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List of works by Parastoo Momeni

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia

scientific article published on 28 February 2006

A familial FTD associated with C9orf72 repeat expansion and dysplastic gangliocytoma.

scientific article published on 4 October 2013

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

scientific article

A presenilin-1 mutation (T245P) in transmembrane domain 6 causes early onset Alzheimer's disease

scientific article published on 15 February 2006

A repository based on a dynamically extensible data model supporting multidisciplinary research in neuroscience

scientific article

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

scientific article

Androgen receptor gene and sex-specific Alzheimer's disease

scientific article

Assessment of common variability and expression quantitative trait loci for genome-wide associations for progressive supranuclear palsy

scientific article

CXCR4 involvement in neurodegenerative diseases

scientific article published on 11 April 2018

Challenges and new opportunities in the investigation of new drug therapies to treat frontotemporal dementia

scholarly article by Edward D Huey et al published November 2008 in Expert Opinion on Therapeutic Targets

Characteristics of frontotemporal dementia patients with a Progranulin mutation

scientific article

Clinical and pathological features of an Alzheimer's disease patient with the MAPT Delta K280 mutation

scientific article published on 27 August 2007

Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

scientific article

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].

scientific article published on 19 October 2015

Elderly individuals with FTLD.

scientific article published in March 2013

FUS and TDP43 genetic variability in FTD and CBS

scientific article published on 23 September 2011

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

scientific article

Familial early onset frontotemporal dementia caused by a novel S356T MAPT mutation, initially diagnosed as schizophrenia

scientific article published on 12 August 2010

Familial frontotemporal dementia associated with C9orf72 repeat expansion and dysplastic gangliocytoma

scientific article published on 27 September 2013

Familial thoracic aortic aneurysm with dissection presenting as flash pulmonary edema in a 26-year-old man.

scientific article

Frontal temporal dementia: dissecting the aetiology and pathogenesis

scientific article published in April 2006

Frontotemporal dementia and its subtypes: a genome-wide association study

scientific article

Frontotemporal dementia in elderly individuals

scientific article published on August 2012

Frontotemporal dementia: from Mendelian genetics towards genome wide association studies

scientific article published on 06 September 2011

Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis

scientific article

Genetic Variability in CHMP2B and Frontotemporal Dementia

article

Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

scientific article

Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

scientific article published on 9 January 2018

Implication of common and disease specific variants in CLU, CR1, and PICALM.

scientific article published on 7 March 2012

Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID).

scientific article published on 7 July 2005

Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia

scientific article published in January 2008

Novel missense mutation in charged multivesicular body protein 2B in a patient with frontotemporal dementia

scientific article

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

scientific article published on 9 October 2006

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative

scientific article published in October 2007

Progranulin (GRN) in two siblings of a Latino family and in other patients with schizophrenia

scientific article

Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

Screening for C9ORF72 repeat expansion in FTLD.

scientific article published on 27 March 2012

Screening of Early and Late Onset Alzheimer's Disease Genetic Risk Factors in a Cohort of Dementia Patients from Liguria, Italy

scientific article published on 10 July 2015

Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum.

scientific article published on 9 April 2018

Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia

scientific article

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

scientific article published on 20 March 2011

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