The Journal of Nuclear Medicine, ISSN 0161-5505, 07/2018, Volume 59, Issue 7, p. 1104
Accurate amyloid PET quantification is necessary for monitoring amyloid-β accumulation and response to therapy. Currently, most of the studies are analyzed...
Computer simulation | Radioactive tracers | Blood | Blood flow | Image acquisition | Interpolation | Windows (intervals) | Simulation | Cerebral blood flow | Correlation analysis | Dementia disorders | Amyloid | Longitudinal studies | Modelling | Kinetics | Validation studies
Computer simulation | Radioactive tracers | Blood | Blood flow | Image acquisition | Interpolation | Windows (intervals) | Simulation | Cerebral blood flow | Correlation analysis | Dementia disorders | Amyloid | Longitudinal studies | Modelling | Kinetics | Validation studies
Journal Article
The Journal of Nuclear Medicine, ISSN 0161-5505, 05/2017, Volume 58, p. 559
Objectives: A common quantitative output value for Aβ imaging across tracers and methods will improve clinical and research use. A method has recently been...
Cerebellum | Elderly people | Neuroimaging | Brain | Nuclear medicine | Transformation | Pons | Cognitive ability | Older people | Tomography | Dementia disorders | Alzheimer's disease | Medical imaging | Neurodegenerative diseases | Cortex | Positron emission | Data processing | Fluorine isotopes | Injection | Disease control | Scaling | Alzheimers disease | Frontotemporal dementia | Elderly | Geriatrics | Tracers
Cerebellum | Elderly people | Neuroimaging | Brain | Nuclear medicine | Transformation | Pons | Cognitive ability | Older people | Tomography | Dementia disorders | Alzheimer's disease | Medical imaging | Neurodegenerative diseases | Cortex | Positron emission | Data processing | Fluorine isotopes | Injection | Disease control | Scaling | Alzheimers disease | Frontotemporal dementia | Elderly | Geriatrics | Tracers
Journal Article
3.
Optimal Reference Region to Measure Longitudinal Amyloid-ß Change with ^sup 18^F-Florbetaben PET
The Journal of Nuclear Medicine, ISSN 0161-5505, 08/2017, Volume 58, Issue 8, p. 1300
Accurate measurement of changes in amyloid-β (Aβ) deposition over time is important in longitudinal studies, particularly in anti-Aβ therapeutic trials. To...
Measurement | Cerebellum | Pons | Medical imaging | Segmentation | Image processing | Change detection | Medical treatment | Cognitive ability | Cortex | Positron emission | Clinical trials | Substantia alba | Substantia grisea | Accumulation | Image segmentation | Magnetic resonance imaging | Correlation analysis | Tomography | Amyloid | Longitudinal studies | Deposition
Measurement | Cerebellum | Pons | Medical imaging | Segmentation | Image processing | Change detection | Medical treatment | Cognitive ability | Cortex | Positron emission | Clinical trials | Substantia alba | Substantia grisea | Accumulation | Image segmentation | Magnetic resonance imaging | Correlation analysis | Tomography | Amyloid | Longitudinal studies | Deposition
Journal Article
The Journal of Nuclear Medicine, ISSN 0161-5505, 05/2017, Volume 58, p. 1253
Objectives: The brain's glymphatic system is implicated in the clearance of toxic waste products such as amyloid-beta peptide (Aβ) x- is more active during...
Cerebellum | Brain | Nuclear medicine | Correlation coefficients | Scanners | Radioactive tracers | Cerebrospinal fluid | Accumulation | Sleep deprivation | Wakefulness | Older people | Aging | Tomography | Alzheimer's disease | Age | Binding | Deprivation | Statistical analysis | Positron emission | Toxic wastes | Cells | Image segmentation | Sleep | Body size | Biomarkers | Alzheimers disease
Cerebellum | Brain | Nuclear medicine | Correlation coefficients | Scanners | Radioactive tracers | Cerebrospinal fluid | Accumulation | Sleep deprivation | Wakefulness | Older people | Aging | Tomography | Alzheimer's disease | Age | Binding | Deprivation | Statistical analysis | Positron emission | Toxic wastes | Cells | Image segmentation | Sleep | Body size | Biomarkers | Alzheimers disease
Journal Article
European Journal of Nuclear Medicine and Molecular Imaging, ISSN 1619-7070, 05/2009, Volume 36, Issue 5, pp. 811 - 822
We report the first clinicopathological series of longitudinal FDG-PET scans in post-mortem (PM) verified cognitively normal elderly (NL) followed to the onset...
