Progranulin mutations result in frontotemporal dementia, but the underlying pathophysiology has remained largely unexplained. New data by Geschwind and colleagues in this issue of Neuron uncovered that the Wnt/FZD2 signaling pathway is an early and critical contributor to disease pathology
Summary: Tauopathies such as frontotemporal dementia (FTD) remain incurable to date, partially due t...
Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both spor...
White matter hyperintensities (WMH) are often seen on MRI brain scans in frontotemporal dementia (FT...
Progranulin mutations result in frontotemporal dementia, but the underlying pathophysiology has rema...
SummaryProgranulin (GRN) mutations cause frontotemporal dementia (FTD), but GRN's function in the CN...
peer reviewedTo understand how haploinsufficiency of progranulin (PGRN) causes frontotemporal dement...
Summary: To understand how haploinsufficiency of progranulin (PGRN) causes frontotemporal dementia (...
SummaryTo understand how haploinsufficiency of progranulin (PGRN) causes frontotemporal dementia (FT...
To understand how haploinsufficiency of progranulin (PGRN) causes frontotemporal dementia (FTD), we ...
Mutations within the granulin (GRN) gene that encodes progranulin (PGRN) cause the neurodegenerative...
Frontotemporal degeneration (FTD) is a complex disease presenting as a spectrum of clinical disorder...
TAR DNA-binding protein 43 (TDP-43) inclusions are pathological hallmarks of patients with frontotem...
Frontotemporal dementia (FTD) is a heterogeneous clinical disorder characterized by progressive abno...
Recently, mutations in the progranulin (PGRN) gene were found to cause familial and apparently spora...
Frontotemporal dementia (FTD) is a neurodegenerative disease, leading to behavioral changes and lang...
Summary: Tauopathies such as frontotemporal dementia (FTD) remain incurable to date, partially due t...
Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both spor...
White matter hyperintensities (WMH) are often seen on MRI brain scans in frontotemporal dementia (FT...
Progranulin mutations result in frontotemporal dementia, but the underlying pathophysiology has rema...
SummaryProgranulin (GRN) mutations cause frontotemporal dementia (FTD), but GRN's function in the CN...
peer reviewedTo understand how haploinsufficiency of progranulin (PGRN) causes frontotemporal dement...
Summary: To understand how haploinsufficiency of progranulin (PGRN) causes frontotemporal dementia (...
SummaryTo understand how haploinsufficiency of progranulin (PGRN) causes frontotemporal dementia (FT...
To understand how haploinsufficiency of progranulin (PGRN) causes frontotemporal dementia (FTD), we ...
Mutations within the granulin (GRN) gene that encodes progranulin (PGRN) cause the neurodegenerative...
Frontotemporal degeneration (FTD) is a complex disease presenting as a spectrum of clinical disorder...
TAR DNA-binding protein 43 (TDP-43) inclusions are pathological hallmarks of patients with frontotem...
Frontotemporal dementia (FTD) is a heterogeneous clinical disorder characterized by progressive abno...
Recently, mutations in the progranulin (PGRN) gene were found to cause familial and apparently spora...
Frontotemporal dementia (FTD) is a neurodegenerative disease, leading to behavioral changes and lang...
Summary: Tauopathies such as frontotemporal dementia (FTD) remain incurable to date, partially due t...
Frontotemporal dementia (FTD) is a heterogeneous group of neurodegenerative disorders with both spor...
White matter hyperintensities (WMH) are often seen on MRI brain scans in frontotemporal dementia (FT...