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1. Full Text Progression of Parkinson's disease pathology is reproduced by intragastric administration of rotenone in mice
by Pan-Montojo, Francisco and Anichtchik, Oleg and Dening, Yanina and Knels, Lilla and Pursche, Stefan and Jung, Roland and Jackson, Sandra and Gille, Gabriele and Spillantini, Maria Grazia and Reichmann, Heinz and Funk, Richard H. W
PLoS ONE, ISSN 1932-6203, 01/2010, Volume 5, Issue 1, pp. e8762 - e8762
In patients with Parkinson's disease (PD), the associated pathology follows a characteristic pattern involving inter alia the enteric nervous system (ENS), the... 
EXTRACELLULAR ALPHA-SYNUCLEIN | GENE | BIOLOGY | NEURONS | DISORDERS | NEURODEGENERATION | MODEL | NEUROPATHOLOGY | SUBSTANTIA-NIGRA | LEWY BODIES | EXPOSURE | Stomach | Enteric Nervous System - drug effects | Parkinson Disease - pathology | Animals | Rotenone - pharmacology | Rotenone - administration & dosage | Mice | Mice, Inbred BALB C | Chromatography, High Pressure Liquid | Disease Models, Animal | registration | Motor vehicles | Analysis | Pesticides | Spinal cord | Phosphorylation | Parkinson's disease | Neuropathology | Substantia nigra | Central nervous system | Parkinsons disease | Nervous system | Synuclein | Nuclei | Electron transport chain | Mitochondria | Motor nuclei | Enteric nervous system | Agrochemicals | Rodents | Movement disorders | NADH-ubiquinone oxidoreductase | Neurodegenerative diseases | Neurons | Environmental factors | Inflammation | Liquid chromatography | Anatomy | High-performance liquid chromatography | Patients | Rotenone | Pathology | Neurology | Musculoskeletal system | Brain research | Mutation | Electron transport | Methods | Index Medicus
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2. Full Text Nonhepatosplenic Extramedullary Hematopoiesis: Associated Diseases, Pathology, Clinical Course, and Treatment
by Koch, Cody A and Li, Chin-Yang and Mesa, Ruben A and Tefferi, Ayalew
Mayo Clinic Proceedings, ISSN 0025-6196, 2003, Volume 78, Issue 10, pp. 1223 - 1233
To define associated clinical conditions, pathology, natural history, and treatment outcome of nonhepatosplenic extramedullary hematopoiesis (NHS-EMH). We... 
EXTRA-MEDULLARY HEMATOPOIESIS | MEDICINE, GENERAL & INTERNAL | STEM-CELLS | COLONY-STIMULATING FACTOR | BONE-MARROW | IN-VIVO | AGNOGENIC MYELOID METAPLASIA | HEREDITARY SPHEROCYTOSIS | MYELOPROLIFERATIVE-SYNDROME | SPINAL-CORD COMPRESSION | RADIATION-THERAPY | Primary Myelofibrosis - complications | Humans | Middle Aged | Male | Primary Myelofibrosis - pathology | Primary Myelofibrosis - radiotherapy | Hematopoiesis, Extramedullary | Adult | Female | Aged | Primary Myelofibrosis - therapy | Retrospective Studies | Biopsy, Needle | Index Medicus | Abridged Index Medicus
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3. Full Text The Homozygote VCPR155H/R155H Mouse Model Exhibits Accelerated Human VCP-Associated Disease Pathology
by Nalbandian, Angèle and Llewellyn, Katrina J and Kitazawa, Masashi and Yin, Hong Z and Badadani, Mallikarjun and Khanlou, Negar and Edwards, Robert and Nguyen, Christopher and Mukherjee, Jogeshwar and Mozaffar, Tahseen and Watts, Giles and Weiss, John and Kimonis, Virginia E
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, p. e46308
Valosin containing protein (VCP) mutations are the cause of hereditary inclusion body myopathy, Paget's disease of bone, frontotemporal dementia (IBMPFD). VCP... 
