A. Villegas

发表

Syntax, action verbs, action semantics, and object semantics in Parkinson's disease: Dissociability, progression, and executive influences

A. Ibáñez, Adolfo M. García, F. Lopera, 2015, Cortex.

A Gain-of-Function Mutation in TRPA1 Causes Familial Episodic Pain Syndrome

G. Bedoya, A. Ruiz-Linares, C. Woods, 2010, Neuron.

The Road Less Traveled: Alternative Pathways for Action-Verb Processing in Parkinson's Disease.

Agustín Ibáñez, Lucas Sedeño, Francisco Lopera, 2016, Journal of Alzheimer's disease : JAD.

Language Deficits as a Preclinical Window into Parkinson’s Disease: Evidence from Asymptomatic Parkin and Dardarin Mutation Carriers

Agustín Ibáñez, Lucas Sedeño, Adolfo M. García, 2016, Journal of the International Neuropsychological Society.

Differential Profile of Systemic Extracellular Vesicles From Sporadic and Familial Alzheimer’s Disease Leads to Neuroglial and Endothelial Cell Degeneration

J. D. Arias-Londoño, I. Zuhorn, G. P. Cardona-Gómez, 2020, Frontiers in Aging Neuroscience.

Language deficits as a preclinical window into Parkinson’s disease: Evidence from asymptomatic parkin and dardarin mutation carriers

A. Ibáñez, L. Sedeño, D. Pineda, 2016 .

Mutations modifying sporadic Alzheimer's disease age of onset

S. Easteal, F. Lopera, H. Patel, 2016, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Familial Alzheimer’s Disease and Recessive Modifiers

F. Lopera, A. Villegas, M. Arcos-Burgos, 2019, Molecular Neurobiology.

Distinct tau neuropathology and cellular profiles of an APOE3 Christchurch homozygote protected against autosomal dominant Alzheimer’s dementia

Justin S. Sanchez, Mark Ellisman, R. Sperling, 2022, Acta Neuropathologica.

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

J. Streffer, M. Mercken, F. Lopera, 2020, Frontiers in Aging Neuroscience.

Evidence of beta amyloid independent small vessel disease in familial Alzheimer's disease

R. Kalaria, Y. Quiroz, M. Glatzel, 2022, Brain pathology.

Distinct tau neuropathology and cellular profiles of an APOE3 Christchurch homozygote protected against autosomal dominant Alzheimer’s dementia

Justin S. Sanchez, Mark Ellisman, R. Sperling, 2022, Acta Neuropathologica.

[Evaluation of amyloid-beta by the E280A mutation in presenilin gene].

G. Bedoya, F. Lopera, A. Villegas, 2007, Biomedica : revista del Instituto Nacional de Salud.

Gliovascular alterations in sporadic and familial Alzheimer's disease: APOE3 Christchurch homozygote glioprotection

G. P. Cardona-Gómez, Jorge Toledo, S. Härtel, 2022, Brain pathology.

Apolipoprotein Eε4 modifies Alzheimer's disease onset in an E280A PS1 kindred

Kenneth S. Kosik, Francisco Lopera, Pau Pastor, 2003 .

Tracking the Cognitive, Social, and Neuroanatomical Profile in Early Neurodegeneration: Type III Cockayne Syndrome

S. Baez, Eduar Herrera, F. Manes, 2013, Front. Aging Neurosci..

Discriminative Accuracy of Plasma Phospho-tau217 for Alzheimer Disease vs Other Neurodegenerative Disorders.

K. Blennow, Yi Su, E. Reiman, 2020, JAMA.

A Mutation in DAOA Modifies the Age of Onset in PSEN1 E280A Alzheimer's Disease

S. Easteal, F. Lopera, H. Patel, 2016, Neural plasticity.

APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer's disease

J. Licinio, S. Easteal, F. Lopera, 2015, Molecular Psychiatry.

APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer's disease

J. Licinio, S. Easteal, F. Lopera, 2015, Molecular Psychiatry.

Extracellular Vesicles From 3xTg-AD Mouse and Alzheimer’s Disease Patient Astrocytes Impair Neuroglial and Vascular Components

F. Lopera, A. Villegas, Juan Villar-Vesga, 2021, Frontiers in Aging Neuroscience.

Plasma neurofilament light chain in the presenilin 1 E280A autosomal dominant Alzheimer's disease kindred: a cross-sectional and longitudinal cohort study

P. Tariot, K. Blennow, Yi Su, 2020, The Lancet Neurology.

Transmissible spongiform encephalopathies: biology of the Prion and current state of the epidemiologic surveillance in Colombia.

A. Villegas, J. Rodas, Juan C Duque-Velásquez, 2010 .

Apolipoprotein E ε 4 Modifies Alzheimer ’ s Disease Onset in an E 280 A PS 1 Kindred

G. Bedoya, A. Goate, K. Kosik, 2003 .

p120‐catenin is necessary for neuroprotection induced by CDK5 silencing in models of Alzheimer's disease

F. Lopera, A. Villegas, C. González-Billault, 2016, Journal of neurochemistry.

Differential cerebral deposition of IDE and NEP in sporadic and familial Alzheimer's disease

J. Troncoso, F. Lopera, L. Pasquini, 2010, Neurobiology of Aging.

Deposition of Hyperphosphorylated Tau in Cerebellum of PS1 E280A Alzheimer's Disease

F. Lopera, B. Puig, I. Ferrer, 2011, Brain pathology.

Familial Alzheimer's disease-associated presenilin-1 alters cerebellar activity and calcium homeostasis.

I. Ferrer, C. D. De Zeeuw, F. Lopera, 2014, The Journal of clinical investigation.

Differential Pattern of Phospholipid Profile in the Temporal Cortex from E280A-Familiar and Sporadic Alzheimer's Disease Brains.

J. D. Arias-Londoño, F. Lopera, A. Villegas, 2017, Journal of Alzheimer's disease : JAD.

The Colombian–German network for neurodegenerative research: UndoAD

M. Glatzel, A. Villegas, D. Sepulveda-Falla, 2019, The Lancet Neurology.

Apolipoprotein Eepsilon4 modifies Alzheimer's disease onset in an E280A PS1 kindred.

G. Bedoya, A. Goate, K. Kosik, 2003, Annals of neurology.

Resilience to autosomal dominant Alzheimer’s disease in a Reelin-COLBOS heterozygous man

Justin S. Sanchez, Keith A. Johnson, R. Sperling, 2023, Nature Medicine.

Phospho‐tau217 and phospho‐tau181 in plasma and CSF as biomarkers for Alzheimer’s disease

K. Blennow, Yi Su, E. Reiman, 2020, Alzheimer's & Dementia.

C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke

M. Frosch, F. Lopera, R. Betensky, 2002, Neurology.

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.

F. Lopera, A. Villegas, M. Arcos-Burgos, 2019, Stem cell research.

Familial Alzheimer's disease-associated presenilin-1 alters cerebellar activity and calcium homeostasis.

I. Ferrer, C. D. De Zeeuw, F. Lopera, 2014, The Journal of clinical investigation.

Characterization of the Handwriting Skills as a Biomarker for Parkinson’s Disease

Jesús Francisco Vargas-Bonilla, Juan R. Orozco-Arroyave, Julian Fiérrez, 2019, 2019 14th IEEE International Conference on Automatic Face & Gesture Recognition (FG 2019).