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Items: 30

1.

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

Cornejo-Olivas M, Inca-Martinez M, Castilhos RM, Furtado GV, Mattos EP, Bampi GB, Leistner-Segal S, Marca V, Mazzetti P, Saraiva-Pereira ML, Jardim LB; Rede Neurogenetica.

Cerebellum. 2020 Apr;19(2):216. doi: 10.1007/s12311-020-01105-x.

PMID:
31940124
2.

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

Cornejo-Olivas M, Inca-Martinez M, Castilhos RM, Furtado GV, Mattos EP, Bampi GB, Leistner-Segal S, Marca V, Mazzetti P, Saraiva-Pereira ML, Jardim LB; Rede Neurogenetica.

Cerebellum. 2020 Apr;19(2):208-215. doi: 10.1007/s12311-019-01098-2. Erratum in: Cerebellum. 2020 Jan 15;:.

PMID:
31900855
3.

Economic burden of Huntington's disease in Peru.

Silva-Paredes G, Urbanos-Garrido RM, Inca-Martinez M, Rabinowitz D, Cornejo-Olivas MR.

BMC Health Serv Res. 2019 Dec 30;19(1):1017. doi: 10.1186/s12913-019-4806-6.

4.

A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington Disease.

Kay C, Collins JA, Caron NS, Agostinho LA, Findlay-Black H, Casal L, Sumathipala D, Dissanayake VHW, Cornejo-Olivas M, Baine F, Krause A, Greenberg JL, Paiva CLA, Squitieri F, Hayden MR.

Am J Hum Genet. 2019 Dec 5;105(6):1112-1125. doi: 10.1016/j.ajhg.2019.10.011. Epub 2019 Nov 7.

PMID:
31708117
5.

Guillain-Barre syndrome outbreak in Peru: Association with polymorphisms in IL-17, ICAM1, and CD1.

Jaramillo-Valverde L, Levano KS, Villanueva I, Hidalgo M, Cornejo M, Mazzetti P, Cornejo-Olivas M, Sanchez C, Poterico JA, Valdivia-Silva J, Guio H.

Mol Genet Genomic Med. 2019 Oct;7(10):e00960. doi: 10.1002/mgg3.960. Epub 2019 Aug 28.

6.

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

Figueroa-Ildefonso E, Bademci G, Rajabli F, Cornejo-Olivas M, Villanueva RDC, Badillo-Carrillo R, Inca-Martinez M, Neyra KM, Sineni C, Tekin M.

Genes (Basel). 2019 Jul 31;10(8). pii: E581. doi: 10.3390/genes10080581.

7.

ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population.

Véliz-Otani D, Inca-Martinez M, Bampi GB, Ortega O, Jardim LB, Saraiva-Pereira ML, Mazzetti P, Cornejo-Olivas M.

Cerebellum. 2019 Oct;18(5):841-848. doi: 10.1007/s12311-019-01057-x.

PMID:
31342269
8.

The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru.

Velez-Pardo C, Lorenzo-Betancor O, Jimenez-Del-Rio M, Moreno S, Lopera F, Cornejo-Olivas M, Torres L, Inca-Martinez M, Mazzetti P, Cosentino C, Yearout D, Waldherr SM, Zabetian CP, Mata IF.

Parkinsonism Relat Disord. 2019 Jun;63:204-208. doi: 10.1016/j.parkreldis.2019.01.030. Epub 2019 Feb 4.

PMID:
30765263
9.

Genetics and genomics in Peru: Clinical and research perspective.

Guio H, Poterico JA, Levano KS, Cornejo-Olivas M, Mazzetti P, Manassero-Morales G, Ugarte-Gil MF, Acevedo-Vásquez E, Dueñas-Roque M, Piscoya A, Fujita R, Sanchez C, Casavilca-Zambrano S, Jaramillo-Valverde L, Sullcahuaman-Allende Y, Iglesias-Pedraz JM, Abarca-Barriga H.

Mol Genet Genomic Med. 2018 Nov;6(6):873-886. doi: 10.1002/mgg3.533. Review.

10.

Palliative Care: Perceptions, Experiences, and Attitudes in a Peruvian Neurologic Hospital.

Vishnevetsky A, Zapata Del Mar C, Luis Cam J, Cornejo-Olivas M, Creutzfeldt CJ.

J Palliat Med. 2019 Mar;22(3):250-257. doi: 10.1089/jpm.2018.0196. Epub 2018 Dec 8.

11.

Neurology outreach clinic for Huntington disease in Peru: Lessons for neurodegenerative diseases.

Vishnevetsky A, Illanes-Manrique M, Inca-Martinez M, Milla-Neyra K, Sarapura-Castro E, Mazzetti P, Cornejo-Olivas M.

