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Rhys H Thomas

Showing results (121-130 of 138) with videos related to

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Frontiers in Cell and Developmental Biology|December 26, 2022
The different clinical facets of <i>SYN1</i>-related neurodevelopmental disordersIlaria Parenti, Elsa Leitão, Alma Kuechler, et al.
Neurology|November 11, 2018
Neurologic phenotypes associated with <i>COL4A1</i>/<i>2</i> mutations: Expanding the spectrum of diseaseSara Zagaglia, Christina Selch, Jelena Radic Nisevic, et al.
Neurology|February 10, 2019
Clinical spectrum of <i>STX1B</i>-related epileptic disordersStefan Wolking, Patrick May, Davide Mei, et al.
Neurology|July 22, 2025
Development and Adaptive Function in Individuals With <i>SCN2A</i>-Related DisordersBeatrice Southby Goad, Jill Rodda, Meagan Allen, et al.
Neuroimage. Clinical|August 2, 2021
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy studyEzequiel Gleichgerrcht, Brent C Munsell, Saud Alhusaini, et al.
Science Advances|November 19, 2020
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA studySara Larivière, Raúl Rodríguez-Cruces, Jessica Royer, et al.
American Journal of Medical Genetics. Part A|October 8, 2020
Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrumYanick J Crow, Heather Marshall, Gillian I Rice, et al.
Human Brain Mapping|May 30, 2020
The ENIGMA-Epilepsy working group: Mapping disease from large data setsSanjay M Sisodiya, Christopher D Whelan, Sean N Hatton, et al.
Nature Communications|July 27, 2022
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expressionSara Larivière, Jessica Royer, Raúl Rodríguez-Cruces, et al.
Brain : a Journal of Neurology|August 21, 2020
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy studySean N Hatton, Khoa H Huynh, Leonardo Bonilha, et al.
Pageof 14

Showing results (121-130 of 138) with videos related to

Sort By:
Pageof 14
Frontiers in Cell and Developmental Biology|December 26, 2022
The different clinical facets of <i>SYN1</i>-related neurodevelopmental disordersIlaria Parenti, Elsa Leitão, Alma Kuechler, et al.
Neurology|November 11, 2018
Neurologic phenotypes associated with <i>COL4A1</i>/<i>2</i> mutations: Expanding the spectrum of diseaseSara Zagaglia, Christina Selch, Jelena Radic Nisevic, et al.
Neurology|February 10, 2019
Clinical spectrum of <i>STX1B</i>-related epileptic disordersStefan Wolking, Patrick May, Davide Mei, et al.
Neurology|July 22, 2025
Development and Adaptive Function in Individuals With <i>SCN2A</i>-Related DisordersBeatrice Southby Goad, Jill Rodda, Meagan Allen, et al.
Neuroimage. Clinical|August 2, 2021
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy studyEzequiel Gleichgerrcht, Brent C Munsell, Saud Alhusaini, et al.
Science Advances|November 19, 2020
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA studySara Larivière, Raúl Rodríguez-Cruces, Jessica Royer, et al.
American Journal of Medical Genetics. Part A|October 8, 2020
Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrumYanick J Crow, Heather Marshall, Gillian I Rice, et al.
Human Brain Mapping|May 30, 2020
The ENIGMA-Epilepsy working group: Mapping disease from large data setsSanjay M Sisodiya, Christopher D Whelan, Sean N Hatton, et al.
Nature Communications|July 27, 2022
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expressionSara Larivière, Jessica Royer, Raúl Rodríguez-Cruces, et al.
Brain : a Journal of Neurology|August 21, 2020
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy studySean N Hatton, Khoa H Huynh, Leonardo Bonilha, et al.
Pageof 14