Plasma Catecholamines and Leukocyte β-Adrenergic Receptors in Response to Anaesthesia and Surgery
6. The Use of Cluster Analysis in Clinical Chemical Diagnosis of Liver Diseases
7. A Colorimetric Assay for the Determination of Acid Nucleoside Triphosphatase Activity
8. HLA Class I-, Complement C4- and 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
9. The Clinical Evaluation of Cobalamin Deficiency by Determination of Methylmalonic Acid in Serum or Urine is not Invalidated by the Presence of Heterozygous Methylmalonic-Acidaemia
10. SHORT COMMUNICATION
11. Tehnical reports