Neurology. 2018 Aug 7;91(6):282-285. doi: 10.1212/WNL.0000000000005940. Epub 2018 Jul 6. Review. No abstract available.

12.

Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease.

Hou X, Fiesel FC, Truban D, Castanedes Casey M, Lin WL, Soto AI, Tacik P, Rousseau LG, Diehl NN, Heckman MG, Lorenzo-Betancor O, Ferrer I, Arbelo JM, Steele JC, Farrer MJ, Cornejo-Olivas M, Torres L, Mata IF, Graff-Radford NR, Wszolek ZK, Ross OA, Murray ME, Dickson DW, Springer W.

Autophagy. 2018;14(8):1404-1418. doi: 10.1080/15548627.2018.1461294. Epub 2018 Jul 28.

13.

Huntington's disease-like disorders in Latin America and the Caribbean.

Walker RH, Gatto EM, Bustamante ML, Bernal-Pacheco O, Cardoso F, Castilhos RM, Chana-Cuevas P, Cornejo-Olivas M, Estrada-Bellmann I, Jardim LB, López-Castellanos R, López-Contreras R, Maia DP, Mazzetti P, Miranda M, Rodríguez-Violante M, Teive H, Tumas V.

Parkinsonism Relat Disord. 2018 Aug;53:10-20. doi: 10.1016/j.parkreldis.2018.05.021. Epub 2018 May 21. Review.

PMID:
29853295
14.

The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population.

Kay C, Collins JA, Wright GEB, Baine F, Miedzybrodzka Z, Aminkeng F, Semaka AJ, McDonald C, Davidson M, Madore SJ, Gordon ES, Gerry NP, Cornejo-Olivas M, Squitieri F, Tishkoff S, Greenberg JL, Krause A, Hayden MR.

Am J Med Genet B Neuropsychiatr Genet. 2018 Apr;177(3):346-357. doi: 10.1002/ajmg.b.32618. Epub 2018 Feb 20.

PMID:
29460498
15.

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.

Cornejo-Olivas M, Torres L, Velit-Salazar MR, Inca-Martinez M, Mazzetti P, Cosentino C, Micheli F, Perandones C, Dieguez E, Raggio V, Tumas V, Borges V, Ferraz HB, Rieder CRM, Shumacher-Schuh A, Velez-Pardo C, Jimenez-Del-Rio M, Lopera F, Chang-Castello J, Andreé-Munoz B, Waldherr S, Yearout D, Zabetian CP, Mata IF.

NPJ Parkinsons Dis. 2018 Jan 19;4:3. doi: 10.1038/s41531-017-0025-1. eCollection 2018.

16.

Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.

Bampi GB, Bisso-Machado R, Hünemeier T, Gheno TC, Furtado GV, Veliz-Otani D, Cornejo-Olivas M, Mazzeti P, Bortolini MC, Jardim LB, Saraiva-Pereira ML; Rede Neurogenetica.

Neuromolecular Med. 2017 Dec;19(4):501-509. doi: 10.1007/s12017-017-8464-8. Epub 2017 Sep 13.

PMID:
28905220
17.

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

Cornejo-Olivas M, Torres L, Velit-Salazar MR, Inca-Martinez M, Mazzetti P, Cosentino C, Micheli F, Perandones C, Dieguez E, Raggio V, Tumas V, Borges V, Ferraz HB, Rieder CRM, Shumacher-Schuh A, Velez-Pardo C, Jimenez-Del-Rio M, Lopera F, Chang-Castello J, Andreé-Munoz B, Waldherr S, Yearout D, Zabetian CP, Mata IF.

NPJ Parkinsons Dis. 2017 Jun 2;3:19. doi: 10.1038/s41531-017-0020-6. eCollection 2017. Erratum in: NPJ Parkinsons Dis. 2018 Jan 19;4:3.

18.

Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil.

Gheno TC, Furtado GV, Saute JAM, Donis KC, Fontanari AMV, Emmel VE, Pedroso JL, Barsottini O, Godeiro-Junior C, van der Linden H, Ternes Pereira E, Cintra VP, Marques W Jr, de Castilhos RM, Alonso I, Sequeiros J, Cornejo-Olivas M, Mazzetti P, Leotti VB, Jardim LB, Saraiva-Pereira ML; Rede Neurogenetica.

Eur J Neurol. 2017 Jul;24(7):892-e36. doi: 10.1111/ene.13281. Epub 2017 May 31.

PMID:
28560845
19.

The First Report of CADASIL in Peru: Olfactory Dysfunction on Initial Presentation.

Vishnevetsky A, Inca-Martinez M, Milla-Neyra K, Barrientos-Iman DM, Cornejo-Herrera I, Cosentino C, Cornejo-Olivas M.

eNeurologicalSci. 2016 Dec;5:15-19. doi: 10.1016/j.ensci.2016.09.001. Epub 2016 Sep 28.

20.

The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America.

