Found: 13

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  • 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.

    Published in:
    2018
    By:
    • Cornejo-Olivas, Mario;
    • Torres, Luis;
    • Velit-Salazar, Mario R.;
    • Inca-Martinez, Miguel;
    • Mazzetti, Pilar;
    • Cosentino, Carlos;
    • Micheli, Federico;
    • Perandones, Claudia;
    • Dieguez, Elena;
    • Raggio, Victor;
    • Tumas, Vitor;
    • Borges, Vanderci;
    • Ferraz, Henrique B.;
    • Rieder, Carlos R. M.;
    • Shumacher-Schuh, Artur;
    • Velez-Pardo, Carlos;
    • Jimenez-Del-Rio, Marlene;
    • Lopera, Francisco;
    • Chang-Castello, Jorge;
    • Andreé-Munoz, Brennie
    Publication type:
    Correction Notice

  • Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.

    Published in:
    NPJ Parkinson's Disease, 2017, v. 3, n. 1, p. N.PAG, doi. 10.1038/s41531-017-0020-6
    By:
    • Cornejo-Olivas, Mario;
    • Torres, Luis;
    • Velit-Salazar, Mario R.;
    • Inca-Martinez, Miguel;
    • Mazzetti, Pilar;
    • Cosentino, Carlos;
    • Micheli, Federico;
    • Perandones, Claudia;
    • Dieguez, Elena;
    • Raggio, Victor;
    • Tumas, Vitor;
    • Borges, Vanderci;
    • Ferraz, Henrique B.;
    • Rieder, Carlos R. M.;
    • Shumacher-Schuh, Artur;
    • Velez-Pardo, Carlos;
    • Jimenez-Del-Rio, Marlene;
    • Lopera, Francisco;
    • Chang-Castello, Jorge;
    • Andreé-Munoz, Brennie
    Publication type:
    Article

  • Juvenile‐Onset Huntington's Disease in Peru: A Case Series of 32 Patients.

    Published in:
    Movement Disorders Clinical Practice, 2023, v. 10, n. 2, p. 238, doi. 10.1002/mdc3.13625
    By:
    • Vishnevetsky, Anastasia;
    • Cornejo‐Olivas, Mario;
    • Sarapura‐Castro, Elison;
    • Inca‐Martinez, Miguel;
    • Rabinowitz, Danielle;
    • Milla‐Neyra, Karina;
    • Mazzetti, Pilar;
    • Bird, Thomas
    Publication type:
    Article

  • Correction to: Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.

    Published in:
    2020
    By:
    • Cornejo-Olivas, Mario;
    • Inca-Martinez, Miguel;
    • Castilhos, Raphael Machado;
    • Furtado, Gabriel Vasata;
    • Mattos, Eduardo Preusser;
    • Bampi, Giovana Bavia;
    • Leistner-Segal, Sandra;
    • Marca, Victoria;
    • Mazzetti, Pilar;
    • Saraiva-Pereira, Maria Luiza;
    • Jardim, Laura Bannach
    Publication type:
    Correction Notice

  • Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.

    Published in:
    Cerebellum, 2020, v. 19, n. 2, p. 208, doi. 10.1007/s12311-019-01098-2
    By:
    • Cornejo-Olivas, Mario;
    • Inca-Martinez, Miguel;
    • Castilhos, Raphael Machado;
    • Furtado, Gabriel Vasata;
    • Mattos, Eduardo Preusser;
    • Bampi, Giovana Bavia;
    • Leistner-Segal, Sandra;
    • Marca, Victoria;
    • Mazzetti, Pilar;
    • Saraiva-Pereira, Maria Luiza;
    • Jardim, Laura Bannach
    Publication type:
    Article

  • ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population.

    Published in:
    Cerebellum, 2019, v. 18, n. 5, p. 841, doi. 10.1007/s12311-019-01057-x
    By:
    • Véliz-Otani, Diego;
    • Inca-Martinez, Miguel;
    • Bampi, Giovana B.;
    • Ortega, Olimpio;
    • Jardim, Laura B.;
    • Saraiva-Pereira, Maria Luiza;
    • Mazzetti, Pilar;
    • Cornejo-Olivas, Mario
    Publication type:
    Article

  • Characterizing the Genetic Architecture of Parkinson's Disease in Latinos.

    Published in:
    Annals of Neurology, 2021, v. 90, n. 3, p. 353, doi. 10.1002/ana.26153
    By:
    • Loesch, Douglas P.;
    • Horimoto, Andrea R. V. R.;
    • Heilbron, Karl;
    • Sarihan, Elif I.;
    • Inca‐Martinez, Miguel;
    • Mason, Emily;
    • Cornejo‐Olivas, Mario;
    • Torres, Luis;
    • Mazzetti, Pilar;
    • Cosentino, Carlos;
    • Sarapura‐Castro, Elison;
    • Rivera‐Valdivia, Andrea;
    • Medina, Angel C.;
    • Dieguez, Elena;
    • Raggio, Victor;
    • Lescano, Andres;
    • Tumas, Vitor;
    • Borges, Vanderci;
    • Ferraz, Henrique B.;
    • Rieder, Carlos R.
    Publication type:
    Article

  • Economic burden of Huntington's disease in Peru.

