Age at onset of alzheimer disease. Medical search. Frequent questions

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Anatomy21

Brain Neurofibrillary Tangles Neurofibrils Hippocampus Cerebral Cortex Neurons Substantia Innominata Lewy Bodies Temporal Lobe Neuropil Threads Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 21 Nerve Fibers, Myelinated CA2 Region, Hippocampal Frontal Lobe Entorhinal Cortex Microglia Astrocytes PC12 Cells Cells, Cultured Cerebral Ventricles

Organisms1

Mice, Transgenic

Diseases48

Alzheimer Disease Plaque, Amyloid Dementia Atrophy Genetic Predisposition to Disease Huntington Disease Dementia, Vascular Disease Progression Prodromal Symptoms Parkinson Disease Frontotemporal Dementia Lewy Body Disease Anticipation, Genetic Spinocerebellar Degenerations Memory Disorders Cerebral Amyloid Angiopathy Disease Models, Animal Nerve Degeneration Diabetes Mellitus, Type 1 Cerebellar Ataxia Neurodegenerative Diseases Tauopathies Down Syndrome Amnesia Psychomotor Agitation Machado-Joseph Disease Marijuana Abuse Epilepsy Parkinsonian Disorders Spinocerebellar Ataxias Dystonia Kluver-Bucy Syndrome Frontotemporal Lobar Degeneration Amyloidosis Alcoholism Recurrence Multiple Sclerosis Legg-Calve-Perthes Disease Postmortem Changes Arthritis, Juvenile Epilepsies, Partial Spastic Paraplegia, Hereditary Syndrome Cerebrovascular Disorders Deafness Gliosis Epilepsy, Temporal Lobe Diseases in Twins

Chemicals and Drugs46

Amyloid beta-Peptides tau Proteins Apolipoprotein E4 Amyloid beta-Protein Precursor Amyloid Precursor Protein Secretases Presenilin-1 Apolipoproteins E Amyloid Presenilin-2 Peptide Fragments Memantine Presenilins Aspartic Acid Endopeptidases Aniline Compounds Cholinesterase Inhibitors Nerve Tissue Proteins Biological Markers Amyloidogenic Proteins Protease Nexins Phenylcarbamates Genetic Markers Nootropic Agents Indans Clioquinol Thiazoles Apolipoprotein E3 Insulysin Tacrine Membrane Proteins Monomeric Clathrin Assembly Proteins Apolipoprotein E2 Galantamine Benzothiazoles Neurocalcin Prions LDL-Receptor Related Proteins Glycogen Synthase Kinase 3 Cyclin-Dependent Kinase 5 Clusterin Microtubule-Associated Proteins PrPC Proteins Aluminum Caspase 6 Anticonvulsants Alzheimer Vaccines Fluorodeoxyglucose F18

Analytical, Diagnostic and Therapeutic Techniques and Equipment51

Pedigree Magnetic Resonance Imaging Risk Factors Cohort Studies Prodromal Symptoms Longitudinal Studies Retrospective Studies Severity of Illness Index Follow-Up Studies Case-Control Studies Genetic Testing DNA Mutational Analysis Autopsy Disease Models, Animal Prospective Studies Incidence Genetic Association Studies Positron-Emission Tomography Prognosis Risk Prevalence Treatment Outcome Analysis of Variance Chromosome Mapping Statistics, Nonparametric Predictive Value of Tests Models, Genetic Proportional Hazards Models Reference Values Odds Ratio Chi-Square Distribution Genome-Wide Association Study Logistic Models Regression Analysis Models, Biological Cross-Sectional Studies Registries Questionnaires Heterozygote Detection Electroencephalography Early Diagnosis Reproducibility of Results Polymerase Chain Reaction Immunohistochemistry Statistics as Topic Risk Assessment Psychosurgery Sensitivity and Specificity Confidence Intervals Linear Models Multivariate Analysis

Psychiatry and Psychology36

Alzheimer Disease Cognition Disorders Dementia Neuropsychological Tests Huntington Disease Dementia, Vascular Mild Cognitive Impairment Cognition Mental Status Schedule Frontotemporal Dementia Lewy Body Disease Psychiatric Status Rating Scales Family Memory Disorders Schizophrenia, Catatonic Cognitive Reserve Psychotic Disorders Schizophrenia, Disorganized Schizophrenia Amnesia Schizophrenia, Childhood Nuclear Family Psychomotor Agitation Fathers Marijuana Abuse Memory Schizophrenia, Paranoid Schizophrenic Psychology Kluver-Bucy Syndrome Frontotemporal Lobar Degeneration Alcoholism Bipolar Disorder Psychosurgery Maze Learning Mothers Siblings

