| Year |
Citation |
Score |
| 2020 |
Sepulveda-Falla D, Chavez-Gutierrez L, Portelius E, Vélez JI, Dujardin S, Barrera-Ocampo A, Dinkel F, Hagel C, Puig B, Mastronardi C, Lopera F, Hyman BT, Blennow K, Arcos-Burgos M, de Strooper B, et al. A multifactorial model of pathology for age of onset heterogeneity in familial Alzheimer's disease. Acta Neuropathologica. PMID 33319314 DOI: 10.1007/s00401-020-02249-0 |
1 |
|
| 2020 |
Vannini P, Hanseeuw BJ, Gatchel JR, Sikkes SAM, Alzate D, Zuluaga Y, Moreno S, Mendez L, Baena A, Ospina-Lopera P, Tirado V, Henao E, Acosta-Baena N, Giraldo M, Lopera F, et al. Trajectory of Unawareness of Memory Decline in Individuals With Autosomal Dominant Alzheimer Disease. Jama Network Open. 3: e2027472. PMID 33263761 DOI: 10.1001/jamanetworkopen.2020.27472 |
0.36 |
|
| 2020 |
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, ... ... Lopera F, et al. Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33150996 DOI: 10.1002/mds.28353 |
0.36 |
|
| 2020 |
Ospina C, Arboleda-Velasquez JF, Aguirre-Acevedo DC, Zuluaga-Castaño Y, Velilla L, Garcia GP, Quiroz YT, Lopera F. Genetic and nongenetic factors associated with CADASIL: A retrospective cohort study. Journal of the Neurological Sciences. 419: 117178. PMID 33091750 DOI: 10.1016/j.jns.2020.117178 |
0.36 |
|
| 2020 |
Vila-Castelar C, Guzmán-Vélez E, Pardilla-Delgado E, Buckley R, Bocanegra Y, Baena A, Fox-Fuller JT, Tirado V, Munoz C, Giraldo M, Acosta-Baena N, Rios-Romenets S, Langbaum JB, Tariot PN, Lopera F, et al. Examining Sex Differences in Markers of Cognition and Neurodegeneration in Autosomal Dominant Alzheimer's Disease: Preliminary Findings from the Colombian Alzheimer's Prevention Initiative Biomarker Study. Journal of Alzheimer's Disease : Jad. PMID 32925067 DOI: 10.3233/JAD-200723 |
0.36 |
|
| 2020 |
Dinkel F, Trujillo-Rodriguez D, Villegas A, Streffer J, Mercken M, Lopera F, Glatzel M, Sepulveda-Falla D. Decreased Deposition of Beta-Amyloid 1-38 and Increased Deposition of Beta-Amyloid 1-42 in Brain Tissue of Presenilin-1 E280A Familial Alzheimer's Disease Patients. Frontiers in Aging Neuroscience. 12: 220. PMID 32848702 DOI: 10.3389/fnagi.2020.00220 |
0.96 |
|
| 2020 |
Palmqvist S, Janelidze S, Quiroz YT, Zetterberg H, Lopera F, Stomrud E, Su Y, Chen Y, Serrano GE, Leuzy A, Mattsson-Carlgren N, Strandberg O, Smith R, Villegas A, Sepulveda-Falla D, et al. Discriminative Accuracy of Plasma Phospho-tau217 for Alzheimer Disease vs Other Neurodegenerative Disorders. Jama. PMID 32722745 DOI: 10.1001/jama.2020.12134 |
0.96 |
|
| 2020 |
Henriquez-Henriquez M, Acosta MT, Martinez AF, Vélez JI, Lopera F, Pineda D, Palacio JD, Quiroga T, Worgall TS, Deckelbaum RJ, Mastronardi C, Molina BSG, Arcos-Burgos M, Muenke M. Mutations in sphingolipid metabolism genes are associated with ADHD. Translational Psychiatry. 10: 231. PMID 32661301 DOI: 10.1038/s41398-020-00881-8 |
0.6 |
|
| 2020 |
Quiroz YT, Zetterberg H, Reiman EM, Chen Y, Su Y, Fox-Fuller JT, Garcia G, Villegas A, Sepulveda-Falla D, Villada M, Arboleda-Velasquez JF, Guzmán-Vélez E, Vila-Castelar C, Gordon BA, Schultz SA, ... ... Lopera F, et al. Plasma neurofilament light chain in the presenilin 1 E280A autosomal dominant Alzheimer's disease kindred: a cross-sectional and longitudinal cohort study. The Lancet. Neurology. 19: 513-521. PMID 32470423 DOI: 10.1016/S1474-4422(20)30137-X |
0.96 |
|
| 2020 |
Rios-Romenets S, Lopera F, Sink KM, Hu N, Lian Q, Guthrie H, Smith J, Cho W, Mackey H, Langbaum JB, Thomas RG, Giraldo-Chica M, Tobon C, Acosta-Baena N, Muñoz C, et al. Baseline demographic, clinical, and cognitive characteristics of the Alzheimer's Prevention Initiative (API) Autosomal-Dominant Alzheimer's Disease Colombia Trial. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 32418361 DOI: 10.1002/alz.12109 |
0.36 |
|
| 2019 |
Villalba AC, García J, Ramos C, Cuastumal AR, Aguillón D, Aguirre-Acevedo DC, Madrigal L, Lopera F. Mental Disorders in Young Adults from Families with the Presenilin-1 Gene Mutation E280A in the Preclinical Stage of Alzheimer's Disease. Journal of Alzheimer's Disease Reports. 3: 241-250. PMID 31754656 DOI: 10.3233/ADR-190139 |
0.36 |
|
| 2019 |
Vélez JI, Lopera F, Silva CT, Villegas A, Espinosa LG, Vidal OM, Mastronardi CA, Arcos-Burgos M. Familial Alzheimer's Disease and Recessive Modifiers. Molecular Neurobiology. PMID 31664702 DOI: 10.1007/s12035-019-01798-0 |
0.64 |
|
| 2019 |
Villalba AC, García J, Ramos C, Cuastumal AR, Aguillón D, Aguirre-Acevedo DC, Madrigal L, Lopera F. Mental Disorders in Young Adults from Families with the Presenilin-1 Gene Mutation E280A in the Preclinical Stage of Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. PMID 31381509 DOI: 10.3233/JAD-181013 |
0.36 |
|
| 2019 |
Torres VL, Vila-Castelar C, Bocanegra Y, Baena A, Guzmán-Vélez E, Aguirre-Acevedo DC, Tirado V, Munoz C, Henao E, Moreno S, Giraldo M, Acosta N, Rios Romenets S, Langbaum JB, Cho W, ... ... Lopera F, et al. Normative data stratified by age and education for a Spanish neuropsychological test battery: Results from the Colombian Alzheimer's prevention initiative registry. Applied Neuropsychology. Adult. 1-15. PMID 31230490 DOI: 10.1080/23279095.2019.1627357 |
0.36 |
|
| 2019 |
Arcos-Burgos M, Lopera F, Sepulveda-Falla D, Mastronardi C. Neural Plasticity during Aging. Neural Plasticity. 2019: 6042132. PMID 31049053 DOI: 10.1155/2019/6042132 |
0.96 |
|
| 2019 |
Vallejo-Diez S, Fleischer A, Martín-Fernández JM, Sánchez-Gilabert A, Castresana M, Aguillón D, Villegas A, Mastronardi CA, Espinosa LG, Arcos-Burgos M, Del Pozo Á, Herrán E, Gainza E, Isaza-Ruget M, Lopera F, et al. Generation of one iPSC line (IMEDEAi006-A) from an early-onset familial Alzheimer's Disease (fAD) patient carrying the E280A mutation in the PSEN1 gene. Stem Cell Research. 37: 101440. PMID 31026686 DOI: 10.1016/j.scr.2019.101440 |
0.64 |
|
| 2019 |
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. The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru. Parkinsonism & Related Disorders. PMID 30765263 DOI: 10.1016/j.parkreldis.2019.01.030 |
0.36 |
|
| 2019 |
Ramirez Aguilar L, Acosta-Uribe J, Giraldo MM, Moreno S, Baena A, Alzate D, Cuastumal R, Aguillón D, Madrigal L, Saldarriaga A, Navarro A, Garcia GP, Aguirre-Acevedo DC, Geier EG, Cochran JN, ... ... Lopera F, et al. Genetic origin of a large family with a novel PSEN1 mutation (Ile416Thr). Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 30745123 DOI: 10.1016/j.jalz.2018.12.010 |
0.36 |
|
