1.
Full Text
Stages of the Pathologic Process in Alzheimer Disease: Age Categories From 1 to 100 Years
Journal of Neuropathology and Experimental Neurology, ISSN 0022-3069, 11/2011, Volume 70, Issue 11, pp. 960 - 969
Two thousand three hundred and thirty two nonselected brains from 1- to 100-year-old individuals were examined using immunocytochemistry (AT8) and Gallyas...
A-amyloid | Pretangles/neurofibrillary tangles | Neuropil threads | Alzheimer disease | Brainstem | Locus coeruleus | Hyperphosphorylated tau protein | TAU-PROTEIN | NEUROFIBRILLARY CHANGES | DEPOSITION | BRAIN-STEM | COGNITIVE IMPAIRMENT | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | DEGENERATION | beta-amyloid | NUCLEUS | TANGLES | LOCUS-COERULEUS | NEURONS | Neurofibrillary Tangles - pathology | Silver Staining - methods | Neurons - pathology | Humans | Middle Aged | Child, Preschool | tau Proteins - metabolism | Infant | Male | Disease Progression | Alzheimer Disease - pathology | Brain - metabolism | Young Adult | Adolescent | Amyloid beta-Peptides - metabolism | Statistics, Nonparametric | Aged, 80 and over | Brain - pathology | Adult | Female | Aged | Neurons - metabolism | Child | Cohort Studies | Brain | Medical research | Cloning
A-amyloid | Pretangles/neurofibrillary tangles | Neuropil threads | Alzheimer disease | Brainstem | Locus coeruleus | Hyperphosphorylated tau protein | TAU-PROTEIN | NEUROFIBRILLARY CHANGES | DEPOSITION | BRAIN-STEM | COGNITIVE IMPAIRMENT | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | DEGENERATION | beta-amyloid | NUCLEUS | TANGLES | LOCUS-COERULEUS | NEURONS | Neurofibrillary Tangles - pathology | Silver Staining - methods | Neurons - pathology | Humans | Middle Aged | Child, Preschool | tau Proteins - metabolism | Infant | Male | Disease Progression | Alzheimer Disease - pathology | Brain - metabolism | Young Adult | Adolescent | Amyloid beta-Peptides - metabolism | Statistics, Nonparametric | Aged, 80 and over | Brain - pathology | Adult | Female | Aged | Neurons - metabolism | Child | Cohort Studies | Brain | Medical research | Cloning
Journal Article
Cell and Tissue Research, ISSN 0302-766X, 7/2018, Volume 373, Issue 1, pp. 267 - 286
It is a well-established fact that the sympathetic, parasympathetic and enteric nervous systems are affected at early stages in Parkinson’s disease (PD)....
Human Genetics | α-Synuclein | Parasympathetic | meta -Iodobenzylguanidine cardiac scintigraphy | Tyrosine hydroxylase | Sympathetic | Enteric nervous system | Biomedicine | Autonomic nervous system | Gastrointestinal system | Proteomics | Cardiovascular autonomic test | Molecular Medicine | Heart rate variability | Parkinson’s disease | Orthostatic hypotension | Lewy body | meta-Iodobenzylguanidine cardiac scintigraphy | LEWY-BODY DISEASE | GLAND NEEDLE-BIOPSY | Parkinson's disease | ALZHEIMERS-DISEASE | SPINAL-CORD | BRAIN-STEM | COLONIC BIOPSIES | EDINGER-WESTPHAL NUCLEUS | SLEEP BEHAVIOR DISORDER | CELL BIOLOGY | ALPHA-SYNUCLEIN PATHOLOGY | IDIOPATHIC PARKINSONS-DISEASE | alpha-Synuclein | Parasympathetic Nervous System - pathology | Parkinson Disease - pathology | Humans | Autonomic Nervous System - pathology | Sympathetic Nervous System - pathology | Organ Specificity | Motor Neurons - pathology | Neurophysiology | Pathology | Neurodegenerative diseases | Central nervous system | Nervous system | Gastrointestinal tract | Parasympathetic nervous system | Movement disorders
