Pages that link to "Q66729652"
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The following pages link to Parastoo Momeni (Q66729652):
Displaying 42 items.
- Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD (Q21261387) (← links)
- Novel missense mutation in charged multivesicular body protein 2B in a patient with frontotemporal dementia (Q30549711) (← links)
- A repository based on a dynamically extensible data model supporting multidisciplinary research in neuroscience (Q30572427) (← links)
- Androgen receptor gene and sex-specific Alzheimer's disease (Q33576938) (← links)
- Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations (Q33771544) (← links)
- Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy (Q33922493) (← links)
- Frontotemporal dementia and its subtypes: a genome-wide association study (Q33955007) (← links)
- Progranulin (GRN) in two siblings of a Latino family and in other patients with schizophrenia (Q33955043) (← links)
- Characteristics of frontotemporal dementia patients with a Progranulin mutation (Q34330746) (← links)
- Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases (Q34546133) (← links)
- Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia (Q34552887) (← links)
- FUS and TDP43 genetic variability in FTD and CBS (Q35811238) (← links)
- A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia (Q36444721) (← links)
- Screening for C9ORF72 repeat expansion in FTLD. (Q37094799) (← links)
- Clinical and pathological features of an Alzheimer's disease patient with the MAPT Delta K280 mutation (Q37151773) (← links)
- Frontotemporal dementia: from Mendelian genetics towards genome wide association studies (Q37928504) (← links)
- Frontotemporal dementia in elderly individuals (Q38005102) (← links)
- The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene (Q38493216) (← links)
- Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis (Q38611043) (← links)
- Screening of Early and Late Onset Alzheimer's Disease Genetic Risk Factors in a Cohort of Dementia Patients from Liguria, Italy (Q40753910) (← links)
- Corrigendum to "Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy." [Neurobiol. Aging 35 (2014) 1514.e1-1514.e12]. (Q42360503) (← links)
- Familial thoracic aortic aneurysm with dissection presenting as flash pulmonary edema in a 26-year-old man. (Q42746422) (← links)
- Implication of common and disease specific variants in CLU, CR1, and PICALM. (Q43747687) (← links)
- Familial frontotemporal dementia associated with C9orf72 repeat expansion and dysplastic gangliocytoma (Q43797929) (← links)
- Elderly individuals with FTLD. (Q45039980) (← links)
- Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID). (Q46590828) (← links)
- Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia (Q46877679) (← links)
- A presenilin-1 mutation (T245P) in transmembrane domain 6 causes early onset Alzheimer's disease (Q46937090) (← links)
- Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies (Q47218394) (← links)
- Familial early onset frontotemporal dementia caused by a novel S356T MAPT mutation, initially diagnosed as schizophrenia (Q48090753) (← links)
- Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome (Q48400376) (← links)
- Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies (Q48509982) (← links)
- Frontal temporal dementia: dissecting the aetiology and pathogenesis (Q48615200) (← links)
- A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia (Q48636005) (← links)
- Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative (Q51971909) (← links)
- CXCR4 involvement in neurodegenerative diseases. (Q52317581) (← links)
- Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum. (Q53513139) (← links)
- A familial FTD associated with C9orf72 repeat expansion and dysplastic gangliocytoma. (Q55359246) (← links)
- Challenges and new opportunities in the investigation of new drug therapies to treat frontotemporal dementia (Q56972630) (← links)
- Genetic Variability in CHMP2B and Frontotemporal Dementia (Q56972704) (← links)
- Protein network analysis reveals selectively vulnerable regions and biological processes in FTD (Q57060450) (← links)
- A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers (Q58698136) (← links)