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2018 1
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2021 4
2022 1
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Page 1
Characterizing the Genetic Architecture of Parkinson's Disease in Latinos.
Loesch DP, Horimoto ARVR, Heilbron K, Sarihan EI, Inca-Martinez M, Mason E, Cornejo-Olivas M, Torres L, Mazzetti P, Cosentino C, Sarapura-Castro E, Rivera-Valdivia A, Medina AC, Dieguez E, Raggio V, Lescano A, Tumas V, Borges V, Ferraz HB, Rieder CR, Schumacher-Schuh A, Santos-Lobato BL, Velez-Pardo C, Jimenez-Del-Rio M, Lopera F, Moreno S, Chana-Cuevas P, Fernandez W, Arboleda G, Arboleda H, Arboleda-Bustos CE, Yearout D, Zabetian CP; 23andMe Research Team, Cannon P, Thornton TA, O'Connor TD, Mata IF; Latin American Research Consortium on the Genetics of Parkinson's Disease (LARGE-PD). Loesch DP, et al. Among authors: sarapura castro e. Ann Neurol. 2021 Sep;90(3):353-365. doi: 10.1002/ana.26153. Epub 2021 Jul 22. Ann Neurol. 2021. PMID: 34227697
Panda with "bright eyes": a rare sign in Wilson disease.
Sarapura-Castro E, RamÍrez-QuiÑones J, Cornejo-Olivas M. Sarapura-Castro E, et al. Arq Neuropsiquiatr. 2020 Jun 29;78(8):525. doi: 10.1590/0004-282X20200036. Arq Neuropsiquiatr. 2020. PMID: 32627810 Free article. No abstract available.
Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients.
Sarihan EI, Pérez-Palma E, Niestroj LM, Loesch D, Inca-Martinez M, Horimoto ARVR, Cornejo-Olivas M, Torres L, Mazzetti P, Cosentino C, Sarapura-Castro E, Rivera-Valdivia A, Dieguez E, Raggio V, Lescano A, Tumas V, Borges V, Ferraz HB, Rieder CR, Schumacher-Schuh AF, Santos-Lobato BL, Velez-Pardo C, Jimenez-Del-Rio M, Lopera F, Moreno S, Chana-Cuevas P, Fernandez W, Arboleda G, Arboleda H, Arboleda-Bustos CE, Yearout D, Zabetian CP, Thornton TA, O'Connor TD, Lal D, Mata IF; Latin American Research Consortium on the Genetics of Parkinson's Disease (LARGE-PD)‡. Sarihan EI, et al. Among authors: sarapura castro e. Mov Disord. 2021 Feb;36(2):434-441. doi: 10.1002/mds.28353. Epub 2020 Nov 5. Mov Disord. 2021. PMID: 33150996 Free PMC article.
Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families.
Sarapura-Castro E, Cosentino C, Landman J, Landman A, Torres L, Nuñez Y, Capellari S, Parchi P, Cornejo-Olivas M. Sarapura-Castro E, et al. Clin Neurol Neurosurg. 2021 Mar;202:106490. doi: 10.1016/j.clineuro.2021.106490. Epub 2021 Jan 12. Clin Neurol Neurosurg. 2021. PMID: 33454496 Free PMC article. No abstract available.
Novel Compound Heterozygous Mutation c.3955_3958dup and c.5825C>T in the ATM Gene: Clinical Evidence of Ataxia-Telangiectasia and Cancer in a Peruvian Family.
Rodriguez RS, Cornejo-Olivas M, Bazalar-Montoya J, Sarapura-Castro E, Torres-Loarte M, Rivera-Valdivia A, Sullcahuaman-Allende Y. Rodriguez RS, et al. Among authors: sarapura castro e. Mol Syndromol. 2021 Aug;12(5):289-293. doi: 10.1159/000515696. Epub 2021 Jun 17. Mol Syndromol. 2021. PMID: 34602955 Free PMC article.
Autosomal Recessive Cerebellar Ataxias in South America: A Multicenter Study of 1338 Patients.
Gama MTD, Braga-Neto P, Rangel DM, Godeiro C Jr, Alencar R, Embiruçu EK, Cornejo-Olivas M, Sarapura-Castro E, Saffie Awad P, Muñoz Chesta D, Kauffman M, Rodriguez-Quiroga S, Jardim LB, da Graça FF, França MC Jr, Tomaselli PJ, Marques W Jr, Teive HAG, Barsottini OGP, Pedroso JL, Synofzik M. Gama MTD, et al. Among authors: sarapura castro e. Mov Disord. 2022 May 4. doi: 10.1002/mds.29046. Online ahead of print. Mov Disord. 2022. PMID: 35507441 No abstract available.