Human Genetics | α-Synuclein | Parasympathetic | meta -Iodobenzylguanidine cardiac scintigraphy | Tyrosine hydroxylase | Sympathetic | Enteric nervous system | Biomedicine | Autonomic nervous system | Gastrointestinal system | Proteomics | Cardiovascular autonomic test | Molecular Medicine | Heart rate variability | Parkinson’s disease | Orthostatic hypotension | Lewy body | meta-Iodobenzylguanidine cardiac scintigraphy | LEWY-BODY DISEASE | GLAND NEEDLE-BIOPSY | Parkinson's disease | ALZHEIMERS-DISEASE | SPINAL-CORD | BRAIN-STEM | COLONIC BIOPSIES | EDINGER-WESTPHAL NUCLEUS | SLEEP BEHAVIOR DISORDER | CELL BIOLOGY | ALPHA-SYNUCLEIN PATHOLOGY | IDIOPATHIC PARKINSONS-DISEASE | alpha-Synuclein | Parasympathetic Nervous System - pathology | Parkinson Disease - pathology | Humans | Autonomic Nervous System - pathology | Sympathetic Nervous System - pathology | Organ Specificity | Motor Neurons - pathology | Neurophysiology | Pathology | Neurodegenerative diseases | Central nervous system | Nervous system | Gastrointestinal tract | Parasympathetic nervous system | Movement disorders
Journal Article
Cell and Tissue Research, ISSN 0302-766X, 10/2004, Volume 318, Issue 1, pp. 121 - 134
The synucleinopathy, idiopathic Parkinson's disease, is a multisystem disorder that involves only a few predisposed nerve cell types in specific regions of the...
Parkinson's disease | Pathoarchitectonics | Staging | Alpha-synuclein | Lewy neurites | Lewy bodies | NERVOUS-SYSTEM | NEURODEGENERATIVE DISORDERS | ALZHEIMERS-DISEASE | BASAL GANGLIA | alpha-synuclein | SUBSTANTIA-NIGRA | PEDUNCULOPONTINE NUCLEUS | CELL BIOLOGY | HUMAN CEREBRAL-CORTEX | FUNCTIONAL-ANATOMY | BODY-CONTAINING NEURONS | staging | pathoarchitectonics | Brain - pathology | Parkinson Disease - pathology | Parkinson Disease - physiopathology | Brain - physiopathology | Humans
Parkinson's disease | Pathoarchitectonics | Staging | Alpha-synuclein | Lewy neurites | Lewy bodies | NERVOUS-SYSTEM | NEURODEGENERATIVE DISORDERS | ALZHEIMERS-DISEASE | BASAL GANGLIA | alpha-synuclein | SUBSTANTIA-NIGRA | PEDUNCULOPONTINE NUCLEUS | CELL BIOLOGY | HUMAN CEREBRAL-CORTEX | FUNCTIONAL-ANATOMY | BODY-CONTAINING NEURONS | staging | pathoarchitectonics | Brain - pathology | Parkinson Disease - pathology | Parkinson Disease - physiopathology | Brain - physiopathology | Humans
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 06/2010, Volume 119, Issue 6, pp. 703 - 713
A retrospective autopsy-based study of the human submandibular gland, one of the three major salivary glands, together with anatomically related peripheral...
