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Emma Palmer

Showing results (51-60 of 64) with videos related to

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Annals of Neurology|June 17, 2026
Cardiovascular Exercise Drives Neuroprotection in a Mouse Model of Spinocerebellar Ataxia 1 Via Rescue of Aberrant SplicingIsabel Soto, Michael Bonomo, Brianna S Nelthrope, et al.
Frontiers in Psychiatry|February 28, 2024
The need for co-educators to drive a new model of inclusive, person-centred and respectful co-healthcare with people with intellectual disabilityChloe Molnar, Iva Strnadová, Manjekah Dunn, et al.
Epilepsia Open|May 4, 2026
KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severityTrupti Jadhav, Sophie E Bouffler, Emily Innes, et al.
Cell Reports|October 26, 2017
A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic EncephalopathySushmitha Gururaj, Elizabeth Emma Palmer, Garrett D Sheehan, et al.
Schizophrenia Bulletin|October 24, 2012
Social disadvantage: cause or consequence of impending psychosis?Simona A Stilo, Marta Di Forti, Valeria Mondelli, et al.
Molecular Genetics and Metabolism|August 31, 2015
Asparagine Synthetase Deficiency causes reduced proliferation of cells under conditions of limited asparagineElizabeth Emma Palmer, Jaclyn Hayner, Rani Sachdev, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 9, 2025
"All doctors should be trained in that": The co-production and mixed-methods evaluation of an educational toolkit to enable safe, high-quality genetic health care for people with intellectual disabilityIva Strnadová, Manjekah Dunn, Chloe Molnar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2025
"All doctors should be trained in that": The coproduction and mixed-methods evaluation of an educational toolkit to enable safe, high-quality genetic health care for people with intellectual disabilityIva Strnadová, Manjekah Dunn, Chloe Molnar, et al.
Orphanet Journal of Rare Diseases|June 30, 2017
Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxiaJessica L Zambonin, Allison Bellomo, Hilla Ben-Pazi, et al.
Epilepsia|September 27, 2016
The molecular and phenotypic spectrum of IQSEC2-related epilepsyAyelet Zerem, Kazuhiro Haginoya, Dorit Lev, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Annals of Neurology|June 17, 2026
Cardiovascular Exercise Drives Neuroprotection in a Mouse Model of Spinocerebellar Ataxia 1 Via Rescue of Aberrant SplicingIsabel Soto, Michael Bonomo, Brianna S Nelthrope, et al.
Frontiers in Psychiatry|February 28, 2024
The need for co-educators to drive a new model of inclusive, person-centred and respectful co-healthcare with people with intellectual disabilityChloe Molnar, Iva Strnadová, Manjekah Dunn, et al.
Epilepsia Open|May 4, 2026
KCNQ2 neonatal epilepsy: Impact of prompt diagnosis and treatment, and early predictors of outcome severityTrupti Jadhav, Sophie E Bouffler, Emily Innes, et al.
Cell Reports|October 26, 2017
A De Novo Mutation in the Sodium-Activated Potassium Channel KCNT2 Alters Ion Selectivity and Causes Epileptic EncephalopathySushmitha Gururaj, Elizabeth Emma Palmer, Garrett D Sheehan, et al.
Schizophrenia Bulletin|October 24, 2012
Social disadvantage: cause or consequence of impending psychosis?Simona A Stilo, Marta Di Forti, Valeria Mondelli, et al.
Molecular Genetics and Metabolism|August 31, 2015
Asparagine Synthetase Deficiency causes reduced proliferation of cells under conditions of limited asparagineElizabeth Emma Palmer, Jaclyn Hayner, Rani Sachdev, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 9, 2025
"All doctors should be trained in that": The co-production and mixed-methods evaluation of an educational toolkit to enable safe, high-quality genetic health care for people with intellectual disabilityIva Strnadová, Manjekah Dunn, Chloe Molnar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2025
"All doctors should be trained in that": The coproduction and mixed-methods evaluation of an educational toolkit to enable safe, high-quality genetic health care for people with intellectual disabilityIva Strnadová, Manjekah Dunn, Chloe Molnar, et al.
Orphanet Journal of Rare Diseases|June 30, 2017
Spinocerebellar ataxia type 29 due to mutations in ITPR1: a case series and review of this emerging congenital ataxiaJessica L Zambonin, Allison Bellomo, Hilla Ben-Pazi, et al.
Epilepsia|September 27, 2016
The molecular and phenotypic spectrum of IQSEC2-related epilepsyAyelet Zerem, Kazuhiro Haginoya, Dorit Lev, et al.
Pageof 7