about
Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.Neurogenetics in Peru: clinical, scientific and ethical perspectives.A Peruvian family with a novel PARK2 mutation: Clinical and pathological characteristicsClinical and molecular studies reveal a PSEN1 mutation (L153V) in a Peruvian family with early-onset Alzheimer's disease.The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America.Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.The First Report of CADASIL in Peru: Olfactory Dysfunction on Initial Presentation.Erratum: Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil.Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body diseaseGenetics and genomics in Peru: Clinical and research perspectiveATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South AmericaThe distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru[Role of government in clinical trials]Huntington's disease-like disorders in Latin America and the CaribbeanNeurology outreach clinic for Huntington disease in Peru: Lessons for neurodegenerative diseasesPalliative Care: Perceptions, Experiences, and Attitudes in a Peruvian Neurologic HospitalA Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington DiseaseATXN10 Microsatellite Distribution in a Peruvian Amerindian PopulationEconomic burden of Huntington's disease in PeruIdentification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian PopulationGenetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete PenetranceCorrection to: Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete PenetranceGuillain-Barre syndrome outbreak in Peru: Association with polymorphisms in IL-17, ICAM1, and CD1
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description
researcher
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wetenschapper
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հետազոտող
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name
M Cornejo-Olivas
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M Cornejo-Olivas
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M Cornejo-Olivas
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M Cornejo-Olivas
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M Cornejo-Olivas
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type
label
M Cornejo-Olivas
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M Cornejo-Olivas
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M Cornejo-Olivas
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M Cornejo-Olivas
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M Cornejo-Olivas
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altLabel
Mario Cornejo
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prefLabel
M Cornejo-Olivas
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M Cornejo-Olivas
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M Cornejo-Olivas
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M Cornejo-Olivas
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M Cornejo-Olivas
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P1053
F-9744-2017
P106
P1153
38360977700
P2798
P31
P3829
P496
0000-0001-6313-5680