Peripheral nervous system | Parkinson's disease | Lewy body disease | Superior cervical ganglion | Submandibular gland | Lewy neuritis | Esophagus | Sialorrhea | Autonomic nervous system/ganglia | Sialopenia | Synucleinopathy | Dysphagia | Alpha-synuclein | ELDERLY SUBJECTS | PATHOLOGY | CARDIAC SYMPATHETIC-NERVE | CLINICAL NEUROLOGY | GASTROINTESTINAL DYSFUNCTION | OLFACTORY DYSFUNCTION | AUTONOMIC DYSFUNCTION | MULTIPLE-SYSTEM-ATROPHY | CONTAINING NEURONS | AMYOTROPHIC-LATERAL-SCLEROSIS | SALIVARY-GLANDS | NEUROSCIENCES | Lewy neurites | Immunohistochemistry | Parkinson Disease - pathology | Vagus Nerve - metabolism | Multiple System Atrophy - pathology | Superior Cervical Ganglion - pathology | Humans | Middle Aged | Lewy Body Disease - pathology | Submandibular Gland - metabolism | Male | Superior Cervical Ganglion - metabolism | Vagus Nerve - pathology | Lewy Body Disease - metabolism | Submandibular Gland - pathology | Multiple System Atrophy - metabolism | Aged, 80 and over | Female | Aged | Parkinson Disease - metabolism | Retrospective Studies | Lewy Bodies - metabolism | Lewy Bodies - pathology | alpha-Synuclein - metabolism | Cohort Studies | Medical colleges | Polyethylene | Neurosciences | Developmental biology | Polyethylene glycol
Peripheral nervous system | Parkinson's disease | Lewy body disease | Superior cervical ganglion | Submandibular gland | Lewy neuritis | Esophagus | Sialorrhea | Autonomic nervous system/ganglia | Sialopenia | Synucleinopathy | Dysphagia | Alpha-synuclein | ELDERLY SUBJECTS | PATHOLOGY | CARDIAC SYMPATHETIC-NERVE | CLINICAL NEUROLOGY | GASTROINTESTINAL DYSFUNCTION | OLFACTORY DYSFUNCTION | AUTONOMIC DYSFUNCTION | MULTIPLE-SYSTEM-ATROPHY | CONTAINING NEURONS | AMYOTROPHIC-LATERAL-SCLEROSIS | SALIVARY-GLANDS | NEUROSCIENCES | Lewy neurites | Immunohistochemistry | Parkinson Disease - pathology | Vagus Nerve - metabolism | Multiple System Atrophy - pathology | Superior Cervical Ganglion - pathology | Humans | Middle Aged | Lewy Body Disease - pathology | Submandibular Gland - metabolism | Male | Superior Cervical Ganglion - metabolism | Vagus Nerve - pathology | Lewy Body Disease - metabolism | Submandibular Gland - pathology | Multiple System Atrophy - metabolism | Aged, 80 and over | Female | Aged | Parkinson Disease - metabolism | Retrospective Studies | Lewy Bodies - metabolism | Lewy Bodies - pathology | alpha-Synuclein - metabolism | Cohort Studies | Medical colleges | Polyethylene | Neurosciences | Developmental biology | Polyethylene glycol
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 06/2008, Volume 115, Issue 6, pp. 599 - 609
Cerebral amyloid angiopathy (CAA) is characterized by the deposition of the amyloid beta-protein (A beta) within cerebral vessels. The involvement of different...
