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Brain Research Bulletin
|
May 2, 2006
Subcortical motor plasticity in patients with sporadic ALS: An fMRI study
A Tessitore, F Esposito, M R Monsurrò, et al.
Neurology
|
April 27, 2005
Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)
P Valentino, F L Conforti, D Pirritano, et al.
Journal of the Neurological Sciences
|
June 19, 2014
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness
M Muglia, L Citrigno, E D'Errico, et al.
Journal of Neurology
|
October 17, 1998
CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity
A Gambardella, G Annesi, F Bono, et al.
Neurology
|
December 6, 2008
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL
M Liguori, R Mazzei, C Ungaro, et al.
Acta Neurologica Scandinavica
|
January 7, 2004
Gene conversion events in adult-onset spinal muscular atrophy
R Mazzei, A Gambardella, F L Conforti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 19, 2005
The spectrum of Notch3 mutations in 28 Italian CADASIL families
M T Dotti, A Federico, R Mazzei, et al.
Neurology
|
October 13, 2004
A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2)
F L Conforti, M Muglia, R Mazzei, et al.
Archives of Neurology
|
September 18, 2001
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings
R L Oliveri, M Muglia, N De Stefano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2007
First evidence of a pathogenic insertion in the NOTCH3 gene causing CADASIL
R Mazzei, D Guidetti, C Ungaro, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Brain Research Bulletin
|
May 2, 2006
Subcortical motor plasticity in patients with sporadic ALS: An fMRI study
A Tessitore, F Esposito, M R Monsurrò, et al.
Neurology
|
April 27, 2005
Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)
P Valentino, F L Conforti, D Pirritano, et al.
Journal of the Neurological Sciences
|
June 19, 2014
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness
M Muglia, L Citrigno, E D'Errico, et al.
Journal of Neurology
|
October 17, 1998
CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity
A Gambardella, G Annesi, F Bono, et al.
Neurology
|
December 6, 2008
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL
M Liguori, R Mazzei, C Ungaro, et al.
Acta Neurologica Scandinavica
|
January 7, 2004
Gene conversion events in adult-onset spinal muscular atrophy
R Mazzei, A Gambardella, F L Conforti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 19, 2005
The spectrum of Notch3 mutations in 28 Italian CADASIL families
M T Dotti, A Federico, R Mazzei, et al.
Neurology
|
October 13, 2004
A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2)
F L Conforti, M Muglia, R Mazzei, et al.
Archives of Neurology
|
September 18, 2001
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings
R L Oliveri, M Muglia, N De Stefano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2007
First evidence of a pathogenic insertion in the NOTCH3 gene causing CADASIL
R Mazzei, D Guidetti, C Ungaro, et al.
Page
of 4