| Tipo Producción |
Título |
Autor |
Año de Producción |
DOI |
Revista |
Fuente |
Cuartil de ScimagoJR o JCR* |
|
Review
|
Advancements in dementia research, diagnostics, and care in Latin America: Highlights from the 2023 Alzheimer's Association International conference satellite symposium in Mexico City
|
Sosa A.L.
|
2024
|
10.1002/ALZ.13850
|
Alzheimer's and Dementia
|
|
2024: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities
|
Tan A.H.
|
2024
|
10.1002/MDC3.13903
|
Movement Disorders Clinical Practice
|
|
2024: No disponible**, 2020: Q2
|
|
Letter
|
A Novel Variant in SQSTM1 Gene Causing Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy in a Peruvian Family
|
Chacaltana-Vinas C.
|
2024
|
10.1002/MDC3.14025
|
Movement Disorders Clinical Practice
|
|
No Aplica
|
|
Review
|
Frequency of Hereditary and GBA1-Related Parkinsonism in Latin America: A Systematic Review and Meta-Analysis
|
Saffie Awad P.
|
2024
|
10.1002/MDS.29614
|
Movement Disorders
|
|
2024: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
The impact of clinical genome sequencing in a global population with suspected rare genetic disease
|
Thorpe E.
|
2024
|
10.1016/J.AJHG.2024.05.006
|
American Journal of Human Genetics
|
|
2024: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
Spinocerebellar ataxia type 2 has multiple ancestral origins
|
Sena L.S.
|
2024
|
10.1016/J.PARKRELDIS.2023.105985
|
Parkinsonism and Related Disorders
|
|
2024: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
|
Kim J.J.
|
2024
|
10.1038/S41588-023-01584-8
|
Nature Genetics
|
|
2024: No disponible**, 2020: Q1
|
|
Editorial
|
Palliative care in neurology: perspectives for the Peruvian healthcare system
|
Cornejo-Olivas M.
|
2024
|
10.20453/RNP.V87I2.5630
|
Revista de Neuro-Psiquiatria
|
|
No Aplica
|
|
Journal - Article
|
Juvenile-Onset Huntington's Disease in Peru: A Case Series of 32 Patients
|
Vishnevetsky, Anastasia | Cornejo-Olivas, Mario | Sarapura-Castro, Elison | Inca-Martinez, Miguel | Rabinowitz, Danielle | Milla-Neyra, Karina | Mazzetti, Pilar | Bird, Thomas
|
2023
|
10.1002/MDC3.13625
|
MOVEMENT DISORDERS CLINICAL PRACTICE
|
|
S/C***
|
|
Journal - Article
|
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
|
Vollstedt, Eva-Juliane | Schaake, Susen | Lohmann, Katja | Padmanabhan, Shalini | Brice, Alexis | Lesage, Suzanne | Tesson, Christelle | Vidailhet, Marie | Wurster, Isabel | Hentati, Faycel | Mirelman, Anat | Giladi, Nir | Marder, Karen | Waters, Cheryl | Fahn, Stanley | Kasten, Meike | Bruggemann, Norbert | Borsche, Max | Foroud, Tatiana | Tolosa, Eduardo | Garrido, Alicia | Annesi, Grazia | Gagliardi, Monica | Bozi, Maria | Stefanis, Leonidas | Ferreira, Joaquim J. | Guedes, Leonor Correia | Avenali, Micol | Petrucci, Simona | Clark, Lorraine | Fedotova, Ekaterina Y. | Abramycheva, Natalya Y. | Alvarez, Victoria | Menendez-Gonzalez, Manuel | Maestre, Silvia Jesus | Gomez-Garre, Pilar | Mir, Pablo | Belin, Andrea Carmine | Ran, Caroline | Lin, Chin-Hsien | Kuo, Ming-Che | Crosiers, David | Wszolek, Zbigniew K. | Ross, Owen A. | Jankovic, Joseph | Nishioka, Kenya | Funayama, Manabu | Clarimon, Jordi | Williams-Gray, Caroline H. | Camacho, Marta | Cornejo-Olivas, Mario | Torres-Ramirez, Luis | Wu, Yih-Ru | Lee-Chen, Guey-Jen | Morgadinho, Ana | Pulkes, Teeratorn | Termsarasab, Pichet | Berg, Daniela | Kuhlenbaumer, Gregor | Kuhn, Andrea A. | Borngraeber, Friederike | de Michele, Giuseppe | De Rosa, Anna | Zimprich, Alexander | Puschmann, Andreas | Mellick, George D. | Dorszewska, Jolanta | Carr, Jonathan | Ferese, Rosangela | Gambardella, Stefano | Chase, Bruce | Markopoulou, Katerina | Satake, Wataru | Toda, Tatsushi | Rossi, Malco | Merello, Marcelo | Lynch, Timothy | Olszewska, Diana A. | Lim, Shen-Yang | Ahmad-Annuar, Azlina | Tan, Ai Huey | Al-Mubarak, Bashayer | Hanagasi, Hasmet | Koziorowski, Dariusz | Ertan, Sibel | Genc, Gencer | Aguiar, Patricia de Carvalho | Barkhuizen, Melinda | Pimentel, Marcia M. G. | Saunders-Pullman, Rachel | van de Warrenburg, Bart | Bressman, Susan | Toft, Mathias | Appel-Cresswell, Silke | Lang, Anthony E. | Skorvanek, Matej | Boon, Agnita J. W. | Kruger, Rejko | Sammler, Esther M. | Tumas, Vitor | Zhang, Bao-Rong | Garraux, Gaetan | Chung, Sun Ju | Kim, Yun Joong | Winkelmann, Juliane | Sue, Carolyn M. | Tan, Eng-King | Damasio, Joana | Klivenyi, Peter | Kostic, Vladimir S. | Arkadir, David | Martikainen, Mika | Borges, Vanderci | Hertz, Jens Michael | Brighina, Laura | Spitz, Mariana | Suchowersky, Oksana | Riess, Olaf | Das, Parimal | Mollenhauer, Brit | Gatto, Emilia M. | Petersen, Maria Skaalum | Hattori, Nobutaka | Wu, Ruey-Meei | Illarioshkin, Sergey N. | Valente, Enza Maria | Aasly, Jan O. | Aasly, Anna | Alcalay, Roy N. | Thaler, Avner | Farrer, Matthew J. | Brockmann, Kathrin | Corvol, Jean-Christophe | Klein, Christine
|
2023
|
10.1002/MDS.29288
|
MOVEMENT DISORDERS
|
|
2023: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinsons Disease
|
Leal T.P.
