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Neuroimage. Clinical
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August 2, 2021
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study
Ezequiel Gleichgerrcht, Brent C Munsell, Saud Alhusaini, et al.
Science Advances
|
November 19, 2020
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study
Sara Larivière, Raúl Rodríguez-Cruces, Jessica Royer, et al.
Neurology
|
January 2, 2024
Molecular and Phenotypic Characterization of the <i>RORB</i>-Related Disorder
Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize, et al.
European Journal of Human Genetics : EJHG
|
February 2, 2020
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature
Sophie Nambot, Laurence Faivre, Ghayda Mirzaa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 31, 2021
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
Gabriel C Dworschak, Jaya Punetha, Jeshurun C Kalanithy, et al.
American Journal of Human Genetics
|
December 25, 2024
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability
Pascale Sabeh, Samantha A Dumas, Claudia Maios, et al.
Biorxiv : the Preprint Server for Biology
|
November 14, 2023
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study
Rebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
Cell Reports
|
March 16, 2022
Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases
Paul C Marcogliese, Samantha L Deal, Jonathan Andrews, et al.
Nature Communications
|
October 31, 2019
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
Mark A Corbett, Thessa Kroes, Liana Veneziano, et al.
The New England Journal of Medicine
|
October 26, 2017
Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
Ingmar Blumcke, Roberto Spreafico, Gerrit Haaker, et al.
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Search research articles
Search
Showing results (571-580 of 611) with videos related to
Sort By:
Page
of 62
Neuroimage. Clinical
|
August 2, 2021
Artificial intelligence for classification of temporal lobe epilepsy with ROI-level MRI data: A worldwide ENIGMA-Epilepsy study
Ezequiel Gleichgerrcht, Brent C Munsell, Saud Alhusaini, et al.
Science Advances
|
November 19, 2020
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study
Sara Larivière, Raúl Rodríguez-Cruces, Jessica Royer, et al.
Neurology
|
January 2, 2024
Molecular and Phenotypic Characterization of the <i>RORB</i>-Related Disorder
Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize, et al.
European Journal of Human Genetics : EJHG
|
February 2, 2020
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature
Sophie Nambot, Laurence Faivre, Ghayda Mirzaa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 31, 2021
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
Gabriel C Dworschak, Jaya Punetha, Jeshurun C Kalanithy, et al.
American Journal of Human Genetics
|
December 25, 2024
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability
Pascale Sabeh, Samantha A Dumas, Claudia Maios, et al.
Biorxiv : the Preprint Server for Biology
|
November 14, 2023
Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study
Rebecca Kerestes, Andrew Perry, Lucy Vivash, et al.
Cell Reports
|
March 16, 2022
Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases
Paul C Marcogliese, Samantha L Deal, Jonathan Andrews, et al.
Nature Communications
|
October 31, 2019
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
Mark A Corbett, Thessa Kroes, Liana Veneziano, et al.
The New England Journal of Medicine
|
October 26, 2017
Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
Ingmar Blumcke, Roberto Spreafico, Gerrit Haaker, et al.
Page
of 62