| 2019 |
Arcos-Burgos M, Vélez JI, Martinez AF, Ribasés M, Ramos-Quiroga JA, Sánchez-Mora C, Richarte V, Roncero C, Cormand B, Fernández-Castillo N, Casas M, Lopera F, Pineda DA, Palacio JD, Acosta-López JE, et al. ADGRL3 (LPHN3) variants predict substance use disorder. Translational Psychiatry. 9: 42. PMID 30696812 DOI: 10.1038/s41398-019-0396-7 |
0.6 |
|
| 2019 |
Sepulveda-Falla D, Villegas A, Lopera F, Glatzel M. The Colombian-German network for neurodegenerative research: UndoAD. The Lancet. Neurology. 18: 29. PMID 30563680 DOI: 10.1016/S1474-4422(18)30458-7 |
0.96 |
|
| 2018 |
Vélez JI, Lopera F, Creagh PK, Piñeros LB, Das D, Cervantes-Henríquez ML, Acosta-López JE, Isaza-Ruget MA, Espinosa LG, Easteal S, Quintero GA, Silva CT, Mastronardi CA, Arcos-Burgos M. Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease. Molecular Neurobiology. PMID 30112632 DOI: 10.1007/s12035-018-1298-z |
0.6 |
|
| 2018 |
Guzmán-Vélez E, Jaimes S, Aguirre-Acevedo DC, Norton DJ, Papp KV, Amariglio R, Rentz D, Baena A, Henao E, Tirado V, Muñoz C, Giraldo M, Sperling RA, Lopera F, Quiroz YT. A Three-Factor Structure of Cognitive Functioning Among Carriers and Non-Carriers of Autosomal-Dominant Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. PMID 30040714 DOI: 10.3233/JAD-180078 |
0.36 |
|
| 2017 |
Villamil-Ortiz JG, Barrera-Ocampo A, Arias-Londoño JD, Villegas A, Lopera F, Cardona-Gómez GP. Differential Pattern of Phospholipid Profile in the Temporal Cortex from E280A-Familiar and Sporadic Alzheimer's Disease Brains. Journal of Alzheimer's Disease : Jad. PMID 29125487 DOI: 10.3233/JAD-170554 |
1 |
|
| 2017 |
Norton DJ, Amariglio R, Protas H, Chen K, Aguirre-Acevedo DC, Pulsifer B, Castrillon G, Tirado V, Munoz C, Tariot P, Langbaum JB, Reiman EM, Lopera F, Sperling RA, Quiroz YT. Subjective memory complaints in preclinical autosomal dominant Alzheimer disease. Neurology. PMID 28878053 DOI: 10.1212/WNL.0000000000004533 |
0.36 |
|
| 2016 |
Barrera-Ocampo A, Lopera F. Amyloid-beta immunotherapy: the hope for Alzheimer disease? Colombia Medica (Cali, Colombia). 47: 203-212. PMID 28293044 |
1 |
|
| 2016 |
Cardona-Gómez GP, Lopera F. Dementia, Preclinical Studies in Neurodegeneration and its Potential for Translational Medicine in South America. Frontiers in Aging Neuroscience. 8: 304. PMID 28066230 DOI: 10.3389/fnagi.2016.00304 |
0.6 |
|
| 2016 |
Abrevaya S, Sedeño L, Fitipaldi S, Pineda D, Lopera F, Buritica O, Villegas A, Bustamante C, Gomez D, Trujillo N, Pautassi R, Ibáñez A, García AM. The Road Less Traveled: Alternative Pathways for Action-Verb Processing in Parkinson's Disease. Journal of Alzheimer's Disease : Jad. PMID 27834777 DOI: 10.3233/JAD-160737 |
0.64 |
|
| 2016 |
Vélez JI, Lopera F, Patel HR, Johar AS, Cai Y, Rivera D, Tobón C, Villegas A, Sepulveda-Falla D, Lehmann SG, Easteal S, Mastronardi CA, Arcos-Burgos M. Mutations modifying sporadic Alzheimer's disease age of onset. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 27573710 DOI: 10.1002/ajmg.b.32493 |
0.96 |
|
| 2016 |
Pietto M, Parra MA, Trujillo N, Flores F, García AM, Bustin J, Richly P, Manes F, Lopera F, Ibáñez A, Baez S. Behavioral and Electrophysiological Correlates of Memory Binding Deficits in Patients at Different Risk Levels for Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. PMID 27372640 DOI: 10.3233/JAD-160056 |
0.96 |
|
| 2016 |
Uribe-Arias A, Posada-Duque RA, González-Billault C, Villegas A, Lopera F, Cardona-Gómez GP. p120-catenin is necessary for neuroprotection induced by CDK5 silencing in models of Alzheimer's disease. Journal of Neurochemistry. PMID 27273428 DOI: 10.1111/jnc.13697 |
0.64 |
|
| 2016 |
Primo V, Graham M, Bigger-Allen AA, Chick JM, Ospina C, Quiroz YT, Manent J, Gygi SP, Lopera F, D'Amore PA, Arboleda-Velasquez JF. Blood Biomarkers in a Mouse Model of CADASIL. Brain Research. PMID 27174004 DOI: 10.1016/j.brainres.2016.05.008 |
0.96 |
|
| 2016 |
Vélez JI, Rivera D, Mastronardi CA, Patel HR, Tobón C, Villegas A, Cai Y, Easteal S, Lopera F, Arcos-Burgos M. A Mutation in DAOA Modifies the Age of Onset in PSEN1 E280A Alzheimer's Disease. Neural Plasticity. 2016: 9760314. PMID 26949549 DOI: 10.1155/2016/9760314 |
0.64 |
|
| 2016 |
Aguirre-Acevedo DC, Lopera F, Henao E, Tirado V, Muñoz C, Giraldo M, Bangdiwala SI, Reiman EM, Tariot PN, Langbaum JB, Quiroz YT, Jaimes F. Cognitive Decline in a Colombian Kindred With Autosomal Dominant Alzheimer Disease: A Retrospective Cohort Study. Jama Neurology. PMID 26902171 DOI: 10.1001/jamaneurol.2015.4851 |
0.96 |
|
| 2016 |
Vélez JI, Rivera D, Mastronardi CA, Patel HR, Tobón C, Villegas A, Cai Y, Easteal S, Lopera F, Arcos-Burgos M. A Mutation in DAOA Modifies the Age of Onset in PSEN1 E280A Alzheimer's Disease Neural Plasticity. 2016. DOI: 10.1155/2016/9760314 |
0.96 |
|
| 2015 |
Giraldo-Chica M, Acosta-Baena N, Urbano L, Velilla L, Lopera F, Pineda N. Novel cerebrotendinous xanthomatosis mutation causes familial early dementia in Colombia. BioméDica : Revista Del Instituto Nacional De Salud. 35: 563-71. PMID 26844446 DOI: 10.7705/biomedica.v35i4.2690 |
0.36 |
|
| 2015 |
Vélez JI, Lopera F, Sepulveda-Falla D, Patel HR, Johar AS, Chuah A, Tobón C, Rivera D, Villegas A, Cai Y, Peng K, Arkell R, Castellanos FX, Andrews SJ, Silva Lara MF, et al. APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer's disease. Molecular Psychiatry. PMID 26619808 DOI: 10.1038/mp.2015.177 |
0.96 |
|
| 2015 |
Mastronardi CA, Pillai E, Pineda DA, Martinez AF, Lopera F, Velez JI, Palacio JD, Patel H, Easteal S, Acosta MT, Castellanos FX, Muenke M, Arcos-Burgos M. Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolate. Molecular Psychiatry. PMID 26598068 DOI: 10.1038/mp.2015.172 |
0.96 |
|
| 2015 |
Aguirre-Acevedo DC, Jaimes-Barragán F, Henao E, Tirado V, Muñoz C, Reiman EM, Tariot PN, Langbaum JB, Lopera F. Diagnostic accuracy of CERAD total score in a Colombian cohort with mild cognitive impairment and Alzheimer's disease affected by E280A mutation on presenilin-1 gene. International Psychogeriatrics / Ipa. 1-8. PMID 26478578 DOI: 10.1017/S1041610215001660 |
0.96 |
|
| 2015 |
Reiman EM, Langbaum JB, Tariot PN, Lopera F, Bateman RJ, Morris JC, Sperling RA, Aisen PS, Roses AD, Welsh-Bohmer KA, Carrillo MC, Weninger S. CAP-advancing the evaluation of preclinical Alzheimer disease treatments. Nature Reviews. Neurology. PMID 26416539 DOI: 10.1038/nrneurol.2015.177 |
0.96 |
|
| 2015 |
