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Neurology
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February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutations
Valentina Cetica, Sara Chiari, Davide Mei, et al.
Plos Genetics
|
May 9, 2018
De novo and inherited private variants in MAP1B in periventricular nodular heterotopia
Erin L Heinzen, Adam C O'Neill, Xiaolin Zhu, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2021
Expanding the genetic and phenotypic spectrum of CHD2-related disease: From early neurodevelopmental disorders to adult-onset epilepsy
Beatrice De Maria, Simona Balestrini, Davide Mei, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
April 4, 2024
Unilateral deep brain stimulation (DBS) of nucleus ventralis intermedius thalami (Vim) for the treatment of post-traumatic tremor in children: a multicentre experience
Simone Peraio, Giorgio Mantovani, Tommaso Araceli, et al.
Annals of Neurology
|
October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1
Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
Communications Biology
|
November 5, 2025
Quantitative cytoarchitectural phenotyping of deparaffinized human brain tissues
Danila Di Meo, Michele Sorelli, Josephine Ramazzotti, et al.
Human Molecular Genetics
|
August 15, 2019
Somatic double-hit in MTOR and RPS6 in hemimegalencephaly with intractable epilepsy
Cristiana Pelorosso, Françoise Watrin, Valerio Conti, et al.
Biorxiv : the Preprint Server for Biology
|
September 24, 2024
Quantitative cytoarchitectural phenotyping of deparaffinized human brain tissues
Danila Di Meo, Michele Sorelli, Josephine Ramazzotti, et al.
Plos Genetics
|
November 30, 2017
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations
Xiaolin Zhu, Raghavendra Padmanabhan, Brett Copeland, et al.
Brain : a Journal of Neurology
|
July 2, 2019
TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model
Kevin Lüthy, Davide Mei, Baptiste Fischer, et al.
Page
of 62
Search research articles
Search
Showing results (371-380 of 611) with videos related to
Sort By:
Page
of 62
Neurology
|
February 17, 2017
Clinical and genetic factors predicting Dravet syndrome in infants with <i>SCN1A</i> mutations
Valentina Cetica, Sara Chiari, Davide Mei, et al.
Plos Genetics
|
May 9, 2018
De novo and inherited private variants in MAP1B in periventricular nodular heterotopia
Erin L Heinzen, Adam C O'Neill, Xiaolin Zhu, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2021
Expanding the genetic and phenotypic spectrum of CHD2-related disease: From early neurodevelopmental disorders to adult-onset epilepsy
Beatrice De Maria, Simona Balestrini, Davide Mei, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
April 4, 2024
Unilateral deep brain stimulation (DBS) of nucleus ventralis intermedius thalami (Vim) for the treatment of post-traumatic tremor in children: a multicentre experience
Simone Peraio, Giorgio Mantovani, Tommaso Araceli, et al.
Annals of Neurology
|
October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1
Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
Communications Biology
|
November 5, 2025
Quantitative cytoarchitectural phenotyping of deparaffinized human brain tissues
Danila Di Meo, Michele Sorelli, Josephine Ramazzotti, et al.
Human Molecular Genetics
|
August 15, 2019
Somatic double-hit in MTOR and RPS6 in hemimegalencephaly with intractable epilepsy
Cristiana Pelorosso, Françoise Watrin, Valerio Conti, et al.
Biorxiv : the Preprint Server for Biology
|
September 24, 2024
Quantitative cytoarchitectural phenotyping of deparaffinized human brain tissues
Danila Di Meo, Michele Sorelli, Josephine Ramazzotti, et al.
Plos Genetics
|
November 30, 2017
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations
Xiaolin Zhu, Raghavendra Padmanabhan, Brett Copeland, et al.
Brain : a Journal of Neurology
|
July 2, 2019
TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model
Kevin Lüthy, Davide Mei, Baptiste Fischer, et al.
Page
of 62