FDG-PET | Alzheimer's disease | Positron emission tomography | Early detection | Dementia | TOMOGRAPHY | DIAGNOSIS | CONVERSION | IMPAIRMENT | PREDICTION | MCI | DETERIORATION | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Dementia, Vascular - diagnostic imaging | Cognition Disorders - diagnostic imaging | Humans | Male | Positron-Emission Tomography - methods | Alzheimer Disease - diagnosis | Brain - metabolism | Lewy Body Disease - metabolism | Cognition Disorders - diagnosis | Hippocampus - metabolism | Dementia, Vascular - diagnosis | Autopsy | Aged, 80 and over | Glucose - metabolism | Female | Aged | Fluorodeoxyglucose F18 - pharmacology | Alzheimer Disease - diagnostic imaging | Medical colleges | Brain | Glucose metabolism | PET imaging | Physiological aspects | Development and progression | Glucose | Dextrose | Nuclear medicine | Neurobiology | Tomography | Alzheimers disease | Medical diagnosis | Metabolism
FDG-PET | Alzheimer's disease | Positron emission tomography | Early detection | Dementia | TOMOGRAPHY | DIAGNOSIS | CONVERSION | IMPAIRMENT | PREDICTION | MCI | DETERIORATION | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Dementia, Vascular - diagnostic imaging | Cognition Disorders - diagnostic imaging | Humans | Male | Positron-Emission Tomography - methods | Alzheimer Disease - diagnosis | Brain - metabolism | Lewy Body Disease - metabolism | Cognition Disorders - diagnosis | Hippocampus - metabolism | Dementia, Vascular - diagnosis | Autopsy | Aged, 80 and over | Glucose - metabolism | Female | Aged | Fluorodeoxyglucose F18 - pharmacology | Alzheimer Disease - diagnostic imaging | Medical colleges | Brain | Glucose metabolism | PET imaging | Physiological aspects | Development and progression | Glucose | Dextrose | Nuclear medicine | Neurobiology | Tomography | Alzheimers disease | Medical diagnosis | Metabolism
Journal Article
1994, ISBN 9780805813654, xiii, 247
Application of analytic discourse techniques to clinical practice is relatively recent. This book's contributors begin with the notion that systematic...
Brain damage | Discourse analysis | Language | Patients | Rome
Brain damage | Discourse analysis | Language | Patients | Rome
Book
Nature Communications, ISSN 2041-1723, 10/2018, Volume 9, Issue 1, pp. 4273 - 16
textabstractThe heterogeneity of neurodegenerative diseases is a key confound to disease understanding and treatment development, as study cohorts typically...