VALOSIN-CONTAINING PROTEIN | INCLUSION-BODY MYOPATHY | MULTIDISCIPLINARY SCIENCES | FRONTOTEMPORAL DEMENTIA | DEGRADATION | BONE | MUTATIONS | AUTOPHAGY | PAGET-DISEASE | CELL-DEATH | FAMILY | Ubiquitin | Neuroimaging | Brain | Pediatrics | Spinal cord | Neurosciences | Disease | Pathogenesis | Neurobiology | Biochemistry | Autophagy | Sclerosis | Proteins | Paget's disease | Mitochondria | Computed tomography | Cell cycle | Dementia disorders | Bones | EMG | Neurodegenerative diseases | Cardiac muscle | Abnormalities | Muscles | Amyotrophic lateral sclerosis | Neurological diseases | Pathology | Neurology | Molecular modelling | Mice | Bone | Mutation | Frontotemporal dementia | Endoplasmic reticulum | Phagocytosis | Apoptosis | Myopathy
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4. Full Text A novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology
by Pasanen, Petra|Myllykangas, Liisa|Siitonen, Maija|Raunio, Anna|Kaakkola, Seppo|Lyytinen, Jukka|Tienari, Pentti J.|Pöyhönen, Minna|Paetau, Anders
Neurobiology of Aging, ISSN 0197-4580, 2014, Volume 35, Issue 9, pp. 2180.e1 - 2180.e5
Abstract We describe the clinical, neuropathological, and genetic features of a Finnish patient with a novel α-synuclein ( SNCA ) mutation A53E. The patient... 
Neurology | Internal Medicine | Parkinsonism | A53E | Genetics | Neuropathology | Synucleinopathy | SNCA | SNCA VARIANTS | DEMENTIA | NEUROSCIENCES | GERIATRICS & GERONTOLOGY | INCREASED RISK | FAMILIES | DUPLICATION | Parkinson Disease - pathology | Spinal Cord - metabolism | Genetic Association Studies | Multiple System Atrophy - pathology | Humans | Middle Aged | Neurites - metabolism | Multiple System Atrophy - genetics | Parkinson Disease - genetics | Brain - metabolism | DNA-Binding Proteins - metabolism | Phenotype | Pedigree | Spinal Cord - pathology | Brain - pathology | Adult | Female | alpha-Synuclein - genetics | Mutation | alpha-Synuclein - metabolism | Index Medicus
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5. Full Text Adhesion molecule L1 binds to amyloid beta and reduces Alzheimer's disease pathology in mice
by Djogo, Nevena|Jakovcevski, Igor|Müller, Christian|Lee, Hyun Joon|Xu, Jin-Chong|Jakovcevski, Mira|Kügler, Sebastian|Loers, Gabriele|Schachner, Melitta
Neurobiology of Disease, ISSN 0969-9961, 2013, Volume 56, pp. 104 - 115
Abstract Alzheimer's disease (AD) is a devastating neurodegenerative disorder and the most common cause of elderly dementia. In an effort to contribute to the... 
Neurology | Astrogliosis | Neural cell adhesion molecule L1 | Amyloid beta peptides | Synaptic terminals | Alzheimer's disease | Adeno-associated virus serotype 5 | Amyloid precursor protein | Hippocampus | APPPS1 mice | FUNCTIONAL RECOVERY | NEUROSCIENCES | NUCLEAR TRANSLOCATION | ENHANCE RECOVERY | PERIPHERAL-NERVE INJURY | NEURITE OUTGROWTH | EMBRYONIC STEM-CELLS | MOUSE MODEL | A-BETA | SPINAL-CORD-INJURY | DENTATE GYRUS | Immunohistochemistry | Dependovirus - genetics | Green Fluorescent Proteins | Humans | Male | Alzheimer Disease - pathology | Gliosis - pathology | Amyloid beta-Peptides - metabolism | Pyramidal Cells - drug effects | Neural Cell Adhesion Molecule L1 - metabolism | Tissue Fixation | Occipital Lobe - metabolism | Enzyme-Linked Immunosorbent Assay | Microglia - drug effects | Plaque, Amyloid - pathology | Alzheimer Disease - drug therapy | Mice, Transgenic | Hippocampus - pathology | Blotting, Western | Neural Cell Adhesion Molecule L1 - therapeutic use | Occipital Lobe - pathology | Hippocampus - metabolism | Receptors, CCR2 - metabolism | Animals | Alzheimer Disease - metabolism | Brain - pathology | Protein Binding | Mice | Fibronectins | Analysis | Amyloid beta-protein | Index Medicus
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6. Full Text Pharmacological inhibition of complement C5a‐C5a1 receptor signalling ameliorates disease pathology in the hSOD1G93A mouse model of amyotrophic lateral sclerosis
by Lee, John D and Kumar, Vinod and Fung, Jenny N T and Ruitenberg, Marc J and Noakes, Peter G and Woodruff, Trent M
British Journal of Pharmacology, ISSN 0007-1188, 04/2017, Volume 174, Issue 8, pp. 689 - 699
Amyotrophic lateral sclerosis (ALS) is a fatal and rapidly progressing motor neuron disease without effective treatment. The complement system is up-regulated... 
