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Deborah Elstein

Showing results (31-40 of 154) with videos related to

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Blood Cells, Molecules & Diseases|November 16, 2016
Liver involvement in Gaucher disease - Review and clinical approachTomer Adar, Yaron Ilan, Deborah Elstein, et al.
Blood Cells, Molecules & Diseases|February 11, 2017
Children with type 1 Gaucher disease: Changing profiles in the 21st centuryDeborah Elstein, Gheona Altarescu, Aya Abrahamov, et al.
Blood Cells, Molecules & Diseases|October 23, 2012
Evolving features in type 3 Gaucher disease on long-term enzyme replacement therapyDeborah Elstein, Ayala Abrahamov, Gheona Altarescu, 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.
Journal of Perinatal Medicine|August 2, 2011
Requests and usage of epidural analgesia in grand-grand multiparous and similar-aged women with lesser parity: prospective observational studyAlexander Ioscovich, Angelika Fadeev, Alina Rivilis, et al.
Gene|June 20, 2012
X-inactivation in Fabry diseaseDeborah Elstein, Ella Schachamorov, Rachel Beeri, 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.
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.
Pageof 16

Showing results (31-40 of 154) with videos related to

Sort By:
Pageof 16
Blood Cells, Molecules & Diseases|November 16, 2016
Liver involvement in Gaucher disease - Review and clinical approachTomer Adar, Yaron Ilan, Deborah Elstein, et al.
Blood Cells, Molecules & Diseases|February 11, 2017
Children with type 1 Gaucher disease: Changing profiles in the 21st centuryDeborah Elstein, Gheona Altarescu, Aya Abrahamov, et al.
Blood Cells, Molecules & Diseases|October 23, 2012
Evolving features in type 3 Gaucher disease on long-term enzyme replacement therapyDeborah Elstein, Ayala Abrahamov, Gheona Altarescu, 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.
Journal of Perinatal Medicine|August 2, 2011
Requests and usage of epidural analgesia in grand-grand multiparous and similar-aged women with lesser parity: prospective observational studyAlexander Ioscovich, Angelika Fadeev, Alina Rivilis, et al.
Gene|June 20, 2012
X-inactivation in Fabry diseaseDeborah Elstein, Ella Schachamorov, Rachel Beeri, 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.
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.
Pageof 16