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Geoffrey Wallace

Showing results (1-10 of 10) with videos related to

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International Journal of Antimicrobial Agents|June 21, 2024
Antimicrobial resistance among clinically significant bacteria in wildlife: An overlooked one health concernXing Li, Shakeel Mowlaboccus, Bethany Jackson, et al.
International Journal of Molecular Sciences|December 8, 2019
The Interplay between the Endocannabinoid System, Epilepsy and CannabinoidsKeith A Kwan Cheung, Hassendrini Peiris, Geoffrey Wallace, et al.
International Journal of Microbiology|November 28, 2025
Genomic Epidemiology of Clonal Complex 1 <i>Staphylococcus aureu</i>s in Remote Western Australian CommunitiesNicholas Wei Tek Yee, Geoffrey Wallace Coombs, Marc Stegger, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|December 6, 2016
Mycobacterium chimaera colonisation of heater-cooler units (HCU) in Western Australia, 2015: investigation of possible iatrogenic infection using whole genome sequencingJames Owen Robinson, Geoffrey Wallace Coombs, David John Speers, et al.
Epilepsia|November 25, 2017
Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45Gemma L Carvill, Aijie Liu, Simone Mandelstam, et al.
Annals of Neurology|December 23, 2011
Rare copy number variants are an important cause of epileptic encephalopathiesHeather C Mefford, Simone C Yendle, Cynthia Hsu, et al.
Brain : a Journal of Neurology|February 1, 2008
Epilepsy and mental retardation limited to females: an under-recognized disorderIngrid E Scheffer, Samantha J Turner, Leanne M Dibbens, et al.
Nature Genetics|May 28, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, et al.
American Journal of Human Genetics|April 26, 2016
Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and SeizuresSlavé Petrovski, Sébastien Küry, Candace T Myers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2020
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patternsHannah Stamberger, Trine B Hammer, Elena Gardella, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
International Journal of Antimicrobial Agents|June 21, 2024
Antimicrobial resistance among clinically significant bacteria in wildlife: An overlooked one health concernXing Li, Shakeel Mowlaboccus, Bethany Jackson, et al.
International Journal of Molecular Sciences|December 8, 2019
The Interplay between the Endocannabinoid System, Epilepsy and CannabinoidsKeith A Kwan Cheung, Hassendrini Peiris, Geoffrey Wallace, et al.
International Journal of Microbiology|November 28, 2025
Genomic Epidemiology of Clonal Complex 1 <i>Staphylococcus aureu</i>s in Remote Western Australian CommunitiesNicholas Wei Tek Yee, Geoffrey Wallace Coombs, Marc Stegger, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|December 6, 2016
Mycobacterium chimaera colonisation of heater-cooler units (HCU) in Western Australia, 2015: investigation of possible iatrogenic infection using whole genome sequencingJames Owen Robinson, Geoffrey Wallace Coombs, David John Speers, et al.
Epilepsia|November 25, 2017
Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45Gemma L Carvill, Aijie Liu, Simone Mandelstam, et al.
Annals of Neurology|December 23, 2011
Rare copy number variants are an important cause of epileptic encephalopathiesHeather C Mefford, Simone C Yendle, Cynthia Hsu, et al.
Brain : a Journal of Neurology|February 1, 2008
Epilepsy and mental retardation limited to females: an under-recognized disorderIngrid E Scheffer, Samantha J Turner, Leanne M Dibbens, et al.
Nature Genetics|May 28, 2013
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1Gemma L Carvill, Sinéad B Heavin, Simone C Yendle, et al.
American Journal of Human Genetics|April 26, 2016
Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and SeizuresSlavé Petrovski, Sébastien Küry, Candace T Myers, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2020
NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patternsHannah Stamberger, Trine B Hammer, Elena Gardella, et al.
Pageof 1