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Showing results (361-370 of 393) with videos related to

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Annals of Neurology|March 6, 2014
SLC25A22 is a novel gene for migrating partial seizures in infancyAnnapurna Poduri, Erin L Heinzen, Vida Chitsazzadeh, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 22, 2003
Complete genome sequence of the Q-fever pathogen Coxiella burnetiiRekha Seshadri, Ian T Paulsen, Jonathan A Eisen, et al.
Brain : a Journal of Neurology|April 20, 2022
Somatic variants in diverse genes leads to a spectrum of focal cortical malformationsDulcie Lai, Meethila Gade, Edward Yang, et al.
Plos Genetics|September 15, 2010
The characterization of twenty sequenced human genomesKimberly Pelak, Kevin V Shianna, Dongliang Ge, et al.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Disrupted O-GalNAc glycosylation as a mechanism and biomarker of <i>SLC35A2</i> -associated epilepsyRobert G Mealer, James J Anderson, Sheridan L Smith, et al.
The New England Journal of Medicine|March 25, 2011
HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in EuropeansMark McCormack, Ana Alfirevic, Stephane Bourgeois, et al.
American Journal of Human Genetics|September 26, 2017
De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with SeizuresCandace T Myers, Nicholas Stong, Emily I Mountier, et al.
Orphanet Journal of Rare Diseases|September 28, 2015
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patientsEleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, et al.
Mayo Clinic Proceedings. Innovations, Quality & Outcomes|October 24, 2022
Rates of Asymptomatic COVID-19 Infection and Associated Factors in Olmsted County, Minnesota, in the Prevaccination EraCeline M Vachon, Aaron D Norman, Kavita Prasad, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsyErin L Heinzen, Chantal Depondt, Gianpiero L Cavalleri, et al.
Pageof 40

Showing results (361-370 of 393) with videos related to

Sort By:
Pageof 40
Annals of Neurology|March 6, 2014
SLC25A22 is a novel gene for migrating partial seizures in infancyAnnapurna Poduri, Erin L Heinzen, Vida Chitsazzadeh, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 22, 2003
Complete genome sequence of the Q-fever pathogen Coxiella burnetiiRekha Seshadri, Ian T Paulsen, Jonathan A Eisen, et al.
Brain : a Journal of Neurology|April 20, 2022
Somatic variants in diverse genes leads to a spectrum of focal cortical malformationsDulcie Lai, Meethila Gade, Edward Yang, et al.
Plos Genetics|September 15, 2010
The characterization of twenty sequenced human genomesKimberly Pelak, Kevin V Shianna, Dongliang Ge, et al.
Biorxiv : the Preprint Server for Biology|March 23, 2026
Disrupted O-GalNAc glycosylation as a mechanism and biomarker of <i>SLC35A2</i> -associated epilepsyRobert G Mealer, James J Anderson, Sheridan L Smith, et al.
The New England Journal of Medicine|March 25, 2011
HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in EuropeansMark McCormack, Ana Alfirevic, Stephane Bourgeois, et al.
American Journal of Human Genetics|September 26, 2017
De Novo Mutations in PPP3CA Cause Severe Neurodevelopmental Disease with SeizuresCandace T Myers, Nicholas Stong, Emily I Mountier, et al.
Orphanet Journal of Rare Diseases|September 28, 2015
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patientsEleni Panagiotakaki, Elisa De Grandis, Michela Stagnaro, et al.
Mayo Clinic Proceedings. Innovations, Quality & Outcomes|October 24, 2022
Rates of Asymptomatic COVID-19 Infection and Associated Factors in Olmsted County, Minnesota, in the Prevaccination EraCeline M Vachon, Aaron D Norman, Kavita Prasad, et al.
American Journal of Human Genetics|August 7, 2012
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsyErin L Heinzen, Chantal Depondt, Gianpiero L Cavalleri, et al.
Pageof 40