Drainage | Cerebral amyloid angiopathy | Amyloid β-protein | Cerebral blood flow | Alzheimer's disease | A-BETA DEPOSITS | FAMILIAL BRITISH DEMENTIA | PATHOLOGY | amyloid beta-protein | MILD COGNITIVE IMPAIRMENT | MENINGOCEREBROVASCULAR AMYLOIDOSIS | NEUROSCIENCES | CLINICAL NEUROLOGY | APOLIPOPROTEIN-E | cerebral amyloid angiopathy | DUTCH TYPE | cerebral blood flow | drainage | PRECURSOR PROTEIN | TRANSGENIC MOUSE MODEL | SMOOTH-MUSCLE CELLS | GIANT-CELL ARTERITIS | Cerebral Amyloid Angiopathy - complications | Cerebral Amyloid Angiopathy - pathology | Alzheimer Disease - complications | Apolipoprotein E4 - genetics | Amyloid - metabolism | Humans | Alzheimer Disease - metabolism | Alzheimer Disease - genetics | Cerebral Amyloid Angiopathy - genetics | Cerebral Amyloid Angiopathy - metabolism | Alzheimer Disease - pathology | Index Medicus
Drainage | Cerebral amyloid angiopathy | Amyloid β-protein | Cerebral blood flow | Alzheimer's disease | A-BETA DEPOSITS | FAMILIAL BRITISH DEMENTIA | PATHOLOGY | amyloid beta-protein | MILD COGNITIVE IMPAIRMENT | MENINGOCEREBROVASCULAR AMYLOIDOSIS | NEUROSCIENCES | CLINICAL NEUROLOGY | APOLIPOPROTEIN-E | cerebral amyloid angiopathy | DUTCH TYPE | cerebral blood flow | drainage | PRECURSOR PROTEIN | TRANSGENIC MOUSE MODEL | SMOOTH-MUSCLE CELLS | GIANT-CELL ARTERITIS | Cerebral Amyloid Angiopathy - complications | Cerebral Amyloid Angiopathy - pathology | Alzheimer Disease - complications | Apolipoprotein E4 - genetics | Amyloid - metabolism | Humans | Alzheimer Disease - metabolism | Alzheimer Disease - genetics | Cerebral Amyloid Angiopathy - genetics | Cerebral Amyloid Angiopathy - metabolism | Alzheimer Disease - pathology | Index Medicus
Journal Article
BRAIN PATHOLOGY, ISSN 1015-6305, 05/2016, Volume 26, Issue 3, pp. 371 - 386
Alzheimer's disease (AD) represents the most frequent progressive neuropsychiatric disorder worldwide leading to dementia. We systematically investigated the...
allocortex | prion-like diseases | AXONAL-TRANSPORT | NEUROANATOMICAL CONNECTIONS | MILD COGNITIVE IMPAIRMENT | HIPPOCAMPAL-FORMATION | NEURODEGENERATIVE DISEASES | entorhinal region | MIDBRAIN PERIAQUEDUCTAL GRAY | NEUROPATHOLOGICAL DIAGNOSIS | NEUROFIBRILLARY DEGENERATION | cytoskeletal pathology | subcortical nuclei | SUBCORTICAL AFFERENTS | DORSAL RAPHE NUCLEUS | Alzheimer's disease | tau protein | prion‐like diseases | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | Cytoskeleton - pathology | Humans | Middle Aged | Brain - pathology | Female | Male | Aged | tau Proteins | Disease Progression | Alzheimer Disease - pathology | Alzheimers disease | Pathology | Rodents
allocortex | prion-like diseases | AXONAL-TRANSPORT | NEUROANATOMICAL CONNECTIONS | MILD COGNITIVE IMPAIRMENT | HIPPOCAMPAL-FORMATION | NEURODEGENERATIVE DISEASES | entorhinal region | MIDBRAIN PERIAQUEDUCTAL GRAY | NEUROPATHOLOGICAL DIAGNOSIS | NEUROFIBRILLARY DEGENERATION | cytoskeletal pathology | subcortical nuclei | SUBCORTICAL AFFERENTS | DORSAL RAPHE NUCLEUS | Alzheimer's disease | tau protein | prion‐like diseases | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | Cytoskeleton - pathology | Humans | Middle Aged | Brain - pathology | Female | Male | Aged | tau Proteins | Disease Progression | Alzheimer Disease - pathology | Alzheimers disease | Pathology | Rodents
Journal Article
JNEN: Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 12/2003, Volume 62, Issue 12, pp. 1287 - 1301
Sporadic, late-onset Alzheimer disease (AD) constitutes the most frequent cause of dementia in the elderly population. AD-related pathology is often...
