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Neurology
|
April 13, 2012
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy
M Fanciulli, L Santulli, L Errichiello, et al.
American Journal of Physiology. Renal Physiology
|
March 25, 2011
Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2
M J Desmond, D Lee, S A Fraser, et al.
Nature Genetics
|
April 1, 1997
Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1
K Virtaneva, E D'Amato, J Miao, et al.
Brain Topography
|
June 21, 2021
fMRI-Based Effective Connectivity in Surgical Remediable Epilepsies: A Pilot Study
A E Vaudano, L Mirandola, F Talami, et al.
Annals of Neurology
|
October 23, 2009
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure
L M Dibbens, R Michelucci, A Gambardella, et al.
Gene
|
January 30, 2002
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia
C Nobile, B Hinzmann, P Scannapieco, et al.
Epilepsy Research
|
May 19, 2006
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy
A Ayerdi-Izquierdo, G Stavrides, J J Sellés-Martínez, et al.
Neuro-Oncology Practice
|
June 3, 2015
Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center?
Alba A Brandes, Enrico Franceschi, Mario Ermani, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 68) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 68 results.
Neurology
|
April 13, 2012
LGI1 microdeletion in autosomal dominant lateral temporal epilepsy
M Fanciulli, L Santulli, L Errichiello, et al.
American Journal of Physiology. Renal Physiology
|
March 25, 2011
Tubular proteinuria in mice and humans lacking the intrinsic lysosomal protein SCARB2/Limp-2
M J Desmond, D Lee, S A Fraser, et al.
Nature Genetics
|
April 1, 1997
Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1
K Virtaneva, E D'Amato, J Miao, et al.
Brain Topography
|
June 21, 2021
fMRI-Based Effective Connectivity in Surgical Remediable Epilepsies: A Pilot Study
A E Vaudano, L Mirandola, F Talami, et al.
Annals of Neurology
|
October 23, 2009
SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure
L M Dibbens, R Michelucci, A Gambardella, et al.
Gene
|
January 30, 2002
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia
C Nobile, B Hinzmann, P Scannapieco, et al.
Epilepsy Research
|
May 19, 2006
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy
A Ayerdi-Izquierdo, G Stavrides, J J Sellés-Martínez, et al.
Neuro-Oncology Practice
|
June 3, 2015
Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center?
Alba A Brandes, Enrico Franceschi, Mario Ermani, et al.
Page
of 7