Quiroz YT, Willment KC, Castrillon G, Muniz M, Lopera F, Budson A, Stern CE. Successful Scene Encoding in Presymptomatic Early-Onset Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. 47: 955-64. PMID 26401774 DOI: 10.3233/JAD-150214 |
0.96 |
|
| 2015 |
Lalli MA, Bettcher BM, Arcila ML, Garcia G, Guzman C, Madrigal L, Ramirez L, Acosta-Uribe J, Baena A, Wojta KJ, Coppola G, Fitch R, de Both MD, Huentelman MJ, Reiman EM, ... ... Lopera F, et al. Whole-genome sequencing suggests a chemokine gene cluster that modifies age at onset in familial Alzheimer's disease. Molecular Psychiatry. PMID 26324103 DOI: 10.1038/mp.2015.131 |
0.96 |
|
| 2015 |
Quiroz YT, Schultz AP, Chen K, Protas HD, Brickhouse M, Fleisher AS, Langbaum JB, Thiyyagura P, Fagan AM, Shah AR, Muniz M, Arboleda-Velasquez JF, Munoz C, Garcia G, Acosta-Baena N, ... ... Lopera F, et al. Brain Imaging and Blood Biomarker Abnormalities in Children With Autosomal Dominant Alzheimer Disease: A Cross-Sectional Study. Jama Neurology. PMID 26121081 DOI: 10.1001/jamaneurol.2015.1099 |
0.96 |
|
| 2015 |
Bocanegra Y, García AM, Pineda D, Buriticá O, Villegas A, Lopera F, Gómez D, Gómez-Arias C, Cardona JF, Trujillo N, Ibáñez A. Syntax, action verbs, action semantics, and object semantics in Parkinson's disease: Dissociability, progression, and executive influences. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 69: 237-54. PMID 26103601 DOI: 10.1016/j.cortex.2015.05.022 |
0.64 |
|
| 2015 |
Suarez I, Burle B, Tobon C, Pineda D, Lopera F, Hasbroucq T, Casini L. Deciphering interference control in adults with ADHD by using distribution analyses and electromyographic activity. Acta Psychologica. 159: 85-92. PMID 26057599 DOI: 10.1016/j.actpsy.2015.05.010 |
0.96 |
|
| 2015 |
Parra MA, Saarimäki H, Bastin ME, Londoño AC, Pettit L, Lopera F, Della Sala S, Abrahams S. Memory binding and white matter integrity in familial Alzheimer's disease. Brain : a Journal of Neurology. 138: 1355-69. PMID 25762465 DOI: 10.1093/brain/awv048 |
0.96 |
|
| 2015 |
Fleisher AS, Chen K, Quiroz YT, Jakimovich LJ, Gutierrez Gomez M, Langois CM, Langbaum JB, Roontiva A, Thiyyagura P, Lee W, Ayutyanont N, Lopez L, Moreno S, Muñoz C, Tirado V, ... ... Lopera F, et al. Associations between biomarkers and age in the presenilin 1 E280A autosomal dominant Alzheimer disease kindred: a cross-sectional study. Jama Neurology. 72: 316-24. PMID 25580592 DOI: 10.1001/jamaneurol.2014.3314 |
0.96 |
|
| 2015 |
Kosik KS, Muñoz C, Lopez L, Arcila ML, García G, Madrigal L, Moreno S, Ríos Romenets S, Lopez H, Gutierrez M, Langbaum JB, Cho W, Suliman S, Tariot PN, Ho C, ... ... Lopera F, et al. Homozygosity of the autosomal dominant Alzheimer disease presenilin 1 E280A mutation. Neurology. 84: 206-8. PMID 25471389 DOI: 10.1212/WNL.0000000000001130 |
0.96 |
|
| 2015 |
MacPherson SE, Parra MA, Moreno S, Lopera F, Della Sala S. Dual memory task impairment in E280A presenilin-1 mutation carriers. Journal of Alzheimer's Disease : Jad. 44: 481-92. PMID 25352452 DOI: 10.3233/JAD-140990 |
0.96 |
|
| 2015 |
Melloni M, Sedeño L, Hesse E, García-Cordero I, Mikulan E, Plastino A, Marcotti A, López JD, Bustamante C, Lopera F, Pineda D, García AM, Manes F, Trujillo N, Ibáñez A. Cortical dynamics and subcortical signatures of motor-language coupling in Parkinson's disease Scientific Reports. 5. DOI: 10.1038/srep11899 |
0.96 |
|
| 2015 |
Bocanegra Y, García AM, Pineda D, Buriticá O, Villegas A, Lopera F, Gómez D, Gómez-Arias C, Cardona JF, Trujillo N, Ibáñez A. Syntax, action verbs, action semantics, and object semantics in Parkinson's disease: Dissociability, progression, and executive influences Cortex. 69: 237-254. DOI: 10.1016/j.cortex.2015.05.022 |
0.96 |
|
| 2015 |
Ochoa J, Sánchez F, Tobón C, Duque J, Quiroz Y, Lopera F, Hernandez M. Effective connectivity changes in presymptomatic alzheimer’s disease with E280A presenilin-1 mutation gene Ifmbe Proceedings. 49: 508-511. DOI: 10.1007/978-3-319-13117-7_130 |
0.96 |
|
| 2015 |
Quiroz YT, Schultz AP, Chen K, Protas HD, Brickhouse M, Fleisher AS, Langbaum JB, Thiyyagura P, Fagan AM, Shah AR, Muniz M, Arboleda-Velasquez JF, Munoz C, Garcia G, Acosta-Baena N, ... ... Lopera F, et al. Brain imaging and blood biomarker abnormalities in children with autosomal dominant Alzheimer disease a cross-sectional study Jama Neurology. 72: 912-919. |
0.96 |
|
| 2014 |
Herrera DA, Vargas J, Ochoa JF, Duque JE, Vargas SA, Lopera F, Castillo M. Alzheimer's disease: initial clinical implementation of automated volumetry. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 41: 651-3. PMID 25373817 DOI: 10.1017/cjn.2014.23 |
0.96 |
|
| 2014 |
Ryman DC, Acosta-Baena N, Aisen PS, Bird T, Danek A, Fox NC, Goate A, Frommelt P, Ghetti B, Langbaum JB, Lopera F, Martins R, Masters CL, Mayeux RP, McDade E, et al. Symptom onset in autosomal dominant Alzheimer disease: a systematic review and meta-analysis. Neurology. 83: 253-60. PMID 24928124 DOI: 10.1212/WNL.0000000000000596 |
0.96 |
|
| 2014 |
Ayutyanont N, Langbaum JB, Hendrix SB, Chen K, Fleisher AS, Friesenhahn M, Ward M, Aguirre C, Acosta-Baena N, Madrigal L, Muñoz C, Tirado V, Moreno S, Tariot PN, Lopera F, et al. The Alzheimer's prevention initiative composite cognitive test score: sample size estimates for the evaluation of preclinical Alzheimer's disease treatments in presenilin 1 E280A mutation carriers. The Journal of Clinical Psychiatry. 75: 652-60. PMID 24816373 DOI: 10.4088/JCP.13m08927 |
0.96 |
|
| 2014 |
Sepulveda-Falla D, Barrera-Ocampo A, Hagel C, Korwitz A, Vinueza-Veloz MF, Zhou K, Schonewille M, Zhou H, Velazquez-Perez L, Rodriguez-Labrada R, Villegas A, Ferrer I, Lopera F, Langer T, De Zeeuw CI, et al. Familial Alzheimer's disease-associated presenilin-1 alters cerebellar activity and calcium homeostasis. The Journal of Clinical Investigation. 124: 1552-67. PMID 24569455 DOI: 10.1172/JCI66407 |
0.96 |
|
| 2014 |
Rodriguez R, Lopera F, Alvarez A, Fernandez Y, Galan L, Quiroz Y, Bobes MA. Spectral Analysis of EEG in Familial Alzheimer's Disease with E280A Presenilin-1 Mutation Gene. International Journal of Alzheimer's Disease. 2014: 180741. PMID 24551475 DOI: 10.1155/2014/180741 |
0.96 |
|
| 2014 |
Lalli MA, Cox HC, Arcila ML, Cadavid L, Moreno S, Garcia G, Madrigal L, Reiman EM, Arcos-Burgos M, Bedoya G, Brunkow ME, Glusman G, Roach JC, Hood L, Kosik KS, ... Lopera F, et al. Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: S277-S283.e10. PMID 24239249 DOI: 10.1016/j.jalz.2013.09.005 |
0.96 |
|
| 2014 |
