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Publications by David S. Geldmacher
Clinical, Imaging, Pathological, and Biochemical Characterization of a Novel Presenilin 1 Mutation (N135Y) Causing Alzheimer's Disease
Neurobiology of Aging
Aging
Gerontology
Developmental Biology
Geriatrics
Neuroscience
Neurology
Characterizing Cognitive Aging in Humans With Links to Animal Models
Frontiers in Aging Neuroscience
Aging
Cognitive Neuroscience
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Novel Presenilin 1 Mutation (S170F) Causing Alzheimer Disease With Lewy Bodies in the Third Decade of Life
Archives of Neurology
A Novel Germline CDKN1B Mutation Causing Multiple Endocrine Tumors: Clinical, Genetic and Functional Characterization
Human Mutation
Genetics
Transcriptional Regulation of the Presenilin-1 Gene: Implication in Alzheimer's Disease
Frontiers in Bioscience - Landmark
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
Variant Alzheimer Disease With Spastic Paraparesis: A Rare Presenilin-1 Mutation
Canadian Journal of Neurological Sciences
Medicine
Neurology
Homozygosity of the Autosomal Dominant Alzheimer Disease Presenilin 1 E280A Mutation
Neurology
Neurology
Prevalence and Clinical Correlates of Pathological Affective Display in Alzheimer's Disease.
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Alzheimer's Disease-Like Alterations in Peripheral Cells From Presenilin-1 Transgenic Mice
Neurobiology of Disease
Neurology
Alzheimer's Disease Neuroimaging Initiative (ADNI): Clinical Characterization
Neurology
Neurology
A Patient With Posterior Cortical Atrophy Possesses a Novel Mutation in the Presenilin 1 Gene
PLoS ONE
Multidisciplinary