COGNITIVE DECLINE | REPEAT EXPANSIONS | DEMENTIA | DEFINED SUBTYPES | MULTIDISCIPLINARY SCIENCES | SPORADIC ALZHEIMERS-DISEASE | ATROPHY PATTERNS | BIOMARKER CHANGES | MODEL | FRONTOTEMPORAL LOBAR DEGENERATION | HUNTINGTONS-DISEASE | Frontotemporal Dementia - genetics | Phenotype | Reproducibility of Results | Neurodegenerative Diseases - pathology | Time Factors | Humans | Genotype | Models, Neurological | Alzheimer Disease - genetics | Alzheimer Disease - pathology | Frontotemporal Dementia - pathology | Neurodegenerative Diseases - classification | Phenotypes | Medical imaging | Disease | Neurodegenerative diseases | Medical treatment | Inference | Trajectories | Patients | Subgroups | Complexity | Diseases | Neurological diseases | Heterogeneity | Learning algorithms | Neurodegeneration | Machine learning | Dementia disorders | Diagnostic systems | Frontotemporal dementia | Genotypes
COGNITIVE DECLINE | REPEAT EXPANSIONS | DEMENTIA | DEFINED SUBTYPES | MULTIDISCIPLINARY SCIENCES | SPORADIC ALZHEIMERS-DISEASE | ATROPHY PATTERNS | BIOMARKER CHANGES | MODEL | FRONTOTEMPORAL LOBAR DEGENERATION | HUNTINGTONS-DISEASE | Frontotemporal Dementia - genetics | Phenotype | Reproducibility of Results | Neurodegenerative Diseases - pathology | Time Factors | Humans | Genotype | Models, Neurological | Alzheimer Disease - genetics | Alzheimer Disease - pathology | Frontotemporal Dementia - pathology | Neurodegenerative Diseases - classification | Phenotypes | Medical imaging | Disease | Neurodegenerative diseases | Medical treatment | Inference | Trajectories | Patients | Subgroups | Complexity | Diseases | Neurological diseases | Heterogeneity | Learning algorithms | Neurodegeneration | Machine learning | Dementia disorders | Diagnostic systems | Frontotemporal dementia | Genotypes
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2007, Volume 104, Issue 48, pp. 19067 - 19072
Having a parent affected with late-onset Alzheimer's disease (AD) is a risk factor for developing AD among cognitively normal subjects. We examined whether...
Neurology | Parents | Predisposing factors | Parietal lobe | Mitochondrial DNA | Alzheimers disease | Family history | Positron emission tomography | Genotypes | Dementia | FDG-PET | POSTERIOR CINGULATE CORTEX | MCI | POSITRON-EMISSION-TOMOGRAPHY | DEMENTIA | GENETIC RISK | ABNORMALITIES | MULTIDISCIPLINARY SCIENCES | HYPOMETABOLISM | MILD COGNITIVE IMPAIRMENT | PREDICTION | Fluorodeoxyglucose F18 - pharmacokinetics | Genomic Imprinting | Apolipoprotein E4 - genetics | Humans | Middle Aged | Male | Risk | Positron-Emission Tomography | Mothers | Cerebral Cortex - metabolism | Fluorine Radioisotopes - pharmacokinetics | Aged, 80 and over | Alzheimer Disease - epidemiology | Female | Retrospective Studies | Genetic Predisposition to Disease | Genes, Mitochondrial | Cerebral Cortex - diagnostic imaging | Genetic Heterogeneity | Magnetic Resonance Imaging | Alzheimer Disease - metabolism | Brain Mapping | Glucose - metabolism | Aged | Alzheimer Disease - diagnostic imaging | Alzheimer Disease - genetics | Glucose metabolism | Research | Genetic susceptibility | Alzheimer's disease | Health aspects | Risk factors | Biological Sciences
Neurology | Parents | Predisposing factors | Parietal lobe | Mitochondrial DNA | Alzheimers disease | Family history | Positron emission tomography | Genotypes | Dementia | FDG-PET | POSTERIOR CINGULATE CORTEX | MCI | POSITRON-EMISSION-TOMOGRAPHY | DEMENTIA | GENETIC RISK | ABNORMALITIES | MULTIDISCIPLINARY SCIENCES | HYPOMETABOLISM | MILD COGNITIVE IMPAIRMENT | PREDICTION | Fluorodeoxyglucose F18 - pharmacokinetics | Genomic Imprinting | Apolipoprotein E4 - genetics | Humans | Middle Aged | Male | Risk | Positron-Emission Tomography | Mothers | Cerebral Cortex - metabolism | Fluorine Radioisotopes - pharmacokinetics | Aged, 80 and over | Alzheimer Disease - epidemiology | Female | Retrospective Studies | Genetic Predisposition to Disease | Genes, Mitochondrial | Cerebral Cortex - diagnostic imaging | Genetic Heterogeneity | Magnetic Resonance Imaging | Alzheimer Disease - metabolism | Brain Mapping | Glucose - metabolism | Aged | Alzheimer Disease - diagnostic imaging | Alzheimer Disease - genetics | Glucose metabolism | Research | Genetic susceptibility | Alzheimer's disease | Health aspects | Risk factors | Biological Sciences
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2013, Volume 110, Issue 12, pp. 4768 - 4773
Aberrant connectivity is implicated in many neurological and psychiatric disorders, including Alzheimer's disease and schizophrenia. However, other than a few...