Medical examination | Neurons | Lymphocytes | Analysis | Amyotrophic lateral sclerosis | Genetic engineering | Blood | Brain | Drinking water | Spinal cord | Complement component C5a | Body weight | Medical treatment | Motor neuron disease | Central nervous system | Lymphocytes T | Pharmacology | Inflammation | Survival | Signaling | Monocytes | Receptors | Peripheral blood | Mice | Grip strength | Leukocytes (granulocytic) | Pharmacokinetics | Index Medicus | Research Papers | Research Paper
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7. Full Text ALS‐Associated Endoplasmic Reticulum Proteins in Denervated Skeletal Muscle: Implications for Motor Neuron Disease Pathology
by Jesse, C. M and Bushuven, E and Tripathi, P and Chandrasekar, A and Simon, C. M and Drepper, C and Yamoah, A and Dreser, A and Katona, I and Johann, S and Beyer, C and Wagner, S and Grond, M and Nikolin, S and Anink, J and Troost, D and Sendtner, M and Goswami, A and Weis, J
Brain Pathology, ISSN 1015-6305, 11/2017, Volume 27, Issue 6, pp. 781 - 794
Alpha‐motoneurons and muscle fibres are structurally and functionally interdependent. Both cell types particularly rely on endoplasmic reticulum (ER/SR)... 
ER chaperones | Neurogenic muscular atrophy (NMA) | VAPB | Neuromuscular junction (NMJ) | ALS | Motor neuron disease (MND) | Sigma Receptor 1 (SigR1) | MOTONEURON SURVIVAL | MARIE-TOOTH-DISEASE | MYOSIN ISOFORMS | MATRIN 3 | REGULAR EXERCISE | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | TUBULAR-AGGREGATE MYOPATHY | DISTAL MYOPATHY | TRANSGENIC MOUSE MODEL | BULBAR MUSCULAR-ATROPHY | Immunohistochemistry | Amyotrophic Lateral Sclerosis - physiopathology | Humans | Muscle Denervation | Mice, Transgenic | Motor Neuron Disease - pathology | Vesicular Transport Proteins - physiology | Motor Neurons - metabolism | Endoplasmic Reticulum - pathology | Animals | Autopsy | Membrane Proteins - physiology | Spinal Cord - pathology | Neuromuscular Junction | Superoxide Dismutase-1 - metabolism | Membrane Proteins - metabolism | Mice | Muscle, Skeletal - pathology | Superoxide Dismutase - metabolism | Disease Models, Animal | Proteins | Neurons | Analysis | Muscles | Heat shock proteins | Amyotrophic lateral sclerosis | Web sites | Animal models | Disintegration | Motor neuron disease | Immunoblotting | Superoxide dismutase | Chaperones | Autophagy | Sclerosis | Fibers | Atrophy | Protein folding | Rodents | Localization | Dynamic response | Motor neurons | Autopsies | Markers | Patients | Skeletal muscle | Pathology | Biopsy | Hsp27 protein | Mutation | Position (location) | Endoplasmic reticulum | Phagocytosis | Denervation | Index Medicus
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8. Full Text Pharmacological inhibition of complement C5a-C5a(1) receptor signalling ameliorates disease pathology in the hSOD1(G93A) mouse model of amyotrophic lateral sclerosis
by Lee, JD and Kumar, V and Fung, JNT and Ruitenberg, MJ and Noakes, PG and Woodruff, TM
BRITISH JOURNAL OF PHARMACOLOGY, ISSN 0007-1188, 04/2017, Volume 174, Issue 8, pp. 689 - 699
BACKGROUND AND PURPOSE Amyotrophic lateral sclerosis (ALS) is a fatal and rapidly progressing motor neuron disease without effective treatment. The complement... 
