Effectiveness of enzyme replacement therapy in 1028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry
Top Cited Papers
- 1 August 2002
- journal article
- Published by Elsevier in The American Journal of Medicine
- Vol. 113 (2) , 112-119
- https://doi.org/10.1016/s0002-9343(02)01150-6
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Low-Dose High-Frequency Enzyme Replacement Therapy Prevents Fractures without Complete Suppression of Painful Bone Crises in Patients with Severe Juvenile Onset Type I Gaucher DiseaseBlood Cells, Molecules, and Diseases, 1998
- Effect of Low-dose Enzyme Replacement Therapy on Bones in Gaucher Disease Patients with Severe Skeletal InvolvementBlood Cells, Molecules, and Diseases, 1996
- Acceleration of retarded growth in children with Gaucher disease after treatment with algluceraseThe Journal of Pediatrics, 1996
- The Clinical Course of Treated and Untreated Gaucher Disease. A Study of 45 PatientsBlood Cells, Molecules, and Diseases, 1995
- Glucocerebrosidase for treatment of Gaucher's disease: first German long-term resultsJournal of Hepatology, 1994
- Enzyme replacement treatment in type 1 and type 3 Gaucher's diseaseThe Lancet, 1994
- Gaucherʼs Disease: A Pilot Study of the Symptomatic Responses to Enzyme Replacement TherapyJournal of Neuroscience Nursing, 1993
- Replacement Therapy for Inherited Enzyme Deficiency — Macrophage-Targeted Glucocerebrosidase for Gaucher's DiseaseNew England Journal of Medicine, 1991
- Hepatopulmonary Syndrome: An Evolving Perspective in the Era of Liver TransplantationHepatology, 1990
- Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's diseaseBiochemical and Biophysical Research Communications, 1965