Neuroimaging | Quantitative genetics | Medical genetics | Connectivity | P values | Alzheimers disease | Twins | Connected regions | Human genetics | Dementia | Graph theory | Neuroimaging genetics | Multiple comparisons correction | HARDI tractography | Diffusion tensor imaging | COMMON VARIANTS | graph theory | multiple comparisons correction | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | NETWORKS | neuroimaging genetics | AMYLOID PRECURSOR PROTEIN | BETA | ORGANIZATION | FLOOR PLATE | F-SPONDIN | diffusion tensor imaging | ASSOCIATION | BRAIN | Autistic Disorder - genetics | Severity of Illness Index | Brain - diagnostic imaging | Genome-Wide Association Study | Autistic Disorder - physiopathology | Brain - physiopathology | Extracellular Matrix Proteins - genetics | Humans | Twins, Dizygotic | Endosomal Sorting Complexes Required for Transport - genetics | Male | Ubiquitin-Conjugating Enzymes - genetics | Chromosomes, Human, Pair 11 - genetics | Twins, Monozygotic | Genetic Variation | Radiography | Magnetic Resonance Imaging | Adult | Female | Nedd4 Ubiquitin Protein Ligases | Alzheimer Disease - genetics | Ubiquitin-Protein Ligases - genetics | Autistic Disorder - diagnostic imaging | Genetic research | Genetic aspects | Mental illness | Methods | Biological Sciences
Neuroimaging | Quantitative genetics | Medical genetics | Connectivity | P values | Alzheimers disease | Twins | Connected regions | Human genetics | Dementia | Graph theory | Neuroimaging genetics | Multiple comparisons correction | HARDI tractography | Diffusion tensor imaging | COMMON VARIANTS | graph theory | multiple comparisons correction | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | NETWORKS | neuroimaging genetics | AMYLOID PRECURSOR PROTEIN | BETA | ORGANIZATION | FLOOR PLATE | F-SPONDIN | diffusion tensor imaging | ASSOCIATION | BRAIN | Autistic Disorder - genetics | Severity of Illness Index | Brain - diagnostic imaging | Genome-Wide Association Study | Autistic Disorder - physiopathology | Brain - physiopathology | Extracellular Matrix Proteins - genetics | Humans | Twins, Dizygotic | Endosomal Sorting Complexes Required for Transport - genetics | Male | Ubiquitin-Conjugating Enzymes - genetics | Chromosomes, Human, Pair 11 - genetics | Twins, Monozygotic | Genetic Variation | Radiography | Magnetic Resonance Imaging | Adult | Female | Nedd4 Ubiquitin Protein Ligases | Alzheimer Disease - genetics | Ubiquitin-Protein Ligases - genetics | Autistic Disorder - diagnostic imaging | Genetic research | Genetic aspects | Mental illness | Methods | Biological Sciences
Journal Article
European Journal of Nuclear Medicine and Molecular Imaging, ISSN 1619-7070, 11/2017, Volume 44, Issue 12, pp. 2053 - 2059
PurposeThe Centiloid (CL) method enables quantitative values from Aβ-amyloid (Aβ) imaging to be expressed in a universal unit providing pathological,...
Florbetaben | Alzheimer’s disease | Centiloid | Amyloid imaging | Standardization | Cerebellum | Binding | Neuroimaging | Neurodegenerative diseases | Positron emission | Image acquisition | Magnetic resonance imaging | β-Amyloid | Tomography | Diagnostic systems | Mathematical models | Alzheimer's disease | Tracers
Florbetaben | Alzheimer’s disease | Centiloid | Amyloid imaging | Standardization | Cerebellum | Binding | Neuroimaging | Neurodegenerative diseases | Positron emission | Image acquisition | Magnetic resonance imaging | β-Amyloid | Tomography | Diagnostic systems | Mathematical models | Alzheimer's disease | Tracers
Journal Article
Anesthesiology, ISSN 0003-3022, 03/2012, Volume 116, Issue 3, pp. 603 - 612
Background: Structural magnetic resonance imaging is used to longitudinally monitor the progression of Alzheimer disease from its presymptomatic to symptomatic...
