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Olimpio Ortega

Biographic Data

ID7984004
NAMEOlimpio Ortega
GIVEN NAMESOlimpio
FAMILY NAMEOrtega
SIGNATUREORTEGA O
AFFILIATIONSInstituto Nacional de Enfermedades Neoplásicas
VERIFIEDNo
TOTAL WORKS3
TOTAL CITATIONS0
WORKS AS AUTHOR3
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2014
LATEST PUBLICATION YEAR2015
H-INDEX0
  • Neurogenetics in Peru

    Open Access•Mario Cornejo‐Olivas, Mario Cornejo-Olivas et al.•ARTICLE•Journal of Community Genetics•2015

  • Enfermedad de Kennedy en el Perú

    Open Access•Víctor Gómez-Calero, Mario Cornejo‐Olivas et al.•ARTICLE•Revista Peruana de Medicina…•2014

    Kennedy's disease is an X-linked recessive disorder with onset in adulthood, characterized by progressive degeneration of spinal motor neurons due to a dynamic mutation in the androgen receptor gene. We report three families (five cases) characterized by progressive weakness involving both limbs and bulbar muscles, atrophy, tremor, cramps and endocrinologic disturbances; the neurophysiological studies demonstrated second motor neuron impairment. …

  • Polimorfismo genético de la apolipoproteína E en una población peruana

    Open Access•Victoria Marca, Oscar Acosta et al.•ARTICLE•Revista Peruana de Medicina…•2014

    Objectives. To determine the allelic and genotypic frequencies of the APOE gene in a sample of a population group in Peru. Materials and methods. Cross-sectional analytic study in 189 apparently healthy volunteers, workers of the Instituto Nacional de Ciencias Neurológicas in Lima, Perú, divided into 5 groups by birth department and two generations ancestry. Genomic DNA was amplified using PCR-RFLP. The resulting fragments were detected by 12 % p…

No prominent works on this page.

  • Enfermedad de Kennedy en el Perú

    Open Access•Víctor Gómez-Calero, Mario Cornejo‐Olivas et al.•ARTICLE•Revista Peruana de Medicina…•2014

    Kennedy's disease is an X-linked recessive disorder with onset in adulthood, characterized by progressive degeneration of spinal motor neurons due to a dynamic mutation in the androgen receptor gene. We report three families (five cases) characterized by progressive weakness involving both limbs and bulbar muscles, atrophy, tremor, cramps and endocrinologic disturbances; the neurophysiological studies demonstrated second motor neuron impairment. …

  • Polimorfismo genético de la apolipoproteína E en una población peruana

    Open Access•Victoria Marca, Oscar Acosta et al.•ARTICLE•Revista Peruana de Medicina…•2014

    Objectives. To determine the allelic and genotypic frequencies of the APOE gene in a sample of a population group in Peru. Materials and methods. Cross-sectional analytic study in 189 apparently healthy volunteers, workers of the Instituto Nacional de Ciencias Neurológicas in Lima, Perú, divided into 5 groups by birth department and two generations ancestry. Genomic DNA was amplified using PCR-RFLP. The resulting fragments were detected by 12 % p…

  • Neurogenetics in Peru

    Open Access•Mario Cornejo‐Olivas, Mario Cornejo-Olivas et al.•ARTICLE•Journal of Community Genetics•2015

Medicine (3 works) · Biology (2 works) · Disease (2 works) · Genetic Neurodegenerative Diseases (2 works) · Genetics (2 works) · Internal Medicine (2 works) · Pathology (2 works) · Population (2 works) · Allele (1 work) · Allele frequency (1 work)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae