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INFECTION OF HUMAN OLFACTORY EPITHELIUM WITH ALPHAHERPESVIRUS ELICITS EXPRESSION OF BETA AMYLOID

IBRO neuroscience reports, 2023-10, Vol.15, p.S484-S484

2023

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Mutations in SORL1 and MTHFDL1 possibly contribute to the development of Alzheimer’s disease in a multigenerational Colombian Family

PloS one, 2022-07, Vol.17 (7), p.e0269955

2022

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First identification and characterization of ovine gammaherpesvirus type 2 in horses and artiodactyla from an outbreak of malignant catarrhal fever in Mexico

PloS one, 2023-09, Vol.18 (9), p.e0290309

2023

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Substance Use-Related Cognitive Decline in Families with Autosomal Dominant Alzheimer's Disease: A Cohort Study

Journal of Alzheimer's disease, 2022-01, Vol.85 (4), p.1423-1439

2022

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Comparison of hemagglutination inhibition tests, immunoperoxidase monolayer assays, and serum neutralizing tests in detecting antibodies against blue eye disease in pigs

Journal of immunological methods, 2021-09, Vol.496, p.113088-113088, Article 113088

2021

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Assessment of the hemagglutinating activity of the Porcine orthorubulavirus

Comparative immunology, microbiology and infectious diseases, 2022-01, Vol.80, p.101736-101736, Article 101736

2022

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Social sustainability, poverty and income: An empirical exploration

Journal of international development, 2024-04, Vol.36 (3), p.1789-1816

2024

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The E280A presenilin 1 Alzheimer mutation produces increased Aβ42 deposition and severe cerebellar pathology

Nature medicine, 1996-10, Vol.2 (10), p.1146-1150

1996

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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, 2014-06, Vol.75 (6), p.652-660

2014

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Exposure to Climatic Risks and Social Sustainability in Vietnam

Sustainability, 2023-02, Vol.15 (4), p.3260

2023

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Genetic origin of a large family with a novel PSEN1 mutation (Ile416Thr)

Alzheimer's & dementia, 2019-05, Vol.15 (5), p.709-719

2019

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Homozygosity of the autosomal dominant Alzheimer disease presenilin 1 E280A mutation

Neurology, 2015-01, Vol.84 (2), p.206-208

2015

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Signatures for viral infection and inflammation in the proximal olfactory system in familial Alzheimer's disease

Neurobiology of aging, 2023-03, Vol.123, p.75-82

2023

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Palliative care in Autosomal Dominant Alzheimer’s disease due to PSEN1‐E280A genetic variant in Colombia

Alzheimer's & dementia, 2023-12, Vol.19 (S24), p.n/a

2023

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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, 2019-07, p.1-10

2019

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Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279 Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings

Molecular neurobiology, 2022-06, Vol.59 (6), p.3845-3858

2022

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APOE3 Christchurch Heterozygosity and Autosomal Dominant Alzheimer’s Disease

The New England journal of medicine, 2024-06, Vol.390 (23), p.2156-2164

2024

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APOE3 Christchurch heterozygosity delays clinical onset in autosomal dominant Alzheimer’s disease

Alzheimer's & dementia, 2023-12, Vol.19 (S12), p.n/a

2023

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Quality of life in early-onset Alzheimer’s disease due to a PSEN1-E280A mutation

Neurological sciences, 2021-11, Vol.42 (11), p.4637-4645

2021

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Equity in Education Expenditure in Thailand

Development policy review, 2014-03, Vol.32 (2), p.239-258

2014

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Correction to: Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279 Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings

Molecular neurobiology, 2022-06, Vol.59 (6), p.3859-3859

2022

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Strategies for activity maintenance in patient and family care and clinical trial adherence of GNA social plan in context of COVID‐19 health emergency

Alzheimer's & dementia, 2021-12, Vol.17 (S7), p.e053105-n/a

2021

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Psychological status in the participants of the API ADAD Colombia trial assisted by a comprehensive mental health program during COVID 19 pandemic

Alzheimer's & dementia, 2021-12, Vol.17 (S10), p.n/a

2021

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INFECTION OF HUMAN OLFACTORY EPITHELIUM WITH ALPHAHERPESVIRUS ELICITS EXPRESSION OF BETA AMYLOID

Mutations in SORL1 and MTHFDL1 possibly contribute to the development of Alzheimer’s disease in a multigenerational Colombian Family

First identification and characterization of ovine gammaherpesvirus type 2 in horses and artiodactyla from an outbreak of malignant catarrhal fever in Mexico

Substance Use-Related Cognitive Decline in Families with Autosomal Dominant Alzheimer's Disease: A Cohort Study

Comparison of hemagglutination inhibition tests, immunoperoxidase monolayer assays, and serum neutralizing tests in detecting antibodies against blue eye disease in pigs

Assessment of the hemagglutinating activity of the Porcine orthorubulavirus

Social sustainability, poverty and income: An empirical exploration

The E280A presenilin 1 Alzheimer mutation produces increased Aβ42 deposition and severe cerebellar pathology

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

Exposure to Climatic Risks and Social Sustainability in Vietnam

Primary lateral sclerosis associated with PSEN1 Pro284Leu variant in a Colombian family: Clinical and neuropathological features

Genetic origin of a large family with a novel PSEN1 mutation (Ile416Thr)

A neurodegenerative disease landscape of rare mutations in Colombia due to founder effects

Homozygosity of the autosomal dominant Alzheimer disease presenilin 1 E280A mutation

Signatures for viral infection and inflammation in the proximal olfactory system in familial Alzheimer's disease

Palliative care in Autosomal Dominant Alzheimer’s disease due to PSEN1‐E280A genetic variant in Colombia

Mental Disorders in Young Adults from Families with the Presenilin-1 Gene Mutation E280A in the Preclinical Stage of Alzheimer’s Disease

Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279 Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings

APOE3 Christchurch Heterozygosity and Autosomal Dominant Alzheimer’s Disease

APOE3 Christchurch heterozygosity delays clinical onset in autosomal dominant Alzheimer’s disease

Quality of life in early-onset Alzheimer’s disease due to a PSEN1-E280A mutation

Equity in Education Expenditure in Thailand

Correction to: Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279 Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings

Strategies for activity maintenance in patient and family care and clinical trial adherence of GNA social plan in context of COVID‐19 health emergency

Psychological status in the participants of the API ADAD Colombia trial assisted by a comprehensive mental health program during COVID 19 pandemic

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