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Neurology. Genetics

Showing results (71-80 of 1,011) with videos related to

Pageof 102
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Neurology. Genetics|October 20, 2018
Increased <i>KCNJ18</i> promoter activity as a mechanism in atypical normokalemic periodic paralysisMuhidien Soufi, Volker Ruppert, Susanne Rinné, et al.
Neurology. Genetics|October 20, 2018
Bioenergetics in fibroblasts of patients with Huntington disease are associated with age at onsetSarah L Gardiner, Chiara Milanese, Merel W Boogaard, et al.
Neurology. Genetics|October 20, 2018
Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunctionRichard G Lee, Maryam Sedghi, Mehri Salari, et al.
Neurology. Genetics|September 14, 2019
Erratum: Missense mutations in DYT-TOR1A dystonia
Neurology. Genetics|September 14, 2019
Erratum: Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts
Neurology. Genetics|August 20, 2016
Rare disease clinical trials: Power in numbersMatthew P Wicklund
Neurology. Genetics|May 20, 2020
Biallelic LINE insertion mutation in <i>HACD1</i> causing congenital myopathyFatema Al Amrani, Carolina Gorodetsky, Lili-Naz Hazrati, et al.
Neurology. Genetics|August 10, 2016
Complex relation of HLA-DRB1*1501, age at menarche, and age at multiple sclerosis onsetRiley Bove, Alicia S Chua, Zongqi Xia, et al.
Neurology. Genetics|August 10, 2016
Trans-pQTL study identifies immune crosstalk between Parkinson and Alzheimer lociGail Chan, Charles C White, Phoebe A Winn, et al.
Neurology. Genetics|July 27, 2016
TREM2 p.R47H substitution is not associated with dementia with Lewy bodiesRonald L Walton, Alexandra I Soto-Ortolaza, Melissa E Murray, et al.
Pageof 102

Showing results (71-80 of 1,011) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|October 20, 2018
Increased <i>KCNJ18</i> promoter activity as a mechanism in atypical normokalemic periodic paralysisMuhidien Soufi, Volker Ruppert, Susanne Rinné, et al.
Neurology. Genetics|October 20, 2018
Bioenergetics in fibroblasts of patients with Huntington disease are associated with age at onsetSarah L Gardiner, Chiara Milanese, Merel W Boogaard, et al.
Neurology. Genetics|October 20, 2018
Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunctionRichard G Lee, Maryam Sedghi, Mehri Salari, et al.
Neurology. Genetics|September 14, 2019
Erratum: Missense mutations in DYT-TOR1A dystonia
Neurology. Genetics|September 14, 2019
Erratum: Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts
Neurology. Genetics|August 20, 2016
Rare disease clinical trials: Power in numbersMatthew P Wicklund
Neurology. Genetics|May 20, 2020
Biallelic LINE insertion mutation in <i>HACD1</i> causing congenital myopathyFatema Al Amrani, Carolina Gorodetsky, Lili-Naz Hazrati, et al.
Neurology. Genetics|August 10, 2016
Complex relation of HLA-DRB1*1501, age at menarche, and age at multiple sclerosis onsetRiley Bove, Alicia S Chua, Zongqi Xia, et al.
Neurology. Genetics|August 10, 2016
Trans-pQTL study identifies immune crosstalk between Parkinson and Alzheimer lociGail Chan, Charles C White, Phoebe A Winn, et al.
Neurology. Genetics|July 27, 2016
TREM2 p.R47H substitution is not associated with dementia with Lewy bodiesRonald L Walton, Alexandra I Soto-Ortolaza, Melissa E Murray, et al.
Pageof 102