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Leukemia Research
|
January 1, 1989
Molecular characterization of Ph' + hybrid acute leukemia
F Lo Coco, G Basso, P F di Celle, et al.
AJNR. American Journal of Neuroradiology
|
March 14, 2007
Whole-brain histogram and voxel-based analyses of apparent diffusion coefficient and magnetization transfer ratio in celiac disease, epilepsy, and cerebral calcifications syndrome
R Della Nave, A Magaudda, R Michelucci, et al.
Brain : a Journal of Neurology
|
April 20, 2004
Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases
F Bisulli, P Tinuper, P Avoni, et al.
Neurology
|
September 19, 2007
Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1
C Tessa, R Michelucci, C Nobile, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
March 21, 2020
Expanding the clinical and EEG spectrum of CNKSR2-related encephalopathy with status epilepticus during slow sleep (ESES)
Claudia M Bonardi, Cyril Mignot, Jose M Serratosa, et al.
Human Molecular Genetics
|
February 5, 1999
A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)
J M Serratosa, P Gómez-Garre, M E Gallardo, 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.
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.
Human Molecular Genetics
|
April 30, 2002
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
José M Morante-Redolat, Ana Gorostidi-Pagola, Salomé Piquer-Sirerol, et al.
Page
of 19
Search research articles
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Showing results (181-190 of 190) with videos related to
Sort By:
Page
of 19
You have reached the last page of results.
This site can display upto 190 results.
Leukemia Research
|
January 1, 1989
Molecular characterization of Ph' + hybrid acute leukemia
F Lo Coco, G Basso, P F di Celle, et al.
AJNR. American Journal of Neuroradiology
|
March 14, 2007
Whole-brain histogram and voxel-based analyses of apparent diffusion coefficient and magnetization transfer ratio in celiac disease, epilepsy, and cerebral calcifications syndrome
R Della Nave, A Magaudda, R Michelucci, et al.
Brain : a Journal of Neurology
|
April 20, 2004
Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases
F Bisulli, P Tinuper, P Avoni, et al.
Neurology
|
September 19, 2007
Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1
C Tessa, R Michelucci, C Nobile, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
March 21, 2020
Expanding the clinical and EEG spectrum of CNKSR2-related encephalopathy with status epilepticus during slow sleep (ESES)
Claudia M Bonardi, Cyril Mignot, Jose M Serratosa, et al.
Human Molecular Genetics
|
February 5, 1999
A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)
J M Serratosa, P Gómez-Garre, M E Gallardo, 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.
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.
Human Molecular Genetics
|
April 30, 2002
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
José M Morante-Redolat, Ana Gorostidi-Pagola, Salomé Piquer-Sirerol, et al.
Page
of 19