Peroxisomal Disorders: Overview
- 17 December 1996
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 804 (1) , 427-441
- https://doi.org/10.1111/j.1749-6632.1996.tb18634.x
Abstract
No abstract availableThis publication has 81 references indexed in Scilit:
- Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groupsThe Journal of Pediatrics, 1995
- Differential protein import deficiencies in human peroxisome assembly disorders.The Journal of cell biology, 1994
- Studies on phytanic acid α-oxidation in rat liver and cultured human skin fibroblastsBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1993
- Adrenoleukodystrophy: Phenotypic variability and implications for therapyJournal of Inherited Metabolic Disease, 1992
- Reversal of Early Neurologic and Neuroradiologic Manifestations of X-Linked Adrenoleukodystrophy by Bone Marrow TransplantationNew England Journal of Medicine, 1990
- Reversal by Liver Transplantation of the Complications of Primary Hyperoxaluria as Well as the Metabolic DefectNew England Journal of Medicine, 1989
- Pseudo-Zellweger syndrome: Deficiencies in several peroxisomal oxidative activitiesThe Journal of Pediatrics, 1986
- The cerebrohepatorenal syndrome of Zellweger, morphologic and metabolic aspectsAmerican Journal of Medical Genetics, 1983
- Infantile phytanic acid storage disease, a possible variant of Refsum's disease: Three cases, including ultrastructural studies of the liverJournal of Inherited Metabolic Disease, 1982
- Bronzekrankheit und sklerosierende EncephalomyelitisArchiv Fur Psychiatrie Und Nervenkrankheiten, 1923