|
2023
|
10.1002/MDS.29508
|
Movement Disorders
|
|
2023: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
An Exploratory Survey on the Care for Ataxic Patients in the American Continents and the Caribbean
|
Jardim L.B.
|
2023
|
10.1007/S12311-022-01442-Z
|
Cerebellum
|
|
2023: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
Machado Joseph-Disease Is Rare in the Peruvian Population
|
Cornejo-Olivas M.
|
2023
|
10.1007/S12311-022-01491-4
|
Cerebellum
|
|
2023: No disponible**, 2020: Q1
|
|
Book Chapter
|
LRRK2: Genetic mechanisms vs genetic subtypes
|
Mata I.
|
2023
|
10.1016/B978-0-323-85555-6.00018-7
|
Handbook of Clinical Neurology
|
|
No Aplica
|
|
Journal - Article
|
Management of rare movement diseases in different world regions
|
Painous, Celia | Marti, Maria J. | Graessner, Holm | Camargo, Andrea Paola | El-Jaafary, Shaimaa Ibrahim | Martinez-Ramirez, Daniel | Ojo, Oluwadamilola O. | Taiwo, Funmilola T. | Rajan, Roopa | Cornejo-Olivas, Mario | Ayele, Biniyam A. | Tibar, Houyam | Kearney, Mary | Gatto, Emilia | Tijssen, Marina AJ.
|
2023
|
10.1016/J.PARKRELDIS.2023.105286
|
PARKINSONISM & RELATED DISORDERS
|
|
2023: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
Identification of genetic risk loci and causal insights associated with Parkinsons disease in African and African admixed populations: a genome-wide association study
|
Rizig M.
|
2023
|
10.1016/S1474-4422(23)00283-1
|
The Lancet Neurology
|
|
2023: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
|
Towns C.
|
2023
|
10.1038/S41531-023-00533-W
|
npj Parkinsons Disease
|
|
2023: No disponible**, 2020: Q1
|
|
Journal - Article
|
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project
|
Vollstedt, Eva-Juliane | Madoev, Harutyun | Aasly, Anna | Ahmad-Annuar, Azlina | Al-Mubarak, Bashayer | Alcalay, Roy N. | Alvarez, Victoria | Amorin, Ignacio | Annesi, Grazia | Arkadir, David | Bardien, Soraya | Barker, Roger A. | Barkhuizen, Melinda | Basak, A. Nazli | Bonifati, Vincenzo | Boon, Agnita | Brighina, Laura | Brockmann, Kathrin | Belin, Andrea Carmine | Carr, Jonathan | Clarimon, Jordi | Cornejo-Olivas, Mario | Guedes, Leonor Correia | Corvol, Jean-Christophe | Crosiers, David | Damasio, Joana | Das, Parimal | de Carvalho Aguiar, Patricia | De Rosa, Anna | Dorszewska, Jolanta | Ertan, Sibel | Ferese, Rosangela | Ferreira, Joaquim | Gatto, Emilia | Genc, Gencer | Giladi, Nir | Gomez-Garre, Pilar | Hanagasi, Hasmet | Hattori, Nobutaka | Hentati, Faycal | Hoffman-Zacharska, Dorota | Illarioshkin, Sergey N. | Jankovic, Joseph | Jesus, Silvia | Kaasinen, Valtteri | Kievit, Anneke | Klivenyi, Peter | Kostic, Vladimir | Koziorowski, Dariusz | Kuehn, Andrea A. | Lang, Anthony E. | Lim, Shen-Yang | Lin, Chin-Hsien | Lohmann, Katja | Markovic, Vladana | Martikainen, Mika Henrik | Mellick, George | Merello, Marcelo | Milanowski, Lukasz | Mir, Pablo | oeztop-cakmak, Oezguer | Pimentel, Marcia Mattos Goncalves | Pulkes, Teeratorn | Puschmann, Andreas | Rogaeva, Ekaterina | Sammler, Esther M. | Skaalum Petersen, Maria | Skorvanek, Matej | Spitz, Mariana | Suchowersky, Oksana | Tan, Ai Huey | Termsarasab, Pichet | Thaler, Avner | Tumas, Vitor | Valente, Enza Maria | van de Warrenburg, Bart | Williams-Gray, Caroline H. | Wu, Ruey-Mei | Zhang, Baorong | Zimprich, Alexander | Solle, Justin | Padmanabhan, Shalini | Klein, Christine
|
2023
|
10.1371/JOURNAL.PONE.0292180
|
PLOS ONE
|
|
2023: No disponible**, 2020: Q2
|
|
Journal-article
|
Embracing Monogenic Parkinsons Disease: The MJFF Global Genetic PD Cohort.
