A new study has identified novel genes involved in sporadic frontotemporal lobar degeneration with neuronal inclusions of TAR DNA-binding protein 43. These findings might enable the elucidation of pathogenic mechanisms of the disease and have implications for the identification of potential therapeutic targets
Abstract Frontotemporal lobar degeneration (FTLD) is a heterogeneous group of disorders characterize...
Through an international consortium, we have collected 37 tau- and TAR DNA-binding protein 43 (TDP-4...
Through an international consortium, we have collected 37 tau- and TAR DNA-binding protein 43 (TDP-4...
It has recently been established that the ubiquitinated neuronal inclusions and neurites observed in...
Frontotemporal lobar degeneration with neuronal inclusions of the TAR DNA-binding protein 43 (FTLD-T...
Frontotemporal lobar degeneration (FTLD) is a highly heterogenous group of progressive neurodegenera...
Frontotemporal lobar degeneration (FTLD) is a heterogeneous group of disorders characterized by dist...
The term frontotemporal lobar degeneration (FTLD) describes a spectrum of neurodegenerative disorder...
Major discoveries have been made in the recent past in the genetics, biochemistry and neuropathology...
Background: Recently, the FUS gene was identified as a new causal gene for amyotrophic lateral scler...
International audienceRecent advances in the genetics of neurodegenerative diseases have substantial...
Frontotemporal Lobar Degeneration (FTLD) is the most frequent neurodegenerative disorder with a pres...
There is a clinical and pathological overlap between amyotrophic lateral sclerosis (ALS) and frontot...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
Abstract Frontotemporal lobar degeneration (FTLD) is a heterogeneous group of disorders characterize...
Through an international consortium, we have collected 37 tau- and TAR DNA-binding protein 43 (TDP-4...
Through an international consortium, we have collected 37 tau- and TAR DNA-binding protein 43 (TDP-4...
It has recently been established that the ubiquitinated neuronal inclusions and neurites observed in...
Frontotemporal lobar degeneration with neuronal inclusions of the TAR DNA-binding protein 43 (FTLD-T...
Frontotemporal lobar degeneration (FTLD) is a highly heterogenous group of progressive neurodegenera...
Frontotemporal lobar degeneration (FTLD) is a heterogeneous group of disorders characterized by dist...
The term frontotemporal lobar degeneration (FTLD) describes a spectrum of neurodegenerative disorder...
Major discoveries have been made in the recent past in the genetics, biochemistry and neuropathology...
Background: Recently, the FUS gene was identified as a new causal gene for amyotrophic lateral scler...
International audienceRecent advances in the genetics of neurodegenerative diseases have substantial...
Frontotemporal Lobar Degeneration (FTLD) is the most frequent neurodegenerative disorder with a pres...
There is a clinical and pathological overlap between amyotrophic lateral sclerosis (ALS) and frontot...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. The ...
Abstract Frontotemporal lobar degeneration (FTLD) is a heterogeneous group of disorders characterize...
Through an international consortium, we have collected 37 tau- and TAR DNA-binding protein 43 (TDP-4...
Through an international consortium, we have collected 37 tau- and TAR DNA-binding protein 43 (TDP-4...