C5A RECEPTOR | ACTIVATION | PUBLICATION | MOTOR-NEURON DEGENERATION | ALZHEIMERS-DISEASE | SPINAL CORD BARRIER | ALS | PHARMACOLOGY & PHARMACY | SOD1 MICE | ANTAGONISTS | RAT MODEL
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9. Pathology of the spinal cord
by Hughes, John Trevor
1978, 2d. ed. --, ISBN 0853241007, xii, 257
Spinal cord | Diseases
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10. Full Text Multi-organ distribution of phosphorylated α-synuclein histopathology in subjects with Lewy body disorders
by Beach, Thomas G and Adler, Charles H and Sue, Lucia I and Vedders, Linda and Lue, Lih Fen and White III, Charles L and Akiyama, Haru and Caviness, John N and Shill, Holly A and Sabbagh, Marwan N and Walker, Douglas G and Arizona Parkinson's Dis Consortium and Arizona Parkinson's Disease Consortium and Arizona Parkinson’s Disease Consortium
Acta Neuropathologica, ISSN 0001-6322, 06/2010, Volume 119, Issue 6, pp. 689 - 702
A sensitive immunohistochemical method for phosphorylated alpha-synuclein was used to stain sets of sections of spinal cord and tissue from 41 different sites... 
Heart | Peripheral nervous system | Stomach | Spinal cord | Parkinson's disease | Submandibular gland | Sympathetic nervous system | Esophagus | Parkinsonism | Incidental lewy bodies | Enteric nervous system | Autonomic nervous system | Dementia with lewy bodies | Gastrointestinal system | Adrenal gland | Alzheimer's disease | α-synuclein | HUMAN BRAIN | ALZHEIMERS-DISEASE | PATHOLOGY | CLINICAL NEUROLOGY | BODIES | IDIOPATHIC PARKINSONS-DISEASE | Incidental Lewy bodies | NIGRAL TRANSPLANTS | NEUROSCIENCES | OLFACTORY-BULB | NEURONS | SALIVARY SECRETION | alpha-Synuclein | Dementia with Lewy bodies | AUTONOMIC NERVOUS-SYSTEM | Immunohistochemistry | Parkinson Disease - pathology | Phosphorylation | Spinal Cord - metabolism | Humans | Lewy Body Disease - pathology | Male | Ganglia, Sympathetic - metabolism | Gastrointestinal Tract - metabolism | Gastrointestinal Tract - pathology | Alzheimer Disease - pathology | Brain - metabolism | Lewy Body Disease - metabolism | Peripheral Nervous System - pathology | Spinal Cord - pathology | Peripheral Nervous System - metabolism | Alzheimer Disease - metabolism | Aged, 80 and over | Brain - pathology | Female | Ganglia, Sympathetic - pathology | Aged | Parkinson Disease - metabolism | alpha-Synuclein - metabolism | Index Medicus | α-Synuclein | Alzheimer’s disease | Parkinson’s disease
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11. Full Text Neurologic complications of gastric bypass surgery for morbid obesity
by Juhasz-Pocsine, Katalin and Rudnicki, Stacy A and Archer, Robert L and Harik, Sami I
Neurology, ISSN 0028-3878, 05/2007, Volume 68, Issue 21, pp. 1843 - 1850
Background: The number of bariatric procedures is rapidly growing as the prevalence of obesity in the USA is increasing. Such procedures are not without... 
