Alfredo Ramirez
Ramírez, Alfredo 1976-
Ramírez Zuñiga, Alfredo Estanislao 1976-
VIAF ID: 67547727 (Personal)
Permalink: http://viaf.org/viaf/67547727
Preferred Forms
- 100 0 _ ‡a Alfredo Ramirez
- 100 1 _ ‡a Ramírez, Alfredo ‡d 1976-
- 100 1 _ ‡a Ramírez Zuñiga, Alfredo Estanislao ‡d 1976-
4xx's: Alternate Name Forms (9)
Works
Title | Sources |
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The association between genome-wide polymorphisms and chronic postoperative pain: a prospective observational study | |
Association of Parkinson disease to PARK16 in a Chilean sample | |
ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome. | |
The BDNFVal66Met SNP modulates the association between beta-amyloid and hippocampal disconnection in Alzheimer's disease | |
Blood-derived integration-free iPS cell line UKBi011-A from a diagnosed male Alzheimer's disease patient with APOE ɛ4/ɛ4 genotype | |
CDH6 and HAGH protein levels in plasma associate with Alzheimer's disease in APOE ε4 carriers | |
Cerebrospinal fluid and blood biomarkers for neurodegenerative dementias: An update of the Consensus of the Task Force on Biological Markers in Psychiatry of the World Federation of Societies of Biological Psychiatry. | |
Characterization of ADAMTS14, a novel member of the ADAMTS metalloproteinase family. | |
Clinical and genetic analysis of a Chilean family with early-onset autosomal dominant Alzheimer's disease. | |
Clinical and molecular characterization of neurodegenerative disorders | |
Clinical spectrum of Kufor-Rakeb syndrome in the Chilean kindred with ATP13A2 mutations | |
Cognitive behavioural therapy for the treatment of late life depression : study protocol of a multicentre, randomized, observer-blinded, controlled trial (CBTlate) | |
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity | |
Corrigendum to "Genome-wide association interaction analysis for Alzheimer's disease." [Neurobiol. Aging 35 (2014) 2436-2443]. | |
Demenz mit Lewy-Körpern: alte und neue Erkenntnisse – Teil 2: Behandlung | |
Design and first baseline data of the DZNE multicenter observational study on predementia Alzheimer's disease (DELCODE). | |
Disentangling the biological pathways involved in early features of Alzheimer's disease in the Rotterdam Study. | |
DNA methylation of the TNF-α promoter region in peripheral blood monocytes and the cortex of human Alzheimer's disease patients. | |
Editorial: Searching for the Holy Grail Will Need Biomarkers | |
Eicosapentaenoic Acid Is Associated with Decreased Incidence of Alzheimer's Dementia in the Oldest Old | |
Elevated HbA1c is associated with increased risk of incident dementia in primary care patients | |
Eye movement disorders in ATP13A2 mutation carriers (PARK9). | |
Frequency of the D620N mutation in VPS35 in Parkinson disease. | |
G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth | |
GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study | |
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease. | |
Genetic estimators of DNA methylation provide insights into the molecular basis of polygenic traits. | |
Genetic interaction of PICALM and APOE is associated with brain atrophy and cognitive impairment in Alzheimer's disease. | |
Genome-wide significant risk factors on chromosome 19 and the APOE locus. | |
Glucocerebrosidase mutations in a Serbian Parkinson's disease population | |
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase | |
Homozygous THAP1 mutations as cause of early-onset generalized dystonia | |
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia. | |
Identifizierung einer neuen Mutation in der kodierenden Region des "Grey-Lethal" Gens OSTM1 bei der humanen malignen infantilen Osteopetrose | |
Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's disease. | |
Influence of genetic variants in SORL1 gene on the manifestation of Alzheimer's disease. | |
Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes | |
Left frontal hub connectivity delays cognitive impairment in autosomal-dominant and sporadic Alzheimer's disease. | |
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove | |
Meta-analysis of genetic association with diagnosed Alzheimer's disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing | |
Methylomic profiling in trisomy 21 identifies cognition- and Alzheimer's disease-related dysregulation | |
Midlife occupational cognitive requirements protect cognitive function in old age by increasing cognitive reserve | |
mind's ratio How the balance between ω-6 and ω-3 fatty acids affects the risk of late-life dementia | |
Minor neuropsychological deficits in patients with subjective cognitive decline | |
Motor pathway excitability in ATP13A2 mutation carriers: a transcranial magnetic stimulation study | |
Multicenter Tract-Based Analysis of Microstructural Lesions within the Alzheimer's Disease Spectrum: Association with Amyloid Pathology and Diagnostic Usefulness | |
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D | |
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease | |
Neurokinin3 receptor as a target to predict and improve learning and memory in the aged organism | |
New insights into the genetic etiology of Alzheimer's disease and related dementias | |
No association of the variant rs11887120 in DNMT3A with cognitive decline in individuals with mild cognitive impairment. | |
A novel Alzheimer disease locus located near the gene encoding tau protein. | |
Novel genetic matching methods for handling population stratification in genome-wide association studies | |
PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment | |
Population-Based Genetic Studies: The Search for Causative Variants in Parkinson's Disease | |
A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2 | |
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration | |
The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk. | |
Rare variant testing of imputed data: an analysis pipeline typified | |
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation | |
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype | |
Reply: POLR3A variants in hereditary spastic paraplegia and ataxia. | |
Resting-State Network Alterations Differ between Alzheimer's Disease Atrophy Subtypes | |
Retraction: Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies | |
[Search for risk genes in Alzheimer's disease]. | |
Structural imaging in the presymptomatic stage of genetically determined parkinsonism. | |
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function | |
SUCLG2 identified as both a determinator of CSF Aβ1–42 levels and an attenuator of cognitive decline in Alzheimer's disease | |
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis | |
Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease | |
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis | |
TREM2 rare variant p.R47H is not associated with Parkinson's disease. | |
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry | |
An unusual neurological syndrome of crawling gait, dystonia, pyramidal signs, and limited speech | |
Which features of subjective cognitive decline are related to amyloid pathology? Findings from the DELCODE study | |
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene |