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Neuropathology and Applied Neurobiology
|
May 4, 2021
MicroRNA-34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesis
Anatoly Korotkov, Nam Suk Sim, Mark J Luinenburg, et al.
Journal of Neuropathology and Experimental Neurology
|
May 31, 2020
Dysregulation of the MMP/TIMP Proteolytic System in Subependymal Giant Cell Astrocytomas in Patients With Tuberous Sclerosis Complex: Modulation of MMP by MicroRNA-320d In Vitro
Anika Bongaarts, Jody M de Jong, Diede W M Broekaart, et al.
American Journal of Human Genetics
|
April 9, 2013
Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria
Benjamin Nota, Eduard A Struys, Ana Pop, et al.
Genome Biology
|
February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Iris E Jansen, Hui Ye, Sasja Heetveld, et al.
Psycho-Oncology
|
March 15, 2025
Efficacy and Budget Impact of a Tailored Psychological Intervention Program Targeting Cancer Patients With Adjustment Disorder: A Randomised Controlled Trial
K Holtmaat, F E van Beek, L M A Wijnhoven, et al.
Annals of Neurology
|
June 10, 2020
SCN3A-Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation
Tariq Zaman, Katherine L Helbig, Jérôme Clatot, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 1, 2018
De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy
F Tran Mau-Them, L Guibaud, L Duplomb, et al.
Nature Communications
|
November 23, 2023
Molecular EPISTOP, a comprehensive multi-omic analysis of blood from Tuberous Sclerosis Complex infants age birth to two years
Franz Huschner, Jagoda Głowacka-Walas, James D Mills, et al.
Translational Psychiatry
|
September 3, 2021
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions
Lianne M Reus, Iris E Jansen, Merel O Mol, et al.
Epilepsia
|
April 23, 2025
Updated classification of epileptic seizures: Position paper of the International League Against Epilepsy
Sándor Beniczky, Eugen Trinka, Elaine Wirrell, et al.
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Showing results (581-590 of 767) with videos related to
Sort By:
Page
of 77
Neuropathology and Applied Neurobiology
|
May 4, 2021
MicroRNA-34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesis
Anatoly Korotkov, Nam Suk Sim, Mark J Luinenburg, et al.
Journal of Neuropathology and Experimental Neurology
|
May 31, 2020
Dysregulation of the MMP/TIMP Proteolytic System in Subependymal Giant Cell Astrocytomas in Patients With Tuberous Sclerosis Complex: Modulation of MMP by MicroRNA-320d In Vitro
Anika Bongaarts, Jody M de Jong, Diede W M Broekaart, et al.
American Journal of Human Genetics
|
April 9, 2013
Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria
Benjamin Nota, Eduard A Struys, Ana Pop, et al.
Genome Biology
|
February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Iris E Jansen, Hui Ye, Sasja Heetveld, et al.
Psycho-Oncology
|
March 15, 2025
Efficacy and Budget Impact of a Tailored Psychological Intervention Program Targeting Cancer Patients With Adjustment Disorder: A Randomised Controlled Trial
K Holtmaat, F E van Beek, L M A Wijnhoven, et al.
Annals of Neurology
|
June 10, 2020
SCN3A-Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation
Tariq Zaman, Katherine L Helbig, Jérôme Clatot, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 1, 2018
De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy
F Tran Mau-Them, L Guibaud, L Duplomb, et al.
Nature Communications
|
November 23, 2023
Molecular EPISTOP, a comprehensive multi-omic analysis of blood from Tuberous Sclerosis Complex infants age birth to two years
Franz Huschner, Jagoda Głowacka-Walas, James D Mills, et al.
Translational Psychiatry
|
September 3, 2021
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions
Lianne M Reus, Iris E Jansen, Merel O Mol, et al.
Epilepsia
|
April 23, 2025
Updated classification of epileptic seizures: Position paper of the International League Against Epilepsy
Sándor Beniczky, Eugen Trinka, Elaine Wirrell, et al.
Page
of 77