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Michal Becker-Cohen

Showing results (21-30 of 31) with videos related to

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International Journal of Molecular Sciences|May 13, 2026
Glucosylsphingosine (Lyso-Gb1) Dynamics in Untreated States in Gaucher DiseaseTama Dinur, Peter Bauer, Sabine Schroeder, et al.
International Journal of Molecular Sciences|June 26, 2019
Glucosylsphingosine (lyso-Gb1) as a Biomarker for Monitoring Treated and Untreated Children with Gaucher DiseaseNoa Hurvitz, Tama Dinur, Michal Becker-Cohen, et al.
International Journal of Molecular Sciences|February 15, 2022
Gaucher Disease Diagnosis Using Lyso-Gb1 on Dry Blood Spot Samples: Time to Change the Paradigm?Tama Dinur, Peter Bauer, Christian Beetz, et al.
Human Molecular Genetics|August 30, 2008
Mitochondrial processes are impaired in hereditary inclusion body myopathyIris Eisenberg, Noa Novershtern, Zohar Itzhaki, et al.
Internal Medicine Journal|July 26, 2023
Rapid home therapy infusion of velaglucerase alfa in naïve patients with Gaucher diseaseMichal Becker-Cohen, Shoshana Revel-Vilk, Dafna Frydman, et al.
Neuromuscular Disorders : NMD|May 29, 2012
Sustained expression and safety of human GNE in normal mice after gene transfer based on AAV8 systemic deliveryStella Mitrani-Rosenbaum, Lena Yakovlev, Michal Becker Cohen, et al.
International Journal of Molecular Sciences|October 27, 2022
A Comprehensive Assessment of Qualitative and Quantitative Prodromal Parkinsonian Features in Carriers of Gaucher Disease-Identifying Those at the Greatest RiskMichal Becker-Cohen, Ari Zimran, Tama Dinur, et al.
Thrombosis and Haemostasis|September 10, 2021
Platelet Activation and Reactivity in a Large Cohort of Patients with Gaucher DiseaseShoshana Revel-Vilk, Mira Naamad, Dafna Frydman, et al.
Life (Basel, Switzerland)|June 26, 2025
Prodromal Parkinsonian Features in Carriers of Gaucher Disease Compared to ControlsMichal Becker-Cohen, Ari Zimran, Tama Dinur, et al.
International Journal of Molecular Sciences|July 13, 2024
<i>GBA1</i>-Associated Parkinson's Disease Is a Distinct EntityAliaksandr Skrahin, Mia Horowitz, Majdolen Istaiti, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
International Journal of Molecular Sciences|May 13, 2026
Glucosylsphingosine (Lyso-Gb1) Dynamics in Untreated States in Gaucher DiseaseTama Dinur, Peter Bauer, Sabine Schroeder, et al.
International Journal of Molecular Sciences|June 26, 2019
Glucosylsphingosine (lyso-Gb1) as a Biomarker for Monitoring Treated and Untreated Children with Gaucher DiseaseNoa Hurvitz, Tama Dinur, Michal Becker-Cohen, et al.
International Journal of Molecular Sciences|February 15, 2022
Gaucher Disease Diagnosis Using Lyso-Gb1 on Dry Blood Spot Samples: Time to Change the Paradigm?Tama Dinur, Peter Bauer, Christian Beetz, et al.
Human Molecular Genetics|August 30, 2008
Mitochondrial processes are impaired in hereditary inclusion body myopathyIris Eisenberg, Noa Novershtern, Zohar Itzhaki, et al.
Internal Medicine Journal|July 26, 2023
Rapid home therapy infusion of velaglucerase alfa in naïve patients with Gaucher diseaseMichal Becker-Cohen, Shoshana Revel-Vilk, Dafna Frydman, et al.
Neuromuscular Disorders : NMD|May 29, 2012
Sustained expression and safety of human GNE in normal mice after gene transfer based on AAV8 systemic deliveryStella Mitrani-Rosenbaum, Lena Yakovlev, Michal Becker Cohen, et al.
International Journal of Molecular Sciences|October 27, 2022
A Comprehensive Assessment of Qualitative and Quantitative Prodromal Parkinsonian Features in Carriers of Gaucher Disease-Identifying Those at the Greatest RiskMichal Becker-Cohen, Ari Zimran, Tama Dinur, et al.
Thrombosis and Haemostasis|September 10, 2021
Platelet Activation and Reactivity in a Large Cohort of Patients with Gaucher DiseaseShoshana Revel-Vilk, Mira Naamad, Dafna Frydman, et al.
Life (Basel, Switzerland)|June 26, 2025
Prodromal Parkinsonian Features in Carriers of Gaucher Disease Compared to ControlsMichal Becker-Cohen, Ari Zimran, Tama Dinur, et al.
International Journal of Molecular Sciences|July 13, 2024
<i>GBA1</i>-Associated Parkinson's Disease Is a Distinct EntityAliaksandr Skrahin, Mia Horowitz, Majdolen Istaiti, et al.
Pageof 4