Londono AC, Castellanos FX, Arbelaez A, Ruiz A, Aguirre-Acevedo DC, Richardson AM, Easteal S, Lidbury BA, Arcos-Burgos M, Lopera F. An 1H-MRS framework predicts the onset of Alzheimer's disease symptoms in PSEN1 mutation carriers. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 552-61. PMID 24239247 DOI: 10.1016/j.jalz.2013.08.282 |
0.96 |
|
| 2014 |
Duque-Velásquez C, Alzate AG, Lanau AV, Velásquez LME, Lopera JZ, Lopera F, González JDR. Human transmissible spongiform encephalopathy: Case report | Encefalopatía espongiforme transmisible humana: Reporte de un caso Iatreia. 27: 330-336. |
0.96 |
|
| 2013 |
Suarez I, Lopera F, Pineda D, Casini L. The cognitive structure of time estimation impairments in adults with attention deficit hyperactivity disorder. Cognitive Neuropsychology. 30: 195-207. PMID 24111987 DOI: 10.1080/02643294.2013.842548 |
0.96 |
|
| 2013 |
Langbaum JB, Fleisher AS, Chen K, Ayutyanont N, Lopera F, Quiroz YT, Caselli RJ, Tariot PN, Reiman EM. Ushering in the study and treatment of preclinical Alzheimer disease. Nature Reviews. Neurology. 9: 371-81. PMID 23752908 DOI: 10.1038/nrneurol.2013.107 |
0.96 |
|
| 2013 |
Giraldo M, Lopera F, Siniard AL, Corneveaux JJ, Schrauwen I, Carvajal J, Muñoz C, Ramirez-Restrepo M, Gaiteri C, Myers AJ, Caselli RJ, Kosik KS, Reiman EM, Huentelman MJ. Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease. Neurobiology of Aging. 34: 2077.e11-8. PMID 23582655 DOI: 10.1016/j.neurobiolaging.2013.02.016 |
0.96 |
|
| 2013 |
Quiroz YT, Stern CE, Reiman EM, Brickhouse M, Ruiz A, Sperling RA, Lopera F, Dickerson BC. Cortical atrophy in presymptomatic Alzheimer's disease presenilin 1 mutation carriers. Journal of Neurology, Neurosurgery, and Psychiatry. 84: 556-61. PMID 23134660 DOI: 10.1136/jnnp-2012-303299 |
0.96 |
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| 2013 |
Vélez JI, Chandrasekharappa SC, Henao E, Martinez AF, Harper U, Jones M, Solomon BD, Lopez L, Garcia G, Aguirre-Acevedo DC, Acosta-Baena N, Correa JC, Lopera-Gómez CM, Jaramillo-Elorza MC, Rivera D, ... ... Lopera F, et al. Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease. Molecular Psychiatry. 18: 568-75. PMID 22710270 DOI: 10.1038/mp.2012.81 |
0.96 |
|
| 2012 |
Fleisher AS, Chen K, Quiroz YT, Jakimovich LJ, Gomez MG, Langois CM, Langbaum JB, Ayutyanont N, Roontiva A, Thiyyagura P, Lee W, Mo H, Lopez L, Moreno S, Acosta-Baena N, ... ... Lopera F, et al. Florbetapir PET analysis of amyloid-β deposition in the presenilin 1 E280A autosomal dominant Alzheimer's disease kindred: a cross-sectional study. The Lancet. Neurology. 11: 1057-65. PMID 23137949 DOI: 10.1016/S1474-4422(12)70227-2 |
0.96 |
|
| 2012 |
Reiman EM, Quiroz YT, Fleisher AS, Chen K, Velez-Pardo C, Jimenez-Del-Rio M, Fagan AM, Shah AR, Alvarez S, Arbelaez A, Giraldo M, Acosta-Baena N, Sperling RA, Dickerson B, Stern CE, ... ... Lopera F, et al. Brain imaging and fluid biomarker analysis in young adults at genetic risk for autosomal dominant Alzheimer's disease in the presenilin 1 E280A kindred: a case-control study. The Lancet. Neurology. 11: 1048-56. PMID 23137948 DOI: 10.1016/S1474-4422(12)70228-4 |
0.96 |
|
| 2012 |
Arcos-Burgos M, Londoño AC, Pineda DA, Lopera F, Palacio JD, Arbelaez A, Acosta MT, Vélez JI, Castellanos FX, Muenke M. Analysis of brain metabolism by proton magnetic resonance spectroscopy (1H-MRS) in attention-deficit/hyperactivity disorder suggests a generalized differential ontogenic pattern from controls. Attention Deficit and Hyperactivity Disorders. 4: 205-12. PMID 23012086 DOI: 10.1007/s12402-012-0088-0 |
0.96 |
|
| 2012 |
Lalli MA, Garcia G, Madrigal L, Arcos-Burgos M, Arcila ML, Kosik KS, Lopera F. Exploratory data from complete genomes of familial alzheimer disease age-at-onset outliers. Human Mutation. 33: 1630-4. PMID 22829467 DOI: 10.1002/humu.22167 |
0.96 |
|
| 2012 |
Sepulveda-Falla D, Glatzel M, Lopera F. Phenotypic profile of early-onset familial Alzheimer's disease caused by presenilin-1 E280A mutation. Journal of Alzheimer's Disease : Jad. 32: 1-12. PMID 22766738 DOI: 10.3233/JAD-2012-120907 |
0.96 |
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| 2012 |
MacPherson SE, Parra MA, Moreno S, Lopera F, Della Sala S. Dual task abilities as a possible preclinical marker of Alzheimer's disease in carriers of the E280A presenilin-1 mutation. Journal of the International Neuropsychological Society : Jins. 18: 234-41. PMID 22133015 DOI: 10.1017/S1355617711001561 |
0.96 |
|
| 2012 |
Jain M, Vélez JI, Acosta MT, Palacio LG, Balog J, Roessler E, Pineda D, Londoño AC, Palacio JD, Arbelaez A, Lopera F, Elia J, Hakonarson H, Seitz C, Freitag CM, et al. A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD. Molecular Psychiatry. 17: 741-7. PMID 21606926 DOI: 10.1038/mp.2011.59 |
0.96 |
|
| 2012 |
Arias WHP, Rojas W, Moreno S, Lopera F, Ruiz-Linares A, Bedoya G. The origin Of the G736A Mutation of Parkin gene in Peque (Northwest of Antioquia) | Origen de la mutación G736A del gen Parkin Revista Colombiana De Antropologia. 48: 81-85. |
0.96 |
|
| 2011 |
Quiroz YT, Lopera F, Budson AE. Charting the path for early diagnosis and prevention of Alzheimer's disease. Expert Review of Neurotherapeutics. 11: 1665-7. PMID 22091590 DOI: 10.1586/ern.11.162 |
0.96 |
|
| 2011 |
Reiman EM, Langbaum JB, Fleisher AS, Caselli RJ, Chen K, Ayutyanont N, Quiroz YT, Kosik KS, Lopera F, Tariot PN. Alzheimer's Prevention Initiative: a plan to accelerate the evaluation of presymptomatic treatments. Journal of Alzheimer's Disease : Jad. 26: 321-9. PMID 21971471 DOI: 10.3233/JAD-2011-0059 |
0.96 |
|
| 2011 |
Pineda DA, Lopera F, Puerta IC, Trujillo-Orrego N, Aguirre-Acevedo DC, Hincapié-Henao L, Arango CP, Acosta MT, Holzinger SI, Palacio JD, Pineda-Alvarez DE, Velez JI, Martinez AF, Lewis JE, Muenke M, et al. Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolate. Attention Deficit and Hyperactivity Disorders. 3: 291-9. PMID 21779842 DOI: 10.1007/s12402-011-0061-3 |
0.96 |
|
| 2011 |
Quiroz YT, Ally BA, Celone K, McKeever J, Ruiz-Rizzo AL, Lopera F, Stern CE, Budson AE. Event-related potential markers of brain changes in preclinical familial Alzheimer disease. Neurology. 77: 469-75. PMID 21775732 DOI: 10.1212/WNL.0b013e318227b1b0 |
0.96 |
|
| 2011 |
Valdés-Sosa M, Bobes MA, Quiñones I, Garcia L, Valdes-Hernandez PA, Iturria Y, Melie-Garcia L, Lopera F, Asencio J. Covert face recognition without the fusiform-temporal pathways. Neuroimage. 57: 1162-76. PMID 21570471 DOI: 10.1016/j.neuroimage.2011.04.057 |
0.96 |
|
| 2011 |
