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Grisel Lopez

Showing results (11-20 of 53) with videos related to

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Movement Disorders Clinical Practice|October 12, 2020
Parkinsonism in Patients with Neuronopathic (Type 3) Gaucher Disease: A Case SeriesEmory Ryan, Dominick Amato, Jennifer J MacKenzie, et al.
Molecular Genetics and Metabolism|July 8, 2018
Alleles with more than one mutation can complicate genotype/phenotype studies in Mendelian disorders: Lessons from Gaucher diseaseShahzeb Hassan, Grisel Lopez, Barbara K Stubblefield, et al.
Journal of Neurology|May 23, 2022
Imaging and genetics in Parkinson's disease: assessment of the GBA1 mutationSweta Ghatti, Esther Yoon, Grisel Lopez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 9, 2009
The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonismJohn DePaolo, Ozlem Goker-Alpan, Ted Samaddar, et al.
American Journal of Medical Genetics. Part A|July 14, 2023
Revisiting the diagnosis of Gaucher disease in a family with multiple GBA1 variantsEmory Ryan, Nahid Tayebi, Andrea D'Souza, et al.
Molecular Genetics and Metabolism|December 2, 2014
The clinical management of Type 2 Gaucher diseaseKarin Weiss, Ashley Gonzalez, Grisel Lopez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 28, 2010
Psychiatric and behavioral manifestations of lysosomal storage disordersOrna Staretz-Chacham, Jae Hyuk Choi, Kazuyo Wakabayashi, 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 CarriersDaniel P Eisenberg, Grisel Lopez, Michael D Gregory, et al.
Archives of Neurology|October 15, 2008
The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutationsOzlem Goker-Alpan, Grisel Lopez, Joseph Vithayathil, et al.
American Journal of Medical Genetics. Part A|November 2, 2017
Type 2 Gaucher disease in an infant despite a normal maternal glucocerebrosidase geneErmias Hagege, Richard J Grey, Grisel Lopez, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
Movement Disorders Clinical Practice|October 12, 2020
Parkinsonism in Patients with Neuronopathic (Type 3) Gaucher Disease: A Case SeriesEmory Ryan, Dominick Amato, Jennifer J MacKenzie, et al.
Molecular Genetics and Metabolism|July 8, 2018
Alleles with more than one mutation can complicate genotype/phenotype studies in Mendelian disorders: Lessons from Gaucher diseaseShahzeb Hassan, Grisel Lopez, Barbara K Stubblefield, et al.
Journal of Neurology|May 23, 2022
Imaging and genetics in Parkinson's disease: assessment of the GBA1 mutationSweta Ghatti, Esther Yoon, Grisel Lopez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 9, 2009
The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonismJohn DePaolo, Ozlem Goker-Alpan, Ted Samaddar, et al.
American Journal of Medical Genetics. Part A|July 14, 2023
Revisiting the diagnosis of Gaucher disease in a family with multiple GBA1 variantsEmory Ryan, Nahid Tayebi, Andrea D'Souza, et al.
Molecular Genetics and Metabolism|December 2, 2014
The clinical management of Type 2 Gaucher diseaseKarin Weiss, Ashley Gonzalez, Grisel Lopez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 28, 2010
Psychiatric and behavioral manifestations of lysosomal storage disordersOrna Staretz-Chacham, Jae Hyuk Choi, Kazuyo Wakabayashi, 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 CarriersDaniel P Eisenberg, Grisel Lopez, Michael D Gregory, et al.
Archives of Neurology|October 15, 2008
The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutationsOzlem Goker-Alpan, Grisel Lopez, Joseph Vithayathil, et al.
American Journal of Medical Genetics. Part A|November 2, 2017
Type 2 Gaucher disease in an infant despite a normal maternal glucocerebrosidase geneErmias Hagege, Richard J Grey, Grisel Lopez, et al.
Pageof 6