Arteriosclerosis/Lipohyalinosis | Cerebral amyloid angiopathy | Amyloid β-protein | Alzheimer disease | Apolipoprotein E | Dementia | HUMAN BRAIN | PROTEIN | RAT | DEPOSITION | INTERSTITIAL FLUID | PATHOLOGY | amyloid beta-protein | NEUROSCIENCES | LESIONS | CLINICAL NEUROLOGY | BETA | THRESHOLD | arteriosclerosis/lipohyalinosis | cerebral amyloid angiopathy | apolipoprotein e | dementia | SIMVASTATIN | Intracranial Arteriosclerosis - pathology | Alzheimer Disease - physiopathology | Cognition Disorders - physiopathology | Cerebral Amyloid Angiopathy - physiopathology | Humans | Middle Aged | Cognition Disorders - pathology | Male | Alzheimer Disease - pathology | Cerebral Amyloid Angiopathy - pathology | Analysis of Variance | Aged, 80 and over | Female | Aged | Intracranial Arteriosclerosis - physiopathology
Arteriosclerosis/Lipohyalinosis | Cerebral amyloid angiopathy | Amyloid β-protein | Alzheimer disease | Apolipoprotein E | Dementia | HUMAN BRAIN | PROTEIN | RAT | DEPOSITION | INTERSTITIAL FLUID | PATHOLOGY | amyloid beta-protein | NEUROSCIENCES | LESIONS | CLINICAL NEUROLOGY | BETA | THRESHOLD | arteriosclerosis/lipohyalinosis | cerebral amyloid angiopathy | apolipoprotein e | dementia | SIMVASTATIN | Intracranial Arteriosclerosis - pathology | Alzheimer Disease - physiopathology | Cognition Disorders - physiopathology | Cerebral Amyloid Angiopathy - physiopathology | Humans | Middle Aged | Cognition Disorders - pathology | Male | Alzheimer Disease - pathology | Cerebral Amyloid Angiopathy - pathology | Analysis of Variance | Aged, 80 and over | Female | Aged | Intracranial Arteriosclerosis - physiopathology
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 12/2009, Volume 118, Issue 6, pp. 777 - 784
Clinical and autopsy studies have consistently reported cardiac sympathetic dysfunction in the left ventricular wall in patients with Parkinson's disease (PD)....
Cardiac conduction system | Tyrosine hydroxylase | Parkinson's disease | Lewy body disease | Sympathetic dysfunction | NERVOUS-SYSTEM | SYMPATHETIC DENERVATION | AUTONOMIC DYSFUNCTION | MIBG | INNERVATION | DISORDERS | SYMPTOMS | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | DEGENERATION | ORTHOSTATIC HYPOTENSION | Immunohistochemistry | Tyrosine 3-Monooxygenase - metabolism | Heart Conduction System - metabolism | Humans | Male | Myocardium - metabolism | Statistics, Nonparametric | Aged, 80 and over | Female | Aged | Neurons - metabolism | Parkinson Disease - metabolism | alpha-Synuclein - metabolism | Heart - innervation
Cardiac conduction system | Tyrosine hydroxylase | Parkinson's disease | Lewy body disease | Sympathetic dysfunction | NERVOUS-SYSTEM | SYMPATHETIC DENERVATION | AUTONOMIC DYSFUNCTION | MIBG | INNERVATION | DISORDERS | SYMPTOMS | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | DEGENERATION | ORTHOSTATIC HYPOTENSION | Immunohistochemistry | Tyrosine 3-Monooxygenase - metabolism | Heart Conduction System - metabolism | Humans | Male | Myocardium - metabolism | Statistics, Nonparametric | Aged, 80 and over | Female | Aged | Neurons - metabolism | Parkinson Disease - metabolism | alpha-Synuclein - metabolism | Heart - innervation
Journal Article
Journal of Neuropathology and Experimental Neurology, ISSN 0022-3069, 05/2010, Volume 69, Issue 5, pp. 442 - 448
Cerebrovascular pathology is a major cause of stroke and mortality. Studies on prevalence of cerebrovascular pathologies in dementia with Lewy bodies (DLBs)...