WHITE-MATTER | NONCARDIAC SURGERY | ALZHEIMERS-DISEASE | HIPPOCAMPAL | GREY-MATTER | ADULTS | ANESTHESIOLOGY | DYSFUNCTION | DECLINE | PREDICTION | Follow-Up Studies | Humans | Middle Aged | Male | Cognitive Dysfunction - pathology | Atrophy | Postoperative Complications - psychology | Aged, 80 and over | Brain - pathology | Cognition - physiology | Cognitive Dysfunction - psychology | Female | Aged | Cohort Studies | Databases, Factual | Postoperative Complications - pathology
WHITE-MATTER | NONCARDIAC SURGERY | ALZHEIMERS-DISEASE | HIPPOCAMPAL | GREY-MATTER | ADULTS | ANESTHESIOLOGY | DYSFUNCTION | DECLINE | PREDICTION | Follow-Up Studies | Humans | Middle Aged | Male | Cognitive Dysfunction - pathology | Atrophy | Postoperative Complications - psychology | Aged, 80 and over | Brain - pathology | Cognition - physiology | Cognitive Dysfunction - psychology | Female | Aged | Cohort Studies | Databases, Factual | Postoperative Complications - pathology
Journal Article
Nature Communications, ISSN 2041-1723, 12/2019, Volume 10, Issue 1, pp. 1766 - 12
The single nucleotide polymorphism (SNP) rs744373 in the bridging integrator-1 gene (BIN1) is a risk factor for Alzheimer's disease (AD). In the brain, BIN1 is...
COGNITIVE RESERVE | PROTEIN | CONNECTIVITY | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | RISK | NEURODEGENERATION | PATHOLOGY | BRAIN | DECLINE | Brain - diagnostic imaging | Humans | Memory | Risk Factors | tau Proteins - metabolism | Male | Cognition | Positron-Emission Tomography | Genetic Variation | Magnetic Resonance Imaging | Endocytosis | Tumor Suppressor Proteins - genetics | Adaptor Proteins, Signal Transducing - genetics | Alleles | Alzheimer Disease - metabolism | Aged, 80 and over | Cytoskeleton - metabolism | Female | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Nuclear Proteins - genetics | Brain | Cognitive ability | Health risks | Single-nucleotide polymorphism | Risk analysis | Gene polymorphism | Risk factors | Pathology | Tau protein | Autopsy | Dementia disorders | β-Amyloid | Cytoskeleton | Positron emission tomography | Alzheimer's disease | Polymorphism
COGNITIVE RESERVE | PROTEIN | CONNECTIVITY | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | RISK | NEURODEGENERATION | PATHOLOGY | BRAIN | DECLINE | Brain - diagnostic imaging | Humans | Memory | Risk Factors | tau Proteins - metabolism | Male | Cognition | Positron-Emission Tomography | Genetic Variation | Magnetic Resonance Imaging | Endocytosis | Tumor Suppressor Proteins - genetics | Adaptor Proteins, Signal Transducing - genetics | Alleles | Alzheimer Disease - metabolism | Aged, 80 and over | Cytoskeleton - metabolism | Female | Aged | Polymorphism, Single Nucleotide | Alzheimer Disease - genetics | Nuclear Proteins - genetics | Brain | Cognitive ability | Health risks | Single-nucleotide polymorphism | Risk analysis | Gene polymorphism | Risk factors | Pathology | Tau protein | Autopsy | Dementia disorders | β-Amyloid | Cytoskeleton | Positron emission tomography | Alzheimer's disease | Polymorphism
Journal Article
06/2013, ISBN 9781138876408, 264
Application of analytic discourse techniques to clinical practice is relatively recent. This book's contributors begin with the notion that systematic...
Psychiatry & Clinical Psychology - Adult | Language, Psychology of | Clinical Neuropsychology | Brain damage | Discourse analysis
Psychiatry & Clinical Psychology - Adult | Language, Psychology of | Clinical Neuropsychology | Brain damage | Discourse analysis
eBook