Arboleda-Velasquez JF, Manent J, Lee JH, Tikka S, Ospina C, Vanderburg CR, Frosch MP, RodrÃguez-Falcón M, Villen J, Gygi S, Lopera F, Kalimo H, Moskowitz MA, Ayata C, Louvi A, et al. Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease. Proceedings of the National Academy of Sciences of the United States of America. 108: E128-35. PMID 21555590 DOI: 10.1073/pnas.1101964108 |
0.96 |
|
| 2011 |
Parra MA, Sala SD, Abrahams S, Logie RH, Méndez LG, Lopera F. Specific deficit of colour-colour short-term memory binding in sporadic and familial Alzheimer's disease. Neuropsychologia. 49: 1943-52. PMID 21435348 DOI: 10.1016/j.neuropsychologia.2011.03.022 |
0.96 |
|
| 2011 |
Acosta-Baena N, Sepulveda-Falla D, Lopera-Gómez CM, Jaramillo-Elorza MC, Moreno S, Aguirre-Acevedo DC, Saldarriaga A, Lopera F. Pre-dementia clinical stages in presenilin 1 E280A familial early-onset Alzheimer's disease: a retrospective cohort study. The Lancet. Neurology. 10: 213-20. PMID 21296022 DOI: 10.1016/S1474-4422(10)70323-9 |
0.96 |
|
| 2011 |
Sepulveda-Falla D, Matschke J, Bernreuther C, Hagel C, Puig B, Villegas A, Garcia G, Zea J, Gomez-Mancilla B, Ferrer I, Lopera F, Glatzel M. Deposition of hyperphosphorylated tau in cerebellum of PS1 E280A Alzheimer's disease. Brain Pathology (Zurich, Switzerland). 21: 452-63. PMID 21159009 DOI: 10.1111/j.1750-3639.2010.00469.x |
0.96 |
|
| 2010 |
Quiroz YT, Budson AE, Celone K, Ruiz A, Newmark R, Castrillón G, Lopera F, Stern CE. Hippocampal hyperactivation in presymptomatic familial Alzheimer's disease. Annals of Neurology. 68: 865-75. PMID 21194156 DOI: 10.1002/ana.22105 |
0.96 |
|
| 2010 |
Parra MA, Abrahams S, Logie RH, Méndez LG, Lopera F, Della Sala S. Visual short-term memory binding deficits in familial Alzheimer's disease. Brain : a Journal of Neurology. 133: 2702-13. PMID 20624814 DOI: 10.1093/brain/awq148 |
0.96 |
|
| 2010 |
Giraldo-Chica MM, RamÃrez JD, Uribe C, Lopera F. [Biopercular syndrome caused by unilateral ischemia. Report of one case]. Revista MéDica De Chile. 138: 341-5. PMID 20556339 |
0.96 |
|
| 2010 |
Kremeyer B, Lopera F, Cox JJ, Momin A, Rugiero F, Marsh S, Woods CG, Jones NG, Paterson KJ, Fricker FR, Villegas A, Acosta N, Pineda-Trujillo NG, Ramírez JD, Zea J, et al. A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. Neuron. 66: 671-80. PMID 20547126 DOI: 10.1016/j.neuron.2010.04.030 |
0.96 |
|
| 2010 |
Pineda DA, Trujillo-Orrego N, Aguirre-Acevedo DC, Arango CP, Hincapié-Henao L, Montoya-Arenas DA, Lopera F, Pineda-Alvarez DE, Arcos-Burgos M, Muenke M. [Utility of the Wender-Utah rating scale and the checklists for the diagnosis of familial attention deficit hyperactivity disorder in adults. Convergent and concurrent validities]. Revista De Neurologia. 50: 207-16. PMID 20198592 |
0.96 |
|
| 2010 |
Arcos-Burgos M, Jain M, Acosta MT, Shively S, Stanescu H, Wallis D, Domené S, Vélez JI, Karkera JD, Balog J, Berg K, Kleta R, Gahl WA, Roessler E, Long R, ... ... Lopera F, et al. A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication. Molecular Psychiatry. 15: 1053-66. PMID 20157310 DOI: 10.1038/mp.2010.6 |
0.96 |
|
| 2010 |
Bobes MA, GarcÃa YF, Lopera F, Quiroz YT, Galán L, Vega M, Trujillo N, Valdes-Sosa M, Valdes-Sosa P. ERP generator anomalies in presymptomatic carriers of the Alzheimer's disease E280A PS-1 mutation. Human Brain Mapping. 31: 247-65. PMID 19650138 DOI: 10.1002/hbm.20861 |
0.96 |
|
| 2010 |
Dorfman VB, Pasquini L, Riudavets M, López-Costa JJ, Villegas A, Troncoso JC, Lopera F, Castaño EM, Morelli L. Differential cerebral deposition of IDE and NEP in sporadic and familial Alzheimer's disease. Neurobiology of Aging. 31: 1743-57. PMID 19019493 DOI: 10.1016/j.neurobiolaging.2008.09.016 |
0.96 |
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| 2009 |
Wallis D, Arcos-Burgos M, Jain M, Castellanos FX, Palacio JD, Pineda D, Lopera F, Stanescu H, Pineda D, Berg K, Palacio LG, Bailey-Wilson JE, Muenke M. Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate. Attention Deficit and Hyperactivity Disorders. 1: 19-24. PMID 21432576 DOI: 10.1007/s12402-009-0003-5 |
0.96 |
|
| 2009 |
Luna-Maldonado E, Aguirre-Acevedo DC, GarcÃa-Ospina GP, Lopera F. [Periodontal disease as an early clinical sign of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)]. Revista De Neurologia. 49: 520-3. PMID 19859875 |
0.96 |
|
| 2009 |
Ruiz-Rizzo AL, Tirado V, Moreno-Carrillo C, Aguirre-Acevedo DC, Murillo O, Lopera F. [Comparison of neuropsychological performance according to the age of onset in subjects with Parkinson's disease and Parkinsonism]. Revista De Neurologia. 49: 123-30. PMID 19621306 |
0.96 |
|
| 2009 |
Trujillo-Orrego N, Pineda DA, Arango CP, Puerta IC, Lopera F, Aguirre-Acevedo DC, Hincapie-Henao L, Pineda-Alvarez DE, Arcos-Burgos M, Muenke M. [Attention deficit hyperactivity behavioral phenotype dimensions of adults from Antioquian families using the Wender-Utah Scale -Spanish version]. Revista De Neurologia. 48: 400-6. PMID 19340779 |
0.96 |
|
| 2008 |
Zhou K, Dempfle A, Arcos-Burgos M, Bakker SC, Banaschewski T, Biederman J, Buitelaar J, Castellanos FX, Doyle A, Ebstein RP, Ekholm J, Forabosco P, Franke B, Freitag C, Friedel S, ... ... Lopera F, et al. Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 1392-8. PMID 18988193 DOI: 10.1002/ajmg.b.30878 |
0.96 |
|
| 2008 |
Tirado V, Motta M, Aguirre-Acevedo DC, Pineda DA, Lopera F. [Analysis of intrusive errors in a memory test as possible pre-clinical marker of familial Alzheimer disease, in E280A presenilin-1 mutation carrier]. Revista De Neurologia. 47: 290-4. PMID 18803154 |
0.96 |
|
| 2008 |
Kosik KS, Lopera F. Genetic testing must recognize impact of bad news on recipient. Nature. 454: 158-9. PMID 18615057 DOI: 10.1038/454158c |
0.96 |
|
| 2008 |
Henao-Arboleda E, Aguirre-Acevedo DC, Muñoz C, Pineda DA, Lopera F. [Prevalence of mild cognitive impairment, amnestic-type, in a Colombian population]. Revista De Neurologia. 46: 709-13. PMID 18543195 |
0.96 |
|
| 2008 |
Valencia C, López-Alzate E, Tirado V, Zea-Herrera MD, Lopera F, Rupprecht R, Oswald WD. [Cognitive effects of combined memory and psychomotor training in elderly adults]. Revista De Neurologia. 46: 465-71. PMID 18428103 |
0.96 |
|
| 2008 |
Van Vickle GD, Esh CL, Kokjohn TA, Patton RL, Kalback WM, Luehrs DC, Beach TG, Newel AJ, Lopera F, Ghetti B, Vidal R, Castaño EM, Roher AE. Presenilin-1 280Glu-->Ala mutation alters C-terminal APP processing yielding longer abeta peptides: implications for Alzheimer's disease. Molecular Medicine (Cambridge, Mass.). 14: 184-94. PMID 18317569 DOI: 10.2119/2007-00094.Van Vickle |