Phenomena and Processes45

Genetic Predisposition to Disease Genotype Alleles Aging Mutation Trinucleotide Repeats Time Factors Genetic Linkage Phenotype Gene Frequency Lod Score Anticipation, Genetic Polymorphism, Single Nucleotide DNA Repeat Expansion Genetic Heterogeneity Heterozygote Polymorphism, Genetic Penetrance Paternal Age Brain Chemistry Genes, Dominant Haplotypes Genetic Markers Risk Puberty Odds Ratio Menarche Chi-Square Distribution Homozygote Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 21 Phosphorylation Point Mutation Linkage Disequilibrium Genetic Variation Mutation, Missense Amino Acid Sequence Sensitivity and Specificity Microsatellite Repeats Oxidative Stress Founder Effect Protein Binding Base Sequence Trinucleotide Repeat Expansion Genes, Recessive

Disciplines and Occupations3

Genetic Counseling Immunohistochemistry Statistics as Topic

Anthropology, Education, Sociology and Social Phenomena10

Family National Institute on Aging (U.S.)Autopsy Nuclear Family Fathers Age Distribution Sex Distribution Demography Mothers Siblings

Information Science9

Incidence Prevalence Molecular Sequence Data Diagnostic and Statistical Manual of Mental Disorders Registries Questionnaires Image Processing, Computer-Assisted Amino Acid Sequence Base Sequence

Named Groups7

Infant, Newborn Fathers European Continental Ancestry Group Caregivers Mothers Siblings Jews

Health Care44

Age of Onset Age Factors Risk Factors Family Health Cohort Studies Longitudinal Studies Retrospective Studies Severity of Illness Index Follow-Up Studies Case-Control Studies Sex Factors Genetic Testing National Institute on Aging (U.S.)Prospective Studies Precipitating Factors Incidence Risk Prevalence Treatment Outcome Analysis of Variance Statistics, Nonparametric Predictive Value of Tests Proportional Hazards Models Comorbidity Odds Ratio Chi-Square Distribution Genome-Wide Association Study Age Distribution Logistic Models Regression Analysis Genetic Counseling Cross-Sectional Studies Registries Sex Distribution Questionnaires Reproducibility of Results Caregivers Statistics as Topic Risk Assessment Sensitivity and Specificity Confidence Intervals Linear Models Demography Multivariate Analysis

Geographicals10

Sweden United States Italy Norway Japan France Finland Dominican Republic Caribbean Region Portugal

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

Alzheimer Disease Age of Onset Amyloid beta-Peptides tau Proteins Apolipoprotein E4 Amyloid beta-Protein Precursor Brain Neurofibrillary Tangles Plaque, Amyloid Cognition Disorders Dementia Atrophy Age Factors Neuropsychological Tests Amyloid Precursor Protein Secretases Genetic Predisposition to Disease Presenilin-1 Huntington Disease Apolipoproteins E Genotype Amyloid Pedigree Dementia, Vascular Magnetic Resonance Imaging Risk Factors Neurofibrils Disease Progression Mild Cognitive Impairment Family Health Cohort Studies Prodromal Symptoms Alleles Aging Mutation Longitudinal Studies Retrospective Studies Trinucleotide Repeats Parkinson Disease Presenilin-2 Severity of Illness Index Peptide Fragments Time Factors Cognition Follow-Up Studies Case-Control Studies Hippocampus Mental Status Schedule Genetic Linkage Sex Factors Frontotemporal Dementia Phenotype Lewy Body Disease Gene Frequency Memantine Presenilins Cerebral Cortex Lod Score Genetic Testing Neurons Anticipation, Genetic Aspartic Acid Endopeptidases Polymorphism, Single Nucleotide Mice, Transgenic Psychiatric Status Rating Scales Aniline Compounds Cholinesterase Inhibitors Family Spinocerebellar Degenerations DNA Repeat Expansion National Institute on Aging (U.S.)Memory Disorders Genetic Heterogeneity Substantia Innominata DNA Mutational Analysis Nerve Tissue Proteins Heterozygote Autopsy Biological Markers Cerebral Amyloid Angiopathy Disease Models, Animal Polymorphism, Genetic Prospective Studies Schizophrenia, Catatonic Penetrance Precipitating Factors Incidence Amyloidogenic Proteins Cognitive Reserve Paternal Age Genetic Association Studies Brain Chemistry Psychotic Disorders Nerve Degeneration Positron-Emission Tomography Diabetes Mellitus, Type 1 Cerebellar Ataxia Protease Nexins Genes, Dominant Neurodegenerative Diseases Phenylcarbamates

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