Coexistence of Deficiencies of Uroporphyrinogen III Synthase and Decarboxylase in a Patient with Congenital Erythropoietic Porphyria and in His Family

Articles in the same Issue

1. Sonstiges
2. Titelei
3. EDITORIAL
4. REVIEW
5. Simplified Sizing of Low-Density Lipoprotein Using Polyacrylamide Gradient Gel Electrophoresis of Plasma
6. Urinary Biotinidase and Alanine Excretion in Patients with Insulin-Dependent Diabetes Mellitus
7. Marginal Folate Deficiency as a Possible Cause of Hyperhomocysteinaemia in Stroke Patients
8. 17β-Estradiol and Tamoxifen Prevent the Over-Glycosylation of Rat Trabecular Bone Collagen Induced by Ovariectomy
9. Coexistence of Deficiencies of Uroporphyrinogen III Synthase and Decarboxylase in a Patient with Congenital Erythropoietic Porphyria and in His Family
10. Discrimination between Normal Wildtype and Carriers of Coagulation Factor V Leiden Mutation by the Activated Protein C Resistance Test in the Presence of Factor V Deficient Plasma
11. Comparison of Sialic Acids Excretion in Spot Urines and 24-Hour-Urines of Children and Adults
12. The Iron Content of Serum Ferritin: Physiological Importance and Diagnostic Value
13. Determination of Vanillylmandelic, 5-Hydroxyindoleacetic and Homovanillic Acid in Urine by Isocratic Liquid Chromatography
14. Comparison of the Clinical Performances of the Immunoenzymometric Assays for N-Terminal and C-Terminal Type I Collagen Telopeptides and the HPLC Assay for Pyridinium Cross-Links