Neuropathology provides clues to the pathophysiology of Gaucher disease
- 9 June 2004
- journal article
- research article
- Published by Elsevier BV in Molecular Genetics and Metabolism
- Vol. 82 (3), 192-207
- https://doi.org/10.1016/j.ymgme.2004.04.011
Abstract
No abstract availableThis publication has 69 references indexed in Scilit:
- Management of neuronopathic Gaucher disease: A European consensusJournal of Inherited Metabolic Disease, 2001
- Late-infantile Gaucher disease in a child with myoclonus and bulbar signs: neuropathological and neurochemical findingsActa Neuropathologica, 1991
- Type 2 and type 3 Gaucher disease: A morphological and biochemical studyAnnals of Neurology, 1986
- Determination of Gaucher's disease phenotypes with monoclonal antibodyClinica Chimica Acta; International Journal of Clinical Chemistry, 1983
- Mutations of glucocerebrosidase: discrimination of neurologic and non-neurologic phenotypes of Gaucher disease.Proceedings of the National Academy of Sciences of the United States of America, 1982
- SphingolipidosesAnnual Review of Biochemistry, 1978
- Gaucher's Disease: Neurologic Disorder in Adult SiblingsAnnals of Internal Medicine, 1973
- Acute infantile Gaucher's disease in identical twinsNeurology, 1969
- Demonstration of a deficiency of glucocerebroside-cleaving enzyme in Gaucher's disease.JCI Insight, 1966
- The neuropathology of infantile Gaucher's diseaseThe Journal of Pathology and Bacteriology, 1956