    Published in:
    2019
    By:
    • Silva-Paredes, Gustavo;
    • Urbanos-Garrido, Rosa M.;
    • Inca-Martinez, Miguel;
    • Rabinowitz, Danielle;
    • Cornejo-Olivas, Mario R.
    Publication type:
    journal article

  • Parkinson's Disease Gene Screening in Familial Cases from Central and South America.

    Published in:
    Movement Disorders, 2024, v. 39, n. 10, p. 1843, doi. 10.1002/mds.29931
    By:
    • Lorenzo‐Betancor, Oswaldo;
    • Mehta, Seysha;
    • Ramchandra, Janvi;
    • Mumuney, Sekinat;
    • Schumacher‐Schuh, Artur F.;
    • Cornejo‐Olivas, Mario;
    • Sarapura‐Castro, Elison H.;
    • Torres, Luis;
    • Inca‐Martinez, Miguel A.;
    • Mazzetti, Pilar;
    • Cosentino, Carlos;
    • Micheli, Federico;
    • Tumas, Vitor;
    • Dieguez, Elena;
    • Raggio, Victor;
    • Borges, Vanderci;
    • Ferraz, Henrique B.;
    • Chana‐Cuevas, Pedro;
    • Jimenez‐Del‐Rio, Marlene;
    • Velez‐Pardo, Carlos
    Publication type:
    Article

  • X‐Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease.

    Published in:
    Movement Disorders, 2023, v. 38, n. 9, p. 1625, doi. 10.1002/mds.29508
    By:
    • Leal, Thiago P.;
    • Rao, Shilpa C.;
    • French‐Kwawu, Jennifer N.;
    • Gouveia, Mateus H.;
    • Borda, Victor;
    • Bandres‐Ciga, Sara;
    • Inca‐Martinez, Miguel;
    • Mason, Emily A.;
    • Horimoto, Andrea R.V.R.;
    • Loesch, Douglas P.;
    • Sarihan, Elif I.;
    • Cornejo‐Olivas, Mario R.;
    • Torres, Luis E.;
    • Mazzetti‐Soler, Pilar E.;
    • Cosentino, Carlos;
    • Sarapura‐Castro, Elison H.;
    • Rivera‐Valdivia, Andrea;
    • Medina, Angel C.;
    • Dieguez, Elena M.;
    • Raggio, Víctor E.
    Publication type:
    Article

  • Genome‐Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients.

    Published in:
    Movement Disorders, 2021, v. 36, n. 2, p. 434, doi. 10.1002/mds.28353
    By:
    • Sarihan, Elif Irem;
    • Pérez‐Palma, Eduardo;
    • Niestroj, Lisa‐Marie;
    • Loesch, Douglas;
    • Inca‐Martinez, Miguel;
    • Horimoto, Andrea R.V.R.;
    • Cornejo‐Olivas, Mario;
    • Torres, Luis;
    • Mazzetti, Pilar;
    • Cosentino, Carlos;
    • Sarapura‐Castro, Elison;
    • Rivera‐Valdivia, Andrea;
    • Dieguez, Elena;
    • Raggio, Victor;
    • Lescano, Andres;
    • Tumas, Vitor;
    • Borges, Vanderci;
    • Ferraz, Henrique B.;
    • Rieder, Carlos R.;
    • Schumacher‐Schuh, Artur F.
    Publication type:
    Article

  • The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease.

    Published in:
    Molecular Neurodegeneration, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13024-015-0045-4
    By:
    • Mata, Ignacio F.;
    • Yongwoo Jang;
    • Chun-Hyung Kim;
    • Hanna, David S.;
    • Dorschner, Michael O.;
    • Samii, Ali;
    • Agarwal, Pinky;
    • Roberts, John W.;
    • Klepitskaya, Olga;
    • Shprecher, David R.;
    • Chung, Kathryn A.;
    • Factor, Stewart A.;
    • Espay, Alberto J.;
    • Revilla, Fredy J.;
    • Higgins, Donald S.;
    • Litvan, Irene;
    • Leverenz, James B.;
    • Yearout, Dora;
    • Inca-Martinez, Miguel;
    • Martinez, Erica
    Publication type:
    Article

  • Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population.

    Published in:
    Genes, 2019, v. 10, n. 8, p. 581, doi. 10.3390/genes10080581
    By:
    • Figueroa-Ildefonso, Erick;
    • Bademci, Guney;
    • Rajabli, Farid;
    • Cornejo-Olivas, Mario;
    • Chacón Villanueva, Ruy Diego;
    • Badillo-Carrillo, Rodolfo;
    • Inca-Martinez, Miguel;
    • Milla Neyra, Karina;
    • Sineni, Claire;
    • Tekin, Mustafa
    Publication type:
    Article