Parkinson disease | Lewy body disease | Cerebrovascular disease | Dementia with Lewy bodies | MORTALITY | CEREBRAL AMYLOID ANGIOPATHY | DEMENTIA | ALZHEIMERS-DISEASE | ATHEROSCLEROSIS | PREVALENCE | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | STROKE | BODIES | BRAIN | PARKINSONS-DISEASE | Neurofibrillary Tangles - pathology | Parkinson Disease - complications | Parkinson Disease - pathology | Humans | Middle Aged | Lewy Body Disease - complications | Lewy Body Disease - pathology | Brain Infarction - pathology | Male | Cerebral Angiography - methods | Chi-Square Distribution | Principal Component Analysis - methods | Case-Control Studies | Cerebrovascular Disorders - etiology | Brain Infarction - etiology | Circle of Willis - pathology | Hemorrhage - etiology | Amyloid beta-Peptides - metabolism | Aged, 80 and over | Female | Aged | Retrospective Studies | Neurologic Examination - methods | Lewy Bodies - pathology
Parkinson disease | Lewy body disease | Cerebrovascular disease | Dementia with Lewy bodies | MORTALITY | CEREBRAL AMYLOID ANGIOPATHY | DEMENTIA | ALZHEIMERS-DISEASE | ATHEROSCLEROSIS | PREVALENCE | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | STROKE | BODIES | BRAIN | PARKINSONS-DISEASE | Neurofibrillary Tangles - pathology | Parkinson Disease - complications | Parkinson Disease - pathology | Humans | Middle Aged | Lewy Body Disease - complications | Lewy Body Disease - pathology | Brain Infarction - pathology | Male | Cerebral Angiography - methods | Chi-Square Distribution | Principal Component Analysis - methods | Case-Control Studies | Cerebrovascular Disorders - etiology | Brain Infarction - etiology | Circle of Willis - pathology | Hemorrhage - etiology | Amyloid beta-Peptides - metabolism | Aged, 80 and over | Female | Aged | Retrospective Studies | Neurologic Examination - methods | Lewy Bodies - pathology
Journal Article
JNEN: Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 03/2002, Volume 61, Issue 3, pp. 282 - 293
Cerebral amyloid angiopathy (CAA) is a type of β-amyloidosis that occurs in leptomeningeal and cortical vessels of the elderly. In a sample of 41 CAA cases...
Cerebral amyloid angiopathy | Dyshoric angiopathy | Leptomeningeal vessels | Apolipoprotein E | Cortical capillaries | Aβ-Protein | cortical capillaries | HEMORRHAGE | ALZHEIMERS-DISEASE | dyshoric angiopathy | PATHOLOGY | APOLIPOPROTEIN-E GENOTYPE | leptomeningeal vessels | NEUROSCIENCES | A beta-protein | CLINICAL NEUROLOGY | cerebral amyloid angiopathy | MOUSE MODEL | apolipoprotein E | BETA-PROTEIN | SMOOTH-MUSCLE-CELLS | PRECURSOR PROTEIN | E-EPSILON 4 | BASEMENT-MEMBRANE | Alzheimer Disease - complications | Blood Vessels - metabolism | Humans | Middle Aged | Male | Reference Values | Cerebral Infarction - complications | Cerebral Amyloid Angiopathy - complications | Amyloid beta-Peptides - metabolism | Aged, 80 and over | Adult | Female | Amyloidosis - complications | Cerebral Amyloid Angiopathy - genetics | Capillaries - metabolism | Severity of Illness Index | Genetic Predisposition to Disease | Cerebral Amyloid Angiopathy - physiopathology | Gene Frequency | Genotype | Cerebrovascular Circulation | Cerebral Amyloid Angiopathy - classification | Aging - physiology | Apolipoproteins E - genetics | Brain Diseases - complications | Alleles | Aged
