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S Sabir

Showing results (51-60 of 59) with videos related to

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Neurology. Genetics|August 13, 2019
<i>MAPT</i> p.V363I mutation: A rare cause of corticobasal degenerationSarah Ahmed, Monica Diez Fairen, Marya S Sabir, et al.
Journal of Neurogastroenterology and Motility|January 3, 2018
Gene Expression Profiling and Assessment of Vitamin D and Serotonin Pathway Variations in Patients With Irritable Bowel SyndromeChristopher M Dussik, Maryam Hockley, Aleksandra Grozić, et al.
Neurobiology of Disease|February 25, 2019
Assessment of APOE in atypical parkinsonism syndromesMarya S Sabir, Cornelis Blauwendraat, Sarah Ahmed, et al.
Journal of Cardiology|January 25, 2022
COVID-19 and arrhythmia: An overviewJoseph A Varney, Vinh S Dong, Tiffany Tsao, et al.
Neurobiology of Aging|December 12, 2018
Genetic analysis of neurodegenerative diseases in a pathology cohortCornelis Blauwendraat, Olga Pletnikova, Joshua T Geiger, et al.
Neuron|November 26, 2020
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral SclerosisRamita Dewan, Ruth Chia, Jinhui Ding, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 30, 2019
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic InsightSara Bandres-Ciga, Sarah Ahmed, Marya S Sabir, et al.
Nature Genetics|February 16, 2021
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architectureRuth Chia, Marya S Sabir, Sara Bandres-Ciga, et al.
JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Neurology. Genetics|August 13, 2019
<i>MAPT</i> p.V363I mutation: A rare cause of corticobasal degenerationSarah Ahmed, Monica Diez Fairen, Marya S Sabir, et al.
Journal of Neurogastroenterology and Motility|January 3, 2018
Gene Expression Profiling and Assessment of Vitamin D and Serotonin Pathway Variations in Patients With Irritable Bowel SyndromeChristopher M Dussik, Maryam Hockley, Aleksandra Grozić, et al.
Neurobiology of Disease|February 25, 2019
Assessment of APOE in atypical parkinsonism syndromesMarya S Sabir, Cornelis Blauwendraat, Sarah Ahmed, et al.
Journal of Cardiology|January 25, 2022
COVID-19 and arrhythmia: An overviewJoseph A Varney, Vinh S Dong, Tiffany Tsao, et al.
Neurobiology of Aging|December 12, 2018
Genetic analysis of neurodegenerative diseases in a pathology cohortCornelis Blauwendraat, Olga Pletnikova, Joshua T Geiger, et al.
Neuron|November 26, 2020
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral SclerosisRamita Dewan, Ruth Chia, Jinhui Ding, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 30, 2019
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic InsightSara Bandres-Ciga, Sarah Ahmed, Marya S Sabir, et al.
Nature Genetics|February 16, 2021
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architectureRuth Chia, Marya S Sabir, Sara Bandres-Ciga, et al.
JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.
Pageof 6