|
|
2023
|
10.17863/CAM.93095
|
|
DataCite a través de ORCID
|
|
|
Review
|
Ataxia telangiectasia: A review from etiopathogenesis to current management with a description of reported cases in Peru
|
Araujo-Aliaga I.
|
2023
|
10.20453/RNP.V86I1.4463
|
Revista de Neuro-Psiquiatria
|
|
S/C***
|
|
Review
|
Friedreichs ataxia, review and literature update with a systematic search for cases in Latin America
|
Alfaro-Olivera M.
|
2023
|
10.20453/RNP.V86I1.4466
|
Revista de Neuro-Psiquiatria
|
|
S/C***
|
|
Artículo en revista científica
|
Juvenile Huntington and intrafamily phenocopy, about two cases
|
Silva-Bullón M.
|
2023
|
10.20453/RNP.V86I3.4560
|
Revista de Neuro-Psiquiatria
|
|
S/C***
|
|
Artículo en revista científica
|
Hot cross bun sign in a Peruvian patient with spinocerebellar ataxia type 2: A case report
|
Tantalean-Gutierrez L.
|
2023
|
10.20453/RNP.V86I3.4561
|
Revista de Neuro-Psiquiatria
|
|
S/C***
|
|
Editorial
|
Advances and challenges in genetics of neurodegenerative disorders in Peru
|
Cornejo-Olivas M.
|
2023
|
10.20453/RNP.V86I4.5186
|
Revista de Neuro-Psiquiatria
|
|
No Aplica
|
|
Artículo en revista científica
|
Disruption of Mitochondrial Complex I Induces Progressive Parkinsonism
|
Cornejo-Olivas M.
|
2022
|
10.1002/mds.28961
|
Movement Disorders
|
|
Q1
|
|
Letter
|
Autosomal Recessive Cerebellar Ataxias in South America: A Multicenter Study of 1338 Patients
|
Gama, Maria Thereza D.
|
2022
|
10.1002/mds.29046
|
MOVEMENT DISORDERS
|
|
No Aplica
|
|
Journal - Review
|
Genotype-Phenotype Correlations for ATX-TBP (SCA17): MDSGene Systematic Review
|
Rossi, Malco | Hamed, Moath | Rodriguez-Antiguedad, Jon | Cornejo-Olivas, Mario | Breza, Marianthi | Lohmann, Katja | Klein, Christine | Rajalingam, Rajasumi | Marras, Connie | van de Warrenburg, Bart P.
|
2022
|
10.1002/MDS.29278
|
MOVEMENT DISORDERS
|
|
2022: No disponible**, 2020: Q1
|
|
Journal - Article
|
Machado Joseph-Disease Is Rare in the Peruvian Population
|
Cornejo-Olivas, Mario | Solis-Ponce, Lesly | Araujo-Aliaga, Ismael | Milla-Neyra, Karina | Ortega, Olimpio | Illanes-Manrique, Maryenela | Mazzetti, Pilar | Manrique-Enciso, Carla | Cubas-Montecino, Diana | Saraiva-Pereira, Maria Luiza | Jardim, Laura B. | Sarapura-Castro, Elison
|
2022
|
10.1007/S12311-022-01491-4
|
CEREBELLUM
|
|
2022: No disponible**, 2020: Q2
|
|
Artículo en revista científica
|
Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinsons disease cohort
|
Loesch D.P.
|
2022
|
10.1016/j.parkreldis.2022.06.010
|
Parkinsonism and Related Disorders
|
|
Q1
|
|
JOURNAL_ARTICLE
|
The next step for neurology education in Peru: A Call for Subspecialty Training
|
|
2022
|
10.20453/rnp.v85i2.4225
|
|
M Cornejo-Olivas a través de ORCID
|
|
|
Article
|
Knowledge and Attitudes for the Management of Behavioral Variant of Frontotemporal Dementia
|
Castro-Suarez, Sheila
|
2022
|
10.3389/fneur.2021.786448
|
FRONTIERS IN NEUROLOGY
|
|
2022: No disponible**, 2020: Q2
|
|
Artículo en revista científica
|
Knowledge and Attitudes for the Management of Behavioral Variant of Frontotemporal Dementia
|
Castro-Suarez S.
|
2022
|
10.3389/FNEUR.2021.786448
|
Frontiers in Neurology
|
|
2022: No disponible**, 2020: Q2
|
|
JOURNAL_ARTICLE
|
Clinical Profile of Frontotemporal Dementia: Case Series from a Neurological Care Center in Peru (P1-6.006)
|
|
2022
|
|
|
M Cornejo-Olivas a través de ORCID
|
|
|
JOURNAL_ARTICLE
|
Cognitive and Neuropsychiatric features of an Alzheimer\textquoterights Disease Cohort in the Peruvian Population (P16-3.004)
|
|
2022
|
|
|
M Cornejo-Olivas a través de ORCID
|
|
|
Article
|
Dopa-responsive dystonia (DRD): systematic search in Latin America
|
Zelada-Ríos, Laura
|
2022
|
|
|
|
No Aplica
|
|
Article
|
MELAS in Latin America
|
Aguirre-Quispe, Wilfor
|
2022
|
|
|
|
No Aplica
|
|
Journal - Meeting Abstract
|
Whole genome sequencing aids in diagnosing GCH1 dopa responsive dystonia in two Peruvian patients and influences medical management
|
Urbina-Ramirez, L. | La Serna-Infantes, J. | Sarapura-Castro, E. | Rivera-Valdivia, A. | Thorpe, E. | Perry, D. | Milla-Neyra, K. | Galarreta, C. | Duenas-Roque, M. | Cornejo-Olivas, M.
