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Daniel M Evans

Showing results (21-30 of 29) with videos related to

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Pediatric Neurology|August 17, 2017
An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2Colin Wilbur, Sarah E Buerki, Ilaria Guella, et al.
RSC Advances|May 6, 2022
Proline derived guanidine catalysts forge extensive H-bonded architectures: a solution and solid state studyZahraa S Al-Taie, Simon R Anetts, Jeppe Christensen, et al.
Neurology. Genetics|November 23, 2016
De novo <i>FGF12</i> mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.
American Journal of Human Genetics|August 5, 2017
De Novo Mutations in YWHAG Cause Early-Onset EpilepsyIlaria Guella, Marna B McKenzie, Daniel M Evans, et al.
European Journal of Pediatrics|June 8, 2019
RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challengesAlison M Elliott, Christèle du Souich, Anna Lehman, et al.
Frontiers in Neurology|June 6, 2019
Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset EpilepsyMichelle Demos, Ilaria Guella, Conrado DeGuzman, et al.
Journal of Natural Products|September 3, 2016
Analogues of Marine Guanidine Alkaloids Are in Vitro Effective against Trypanosoma cruzi and Selectively Eliminate Leishmania (L.) infantum Intracellular AmastigotesLigia F Martins, Juliana T Mesquita, Erika G Pinto, et al.
American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Human Molecular Genetics|November 13, 2013
DNAJC13 mutations in Parkinson diseaseCarles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Pediatric Neurology|August 17, 2017
An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2Colin Wilbur, Sarah E Buerki, Ilaria Guella, et al.
RSC Advances|May 6, 2022
Proline derived guanidine catalysts forge extensive H-bonded architectures: a solution and solid state studyZahraa S Al-Taie, Simon R Anetts, Jeppe Christensen, et al.
Neurology. Genetics|November 23, 2016
De novo <i>FGF12</i> mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.
American Journal of Human Genetics|August 5, 2017
De Novo Mutations in YWHAG Cause Early-Onset EpilepsyIlaria Guella, Marna B McKenzie, Daniel M Evans, et al.
European Journal of Pediatrics|June 8, 2019
RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challengesAlison M Elliott, Christèle du Souich, Anna Lehman, et al.
Frontiers in Neurology|June 6, 2019
Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset EpilepsyMichelle Demos, Ilaria Guella, Conrado DeGuzman, et al.
Journal of Natural Products|September 3, 2016
Analogues of Marine Guanidine Alkaloids Are in Vitro Effective against Trypanosoma cruzi and Selectively Eliminate Leishmania (L.) infantum Intracellular AmastigotesLigia F Martins, Juliana T Mesquita, Erika G Pinto, et al.
American Journal of Human Genetics|July 19, 2011
VPS35 mutations in Parkinson diseaseCarles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Human Molecular Genetics|November 13, 2013
DNAJC13 mutations in Parkinson diseaseCarles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, et al.
Pageof 3