Pages that link to "Q51971909"
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The following pages link to Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative (Q51971909):
Displaying 50 items.
- The genetics and neuropathology of frontotemporal lobar degeneration (Q24615201) (← links)
- Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features (Q24630410) (← links)
- Molecular Pathways Bridging Frontotemporal Lobar Degeneration and Psychiatric Disorders (Q26766487) (← links)
- The epidemiology of frontotemporal dementia (Q26823243) (← links)
- Mechanisms of granulin deficiency: lessons from cellular and animal models (Q26824221) (← links)
- Potential mechanisms of progranulin-deficient FTLD (Q26863702) (← links)
- Diagnosis and management of behavioral variant frontotemporal dementia (Q27006258) (← links)
- Primary progressive aphasia and the evolving neurology of the language network (Q27011657) (← links)
- Structure dissection of human progranulin identifies well-folded granulin/epithelin modules with unique functional activities (Q27650138) (← links)
- Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis (Q28079852) (← links)
- TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia (Q28294001) (← links)
- Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families (Q28732285) (← links)
- TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy (Q28749802) (← links)
- Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration (Q30503638) (← links)
- Biology and genetics of prions causing neurodegeneration (Q33567229) (← links)
- ALS and FTLD: two faces of TDP-43 proteinopathy (Q33571116) (← links)
- Accumulation of multiple neurodegenerative disease-related proteins in familial frontotemporal lobar degeneration associated with granulin mutation (Q33685394) (← links)
- Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease (Q33742148) (← links)
- The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics (Q33778423) (← links)
- A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition (Q33808422) (← links)
- Progranulin (GRN) in two siblings of a Latino family and in other patients with schizophrenia (Q33955043) (← links)
- Frontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management (Q34046590) (← links)
- Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations (Q34059809) (← links)
- Are there susceptibility factors for primary progressive aphasia? (Q34332931) (← links)
- An algorithm for genetic testing of frontotemporal lobar degeneration (Q34555422) (← links)
- Genetics of frontotemporal lobar degeneration (Q34574931) (← links)
- A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia (Q34658918) (← links)
- Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels (Q34959322) (← links)
- Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72 (Q35752001) (← links)
- The non-fluent/agrammatic variant of primary progressive aphasia (Q35992776) (← links)
- Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage (Q36017101) (← links)
- Arizona Study of Aging and Neurodegenerative Disorders and Brain and Body Donation Program (Q36121377) (← links)
- Progranulin: a proteolytically processed protein at the crossroads of inflammation and neurodegeneration (Q36294670) (← links)
- Amyloid in dementia associated with familial FTLD: not an innocent bystander (Q36327682) (← links)
- Prion protein codon 129 polymorphism modifies age at onset of frontotemporal dementia with the C.709-1G>A progranulin mutation (Q36520890) (← links)
- Tau pathology in frontotemporal lobar degeneration with C9ORF72 hexanucleotide repeat expansion (Q36553164) (← links)
- C9ORF72 repeat expansions and other FTD gene mutations in a clinical AD patient series from Mayo Clinic (Q36576421) (← links)
- Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis (Q36725198) (← links)
- Update on frontotemporal dementia (Q36784381) (← links)
- C9orf72 hexanucleotide repeat expansions in clinical Alzheimer disease (Q36926919) (← links)
- A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series (Q36960858) (← links)
- Progranulin mutations as risk factors for Alzheimer disease (Q37095837) (← links)
- Apolipoprotein E epsilon4 is associated with disease-specific effects on brain atrophy in Alzheimer's disease and frontotemporal dementia (Q37100964) (← 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)
- Molecular genetics of Alzheimer's disease: an update (Q37209771) (← links)
- A decade of genetic counseling in frontotemporal dementia affected families: few counseling requests and much familial opposition to testing (Q37253462) (← links)
- Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia (Q37260852) (← links)
- Frontotemporal lobar degeneration: current perspectives (Q37591327) (← links)
- Neurodegenerative dementia and parkinsonism. (Q37676947) (← links)