|
2021
|
|
MOVEMENT DISORDERS
|
|
2021: No disponible**, 2020: Q1
|
|
Article
|
Characterizing the Genetic Architecture of Parkinson's Disease in Latinos
|
Loesch, Douglas P.
|
2021
|
10.1002/ana.26153
|
ANNALS OF NEUROLOGY
|
|
2021: No disponible**, 2020: Q1
|
|
Article
|
Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients
|
Sarihan, Elif Irem
|
2021
|
10.1002/mds.28353
|
MOVEMENT DISORDERS
|
|
2021: No disponible**, 2020: Q1
|
|
Article
|
MLPA followed by target-NGS to detect mutations in the dystrophin gene of Peruvian patients suspected of DMD/DMB
|
Guevara-Fujita, Maria Luisa
|
2021
|
10.1002/mgg3.1759
|
MOLECULAR GENETICS & GENOMIC MEDICINE
|
|
2021: No disponible**, 2020: Q3
|
|
Letter
|
Response to ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population
|
Veliz-Otani, Diego
|
2021
|
10.1007/s12311-021-01258-3
|
CEREBELLUM
|
|
No Aplica
|
|
Letter
|
Response to ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population
|
Véliz-Otani D.
|
2021
|
10.1007/S12311-021-01258-3
|
Cerebellum
|
|
No Aplica
|
|
Journal-article
|
Response to ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population.
|
|
2021
|
10.1007/S12311-021-01258-3
|
|
M Cornejo-Olivas a través de ORCID
|
|
|
Artículo en revista científica
|
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.
|
2021
|
10.1016/j.clineuro.2021.106490
|
Clinical Neurology and Neurosurgery
|
|
Q2
|
|
Article
|
Dissecting the role of Amerindian genetic ancestry and the ApoE epsilon 4 allele on Alzheimer disease in an admixed Peruvian population
|
Marca-Ysabel, Maria Victoria
|
2021
|
10.1016/j.neurobiolaging.2020.10.003
|
NEUROBIOLOGY OF AGING
|
|
2021: No disponible**, 2020: Q2
|
|
Article
|
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, Richard S.
|
2021
|
10.1159/000515696
|
MOLECULAR SYNDROMOLOGY
|
|
2021: No disponible**, 2020: Q4
|
|
Article
|
Prevalence of stroke survival in rural communities living in northern Peru
|
Moyano, Luz M.
|
2021
|
10.1371/journal.pone.0254440
|
PLOS ONE
|
|
2021: No disponible**, 2020: Q2
|
|
Editorial
|
Editorial: Monogenic vs. Oligogenic Reclassification
|
Messaoud O.
|
2021
|
10.3389/fgene.2021.821591
|
Frontiers in Genetics
|
|
No Aplica
|
|
Review
|
Mapping the Diverse and Inclusive Future of Parkinson's Disease Genetics and Its Widespread Impact
|
Elsayed, Inas
|
2021
|
10.3390/genes12111681
|
GENES
|
|
2021: No disponible**, 2020: Q2
|
|
Article
|
Advances in genetics and genomics in inherited neurological diseases in Peru.
|
Cornejo-Olivas, Mario
|
2021
|
|
|
|
No Aplica
|
|
Article
|
Genetic counseling to a DMD asymptomatic carrier: First case report in the Peruvian public healthcare system
|
Bazalar-Montoya, Jeny
|
2021
|
|
|
|
No Aplica
|
|
Meeting Abstract
|
Characterizing the genetic architecture of Parkinson's disease in Latinos
|
Loesch, D.
|
2020
|
|
MOVEMENT DISORDERS
|
|
No Aplica
|
|
Article
|
Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance
|
Cornejo-Olivas, Mario
|
2020
|
10.1007/s12311-019-01098-2
|
CEREBELLUM
|
|
Q2
|
|
Erratum
|
Correction to: Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance (The Cerebellum, (2020), 19, 2, (208-215), 10.1007/s12311-019-01098-2)
|
Cornejo-Olivas M.
|
2020
|
10.1007/s12311-020-01105-x
|
Cerebellum
|
|
No Aplica
|
|
Correction
|
Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance (vol 45, pg 231, 2020)
|
Cornejo-Olivas, Mario
|
2020
|
10.1007/s12311-020-01105-x
|
CEREBELLUM
|
|
No Aplica
|
|
Artículo en revista científica
|
Distribution of the CAG Triplet Repeat in ATXN1, ATXN3, and CACNA1A Loci in Peruvian Population
|
Gonzales-Sáenz C.
|
2020
|
10.1007/s12311-020-01129-3
|
Cerebellum
|
|
Q1
|
|
Article
|
Distribution of the CAG Triplet Repeat in ATXN1, ATXN3, and CACNA1A Loci in Peruvian Population
|
Gonzales-Saenz, Claudia
|
2020
|
10.1007/s12311-020-01129-3
|
CEREBELLUM
|
|
Q2
|
|
Journal-article
|
Dissecting the role of Amerindian genetic ancestry and the ApoE ε4 allele on Alzheimer disease in an admixed Peruvian population.
|
|
2020
|
10.1016/J.NEUROBIOLAGING.2020.10.003
|
|
M Cornejo-Olivas a través de ORCID
|
|
|
Editorial Material
|
Panda with "bright eyes": a rare sign in Wilson disease
|
Sarapura-Castro, Elison
|
2020
|
10.1590/0004-282X20200036
|
ARQUIVOS DE NEURO-PSIQUIATRIA
|
|
No Aplica
|
|
Note
|
Panda with “bright eyes”: A rare sign in Wilson disease
|
Sarapura-Castro E.
