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Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2011
Osteopontin polymorphic susceptibility factor for Parkinson's disease among patients with Gaucher diseaseAvigayil Ribner, Gheona Altarescu, Ari Zimran, et al.
American Journal of Hematology|July 25, 2003
D-dimer assay in Gaucher disease: correlation with severity of bone and lung involvementDavid Shitrit, Bernard Rudensky, Ari Zimran, et al.
Blood Cells, Molecules & Diseases|March 30, 2007
A pharmacokinetic analysis of a novel enzyme replacement therapy with Gene-Activated human glucocerebrosidase (GA-GCB) in patients with type 1 Gaucher diseaseAri Zimran, Kenneth Loveday, Candida Fratazzi, et al.
Clinical Rheumatology|April 27, 2010
Effect of vitamin D receptor (VDR) genotypes on the risk for osteoporosis in type 1 Gaucher diseaseAllen Greenwood, Deborah Elstein, Ari Zimran, et al.
Drugs|September 23, 2025
Pharmacological Therapies in Paroxysmal Nocturnal Haemoglobinuria: Focus on Complement InhibitionRichard J Kelly, Matthew Holt, Jeff Szer
Ejhaem|August 21, 2023
Normalisation of haemoglobin and control of breakthrough haemolysis with increased frequency pegcetacoplan dosing in treated paroxysmal nocturnal haemoglobinuriaAmanda K Davis, Nicholas Bingham, Jeff Szer
Clinical Advances in Hematology & Oncology : H&O|December 29, 2012
Clinical roundtable monograph: Paroxysmal nocturnal hemoglobinuria: a case-based discussionJeff Szer, Anita Hill, Ilene Ceil Weitz
Clinical Therapeutics|October 9, 2007
Effect of miglustat on bone disease in adults with type 1 Gaucher disease: a pooled analysis of three multinational, open-label studiesGregory M Pastores, Deborah Elstein, Martin Hrebícek, et al.
Surgical Laparoscopy, Endoscopy & Percutaneous Techniques|March 10, 2018
Splenectomy in Gaucher Disease: A Call for Minimally Invasive SurgeryMichael R Freund, Petachia Reissman, Ari Zimran, et al.
Blood Cells, Molecules & Diseases|December 9, 2009
Proteinase-activated receptor (PAR1) polymorphic variant correlates with thrombocytopenia in Gaucher diseaseGheona Altarescu, Orit Seror-Bukris, Ari Zimran, et al.
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