0.96 |
|
| 2008 |
Villegas A, Castañeda MM, Arias LF, Vieco B, Lopera F, Bedoya G. Evaluation of amyloid-β by the E280A mutation in presenillin gene | Evaluación de la producción de β-amiloide por la mutación E280A en el gen de la presenilina 1 Biomedica. 27: 372-384. |
0.96 |
|
| 2007 |
Villegas A, Castañeda MM, Arias LF, Vieco B, Lopera F, Bedoya G. [Evaluation of amyloid-beta by the E280A mutation in presenilin gene]. BioméDica : Revista Del Instituto Nacional De Salud. 27: 372-84. PMID 18320103 |
0.96 |
|
| 2007 |
Henao-Arboleda E, Aguirre-Acevedo DC, Pacheco C, Yamile-Bocanegra O, Lopera F. [Monitoring cognitive characteristics in a population with hereditary cerebrovascular disease (CADASIL) in Colombia]. Revista De Neurologia. 45: 729-33. PMID 18075987 |
0.96 |
|
| 2007 |
Aguirre-Acevedo DC, Gómez RD, Moreno S, Henao-Arboleda E, Motta M, Muñoz C, Arana A, Pineda DA, Lopera F. [Validity and reliability of the CERAD-Col neuropsychological battery]. Revista De Neurologia. 45: 655-60. PMID 18050096 |
0.96 |
|
| 2007 |
Arango-Lasprilla JC, Cuetos F, Valencia C, Uribe C, Lopera F. Cognitive changes in the preclinical phase of familial Alzheimer's disease. Journal of Clinical and Experimental Neuropsychology. 29: 892-900. PMID 17852592 DOI: 10.1080/13803390601174151 |
0.96 |
|
| 2007 |
Arboleda-RamÃrez A, Lopera-Vásquez JP, Hincapié-Henao L, Giraldo-Prieto M, Pineda DA, Lopera F, Lopera-Echeverri E. [Specific impaired language development: a selective or generalised cognition problem]. Revista De Neurologia. 44: 596-600. PMID 17523117 |
0.96 |
|
| 2007 |
Pineda DA, Palacio LG, Puerta IC, Merchán V, Arango CP, Galvis AY, Gómez M, Aguirre DC, Lopera F, Arcos-Burgos M. Environmental influences that affect attention deficit/hyperactivity disorder: study of a genetic isolate. European Child & Adolescent Psychiatry. 16: 337-46. PMID 17487441 DOI: 10.1007/s00787-007-0605-4 |
0.96 |
|
| 2007 |
Cuetos F, Arango-Lasprilla JC, Uribe C, Valencia C, Lopera F. Linguistic changes in verbal expression: a preclinical marker of Alzheimer's disease. Journal of the International Neuropsychological Society : Jins. 13: 433-9. PMID 17445292 DOI: 10.1017/S1355617707070609 |
0.96 |
|
| 2007 |
Jain M, Palacio LG, Castellanos FX, Palacio JD, Pineda D, Restrepo MI, Muñoz JF, Lopera F, Wallis D, Berg K, Bailey-Wilson JE, Arcos-Burgos M, Muenke M. Attention-deficit/hyperactivity disorder and comorbid disruptive behavior disorders: evidence of pleiotropy and new susceptibility loci. Biological Psychiatry. 61: 1329-39. PMID 16950213 DOI: 10.1016/j.biopsych.2006.06.026 |
0.96 |
|
| 2007 |
Pineda DA, Aguirre-Acevedo DC, Lopera F, Arcos-Burgos M. Cluster taxometry of attention deficit/hyperactivity disorder with latent class and correspondence analysis | Taxometría de conglomerados del trastorno por déficit de atención/hiperactividad con análisis de clases latentes y de correspondencias Universitas Psychologica. 6: 409-423. |
0.96 |
|
| 2007 |
Hincapié L, Giraldo M, Castro R, Lopera F, Pineda D, Lopera E. Linguistic properties of specific language impairment | Propiedades lingüísticas de los trastornos Específicos del desarrollo del lenguaje Revista Latinoamericana De Psicologia. 39: 47-61. |
0.96 |
|
| 2006 |
Pineda DA, Kamphaus RW, Restrepo MA, Puerta IC, Arango CP, Lopera FJ, GarcÃa-Barrera MA, Dowdy ET. Screening for conduct disorder in an adolescent male sample from Colombia. Transcultural Psychiatry. 43: 362-82. PMID 17090623 DOI: 10.1177/1363461506066983 |
0.96 |
|
| 2006 |
Pineda-Trujillo N, Apergi M, Moreno S, Arias W, Lesage S, Franco A, Sepulveda-Falla D, Cano D, Buriticá O, Pineda D, Uribe CS, de Yebenes JG, Lees AJ, Brice A, Bedoya G, ... Lopera F, et al. A genetic cluster of early onset Parkinson's disease in a Colombian population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 885-9. PMID 16941654 DOI: 10.1002/ajmg.b.30375 |
0.96 |
|
| 2006 |
Muñoz AM, Agudelo GM, Lopera FJ. [Nutritional condition in patients with Alzheimer-type dementia from the neurosciences' group, MedellÃn 2004]. BioméDica : Revista Del Instituto Nacional De Salud. 26: 113-25. PMID 16929909 |
0.96 |
|
| 2006 |
Bustamante J, Lopera F. [Tumour of the corpus callosum: the association between interhemispheric disconnection and an anterograde amnesia syndrome]. Revista De Neurologia. 43: 207-12. PMID 16883509 |
0.96 |
|
| 2006 |
Lara-Useche E, Pineda DA, Henao-Arboleda E, Arboleda-RamÃrez A, Aguirre-Acevedo DC, Lopera F. [A description of semantic memory performance in a sample of the Antioquian population]. Revista De Neurologia. 42: 272-6. PMID 16538589 |
0.96 |
|
| 2006 |
Arango-Lasprilla JC, Rogers H, Lengenfelder J, Deluca J, Moreno S, Lopera F. Cortical and subcortical diseases: do true neuropsychological differences exist? Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists. 21: 29-40. PMID 16143493 DOI: 10.1016/j.acn.2005.07.004 |
0.96 |
|
| 2005 |
Pineda DA, Aguirre DC, Garcia MA, Lopera FJ, Palacio LG, Kamphaus RW. Validation of two rating scales for attention-deficit hyperactivity disorder diagnosis in Colombian children. Pediatric Neurology. 33: 15-25. PMID 15993319 DOI: 10.1016/j.pediatrneurol.2005.02.001 |
0.96 |
|
| 2005 |
RÃos-Romenets S, Tirado V, Arbeláez A, RÃos A, Lopera F. [Semantic dementia: a case report]. Revista De Neurologia. 40: 253-4. PMID 15765320 |
0.96 |
|
| 2004 |
Bobes MA, Lopera F, Comas LD, Galan L, Carbonell F, Bringas ML, Valdes-Sosa M. Brain potentials reflect residual face processing in a case of prosopagnosia. Cognitive Neuropsychology. 21: 691-718. PMID 21038228 DOI: 10.1080/02643290342000258 |
0.96 |
|
| 2004 |
Castro-Rebolledo R, Giraldo-Prieto M, Hincapié-Henao L, Lopera F, Pineda DA. [Specific developmental language disorder: a theoretical approach to its diagnosis, aetiology and clinical symptoms]. Revista De Neurologia. 39: 1173-81. PMID 15625638 |
0.96 |
|
| 2004 |
Palacio JD, Castellanos FX, Pineda DA, Lopera F, Arcos-Burgos M, Quiroz YT, Henao GC, Puerta IC, RamÃrez DL, Rapoport JL, Bailey-Wilson J, Berg K, Muenke M. Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families. Journal of the American Academy of Child and Adolescent Psychiatry. 43: 1506-15. PMID 15564820 DOI: 10.1097/01.chi.0000142279.79805.dc |
0.96 |
|
| 2004 |
Arcos-Burgos M, Castellanos FX, Pineda D, Lopera F, Palacio JD, Palacio LG, Rapoport JL, Berg K, Bailey-Wilson JE, Muenke M. Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11. American Journal of Human Genetics. 75: 998-1014. PMID 15497111 DOI: 10.1086/426154 |