|
2020
|
10.1590/0004-282X20200036
|
Arquivos de Neuro-Psiquiatria
|
|
No Aplica
|
|
Note
|
Panda with “bright eyes”: A rare sign in Wilson disease
|
Sarapura-Castro E.
|
2020
|
10.2590/0004-282x20200036
|
Arquivos de Neuro-Psiquiatria
|
|
No Aplica
|
|
Review
|
C9orf72 Hexanucleotide Repeat in Huntington-Like Patients: Systematic Review and Meta-Analysis
|
Alva-Diaz, Carlos
|
2020
|
10.3389/fgene.2020.551780
|
Frontiers in Genetics
|
|
Q2
|
|
Review
|
C9orf72 Hexanucleotide Repeat in Huntington-Like Patients: Systematic Review and Meta-Analysis
|
Alva-Diaz C.
|
2020
|
10.3389/fgene.2020.551780
|
Frontiers in Genetics
|
|
Q2
|
|
Article
|
Neurologic healthcare during COVID emergency
|
Cornejo-Olivas, Mario
|
2020
|
|
|
|
No Aplica
|
|
Journal - Meeting Abstract
|
Prevalence of Parkinson's disease in a district of central highlands of Peru: Preliminary report
|
Sarapura-Castro, E. | Milla-Neyra, K. | Montano, S. | Mata, I. | Inca-Martinez, M. | Rios-Pinto, J. | Cosentino, C. | Mazzetti, P. | Cornejo-Olivas, M.
|
2019
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Editorial Material
|
Using global team science to identify genetic parkinson's disease worldwide
|
Vollstedt, Eva-Juliane
|
2019
|
10.1002/ana.25514
|
ANNALS OF NEUROLOGY
|
|
No Aplica
|
|
Editorial
|
Using global team science to identify genetic parkinsons disease worldwide
|
Vollstedt E.J.
|
2019
|
10.1002/ANA.25514
|
Annals of Neurology
|
|
No Aplica
|
|
Article
|
Guillain-Barre syndrome outbreak in Peru: Association with polymorphisms in IL-17, ICAM1, and CD1
|
Jaramillo-Valverde, Luis
|
2019
|
10.1002/mgg3.960
|
Molecular Genetics & Genomic Medicine
|
|
Q3
|
|
Artículo en revista científica
|
Guillain–Barre syndrome outbreak in Peru: Association with polymorphisms in IL-17, ICAM1, and CD1
|
Jaramillo-Valverde L.
|
2019
|
10.1002/mgg3.960
|
Molecular genetics & genomic medicine
|
|
Q2
|
|
Artículo en revista científica
|
ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population
|
Véliz-Otani D.
|
2019
|
10.1007/s12311-019-01057-x
|
Cerebellum
|
|
Q1
|
|
Article
|
ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population
|
Veliz-Otani, Diego
|
2019
|
10.1007/s12311-019-01057-x
|
CEREBELLUM
|
|
Q2
|
|
Artículo en revista científica
|
A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington Disease
|
Kay C.
|
2019
|
10.1016/j.ajhg.2019.10.011
|
American Journal of Human Genetics
|
|
Q1
|
|
Article
|
A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington Disease
|
Kay, Chris
|
2019
|
10.1016/j.ajhg.2019.10.011
|
AMERICAN JOURNAL OF HUMAN GENETICS
|
|
Q1
|
|
Artículo en revista científica
|
The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru
|
Velez-Pardo C.
|
2019
|
10.1016/j.parkreldis.2019.01.030
|
Parkinsonism and Related Disorders
|
|
Q1
|
|
Article
|
The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru
|
Velez-Pardo, Carlos
|
2019
|
10.1016/j.parkreldis.2019.01.030
|
PARKINSONISM & RELATED DISORDERS
|
|
Q1
|
|
Artículo en revista científica
|
Palliative Care: Perceptions, Experiences, and Attitudes in a Peruvian Neurologic Hospital
|
Vishnevetsky A.
|
2019
|
10.1089/jpm.2018.0196
|
Journal of Palliative Medicine
|
|
Q1
|
|
Article
|
Palliative Care: Perceptions, Experiences, and Attitudes in a Peruvian Neurologic Hospital
|
Vishnevetsky, Anastasia
|
2019
|
10.1089/jpm.2018.0196
|
JOURNAL OF PALLIATIVE MEDICINE
|
|
Q2
|
|
Article
|
Economic burden of Huntington's disease in Peru
|
Silva-Paredes, Gustavo
|
2019
|
10.1186/s12913-019-4806-6
|
BMC HEALTH SERVICES RESEARCH
|
|
Q3
|
|
Artículo en revista científica
|
Economic burden of Huntingtons disease in Peru
|
Silva-Paredes G.
|
2019
|
10.1186/s12913-019-4806-6
|
BMC Health Services Research
|
|
Q1
|
|
Article
|
Identification of Main Genetic Causes Responsible for Non-Syndromic Hearing Loss in a Peruvian Population
|
Figueroa-Ildefonso, Erick
|
2019
|
10.3390/genes10080581
|
Genes
|
|
Q2
|
|
Artículo en revista científica
|
Identification of main genetic causes responsible for non-syndromic hearing loss in a Peruvian population
|
Figueroa-Ildefonso E.