Kay C, Tirado-Hurtado I, Cornejo-Olivas M, Collins JA, Wright G, Inca-Martinez M, Veliz-Otani D, Ketelaar ME, Slama RA, Ross CJ, Mazzetti P, Hayden MR.

Eur J Hum Genet. 2017 Feb;25(3):332-340. doi: 10.1038/ejhg.2016.169. Epub 2016 Dec 21.

21.

[Neurogenetics in Peru, example of translational research].

Mazzetti P, Inca-Martínez M, Tirado-Hurtado I, Milla-Neyra K, Silva-Paredes G, Vishnevetsky A, Cornejo-Olivas M.

Rev Peru Med Exp Salud Publica. 2015 Oct;32(4):787-93. Spanish.

22.

Clinical and Molecular Features of Late Onset Huntington Disease in a Peruvian Cohort.

Cornejo-Olivas MR, Inca-Martinez MA, Espinoza-Huertas K, Veliz-Otani D, Velit-Salazar MR, Marca V, Ortega O, Cornejo-Herrera IF, Lindo-Samanamud S, Mora-Alferez P, Mazzetti P.

J Huntingtons Dis. 2015;4(1):99-105.

PMID:
26333261
23.

Neurogenetics in Peru: clinical, scientific and ethical perspectives.

Cornejo-Olivas M, Espinoza-Huertas K, Velit-Salazar MR, Veliz-Otani D, Tirado-Hurtado I, Inca-Martinez M, Silva-Paredes G, Milla-Neyra K, Marca V, Ortega O, Mazzetti P.

J Community Genet. 2015 Jul;6(3):251-7. doi: 10.1007/s12687-015-0239-z. Epub 2015 May 27.

24.

ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America.

Pereira FS, Monte TL, Locks-Coelho LD, Silva AS, Barsottini O, Pedroso JL, Cornejo-Olivas M, Mazzetti P, Godeiro C, Vargas FR, Lima MA, van der Linden H Jr, Toralles MB, Medeiros PF, Ribeiro E, Braga-Neto P, Salarini D, Castilhos RM, Saraiva-Pereira ML, Jardim LB; Rede Neurogenetica.

Cerebellum. 2015 Dec;14(6):728-30. doi: 10.1007/s12311-015-0666-8. No abstract available.

PMID:
25869926
25.

A Peruvian family with a novel PARK2 mutation: Clinical and pathological characteristics.

Cornejo-Olivas MR, Torres L, Mata IF, Mazzetti P, Rivas D, Cosentino C, Inca-Martinez M, Cuba JM, Zabetian CP, Leverenz JB.

Parkinsonism Relat Disord. 2015 May;21(5):444-8. doi: 10.1016/j.parkreldis.2015.01.005. Epub 2015 Jan 15.

26.

Clinical and molecular studies reveal a PSEN1 mutation (L153V) in a Peruvian family with early-onset Alzheimer's disease.

Cornejo-Olivas MR, Yu CE, Mazzetti P, Mata IF, Meza M, Lindo-Samanamud S, Leverenz JB, Bird TD.

Neurosci Lett. 2014 Mar 20;563:140-3. doi: 10.1016/j.neulet.2014.01.016. Epub 2014 Feb 2.

27.

[Kennedy disease in Peru: first cases with molecular diagnosis].

Gómez-Calero V, Cornejo-Olivas M, Ortega O, Marca V, Lindo-Samanamud S, Flores M, Torres-Ramírez L, Mazzetti P.

Rev Peru Med Exp Salud Publica. 2013 Apr;30(2):331-5. Spanish.

28.

[Role of government in clinical trials].

Mazzetti P, Silva-Paredes G, Cornejo-Olivas M.

Rev Peru Med Exp Salud Publica. 2012 Oct-Dec;29(4):509-15. Spanish.

29.

[Genetic polymorphism of apolipoprotein E in a Peruvian population].

Marca V, Acosta O, Cornejo-Olivas M, Ortega O, Huerta D, Mazzetti P.

Rev Peru Med Exp Salud Publica. 2011 Dec;28(4):589-94. Spanish.

30.

Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin America.

Mata IF, Wilhoite GJ, Yearout D, Bacon JA, Cornejo-Olivas M, Mazzetti P, Marca V, Ortega O, Acosta O, Cosentino C, Torres L, Medina AC, Perez-Pastene C, Díaz-Grez F, Vilariño-Güell C, Venegas P, Miranda M, Trujillo-Godoy O, Layson L, Avello R, Dieguez E, Raggio V, Micheli F, Perandones C, Alvarez V, Segura-Aguilar J, Farrer MJ, Zabetian CP, Ross OA.

Parkinsonism Relat Disord. 2011 Sep;17(8):629-31. doi: 10.1016/j.parkreldis.2011.05.003. Epub 2011 May 31.

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