0.96 |
|
| 2004 |
Tirado V, Muñoz C, Aguirre C, Pineda DA, Lopera F. [Performance of carriers and non-carriers of the E280A mutation for familial Alzheimer's disease in a naming test]. Revista De Neurologia. 39: 322-6. PMID 15340889 |
0.96 |
|
| 2004 |
Velez-Pardo C, Rio MJ, Moreno S, RamÃrez-Gomez L, Correa G, Lopera F. New mutation (T1232P) of the ATP-7B gene associated with neurologic and neuropsychiatric dominance onset of Wilson's disease in three unrelated Colombian kindred. Neuroscience Letters. 367: 360-4. PMID 15337266 DOI: 10.1016/j.neulet.2004.06.032 |
0.96 |
|
| 2004 |
Velez-Pardo C, Arellano JI, Cardona-Gomez P, Jimenez Del Rio M, Lopera F, De Felipe J. CA1 hippocampal neuronal loss in familial Alzheimer's disease presenilin-1 E280A mutation is related to epilepsy. Epilepsia. 45: 751-6. PMID 15230697 DOI: 10.1111/j.0013-9580.2004.55403.x |
0.96 |
|
| 2004 |
Arcos-Burgos M, Castellanos FX, Konecki D, Lopera F, Pineda D, Palacio JD, Rapoport JL, Berg K, Bailey-Wilson J, Muenke M. Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolate. Molecular Psychiatry. 9: 252-9. PMID 15094785 DOI: 10.1038/sj.mp.4001396 |
0.96 |
|
| 2004 |
Jimenez Del Rio M, Moreno S, Garcia-Ospina G, Buritica O, Uribe CS, Lopera F, Velez-Pardo C. Autosomal recessive juvenile parkinsonism Cys212Tyr mutation in parkin renders lymphocytes susceptible to dopamine- and iron-mediated apoptosis. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 324-30. PMID 15022188 DOI: 10.1002/mds.10670 |
0.96 |
|
| 2003 |
MejÃa S, Giraldo M, Pineda D, Ardila A, Lopera F. Nongenetic factors as modifiers of the age of onset of familial Alzheimer's disease. International Psychogeriatrics / Ipa. 15: 337-49. PMID 15000414 DOI: 10.1017/S1041610203009591 |
0.96 |
|
| 2003 |
Arango-Lasprilla JC, Iglesias-Dorado J, Lopera F. [Clinical and neuropsychological characteristics of Huntington's disease: a review]. Revista De Neurologia. 37: 758-65. PMID 14593636 |
0.96 |
|
| 2003 |
Pastor P, Roe CM, Villegas A, Bedoya G, Chakraverty S, GarcÃa G, Tirado V, Norton J, RÃos S, MartÃnez M, Kosik KS, Lopera F, Goate AM. Apolipoprotein Eepsilon4 modifies Alzheimer's disease onset in an E280A PS1 kindred. Annals of Neurology. 54: 163-9. PMID 12891668 DOI: 10.1002/ana.10636 |
0.96 |
|
| 2003 |
Arango-Lasprilla JC, Iglesias-Dorado J, Moreno S, Lopera F. [A neuropsychological study of Huntington's disease in families in Antioquia, Colombia]. Revista De Neurologia. 37: 7-13. PMID 12861500 |
0.96 |
|
| 2003 |
Arango Lasprilla JC, Iglesias J, Lopera F. Neuropsychological study of familial Alzheimer's disease caused by mutation E280A in the presenilin 1 gene. American Journal of Alzheimer's Disease and Other Dementias. 18: 137-46. PMID 12811988 |
0.96 |
|
| 2003 |
GarcÃa-Ospina GP, JÃmenez-Del RÃo M, Lopera F, Vélez-Pardo C. [Neuronal DNA damage correlates with a positive detection of c-Jun, nuclear factor kB, p53 and Par-4 transcription factors in Alzheimer's disease]. Revista De Neurologia. 36: 1004-10. PMID 12808492 |
0.96 |
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| 2003 |
Pineda DA, Lopera F, Palacio JD, Ramirez D, Henao GC. Prevalence estimations of attention-deficit/hyperactivity disorder: differential diagnoses and comorbidities in a Colombian sample. The International Journal of Neuroscience. 113: 49-71. PMID 12691001 DOI: 10.1080/00207450390161921 |
0.96 |
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| 2003 |
Pineda DA, Puerta IC, Merchán V, Arango CP, Galvis AY, Velásquez B, Gómez M, Builes A, Zapata M, Montoya P, MartÃnez J, Salazar EO, Lopera F. [Perinatal factors associated with attention deficit/hyperactivity diagnosis in Colombian Paisa children]. Revista De Neurologia. 36: 609-13. PMID 12666038 |
0.96 |
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| 2003 |
Bobes MA, Lopera F, Garcia M, DÃaz-Comas L, Galan L, Valdes-Sosa M. Covert matching of unfamiliar faces in a case of prosopagnosia: an ERP study. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 39: 41-56. PMID 12627752 |
0.96 |
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| 2003 |
García A, Lopera F, Madrigal L, Ossa J. Towards the enunciation of ethical dilemmas regarding early onset Alzheimer's disease in Antioquia, Colombia | Hacia el enunciado de dilemas éticos sobre la enfermedad de Alzheimer precoz, en Antioquia, Colombia Iatreia. 16: 174-182. |
0.96 |
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| 2002 |
Arboleda-Velasquez JF, Lopera F, Lopez E, Frosch MP, Sepulveda-Falla D, Gutierrez JE, Vargas S, Medina M, Martinez De Arrieta C, Lebo RV, Slaugenhaupt SA, Betensky RA, Villegas A, Arcos-Burgos M, Rivera D, et al. C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke. Neurology. 59: 277-9. PMID 12136071 |
0.96 |
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| 2002 |
Arcos-Burgos M, Castellanos FX, Lopera F, Pineda D, Palacio JD, Garcia M, Henao GC, Palacio LG, Berg K, Bailey-Wilson JE, Muenke M. Attention-deficit/hyperactivity disorder (ADHD): feasibility of linkage analysis in a genetic isolate using extended and multigenerational pedigrees. Clinical Genetics. 61: 335-43. PMID 12081716 DOI: 10.1034/j.1399-0004.2002.610503.x |
0.96 |
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| 2002 |
Sierra M, Lopera F, Lambert MV, Phillips ML, David AS. Separating depersonalisation and derealisation: the relevance of the "lesion method". Journal of Neurology, Neurosurgery, and Psychiatry. 72: 530-2. PMID 11909918 DOI: 10.1136/jnnp.72.4.530 |
0.96 |
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| 2001 |
Velez-Pardo C, Arroyave ST, Lopera F, Castaño AD, Jimenez Del Rio M. Ultrastructure evidence of necrotic neural cell death in familial Alzheimer's disease brains bearing presenilin-1 E280A mutation. Journal of Alzheimer's Disease : Jad. 3: 409-415. PMID 12214045 |
0.96 |
|
| 2001 |
Lopera F. [Clinical history in the study of a patient with dementia]. Revista De Neurologia. 32: 1187-91. PMID 11708253 |
0.96 |
|
| 2001 |
Johnson KA, Lopera F, Jones K, Becker A, Sperling R, Hilson J, Londono J, Siegert I, Arcos M, Moreno S, Madrigal L, Ossa J, Pineda N, Ardila A, Roselli M, et al. Presenilin-1-associated abnormalities in regional cerebral perfusion. Neurology. 56: 1545-51. PMID 11402113 |
0.96 |
|
| 2001 |
