PROLIDASE DEFICIENCY
- 1 September 1983
- journal article
- case report
- Published by Wiley in Acta Paediatrica
- Vol. 72 (5), 785-788
- https://doi.org/10.1111/j.1651-2227.1983.tb09815.x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Prolidase Deficiency: An Inborn Error of Metabolism with Major Dermatological ManifestationsDermatology, 1982
- Prolidase deficiency with iminodipeptiduria: Biochemical investigations and first results of attempted therapyJournal of Inherited Metabolic Disease, 1981
- Prolidase deficiency: its dermatological manifestations and some additional biochemical studiesArchives of Dermatology, 1979
- Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiencyThe Journal of Pediatrics, 1977
- Prolidase deficiency: Report of a second case with quantitation of the excessively excreted amino acidsThe Journal of Pediatrics, 1977
- The mass spectrometric identification of dipeptides in the urine of a patient suffering from chronic skin ulceration and oedemaClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- A prolidase deficiency in man with iminopeptiduriaMetabolism, 1974
- Determination of dipeptides in urineClinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- Further studies on a patient with iminodipeptiduria: A probable case of prolidase deficiencyMetabolism, 1972
- A syndrome resembling lathyrism associated with iminodipeptiduriaAmerican Journal Of Medicine, 1968