|
2019
|
10.3390/GENES10080581
|
|
|
2019: No disponible**, 2020: Q2
|
|
Article
|
Guías de práctica clínica basadas en evidencia: Desarrollo y aplicación en neurología clínica en el Perú
|
Cornejo-Olivas, Mario
|
2019
|
|
|
|
No Aplica
|
|
Journal - Meeting Abstract
|
Huntington's Disease-like Disorders in Latin America and the Caribbean
|
Walker, Ruth | Gatto, Emilia | Bernal-Pacheco, Oscar | Cardoso, Francisco | Castilhos, Raphael | Chana-Cuevas, Pedro | Cornejo-Olivas, Mario | Bellmann, Ingrid Estrada | Jardim, Laura | Lopez-Castellanos, Jose Ricardo | Lopez-Contreras, Jose | Maia, Debora | Soler, Pilar Mazzetti | Miranda, Marcelo | Violante, Mayela Rodriguez | Teive, Helio | Tumas, Vitor
|
2018
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Journal - Meeting Abstract
|
Proximal Motor Sensory Hereditary Neuropathy (HMSN-P) in a Peruvian Family with Japanese Ancestry
|
Sarapura-Castro, Elison | Quispe, Darko | Illanes-Manrique, Maryenela | Milla-Neyra, Karina | Inca-Martinez, Miguel | Figueroa-Ildefonso, Erick | Marca, Victoria | Takashima, Hiroshi | Mazzetti, Pilar | Cornejo-Olivas, Mario
|
2018
|
|
NEUROLOGY
|
|
Q1
|
|
Journal - Meeting Abstract
|
Screening of Parkinson's disease genes in Latino families from LARGE-PD
|
Lorenzo-Betancor, Oswaldo | Cornejo-Olivas, Mario | Sarapura, Elison | Torres, Luis | Inca-Martinez, Miguel | Mazzetti, Pilar | Cosentino, Carlos | Micheli, Federico | Tumas, Vitor | Zabetian, Cyrus | Mata, Ignacio
|
2018
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Journal - Meeting Abstract
|
Spinocerebellar Ataxia Type 2 with Infantile onset in Peru: A Case Report
|
Cornejo-Olivas, Mario | Figueroa-Ildefonso, Erick | Sarapura-Castro, Elison | Milla-Neyra, Karina | Solis-Ponce, Lesly | Marca, Victoria | Illanes-Manrique, Maryenela | Inca-Martinez, Miguel | Mazzetti, Pilar
|
2018
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Artículo en revista científica
|
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population
|
Kay C.
|
2018
|
10.1002/ajmg.b.32618
|
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
|
|
Q1
|
|
Article
|
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general population
|
Kay, Chris
|
2018
|
10.1002/ajmg.b.32618
|
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
|
|
Q2
|
|
Article
|
Genetics and genomics in Peru: Clinical and research perspective
|
Guio, Heinner
|
2018
|
10.1002/mgg3.533
|
Molecular Genetics & Genomic Medicine
|
|
Q3
|
|
Artículo en revista científica
|
Genetics and genomics in Peru: Clinical and research perspective
|
Guio H.
|
2018
|
10.1002/mgg3.533
|
Molecular genetics & genomic medicine
|
|
Q3
|
|
Review
|
Huntington's disease-like disorders in Latin America and the Caribbean
|
Walker, Ruth H.
|
2018
|
10.1016/j.parkreldis.2018.05.021
|
PARKINSONISM & RELATED DISORDERS
|
|
Q1
|
|
Review
|
Huntingtons disease-like disorders in Latin America and the Caribbean
|
Walker R.H.
|
2018
|
10.1016/j.parkreldis.2018.05.021
|
Parkinsonism and Related Disorders
|
|
Q1
|
|
Erratum
|
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 (npj Parkinsons Disease, (2017), 3, 1, (19), 10.1038/s41531-017-0020-6)
|
Cornejo-Olivas M.
|
2018
|
10.1038/s41531-017-0025-1
|
npj Parkinson's Disease
|
|
No Aplica
|
|
Correction
|
Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry (vol 3, 19, 2017)
|
Cornejo-Olivas, Mario
|
2018
|
10.1038/s41531-017-0025-1
|
|
|
|
|
Article
|
Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease
|
Hou, Xu
|
2018
|
10.1080/15548627.2018.1461294
|
Autophagy
|
|
Q1
|
|
Artículo en revista científica
|
Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease
|
Hou X.
|
2018
|
10.1080/15548627.2018.1461294
|
Autophagy
|
|
Q1
|
|
Review
|
Neurology outreach clinic for Huntington disease in Peru
|
Vishnevetsky A.
|
2018
|
10.1212/WNL.0000000000005940
|
Neurology
|
|
Q1
|
|
Editorial Material
|
Neurology outreach clinic for Huntington disease in Peru Lessons for neurodegenerative diseases
|
Vishnevetsky, Anastasia
|
2018
|
10.1212/WNL.0000000000005940
|
NEUROLOGY
|
|
No Aplica
|
|
Article
|
Ausencia de la mutación A53T del gen SNCA en una muestra de pacientes con Enfermedad de Parkinson en el Perú
|
Milla-Neyra, Karina
|
2018
|
|
|
|
No Aplica
|
|
Journal - Meeting Abstract
|
Clinical features of Wilson's disease in Peru: Review of eight cases
|
Sarapura, Elison | Ramirez-Quinones, Jorge | Cornejo-Olivas, Mario | Torres, Luis
|
2017
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Journal - Meeting Abstract
|
Familial Creutzfeldt-Jakob disease with an E200K mutation in Peru: a case report
|
Sarapura-Castro, H. | Cosentino, C. | Torres-Ramirez, L. | Parchi, P. | Vishnevetsky, A. | Inca-Martinez, M. | Figueroa-Ildefonso, E. | Mazzetti, P. | Cornejo-Olivas, M.
