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frontotemporal degeneration
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
VCP
GRN
C9orf72
RPE65
NPTX2
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
BLALOCK_ALZHEIMERS_DISEASE_DN
mitochondrion
GGGCGGR_SP1_Q6
FLECHNER_BIOPSY_KIDNEY_TRANSPLANT_REJECTED_VS_OK_DN
cytosol
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Curated Studies
Most Correlated Studies
Neurons differentiated from iPSCs of frontotemporal dementia patients with or without GRN mutations
Cortical neurons derived from iPSc's from FMD patients with PGRN mutation or corrected PGRN defect
Neurons from differentiated iPSCs of frontotemporal dementia patients with mutant CHMP2B gene
Frontal cortices, hippocampi and cerebella of patients with frontotemporal lobar degeneration
OMIM - Frontotemporal dementia
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Literature
Most Relevant Literature
Frontotemporal degeneration in the patient with amyotrophic lateral sclerosis: helping the caregiver…
Caring for loved ones with frontotemporal degeneration: the lived experiences of spouses.
Frontotemporal degeneration.
Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion.
New approaches to genetic counseling and testing for Alzheimer's disease and frontotemporal degenera…
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Clinical Trials
Most Relevant Clinical Trials
ARTFL LEFFTDS Longitudinal Frontotemporal Lobar Degeneration (ALLFTD)
DAPHNE Scale Validation in Frontotemporal Lobar Degeneration
Social Cognition in Ageing and in Frontotemporal Lobar Degeneration
Advancing Research and Treatment for Frontotemporal Lobar Degeneration (ARTFL)
A 52 Week Open Label Trial of Memantine for Frontotemporal Lobar Degeneration
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