Cerebral amyloid angiopathy | Dyshoric angiopathy | Leptomeningeal vessels | Apolipoprotein E | Cortical capillaries | Aβ-Protein | cortical capillaries | HEMORRHAGE | ALZHEIMERS-DISEASE | dyshoric angiopathy | PATHOLOGY | APOLIPOPROTEIN-E GENOTYPE | leptomeningeal vessels | NEUROSCIENCES | A beta-protein | CLINICAL NEUROLOGY | cerebral amyloid angiopathy | MOUSE MODEL | apolipoprotein E | BETA-PROTEIN | SMOOTH-MUSCLE-CELLS | PRECURSOR PROTEIN | E-EPSILON 4 | BASEMENT-MEMBRANE | Alzheimer Disease - complications | Blood Vessels - metabolism | Humans | Middle Aged | Male | Reference Values | Cerebral Infarction - complications | Cerebral Amyloid Angiopathy - complications | Amyloid beta-Peptides - metabolism | Aged, 80 and over | Adult | Female | Amyloidosis - complications | Cerebral Amyloid Angiopathy - genetics | Capillaries - metabolism | Severity of Illness Index | Genetic Predisposition to Disease | Cerebral Amyloid Angiopathy - physiopathology | Gene Frequency | Genotype | Cerebrovascular Circulation | Cerebral Amyloid Angiopathy - classification | Aging - physiology | Apolipoproteins E - genetics | Brain Diseases - complications | Alleles | Aged
Journal Article
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 11/2005, Volume 289, Issue 5, pp. 1075 - 1084
Tryptophan metabolites such as kynurenate (KYNA), xanthurenate (XA), and quinolinate are considered to have an important impact on many physiological...
N-methyl-D-aspartate receptor | Brain | Kidneys | Macula densa | Transforming growth factor | ENZYME-ACTIVITIES | PHYSIOLOGY | KYNURENINE PATHWAY | macula densa | FUNCTIONAL-CHARACTERIZATION | kidneys | brain | BLOOD-BRAIN-BARRIER | CELL BIOLOGY | QUINOLINIC ACID | ABLUMINAL MEMBRANE | HOMOVANILLIC-ACID | AMINOHIPPURATE SECRETION | CHOROID-PLEXUS | transforming growth factor | RABBIT PROXIMAL TUBULES | Gene Expression | Cercopithecus aethiops | Tryptophan - metabolism | Brain - metabolism | Organic Anion Transport Protein 1 - physiology | Biological Transport, Active | Kidney - metabolism | Animals | Tryptophan - analogs & derivatives | Mice | Molecular Structure | COS Cells | Organic Anion Transporters, Sodium-Independent - physiology
N-methyl-D-aspartate receptor | Brain | Kidneys | Macula densa | Transforming growth factor | ENZYME-ACTIVITIES | PHYSIOLOGY | KYNURENINE PATHWAY | macula densa | FUNCTIONAL-CHARACTERIZATION | kidneys | brain | BLOOD-BRAIN-BARRIER | CELL BIOLOGY | QUINOLINIC ACID | ABLUMINAL MEMBRANE | HOMOVANILLIC-ACID | AMINOHIPPURATE SECRETION | CHOROID-PLEXUS | transforming growth factor | RABBIT PROXIMAL TUBULES | Gene Expression | Cercopithecus aethiops | Tryptophan - metabolism | Brain - metabolism | Organic Anion Transport Protein 1 - physiology | Biological Transport, Active | Kidney - metabolism | Animals | Tryptophan - analogs & derivatives | Mice | Molecular Structure | COS Cells | Organic Anion Transporters, Sodium-Independent - physiology
Journal Article
Journal of Electromyography and Kinesiology, ISSN 1050-6411, 2015, Volume 25, Issue 5, pp. 749 - 753
Abstract Introduction: Mechanomyography (MMG) has recently shown promise in monitoring recovery of injured muscles. However, delivering a maximal percutaneous...
