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Expert Opinion on Therapeutic Targets
|
February 29, 2020
Glucocerebrosidase as a therapeutic target for Parkinson's disease
Yu Chen, Richard Sam, Pankaj Sharma, et al.
Pediatrics
|
April 2, 2009
Lysosomal storage disorders in the newborn
Orna Staretz-Chacham, Tess C Lang, Mary E LaMarca, et al.
Biochemistry
|
September 28, 2013
Saposin C protects glucocerebrosidase against α-synuclein inhibition
Thai Leong Yap, James M Gruschus, Arash Velayati, et al.
Archives of Neurology
|
October 15, 2008
The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutations
Ozlem Goker-Alpan, Grisel Lopez, Joseph Vithayathil, et al.
Expert Opinion on Pharmacotherapy
|
May 19, 2026
Pharmacotherapies for Gaucher disease: What's New on the horizon?
Maya Bhattiprolu, Max Kappler, Tae-Un Han, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 11, 2021
Comparison of Transcranial Sonography and [<sup>18</sup> F]-Fluorodopa PET Imaging in GBA1 Mutation Carriers
Daniel P Eisenberg, Grisel Lopez, Michael D Gregory, et al.
Journal of Movement Disorders
|
June 13, 2023
Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease
Ellen Hertz, Grisel Lopez, Jens Lichtenberg, et al.
Molecular Genetics and Metabolism
|
October 19, 2021
Investigation of a dysmorphic facial phenotype in patients with Gaucher disease types 2 and 3
Emily Daykin, Nicole Fleischer, Magy Abdelwahab, et al.
Frontiers in Neurology
|
November 4, 2022
Longitudinal evaluation of olfactory function in individuals with Gaucher disease and <i>GBA1</i> mutation carriers with and without Parkinson's disease
Grisel J Lopez, Jens Lichtenberg, Nahid Tayebi, et al.
American Journal of Medical Genetics. Part A
|
November 2, 2017
Type 2 Gaucher disease in an infant despite a normal maternal glucocerebrosidase gene
Ermias Hagege, Richard J Grey, Grisel Lopez, et al.
Page
of 17
Search research articles
Search
Showing results (61-70 of 166) with videos related to
Sort By:
Page
of 17
Expert Opinion on Therapeutic Targets
|
February 29, 2020
Glucocerebrosidase as a therapeutic target for Parkinson's disease
Yu Chen, Richard Sam, Pankaj Sharma, et al.
Pediatrics
|
April 2, 2009
Lysosomal storage disorders in the newborn
Orna Staretz-Chacham, Tess C Lang, Mary E LaMarca, et al.
Biochemistry
|
September 28, 2013
Saposin C protects glucocerebrosidase against α-synuclein inhibition
Thai Leong Yap, James M Gruschus, Arash Velayati, et al.
Archives of Neurology
|
October 15, 2008
The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutations
Ozlem Goker-Alpan, Grisel Lopez, Joseph Vithayathil, et al.
Expert Opinion on Pharmacotherapy
|
May 19, 2026
Pharmacotherapies for Gaucher disease: What's New on the horizon?
Maya Bhattiprolu, Max Kappler, Tae-Un Han, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 11, 2021
Comparison of Transcranial Sonography and [<sup>18</sup> F]-Fluorodopa PET Imaging in GBA1 Mutation Carriers
Daniel P Eisenberg, Grisel Lopez, Michael D Gregory, et al.
Journal of Movement Disorders
|
June 13, 2023
Rapid-Onset Dystonia and Parkinsonism in a Patient With Gaucher Disease
Ellen Hertz, Grisel Lopez, Jens Lichtenberg, et al.
Molecular Genetics and Metabolism
|
October 19, 2021
Investigation of a dysmorphic facial phenotype in patients with Gaucher disease types 2 and 3
Emily Daykin, Nicole Fleischer, Magy Abdelwahab, et al.
Frontiers in Neurology
|
November 4, 2022
Longitudinal evaluation of olfactory function in individuals with Gaucher disease and <i>GBA1</i> mutation carriers with and without Parkinson's disease
Grisel J Lopez, Jens Lichtenberg, Nahid Tayebi, et al.
American Journal of Medical Genetics. Part A
|
November 2, 2017
Type 2 Gaucher disease in an infant despite a normal maternal glucocerebrosidase gene
Ermias Hagege, Richard J Grey, Grisel Lopez, et al.
Page
of 17