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Neurogenetics

Showing results (881-890 of 949) with videos related to

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Neurogenetics|February 17, 2009
Association between migraine and a functional polymorphism at the dopamine beta-hydroxylase locusF Fernandez, N Colson, S Quinlan, et al.
Neurogenetics|January 19, 2024
Bi-allelic variants in HCRT cause autosomal recessive narcolepsyWejdan Hakami, Farah Thabet, Amal Alhashem, et al.
Neurogenetics|December 20, 2023
Dem-Aging: autophagy-related pathologies and the "two faces of dementia"N Gammaldi, S Doccini, S Bernardi, et al.
Neurogenetics|December 17, 2023
Atypical retinopathy in ataxia with vitamin E deficiency: report of a sibshipStéphane Abramowicz, Alexandre Dentel, Maxime Chouraqui, et al.
Neurogenetics|July 27, 2024
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.
Neurogenetics|July 3, 2024
Unveiling the therapeutic prospects of IFNW1 and IFNA21: insights into glioma pathogenesis and clinical significanceHong Cheng, Yingjie Zhao, Xiaoli Hou, et al.
Neurogenetics|May 25, 2024
Clinical genomics expands the link between erroneous cell division, primary microcephaly and intellectual disabilitySaima, Amjad Khan, Sajid Ali, et al.
Neurogenetics|June 8, 2024
Investigation of genotype-phenotype and familial features of Turkish dystrophinopathy patientsHande Ozkalayci, Elcin Bora, Tufan Cankaya, et al.
Neurogenetics|July 5, 2024
A perspective on epigenomic aging processes in the human brain and their plasticity in patients with mental disorders - a systematic reviewJan Postberg, Michèle Tina Schubert, Vincent Nin, et al.
Neurogenetics|August 19, 2023
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, et al.
Pageof 95

Showing results (881-890 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|February 17, 2009
Association between migraine and a functional polymorphism at the dopamine beta-hydroxylase locusF Fernandez, N Colson, S Quinlan, et al.
Neurogenetics|January 19, 2024
Bi-allelic variants in HCRT cause autosomal recessive narcolepsyWejdan Hakami, Farah Thabet, Amal Alhashem, et al.
Neurogenetics|December 20, 2023
Dem-Aging: autophagy-related pathologies and the "two faces of dementia"N Gammaldi, S Doccini, S Bernardi, et al.
Neurogenetics|December 17, 2023
Atypical retinopathy in ataxia with vitamin E deficiency: report of a sibshipStéphane Abramowicz, Alexandre Dentel, Maxime Chouraqui, et al.
Neurogenetics|July 27, 2024
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changesKyle P Flannery, Sylvia Safwat, Eli Matsell, et al.
Neurogenetics|July 3, 2024
Unveiling the therapeutic prospects of IFNW1 and IFNA21: insights into glioma pathogenesis and clinical significanceHong Cheng, Yingjie Zhao, Xiaoli Hou, et al.
Neurogenetics|May 25, 2024
Clinical genomics expands the link between erroneous cell division, primary microcephaly and intellectual disabilitySaima, Amjad Khan, Sajid Ali, et al.
Neurogenetics|June 8, 2024
Investigation of genotype-phenotype and familial features of Turkish dystrophinopathy patientsHande Ozkalayci, Elcin Bora, Tufan Cankaya, et al.
Neurogenetics|July 5, 2024
A perspective on epigenomic aging processes in the human brain and their plasticity in patients with mental disorders - a systematic reviewJan Postberg, Michèle Tina Schubert, Vincent Nin, et al.
Neurogenetics|August 19, 2023
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, et al.
Pageof 95