Pages that link to "Q80162804"
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The following pages link to Progranulin null mutations in both sporadic and familial frontotemporal dementia (Q80162804):
Displaying 50 items.
- Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study (Q24600803) (← links)
- The genetics and neuropathology of frontotemporal lobar degeneration (Q24615201) (← links)
- Understanding Neuropsychiatric Diseases, Analyzing the Peptide Sharing between Infectious Agents and the Language-Associated NMDA 2A Protein (Q26752661) (← links)
- Mechanisms of granulin deficiency: lessons from cellular and animal models (Q26824221) (← links)
- Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis (Q28079852) (← links)
- Targeted manipulation of the sortilin-progranulin axis rescues progranulin haploinsufficiency (Q28587955) (← links)
- Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families (Q28732285) (← links)
- The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration (Q30495415) (← links)
- A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells (Q30498840) (← links)
- Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration (Q30503638) (← links)
- Progranulin is expressed within motor neurons and promotes neuronal cell survival (Q33513028) (← links)
- Mitochondrial DNA haplogroups in early-onset Alzheimer's disease and frontotemporal lobar degeneration (Q33698557) (← links)
- Frontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management (Q34046590) (← links)
- Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders (Q34170998) (← links)
- An algorithm for genetic testing of frontotemporal lobar degeneration (Q34555422) (← links)
- Genetics of frontotemporal lobar degeneration (Q34574931) (← links)
- Brain progranulin expression in GRN-associated frontotemporal lobar degeneration (Q35014879) (← links)
- A network of RNA and protein interactions in Fronto Temporal Dementia (Q35194634) (← links)
- Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia Patients (Q36134488) (← links)
- New approaches to genetic counseling and testing for Alzheimer's disease and frontotemporal degeneration (Q36218610) (← links)
- Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival (Q36527176) (← links)
- Novel GRN Mutations in Patients with Corticobasal Syndrome (Q36671072) (← links)
- Advances in understanding the molecular basis of frontotemporal dementia (Q36775677) (← links)
- Progranulin: an emerging target for FTLD therapies (Q36826623) (← links)
- The genetics of frontotemporal lobar degeneration (Q36926070) (← links)
- The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments (Q36931728) (← links)
- Novel progranulin mutation detected in 2 patients with FTLD. (Q37008874) (← links)
- Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members (Q37148011) (← links)
- Update on recent molecular and genetic advances in frontotemporal lobar degeneration (Q37205729) (← links)
- Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration (Q37235164) (← links)
- FTD and ALS: A Tale of Two Diseases (Q37241079) (← links)
- Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy. (Q37248850) (← links)
- Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia (Q37260852) (← links)
- The heritability and genetics of frontotemporal lobar degeneration. (Q37425094) (← links)
- Development and validation of pedigree classification criteria for frontotemporal lobar degeneration (Q37531130) (← links)
- Neurodegenerative dementia and parkinsonism. (Q37676947) (← links)
- Frontotemporal dementia: from Mendelian genetics towards genome wide association studies (Q37928504) (← links)
- Frontotemporal lobar degeneration: epidemiology, pathology, diagnosis and management (Q38040822) (← links)
- TARDBP and FUS mutations associated with amyotrophic lateral sclerosis: summary and update (Q38096349) (← links)
- Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern Italy. (Q38379891) (← links)
- Psychotic symptoms in frontotemporal dementia (Q38501875) (← links)
- Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation (Q38922949) (← links)
- Targeting the low-hanging fruit of neurodegeneration (Q41867906) (← links)
- A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration (Q42490354) (← links)
- Disease and Region Specificity of Granulin Immunopositivities in Alzheimer Disease and Frontotemporal Lobar Degeneration (Q45873297) (← links)
- Targeting Tyro3 ameliorates a model of PGRN-mutant FTLD-TDP via tau-mediated synaptic pathology. (Q47830754) (← links)
- Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family. (Q47839519) (← links)
- Frequency of progranulin mutations in a German cohort of 79 frontotemporal dementia patients (Q48515203) (← links)
- Prevalence of primitive reflexes and Parkinsonian signs in dementia (Q51031058) (← links)
- Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. (Q51971909) (← links)