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Publications by M. L. Arcila

Homozygosity of the Autosomal Dominant Alzheimer Disease Presenilin 1 E280A Mutation

English

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Phenotypic Variability in Autosomal Dominant Familial Alzheimer Disease Due to the S170F Mutation of Presenilin-1

Neurodegenerative Diseases

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Variant Alzheimer Disease With Spastic Paraparesis: A Rare Presenilin-1 Mutation

Canadian Journal of Neurological Sciences

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Cortical Microstructural Correlates of Astrocytosis in Autosomal Dominant Alzheimer Disease

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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 Reports

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Novel Presenilin 1 Mutation (S170F) Causing Alzheimer Disease With Lewy Bodies in the Third Decade of Life

Archives of Neurology

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Wide Range of Disease Onset in a Family With Alzheimer Disease and a His163Tyr Mutation in the Presenilin-1 Gene

Archives of Neurology

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Alzheimer Disease: Presenilin Springs a Leak

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Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation

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Formation of Tau Inclusions in Knock-In Mice With Familial Alzheimer Disease (FAD) Mutation of Presenilin 1 (PS1)

Journal of Biological Chemistry

Molecular Biology

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