Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Neurology. Genetics

Showing results (151-160 of 1,011) with videos related to

Pageof 102
Sort By:
Neurology. Genetics|April 24, 2023
Transcriptome and Genome Analysis Uncovers a <i>DMD</i> Structural Variant: A Case ReportChiara Folland, Vijay Ganesh, Ben Weisburd, et al.
Neurology. Genetics|April 24, 2023
New-Onset Refractory Status Epilepticus Due to a Novel MT-TF Variant: Time for Acute Genetic Testing Before Treatment?Elisabetta Indelicato, Johannes Pfeilstetter, Michael Zech, et al.
Neurology. Genetics|April 22, 2021
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1Stephan Wenninger, Sarah A Cumming, Kristina Gutschmidt, et al.
Neurology. Genetics|April 26, 2021
Interactive Effects of HLA and GM Alleles on the Development of Alzheimer DiseaseJanardan P Pandey, Paul J Nietert, Ronald T Kothera, et al.
Neurology. Genetics|April 26, 2021
Novel Cysteine-Sparing Hypomorphic <i>NOTCH3</i> A1604T Mutation Observed in a Family With Migraine and White Matter LesionsSnjolaug Arnardottir, Francesca Del Gaudio, Stefanos Klironomos, et al.
Neurology. Genetics|April 15, 2021
Progressive Ataxia and Neurologic Regression in <i>RFXANK</i>-Associated Bare Lymphocyte SyndromeEssa Alharby, Mona Obaid, Mohammed A O Elamin, et al.
Neurology. Genetics|August 18, 2020
Integrated sequencing and array comparative genomic hybridization in familial Parkinson diseaseLaurie A Robak, Renqian Du, Bo Yuan, et al.
Neurology. Genetics|August 22, 2020
Erratum: Neuraxial dysraphism in <i>EPAS1</i>-associated syndrome due to improper mesenchymal transition
Neurology. Genetics|May 1, 2023
Identifying Aging and Alzheimer Disease-Associated Somatic Variations in Excitatory Neurons From the Human Frontal CortexMeng Zhang, Gerard A Bouland, Henne Holstege, et al.
Neurology. Genetics|May 8, 2023
CircPDS5B Reduction Improves Angiogenesis Following Ischemic Stroke by Regulating MicroRNA-223-3p/NOTCH2 AxisLing Kui, Zongyu Li, Guoyun Wang, et al.
Pageof 102

Showing results (151-160 of 1,011) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|April 24, 2023
Transcriptome and Genome Analysis Uncovers a <i>DMD</i> Structural Variant: A Case ReportChiara Folland, Vijay Ganesh, Ben Weisburd, et al.
Neurology. Genetics|April 24, 2023
New-Onset Refractory Status Epilepticus Due to a Novel MT-TF Variant: Time for Acute Genetic Testing Before Treatment?Elisabetta Indelicato, Johannes Pfeilstetter, Michael Zech, et al.
Neurology. Genetics|April 22, 2021
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1Stephan Wenninger, Sarah A Cumming, Kristina Gutschmidt, et al.
Neurology. Genetics|April 26, 2021
Interactive Effects of HLA and GM Alleles on the Development of Alzheimer DiseaseJanardan P Pandey, Paul J Nietert, Ronald T Kothera, et al.
Neurology. Genetics|April 26, 2021
Novel Cysteine-Sparing Hypomorphic <i>NOTCH3</i> A1604T Mutation Observed in a Family With Migraine and White Matter LesionsSnjolaug Arnardottir, Francesca Del Gaudio, Stefanos Klironomos, et al.
Neurology. Genetics|April 15, 2021
Progressive Ataxia and Neurologic Regression in <i>RFXANK</i>-Associated Bare Lymphocyte SyndromeEssa Alharby, Mona Obaid, Mohammed A O Elamin, et al.
Neurology. Genetics|August 18, 2020
Integrated sequencing and array comparative genomic hybridization in familial Parkinson diseaseLaurie A Robak, Renqian Du, Bo Yuan, et al.
Neurology. Genetics|August 22, 2020
Erratum: Neuraxial dysraphism in <i>EPAS1</i>-associated syndrome due to improper mesenchymal transition
Neurology. Genetics|May 1, 2023
Identifying Aging and Alzheimer Disease-Associated Somatic Variations in Excitatory Neurons From the Human Frontal CortexMeng Zhang, Gerard A Bouland, Henne Holstege, et al.
Neurology. Genetics|May 8, 2023
CircPDS5B Reduction Improves Angiogenesis Following Ischemic Stroke by Regulating MicroRNA-223-3p/NOTCH2 AxisLing Kui, Zongyu Li, Guoyun Wang, et al.
Pageof 102