MALNUTRITION | POLYNEUROPATHY | VERTICAL BANDED GASTROPLASTY | DISORDER | BERIBERI | PERIPHERAL NEUROPATHY | BARIATRIC SURGERY | WERNICKE-KORSAKOFF ENCEPHALOPATHY | DEFICIENCIES | WEIGHT | CLINICAL NEUROLOGY | Brain Diseases, Metabolic - pathology | Postoperative Complications - etiology | Spinal Cord - metabolism | Obesity, Morbid - surgery | Vitamin B 12 Deficiency - etiology | Neurodegenerative Diseases - etiology | Spinal Cord Diseases - physiopathology | Humans | Middle Aged | Male | Peripheral Nervous System Diseases - physiopathology | Wernicke Encephalopathy - physiopathology | Brain - metabolism | Obesity, Morbid - physiopathology | Thiamine Deficiency - etiology | Spinal Cord - pathology | Wernicke Encephalopathy - pathology | Adult | Female | Avitaminosis - pathology | Gastric Bypass - methods | Peripheral Nerves - metabolism | Peripheral Nervous System Diseases - pathology | Copper - deficiency | Postoperative Complications - pathology | Peripheral Nervous System Diseases - etiology | Reoperation | Neurodegenerative Diseases - pathology | Postoperative Complications - physiopathology | Wernicke Encephalopathy - etiology | Brain - physiopathology | Gastric Bypass - adverse effects | Vitamin B 12 Deficiency - physiopathology | Thiamine Deficiency - physiopathology | Peripheral Nerves - pathology | Peripheral Nerves - physiopathology | Avitaminosis - complications | Neurodegenerative Diseases - physiopathology | Spinal Cord Diseases - etiology | Brain Diseases, Metabolic - physiopathology | Dietary Supplements - standards | Avitaminosis - physiopathology | Brain - pathology | Brain Diseases, Metabolic - etiology | Spinal Cord - physiopathology | Spinal Cord Diseases - pathology | Index Medicus | Abridged Index Medicus
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12. Full Text Profiles of extracellular miRNA in cerebrospinal fluid and serum from patients with Alzheimer's and Parkinson's diseases correlate with disease status and features of pathology
by Burgos, Kasandra and Malenica, Ivana and Metpally, Raghu and Courtright, Amanda and Rakela, Benjamin and Beach, Thomas and Shill, Holly and Adler, Charles and Sabbagh, Marwan and Villa, Stephen and Tembe, Waibhav and Craig, David and Van Keuren-Jensen, Kendall
PLoS ONE, ISSN 1932-6203, 05/2014, Volume 9, Issue 5, pp. e94839 - e94839
The discovery and reliable detection of markers for neurodegenerative diseases have been complicated by the inaccessibility of the diseased tissue-such as the... 
CIRCULATING MICRORNAS | BIOMARKERS | SYSTEM | PROTEIN | DEMENTIA | MULTIDISCIPLINARY SCIENCES | DOPAMINE | ALPHA-SYNUCLEIN | DIFFERENTIATION | IDENTIFICATION | EXPRESSION | Parkinson Disease - therapy | Parkinson Disease - pathology | MicroRNAs - cerebrospinal fluid | Humans | Alzheimer Disease - therapy | Male | Alzheimer Disease - cerebrospinal fluid | Alzheimer Disease - pathology | Parkinson Disease - cerebrospinal fluid | Aged, 80 and over | Female | Aged | MicroRNAs - blood | Parkinson Disease - blood | Alzheimer Disease - blood | Proteins | Development and progression | MicroRNA | Alzheimer's disease | Protein binding | Brain | Spinal cord | Deregulation | Parkinson's disease | Neuropathology | Genomics | Central nervous system | Parkinsons disease | Nervous system | Cerebrospinal fluid | Tissues | Gene sequencing | Neurodegeneration | Dementia disorders | Age | Movement disorders | Peripheral circulation | Medical research | Neurodegenerative diseases | Fluid | MiRNA | Gene expression | Patients | Disease control | Diseases | Lewy bodies | Neurological diseases | Pathology | Neurology | RNA-binding protein | Brain research | Ribonucleic acids | Biopsy | MicroRNAs | Stem cells | Protein expression | Alzheimers disease | Dementia | Index Medicus
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