|
2017
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Journal - Meeting Abstract
|
LRRK2 analysis in the largest Latin American PD cohort: The LARGE-PD consortium
|
Cornejo-Olivas, Mario | Torres, Luis | Velit-Salazar, Mario | Inca-Martinez, Miguel | Soler, Pilar Mazzetti | Cosentino, Carlos | Micheli, Federico | Perandones, Claudia | Dieguez, Elena | Raggio, Victor | Tumas, Vitor | Borges, Van-derci | Ferraz, Henrique | Rieder, Carlos Roberto | Schuh, Artur Schu-macher | Velez-Pardo, Carlos | Jimenez-Del-Rio, Marlene | Lopera, Francisco | Castello, Jorge Chang | Andree-Munoz, Brennie | Mata, Igna-cio Fernandez | Waldherr, Sarah | Yearout, Dora | Zabetian, Cyrus
|
2017
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Journal - Meeting Abstract
|
Myths and misconceptions regarding Huntington's disease in Peru
|
Vishnevetsky, A. | Illanes-Manrique, M. | Inca-Martinez, M. | Cornejo-Olivas, M.
|
2017
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Article
|
Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation
|
Bampi, Giovana B.
|
2017
|
10.1007/s12017-017-8464-8
|
NEUROMOLECULAR MEDICINE
|
|
Q3
|
|
Artículo en revista científica
|
Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation
|
Bampi G.B.
|
2017
|
10.1007/s12017-017-8464-8
|
NeuroMolecular Medicine
|
|
Q2
|
|
Artículo en revista científica
|
The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America
|
Kay C.
|
2017
|
10.1038/ejhg.2016.169
|
European Journal of Human Genetics
|
|
Q1
|
|
Article
|
The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin America
|
Kay, Chris
|
2017
|
10.1038/ejhg.2016.169
|
EUROPEAN JOURNAL OF HUMAN GENETICS
|
|
Q2
|
|
Article
|
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, Mario
|
2017
|
10.1038/s41531-017-0020-6
|
|
|
2017: No disponible**, 2020: Q1
|
|
JOURNAL_ARTICLE
|
Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinsons disease (LARGE-PD), a case of ancestry.
|
|
2017
|
10.1038/s41531-017-0020-6
|
|
Europe PubMed Central a través de ORCID
|
|
|
Artículo en revista científica
|
Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinsons disease (LARGE-PD), a case of ancestry /692/617/375/1718 /631/208/1516 article
|
Cornejo-Olivas M.
|
2017
|
10.1038/s41531-017-0020-6
|
npj Parkinson's Disease
|
|
2017: No disponible**, 2020: Q1
|
|
Artículo en revista científica
|
Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil
|
Gheno T.C.
|
2017
|
10.1111/ene.13281
|
European Journal of Neurology
|
|
Q1
|
|
Article
|
Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil
|
Gheno, T. C.
|
2017
|
10.1111/ene.13281
|
EUROPEAN JOURNAL OF NEUROLOGY
|
|
Q1
|
|
Journal - Meeting Abstract
|
A health cost analysis for Huntington disease in Peru
|
Silva-Paredes, G. | Cornejo-Olivas, M. | Inca-Martinez, M. | Espinoza-Huertas, K. | Vishnevetsky, A. | Mazzetti, P. | Urbanos-Garrido, R.
|
2016
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Journal - Meeting Abstract
|
Clinical and molecular features of DYT1 primary dystonia in a Peruvian population
|
Inca-Martinez, M. | Milla-Neyra, K. | Cosentino, C. C. | Mori, N. | Marca, V. | Flores, M. | Guevara-Silva, E. | Nunez-Coronado, Y. | Vasquez, C. M. | Torres-Ramirez, L. | Mazzetti, P. | Cornejo-Olivas, M.
|
2016
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Journal - Meeting Abstract
|
Preliminary results for a study on quality of life in Huntington's disease patients and their caregivers in Peru
|
Vishnevetsky, A. | Inca-Martinez, M. A. | Illanes-Manrique, M. | Cornejo-Olivas, M.
|
2016
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Artículo en revista científica
|
The first report of CADASIL in Peru: Olfactory dysfunction on initial presentation
|
Vishnevetsky A.
|
2016
|
10.1016/j.ensci.2016.09.001
|
eNeurologicalSci
|
|
Q4
|
|
Journal - Meeting Abstract
|
Clinical and genetic features of an early-onset Parkinson's disease Peruvian cohort
|
Sarapura, E. H. | Cosentino, C. | Inca-Martinez, M. A. | Cornejo-Olivas, M. R. | Torres, L. | Marca, V. | Ortega, O. | Velit-Otani, D. M. | Espinoza-Huertas, K. A. | Yearout, D. | Huston, H. | Zabetian, C. | Mata, I. F. | Mazzetti, P.
|
2015
|
|
MOVEMENT DISORDERS
|
|
Q1
|
|
Meeting Abstract
|
Spinocerebellar ataxia type 10 in Peruvian population: Clinical features of 17 families
|
Cornejo-Herrera, I. F.
|
2015
|
|
MOVEMENT DISORDERS
|
|
No Aplica
|
|
Letter
|
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 F.S.
|
2015
|
10.1007/s12311-015-0666-8
|
Cerebellum
|
|
No Aplica
|
|
Letter
|
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, Fernanda S.
|
2015
|
10.1007/s12311-015-0666-8
|
CEREBELLUM
|
|
No Aplica
|
|
Artículo en revista científica
|
Neurogenetics in Peru: clinical, scientific and ethical perspectives
|
Cornejo-Olivas M.
|
2015
|
10.1007/s12687-015-0239-z
|
Journal of Community Genetics
|
|
Q2
|
|
Article
|
Neurogenetics in Peru: clinical, scientific and ethical perspectives
|
Cornejo-Olivas, Mario
|
2015
|
10.1007/s12687-015-0239-z
|
|
|
S/C***
|
|
Artículo en revista científica
|
A Peruvian family with a novel PARK2 mutation: Clinical and pathological characteristics
|
Cornejo-Olivas M.R.
