Ari Zimran
Researcher Next ID · RN-042344
Researcher · Biochemistry, Genetics and Molecular Biology
Hebrew University of Jerusalem
Jerusalem, Israel
- Works count
- 391
- Citation count
- 11,471
- H-index
- 55
- i10-index
- 188
Research interests
Publications
Management goals for type 1 Gaucher disease: An expert consensus document from the European working group on Gaucher disease
Blood Cells Molecules and Diseases · 2016 · 10.1016/j.bcmd.2016.10.008
Gaucher disease types 1 and 3: Phenotypic characterization of large populations from the ICGG Gaucher Registry
American Journal of Hematology · 2015 · 10.1002/ajh.24063
Glucosylsphingosine Is a Highly Sensitive and Specific Biomarker for Primary Diagnostic and Follow-Up Monitoring in Gaucher Disease in a Non-Jewish, Caucasian Cohort of Gaucher Disease Patients
PLoS ONE · 2013 · 10.1371/journal.pone.0079732
Pilot study using ambroxol as a pharmacological chaperone in type 1 Gaucher disease
Blood Cells Molecules and Diseases · 2012 · 10.1016/j.bcmd.2012.09.006
How I treat Gaucher disease
Blood · 2011 · 10.1182/blood-2011-04-308890
Pivotal trial with plant cell–expressed recombinant glucocerebrosidase, taliglucerase alfa, a novel enzyme replacement therapy for Gaucher disease
Blood · 2011 · 10.1182/blood-2011-07-366955
The incidence of Parkinsonism in patients with type 1 Gaucher disease: Data from the ICGG Gaucher Registry
Blood Cells Molecules and Diseases · 2010 · 10.1016/j.bcmd.2010.10.006
Phase 1/2 and extension study of velaglucerase alfa replacement therapy in adults with type 1 Gaucher disease: 48-month experience
Blood · 2010 · 10.1182/blood-2010-02-268649
A Plant-Derived Recombinant Human Glucocerebrosidase Enzyme—A Preclinical and Phase I Investigation
PLoS ONE · 2009 · 10.1371/journal.pone.0004792
Oral maintenance clinical trial with miglustat for type I Gaucher disease: switch from or combination with intravenous enzyme replacement
Blood · 2007 · 10.1182/blood-2007-02-075960
Effect of Enzyme Replacement Therapy With Imiglucerase on BMD in Type 1 Gaucher Disease
Journal of Bone and Mineral Research · 2006 · 10.1359/jbmr.061004
Increased incidence of Parkinson disease among relatives of patients with Gaucher disease
Blood Cells Molecules and Diseases · 2006 · 10.1016/j.bcmd.2006.02.004
Gaucher disease and cancer incidence: a study from the Gaucher Registry
Blood · 2005 · 10.1182/blood-2004-12-4672
Gaucher disease type 1: Revised recommendations on evaluations and monitoring for adult patients
Seminars in Hematology · 2004 · 10.1053/j.seminhematol.2004.07.010
Sustained therapeutic effects of oral miglustat (Zavesca, N‐butyldeoxynojirimycin, OGT 918) in type I Gaucher disease
Journal of Inherited Metabolic Disease · 2004 · 10.1023/b:boli.0000045756.54006.17
The role of the iminosugar N‐butyldeoxynojirimycin (miglustat) in the management of type I (non‐neuronopathic) Gaucher disease: A position statement
Journal of Inherited Metabolic Disease · 2003 · 10.1023/a:1025902113005
Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapy
Journal of Inherited Metabolic Disease · 2001 · 10.1023/a:1010335505357
Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis
The Lancet · 2000 · https://doi.org/10.1016/s0140-6736(00)02161-9
The Gaucher Registry
Archives of Internal Medicine · 2000 · https://doi.org/10.1001/archinte.160.18.2835
Occurrence of Parkinson's syndrome in type 1 Gaucher disease
QJM · 1996 · https://doi.org/10.1093/qjmed/89.9.691
Mutations in Jewish patients with Gaucher disease
Blood · 1992 · 10.1182/blood.v79.7.1662.bloodjournal7971662
Current projects
No projects listed.