Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers—a developmental disorder
Background A mutation in C9orf72 constitute a cross-link between amyotrophic lateral
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers-a developmental disorder
DE Lule, J Kassubek, AC Ludolph… - Journal of Neurology …, 2020 - hero.epa.gov
Background A mutation in C9orf72 constitute a cross-link between amyotrophic lateral
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers—a developmental disorder
DE Lulé, HP Müller, J Finsel, P Weydt… - Journal of …, 2020 - search.proquest.com
Background A mutation in C9orf72 constitute a cross-link between amyotrophic lateral
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers-a developmental disorder.
DE Lulé, HP Müller, J Finsel, P Weydt… - Journal of Neurology …, 2020 - europepmc.org
Background A mutation in C9orf72 constitute a cross-link between amyotrophic lateral
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
[引用][C] Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers-a developmental disorder
DE Lule, HP Müller, J Finsel, P Weydt… - Journal of Neurology …, 2020 - oparu.uni-ulm.de
Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers-a
developmental disorder Toggle navigation English Deutsch Deutsch English Deutsch …
developmental disorder Toggle navigation English Deutsch Deutsch English Deutsch …
[HTML][HTML] Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers—a developmental disorder
DE Lulé, HP Müller, J Finsel, P Weydt… - Journal of Neurology …, 2020 - ncbi.nlm.nih.gov
Background A mutation in C9orf72 constitute a cross-link between amyotrophic lateral
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
[PDF][PDF] Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers—a developmental disorder
DE Lulé, HP Müller, J Finsel, P Weydt… - Journal of Neurology …, 2020 - jnnp.bmj.com
Background A mutation in C9orf72 constitute a cross-link between amyotrophic lateral
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers-a developmental disorder
DE Lulé, HP Müller, J Finsel, P Weydt… - Journal of Neurology …, 2020 - diva-portal.org
Background: A mutation in C9orf72 constitute a cross-link between amyotrophic lateral
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
[PDF][PDF] Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers—a developmental disorder
DE Lulé, HP Müller, J Finsel, P Weydt, A Knehr… - scholar.archive.org
Background A mutation in C9orf72 constitute a cross-link between amyotrophic lateral
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
Deficits in verbal fluency in presymptomatic C9orf72 mutation gene carriers-a developmental disorder
DE Lulé, HP Müller, J Finsel… - Journal of …, 2020 - pubmed.ncbi.nlm.nih.gov
Background A mutation in C9orf72 constitute a cross-link between amyotrophic lateral
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …
sclerosis (ALS) and fronto-temporal dementia (FTD). At clinical manifestation, both patient …