Arcos-Burgos M, Restrepo T, Rivera D, Palacio LG, Castañeda M, Palacio O, Arboleda J, Lopera F. Vascular hereditary dementia CADASIL type in Colombia. III. Linkage analysis to Notch3 gene | Demencia vascular hereditaria tipo CADASIL en Colombia. III. Análisis de ligamiento a Notch3 Revista De Neurologia. 32: 701-704. PMID 11391502 |
0.96 |
|
| 2001 |
Lopera F, Rivera N, Arboleda J, Restrepo T, Arcos-Burgos M. [Analysis of complex segregation in a large family with hereditary cerebrovascular disease in Antioquia, Colombia]. Revista De Neurologia. 32: 222-5. PMID 11310272 |
0.96 |
|
| 2001 |
Pineda DA, Lopera F, Henao GC, Palacio JD, Castellanos FX. [Confirmation of the high prevalence of attention deficit disorder in a Colombian community]. Revista De Neurologia. 32: 217-22. PMID 11310271 |
0.96 |
|
| 2001 |
Pineda-Trujillo N, Carvajal-Carmona LG, Buriticá O, Moreno S, Uribe C, Pineda D, Toro M, GarcÃa F, Arias W, Bedoya G, Lopera F, Ruiz-Linares A. A novel Cys212Tyr founder mutation in parkin and allelic heterogeneity of juvenile Parkinsonism in a population from North West Colombia. Neuroscience Letters. 298: 87-90. PMID 11163284 DOI: 10.1016/S0304-3940(00)01733-X |
0.96 |
|
| 2000 |
Ardila A, Lopera F, Rosselli M, Moreno S, Madrigal L, Arango-Lasprilla JC, Arcos M, Murcia C, Arango-Viana JC, Ossa J, Goate A, Kosik KS. Neuropsychological profile of a large kindred with familial Alzheimer's disease caused by the E280A single presenilin-1 mutation. Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists. 15: 515-28. PMID 14590205 DOI: 10.1016/S0887-6177(99)00041-4 |
0.96 |
|
| 2000 |
Lopera F, Arboleda J, Moreno S, Almeida N, Cuartas M, Arcos-Burgos M. [Clinical characteristics of hereditary cerebrovascular disease in a large family from Colombia]. Revista De Neurologia. 31: 901-7. PMID 11244680 |
0.96 |
|
| 2000 |
Escobar R, Rios A, Montoya ID, Lopera F, Ramos D, Carvajal C, Constain G, Gutierrez JE, Vargas S, Herrera CP. Clinical and cerebral blood flow changes in catatonic patients treated with ECT. Journal of Psychosomatic Research. 49: 423-9. PMID 11182435 DOI: 10.1016/S0022-3999(00)00190-2 |
0.96 |
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| 2000 |
Velásquez M, Arcos-Burgos M, Toro ME, Castaño A, Madrigal L, Moreno S, Jaramillo N, Lopera F. [Factorial and discriminant analyses of neuropsychological variables in familial and sporadic late onset Alzheimer disease]. Revista De Neurologia. 31: 501-6. PMID 11055049 |
0.96 |
|
| 2000 |
Rosselli MC, Ardila AC, Moreno SC, Standish VC, Arango-Lasprilla JC, Tirado VM, Ossa JM, Goate AM, Kosik KS, Lopera F. Cognitive decline in patients with familial Alzheimer's disease associated with E280a presenilin-1 mutation: a longitudinal study. Journal of Clinical and Experimental Neuropsychology. 22: 483-95. PMID 10923058 DOI: 10.1076/1380-3395(200008)22:4;1-0;FT483 |
0.96 |
|
| 2000 |
Lopera F. [Procesing of faces: neurological bases, disorders and evaluation]. Revista De Neurologia. 30: 486-90. PMID 10775980 |
0.96 |
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| 2000 |
Mangone CA, Bueno AA, Allegri R, Arizaga R, Nitrini R, Ventura R, Lopera F. Behavioral and psychological symptoms of dementia in Latin America International Psychogeriatrics. 12: 415-418. |
0.96 |
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| 2000 |
Velez-Pardo C, Lopera F, Jimenez Del Rio M. DNA damage does not correlate with amyloid-β-plaques and neurofibrillary tangles in familial Alzheimer's disease presenilin-1 [E280A] mutation Journal of Alzheimer's Disease. 2: 47-57. |
0.96 |
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| 1999 |
Toro F, Lopera F, Ossa J, Madrigal L, Mira A, DÃaz A, Parra S. [Detection of antibodies to beta-amyloid in carriers of E280A mutation in the presenilin-1 gene]. Revista De Neurologia. 29: 1104-7. PMID 10652730 |
0.96 |
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| 1999 |
Lopera F, Tobón N, Arcos-Burgos M, Vargas S, Gutiérrez JE, Rosselli M, Ardila A. [Image characterization of Alzheimer's disease associated with the E280A-PS1 mutation. Case-control study: MRI findings]. Revista De Neurologia. 29: 6-12. PMID 10528301 |
0.96 |
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| 1999 |
Duque-Castaño A, Roldán MI, Arango-Viana JC, Arcos-Burgos M, Cubillo H, Lopera F. [Neuropathological findings in early-onset Alzheimer's disease (E280a-PS1 mutation)]. Revista De Neurologia. 29: 1-6. PMID 10528300 |
0.96 |
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| 1999 |
Lopera F, Palacio LG, Jiménez I, Villegas P, Puerta IC, Pineda D, Jiménez M, Arcos-Burgos M. [Discrimination between genetic factors in attention deficit]. Revista De Neurologia. 28: 660-4. PMID 10363289 |
0.6 |
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| 1999 |
Bobes MA, Valdes-Sosa M, García M, Gómez JF, Lopera F. ERP signs of abnormal face processing in prosopagnosia Brain and Cognition. 40: 52-57. |
0.96 |
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| 1998 |
Velez-Pardo C, Jimenez Del Rio M, Lopera F. Familial Alzheimer's disease: oxidative stress, beta-amyloid, presenilins, and cell death. General Pharmacology. 31: 675-81. PMID 9809462 DOI: 10.1016/S0306-3623(98)00189-X |
0.96 |
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| 1997 |
Lendon CL, Martinez A, Behrens IM, Kosik KS, Madrigal L, Norton J, Neuman R, Myers A, Busfield F, Wragg M, Arcos M, Arango Viana JC, Ossa J, Ruiz A, Goate AM, ... Lopera F, et al. E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles. Human Mutation. 10: 186-95. PMID 9298817 DOI: 10.1002/(SICI)1098-1004(1997)10:3<186::AID-HUMU2>3.0.CO;2-H |
0.96 |
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| 1997 |
Lopera F, Ardilla A, MartÃnez A, Madrigal L, Arango-Viana JC, Lemere CA, Arango-Lasprilla JC, HincapÃe L, Arcos-Burgos M, Ossa JE, Behrens IM, Norton J, Lendon C, Goate AM, Ruiz-Linares A, et al. Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation. Jama. 277: 793-9. PMID 9052708 |
0.96 |
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| 1996 |
Lemere CA, Lopera F, Kosik KS, Lendon CL, Ossa J, Saido TC, Yamaguchi H, Ruiz A, Martinez A, Madrigal L, Hincapie L, Arango JC, Anthony DC, Koo EH, Goate AM, et al. The E280A presenilin 1 Alzheimer mutation produces increased A beta 42 deposition and severe cerebellar pathology. Nature Medicine. 2: 1146-50. PMID 8837617 DOI: 10.1038/nm1096-1146 |
0.96 |
|
| 1992 |
Lopera F, Ardila A. Prosopamnesia and Visuolimbic Disconnection Syndrome: A Case Study Neuropsychology. 6: 3-12. |
0.96 |
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