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Daniel du Plessis

Showing results (31-40 of 44) with videos related to

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Dementia and Geriatric Cognitive Disorders Extra|June 29, 2016
Co-Occurrence of Language and Behavioural Change in Frontotemporal Lobar DegenerationJennifer M Harris, Matthew Jones, Claire Gall, et al.
American Journal of Medical Genetics. Part A|November 13, 2020
The importance of genetic counseling and screening for people with pathogenic SMARCE1 variants: A family studyAlireza Shoakazemi, Alan Hewitt, Miriam J Smith, et al.
Journal of Alzheimer'S Disease : JAD|December 5, 2019
A Comparative Study of Pathological Outcomes in The University of Manchester Longitudinal Study of Cognition in Normal Healthy Old Age and Brains for Dementia Research CohortsAndrew C Robinson, Stephen Chew-Graham, Yvonne S Davidson, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|October 25, 2017
Assessing Inflammation in Acute Intracerebral Hemorrhage with PK11195 PET and Dynamic Contrast-Enhanced MRIKamran A Abid, Oluwaseun A Sobowale, Laura M Parkes, et al.
Human Molecular Genetics|March 24, 2017
Genetic regulation of gene expression in the epileptic human hippocampusNasir Mirza, Richard Appleton, Sasha Burn, et al.
Nature Genetics|February 5, 2013
Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomasMiriam J Smith, James O'Sullivan, Sanjeev S Bhaskar, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|February 28, 2015
The 18-kDa mitochondrial translocator protein in human gliomas: an 11C-(R)PK11195 PET imaging and neuropathology studyZhangjie Su, Federico Roncaroli, Pascal F Durrenberger, et al.
Human Molecular Genetics|May 6, 2015
Identifying the biological pathways underlying human focal epilepsy: from complexity to coherence to centralityNasir Mirza, Richard Appleton, Sasha Burn, et al.
Molecular Genetics and Metabolism Reports|October 23, 2025
Long-term neuromuscular, cardiac and liver outcomes in an adult man affected with Chanarin-Dorfman syndromeKinza Noman, Andreas Tridimas, James B Lilleker, et al.
Epilepsia|July 17, 2016
An integrative in silico system for predicting dysregulated genes in the human epileptic focus: Application to SLC transportersNasir Mirza, Olga Vasieva, Richard Appleton, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Dementia and Geriatric Cognitive Disorders Extra|June 29, 2016
Co-Occurrence of Language and Behavioural Change in Frontotemporal Lobar DegenerationJennifer M Harris, Matthew Jones, Claire Gall, et al.
American Journal of Medical Genetics. Part A|November 13, 2020
The importance of genetic counseling and screening for people with pathogenic SMARCE1 variants: A family studyAlireza Shoakazemi, Alan Hewitt, Miriam J Smith, et al.
Journal of Alzheimer'S Disease : JAD|December 5, 2019
A Comparative Study of Pathological Outcomes in The University of Manchester Longitudinal Study of Cognition in Normal Healthy Old Age and Brains for Dementia Research CohortsAndrew C Robinson, Stephen Chew-Graham, Yvonne S Davidson, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|October 25, 2017
Assessing Inflammation in Acute Intracerebral Hemorrhage with PK11195 PET and Dynamic Contrast-Enhanced MRIKamran A Abid, Oluwaseun A Sobowale, Laura M Parkes, et al.
Human Molecular Genetics|March 24, 2017
Genetic regulation of gene expression in the epileptic human hippocampusNasir Mirza, Richard Appleton, Sasha Burn, et al.
Nature Genetics|February 5, 2013
Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomasMiriam J Smith, James O'Sullivan, Sanjeev S Bhaskar, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|February 28, 2015
The 18-kDa mitochondrial translocator protein in human gliomas: an 11C-(R)PK11195 PET imaging and neuropathology studyZhangjie Su, Federico Roncaroli, Pascal F Durrenberger, et al.
Human Molecular Genetics|May 6, 2015
Identifying the biological pathways underlying human focal epilepsy: from complexity to coherence to centralityNasir Mirza, Richard Appleton, Sasha Burn, et al.
Molecular Genetics and Metabolism Reports|October 23, 2025
Long-term neuromuscular, cardiac and liver outcomes in an adult man affected with Chanarin-Dorfman syndromeKinza Noman, Andreas Tridimas, James B Lilleker, et al.
Epilepsia|July 17, 2016
An integrative in silico system for predicting dysregulated genes in the human epileptic focus: Application to SLC transportersNasir Mirza, Olga Vasieva, Richard Appleton, et al.
Pageof 5