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Neurogenetics

Showing results (891-900 of 949) with videos related to

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Neurogenetics|July 5, 2023
Novel potentially pathogenic variants detected in genes causing intellectual disability and epilepsy in Polish familiesS Skoczylas, P Jakiel, T Płoszaj, et al.
Neurogenetics|January 26, 2019
Clinical and molecular studies in two new cases of ARSACSIvana Ricca, Federica Morani, Giacomo Maria Bacci, et al.
Neurogenetics|December 12, 2019
Neurodevelopmental phenotype associated with CHD8-SUPT16H duplicationThomas Smol, Caroline Thuillier, Elise Boudry-Labis, et al.
Neurogenetics|January 5, 2020
Mitochondrial epilepsy: a cross-sectional nationwide Italian surveyChiara Ticci, Federico Sicca, Anna Ardissone, et al.
Neurogenetics|January 14, 2020
Changes in global gene expression indicate disordered autophagy, apoptosis and inflammatory processes and downregulation of cytoskeletal signalling and neuronal development in patients with Niemann-Pick C diseaseKatarzyna Hetmańczyk-Sawicka, Roksana Iwanicka-Nowicka, Anna Fogtman, et al.
Neurogenetics|March 28, 2020
Cognitive decline and depressive symptoms: early non-motor presentations of parkinsonism among Egyptian Gaucher patientsAzza Abdel Gawad Tantawy, Amira Abdel Moneam Adly, Mai Seif El Din Abdeen, et al.
Neurogenetics|June 8, 2021
Age-dependent neurological phenotypes in a mouse model of PRRT2-related diseasesFay Aj, McMahon T, Im C, et al.
Neurogenetics|April 9, 2022
Inherited metabolic diseases mimicking hereditary spastic paraplegia (HSP): a chance for treatmentHélio A G Teive, Carlos Henrique F Camargo, Eduardo R Pereira, et al.
Neurogenetics|February 12, 2016
Multiple sclerosis in families: risk factors beyond known genetic polymorphismsDenis A Akkad, De-Hyung Lee, Kathrin Bruch, et al.
Neurogenetics|January 19, 2016
Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescenceKarina Carvalho Donis, Jonas Alex Morales Saute, Ana Carolina Krum-Santos, et al.
Pageof 95

Showing results (891-900 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|July 5, 2023
Novel potentially pathogenic variants detected in genes causing intellectual disability and epilepsy in Polish familiesS Skoczylas, P Jakiel, T Płoszaj, et al.
Neurogenetics|January 26, 2019
Clinical and molecular studies in two new cases of ARSACSIvana Ricca, Federica Morani, Giacomo Maria Bacci, et al.
Neurogenetics|December 12, 2019
Neurodevelopmental phenotype associated with CHD8-SUPT16H duplicationThomas Smol, Caroline Thuillier, Elise Boudry-Labis, et al.
Neurogenetics|January 5, 2020
Mitochondrial epilepsy: a cross-sectional nationwide Italian surveyChiara Ticci, Federico Sicca, Anna Ardissone, et al.
Neurogenetics|January 14, 2020
Changes in global gene expression indicate disordered autophagy, apoptosis and inflammatory processes and downregulation of cytoskeletal signalling and neuronal development in patients with Niemann-Pick C diseaseKatarzyna Hetmańczyk-Sawicka, Roksana Iwanicka-Nowicka, Anna Fogtman, et al.
Neurogenetics|March 28, 2020
Cognitive decline and depressive symptoms: early non-motor presentations of parkinsonism among Egyptian Gaucher patientsAzza Abdel Gawad Tantawy, Amira Abdel Moneam Adly, Mai Seif El Din Abdeen, et al.
Neurogenetics|June 8, 2021
Age-dependent neurological phenotypes in a mouse model of PRRT2-related diseasesFay Aj, McMahon T, Im C, et al.
Neurogenetics|April 9, 2022
Inherited metabolic diseases mimicking hereditary spastic paraplegia (HSP): a chance for treatmentHélio A G Teive, Carlos Henrique F Camargo, Eduardo R Pereira, et al.
Neurogenetics|February 12, 2016
Multiple sclerosis in families: risk factors beyond known genetic polymorphismsDenis A Akkad, De-Hyung Lee, Kathrin Bruch, et al.
Neurogenetics|January 19, 2016
Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescenceKarina Carvalho Donis, Jonas Alex Morales Saute, Ana Carolina Krum-Santos, et al.
Pageof 95