Search research articles
Contact Us
Filters
Showing results (51-60 of 58) with videos related to
Page
of 6
Sort By:
You have reached the last page of results.
This site can display upto 58 results.
European Journal of Neurology
|
December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration
E Venturelli, C Villa, C Fenoglio, et al.
European Journal of Neurology
|
May 29, 2009
DCUN1D1 is a risk factor for frontotemporal lobar degeneration
C Villa, E Venturelli, C Fenoglio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 22, 2014
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy
B Borroni, R Turrone, D Galimberti, et al.
Neurology
|
November 1, 1993
Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease
E I Rogaev, W J Lukiw, G Vaula, et al.
Nature Genetics
|
December 1, 1992
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14
P St George-Hyslop, J Haines, E Rogaev, et al.
Neurology
|
February 19, 2010
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation
A C Bruni, L Bernardi, R Colao, et al.
Nature
|
September 13, 1990
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder
P H St George-Hyslop, J L Haines, L A Farrer, et al.
Nature
|
June 29, 1995
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
R Sherrington, E I Rogaev, Y Liang, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 58) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 58 results.
European Journal of Neurology
|
December 18, 2008
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration
E Venturelli, C Villa, C Fenoglio, et al.
European Journal of Neurology
|
May 29, 2009
DCUN1D1 is a risk factor for frontotemporal lobar degeneration
C Villa, E Venturelli, C Fenoglio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 22, 2014
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy
B Borroni, R Turrone, D Galimberti, et al.
Neurology
|
November 1, 1993
Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease
E I Rogaev, W J Lukiw, G Vaula, et al.
Nature Genetics
|
December 1, 1992
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14
P St George-Hyslop, J Haines, E Rogaev, et al.
Neurology
|
February 19, 2010
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation
A C Bruni, L Bernardi, R Colao, et al.
Nature
|
September 13, 1990
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder
P H St George-Hyslop, J L Haines, L A Farrer, et al.
Nature
|
June 29, 1995
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
R Sherrington, E I Rogaev, Y Liang, et al.
Page
of 6