Physical Medicine and Rehabilitation | Mechanomyography | Stimulation | Contraction time | Muscle | Injury | SIGNAL | SPORT SCIENCES | PHYSIOLOGY | MUSCLE INJURIES | REHABILITATION | NEUROSCIENCES | Myography - methods | Muscle Contraction | Muscle, Skeletal - physiology | Humans | Myography - standards
Physical Medicine and Rehabilitation | Mechanomyography | Stimulation | Contraction time | Muscle | Injury | SIGNAL | SPORT SCIENCES | PHYSIOLOGY | MUSCLE INJURIES | REHABILITATION | NEUROSCIENCES | Myography - methods | Muscle Contraction | Muscle, Skeletal - physiology | Humans | Myography - standards
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 08/2010, Volume 120, Issue 2, pp. 169 - 183
Journal Article
Journal of Alzheimer's Disease, ISSN 1387-2877, 10/2015, Volume 49, Issue 4, pp. 905 - 915
Journal Article
Journal of Alzheimer's Disease, ISSN 1387-2877, 12/2015, Volume 49, Issue 4, pp. 905 - 915
In spite of considerable progress in neuropathological research on Alzheimer's disease (AD), knowledge regarding the exact pathoanatomical distribution of the...
tau | cytoskeletal pathology | pathoanatomy | Alzheimer's disease | thalamus | SYSTEM | NEUROFIBRILLARY TANGLES | RETICULAR NUCLEUS | CONNECTIONS | NEUROSCIENCES | NEURODEGENERATIVE DISEASES | DEGENERATION | PROPAGATION | BRAIN | HISTORY | Thalamus - metabolism | Humans | Alzheimer Disease - metabolism | Cytoskeleton - metabolism | tau Proteins - metabolism | Thalamus - pathology | Alzheimer Disease - pathology
tau | cytoskeletal pathology | pathoanatomy | Alzheimer's disease | thalamus | SYSTEM | NEUROFIBRILLARY TANGLES | RETICULAR NUCLEUS | CONNECTIONS | NEUROSCIENCES | NEURODEGENERATIVE DISEASES | DEGENERATION | PROPAGATION | BRAIN | HISTORY | Thalamus - metabolism | Humans | Alzheimer Disease - metabolism | Cytoskeleton - metabolism | tau Proteins - metabolism | Thalamus - pathology | Alzheimer Disease - pathology
Journal Article
Annals of Clinical and Translational Neurology, ISSN 2328-9503, 07/2018, Volume 5, Issue 7, pp. 815 - 831
Objective Amyloid β (Aβ) depositions in plaques and cerebral amyloid angiopathy (CAA) represent common features of Alzheimer's disease (AD). Sequential...
MAJOR COMPONENT | ALZHEIMERS ASSOCIATION GUIDELINES | NATIONAL INSTITUTE | HUMAN BRAIN | CEREBRAL-HEMORRHAGE | A-BETA | TERMINAL HETEROGENEITY | NEUROSCIENCES | CLINICAL NEUROLOGY | NEUROPATHOLOGIC ASSESSMENT | SENILE PLAQUES | APOLIPOPROTEIN-E | Hypertension | Pathology | Alzheimers disease | Dementia
MAJOR COMPONENT | ALZHEIMERS ASSOCIATION GUIDELINES | NATIONAL INSTITUTE | HUMAN BRAIN | CEREBRAL-HEMORRHAGE | A-BETA | TERMINAL HETEROGENEITY | NEUROSCIENCES | CLINICAL NEUROLOGY | NEUROPATHOLOGIC ASSESSMENT | SENILE PLAQUES | APOLIPOPROTEIN-E | Hypertension | Pathology | Alzheimers disease | Dementia
Journal Article