|
2015
|
10.1016/j.parkreldis.2015.01.005
|
Parkinsonism and Related Disorders
|
|
Q1
|
|
Article
|
A Peruvian family with a novel PARK2 mutation: Clinical and pathological characteristics
|
Cornejo-Olivas, Mario R.
|
2015
|
10.1016/j.parkreldis.2015.01.005
|
PARKINSONISM & RELATED DISORDERS
|
|
Q1
|
|
Artículo en revista científica
|
Neurogenetics in peru, example of translational research
|
Mazzetti P.
|
2015
|
10.17843/rpmesp.2015.324.1773
|
Revista Peruana de Medicina de Experimental y Salud Publica
|
|
Q3
|
|
Article
|
Clinical and Molecular Features of Late Onset Huntington Disease in a Peruvian Cohort
|
Cornejo-Olivas, Mario R.
|
2015
|
10.3233/JHD-140119
|
|
|
S/C***
|
|
Artículo en revista científica
|
Clinical and Molecular Features of Late Onset Huntington Disease in a Peruvian Cohort
|
Cornejo-Olivas M.
|
2015
|
10.3233/JHD-140119
|
Journal of Huntington's disease
|
|
Q2
|
|
Article
|
Homocistinuria, una enfermedad metabólica de diagnóstico tardío en el Perú.
|
Cornejo-Olivas, Mario R.
|
2015
|
|
|
|
No Aplica
|
|
Meeting Abstract
|
Allelic distribution of the normal ATXN3 gene in a Peruvian mestizo population
|
Cornejo-Olivas, M. R.
|
2014
|
|
MOVEMENT DISORDERS
|
|
No Aplica
|
|
Meeting Abstract
|
Analysis of the GBA gene in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD)
|
Waldherr, S. M.
|
2014
|
|
MOVEMENT DISORDERS
|
|
No Aplica
|
|
Article
|
Clinical and molecular studies reveal a PSEN1 mutation (L153V) in a Peruvian family with early-onset Alzheimer's disease
|
Cornejo-Olivas, Mario R.
|
2014
|
10.1016/j.neulet.2014.01.016
|
NEUROSCIENCE LETTERS
|
|
Q3
|
|
Artículo en revista científica
|
Clinical and molecular studies reveal a PSEN1 mutation (L153V) in a Peruvian family with early-onset Alzheimers disease
|
Cornejo-Olivas M.R.
|
2014
|
10.1016/j.neulet.2014.01.016
|
Neuroscience Letters
|
|
Q2
|
|
Meeting Abstract
|
Clinical Characteristics and Progression Rate of Brazilian and Peruvian Patients with SCA10
|
Jardim, Laura
|
2013
|
|
NEUROLOGY
|
|
No Aplica
|
|
Meeting Abstract
|
Variable penetrance of the LRRK2-R1441G mutation in a Peruvian family
|
Cornejo-Olivas, M. R.
|
2013
|
|
MOVEMENT DISORDERS
|
|
No Aplica
|
|
Article
|
Association between apolipoprotein E (ApoE) genetic polymorphism and Parkinson’s disease
|
Marca, Victoria
|
2013
|
|
|
|
No Aplica
|
|
Article
|
Estrategia de genotipado del gen FMR1: Método de diagnóstico alternativo para el Síndrome X Frágil y otras enfermedades por expansión de trinucleotidos
|
Lindo-Samanamud, Saúl
|
2013
|
|
|
|
No Aplica
|
|
Artículo en revista científica
|
Kennedy disease in Peru: First cases with molecular diagnosis
|
Gómez-Calero V.
|
2013
|
|
Revista Peruana de Medicina de Experimental y Salud Publica
|
|
Q3
|
|
Meeting Abstract
|
Huntington's disease in an indigneous village in the Peruvian Amazon jungle
|
Cornejo-Olivas, M. R.
|
2012
|
|
MOVEMENT DISORDERS
|
|
No Aplica
|
|
Artículo en revista científica
|
Role of government in clinical trial
|
Mazzetti P.
|
2012
|
10.1590/S1726-46342012000400014
|
Revista Peruana de Medicina de Experimental y Salud Publica
|
|
Q3
|
|
Journal-article
|
Ataxia espinocerebelosa tipo 3 (Enfermedad de Machado Joseph) A propósito de un caso
|
|
2012
|
|
|
M Cornejo-Olivas a través de ORCID
|
|
|
Journal-article
|
Histopatoloǵıa de la enfermedad de Lhermitte-Duclos: a propósito de un caso
|
|
2012
|
|
|
M Cornejo-Olivas a través de ORCID
|
|
|
Article
|
Lrrk2 p.Q1111H substitution and Parkinson's disease in Latin America
|
Mata, Ignacio F.
|
2011
|
10.1016/j.parkreldis.2011.05.003
|
PARKINSONISM & RELATED DISORDERS
|
|
Q1
|
|
Artículo en revista científica
|
Lrrk2 p.Q1111H substitution and Parkinsons disease in Latin America
|
Mata I.F.
|
2011
|
10.1016/j.parkreldis.2011.05.003
|
Parkinsonism and Related Disorders
|
|
Q1
|
|
Journal-article
|
Epilepsia por glioma de bajo grado de larga evolución: reporte de un caso
|
|
2011
|
|
|
M Cornejo-Olivas a través de ORCID
|
|
|
Artículo en revista científica
|
Genetic polymorphism of Apolipoprotein e in a Peruvian population
|
Marca V.
|
2011
|
|
Revista Peruana de Medicina de Experimental y Salud Publica
|
|
Q3
|