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1. Motor neuron disease in adults
by Bromberg, M. B. editor. (Mark B.)
2015, Contemporary neurology series, ISBN 019978311X, Volume 88, xxviii, 336
Motor neurons | Amyotrophic lateral sclerosis | Adult | Motor Neuron Disease | Diseases
Book
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2. Motor neuron disease
by Talbot, Kevin and Marsden, Rachael
2008, Facts (Oxford, England), ISBN 0199206910, viii, 151
Amyotrophic lateral sclerosis | Motor Neuron Disease
Book
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3. Motor neuron disease
by Weiss, Michael D. M. D and Carter, Gregory T
2008, Physical medicine and rehabilitation clinics of North America, ISBN 9781416063377, Volume 19, no. 3., xxii, p. 429-690
Motor neurons | Amyotrophic lateral sclerosis | Diseases
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4. Amyotrophic lateral sclerosis
: official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
by Swash, Michael and Hardiman, Orla and World Federation of Neurology. Research Group on Motor Neuron Diseases and World Federation of Neurology and Research Group on Motor Neuron Diseases
Amyotrophic lateral sclerosis, ISSN 1748-2968, 2006
Motor neurons | Amyotrophic lateral sclerosis | Diseases | periodicals
Journal
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5. Dementia and motor neuron disease
by Strong, Michael J
2006, ISBN 0415391660, xiv, 242
physiopathology | Amyotrophic Lateral Sclerosis | complications | therapy | Dementia
Book
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6. Full Text The frontotemporal dementia-motor neuron disease continuum
by Burrell, James R, PhD and Halliday, Glenda M, Prof and Kril, Jillian J, Prof and Ittner, Lars M, Prof and Götz, Jürgen, Prof and Kiernan, Matthew C, Prof and Hodges, John R, Prof
Lancet, The, ISSN 0140-6736, 2016, Volume 388, Issue 10047, pp. 919 - 931
Summary Early reports of cognitive and behavioural deficits in motor neuron disease might have been overlooked initially, but the concept of a frontotemporal... 
Internal Medicine | HEXANUCLEOTIDE REPEAT EXPANSION | MEDICINE, GENERAL & INTERNAL | PTDP-43 PATHOLOGY | LOBAR DEGENERATION | EXPANDED C9ORF72 | ANTISENSE TRANSCRIPTS | BRAIN NETWORK CONNECTIVITY | C9ORF72 EXPANSION | COGNITIVE IMPAIRMENT | AMYOTROPHIC-LATERAL-SCLEROSIS | RNA FOCI | Neuroimaging | Neuroprotective Agents - therapeutic use | Prognosis | Humans | Patient Care Team | Cognition | Frontotemporal Dementia - psychology | Activities of Daily Living | Brain - metabolism | DNA-Binding Proteins - metabolism | DNA Repeat Expansion | DNA Methylation | Motor Neuron Disease - therapy | Motor Neuron Disease - genetics | Riluzole - therapeutic use | C9orf72 Protein | Executive Function | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | DNA-Binding Proteins - genetics | Frontotemporal Dementia - therapy | Motor Neuron Disease - pathology | Neuropsychological Tests | Proteins - genetics | Proteins - metabolism | Image Processing, Computer-Assisted | Brain - pathology | Motor Neuron Disease - psychology | Mutation | Medical colleges | Neurosciences | Neurons | Epidemiology | Dementia | Protein binding | Brain | Gene expression | Patients | Studies | Pathology | Stem cells | DNA methylation | Epigenetics | Genetics | Chromosomes | Deoxyribonucleic acid--DNA
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7. Human motor neuron diseases
by Rowland, Lewis P and Muscular Dystrophy Association
1982, ISBN 9780890047378, Volume 36, xiv, 577
Motor neurons | Amyotrophic lateral sclerosis | Congresses | Diseases
Book
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8. Motor neuron disease
: biology and management
by Leigh, P. Nigel and Swash, Michael
1995, ISBN 3540196854, xviii, 468
Motor neurons | Amyotrophic lateral sclerosis | Motor Neuron Disease | Diseases
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9. Full Text miRNA malfunction causes spinal motor neuron disease
by Sharon Haramati and Elik Chapnik and Yehezkel Sztainberg and Raya Eilam and Raaya Zwang and Noga Gershoni and Edwina McGlinn and Patrick W. Heiser and Anne-Marie Wills and Itzhak Wirguin and Lee L. Rubin and Hidemi Misawa and Clifford J. Tabin and Robert Brown and Alon Chen and Eran Hornstein
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2010, Volume 107, Issue 29, pp. 13111 - 13116
Defective RNA metabolism is an emerging mechanism involved in ALS pathogenesis and possibly in other neurodegenerative disorders. Here, we show that microRNA... 
Nervous system diseases | MicroRNA | Messenger RNA | RNA | Neurodegenerative diseases | Neurons | Amyotrophic lateral sclerosis | Mice | Gene expression regulation | Genetic mutation | ALS | microRNA | Motor neuron | Dicer | Neurodegeneration | MULTIDISCIPLINARY SCIENCES | neurodegeneration | MICROPROCESSOR COMPLEX | AMYOTROPHIC-LATERAL-SCLEROSIS | MUSCULAR-ATROPHY | RNA-BINDING PROTEIN | MESSENGER-RNA | motor neuron | HEAVY NEUROFILAMENT SUBUNIT | MOUSE MODEL | SELECTIVE LOSS | INTERMEDIATE-FILAMENTS | TRANSGENIC MICE | Motor Activity - physiology | Ribonuclease III - metabolism | Axons - metabolism | Muscle Denervation | MicroRNAs - metabolism | Down-Regulation - genetics | Motor Neurons - pathology | Protein Subunits - metabolism | Motor Neurons - metabolism | Muscular Atrophy, Spinal - genetics | Animals | Mice, Mutant Strains | Axons - pathology | Survival Analysis | MicroRNAs - genetics | Neurofilament Proteins - metabolism | Muscular Atrophy, Spinal - physiopathology | Disease Models, Animal | Motor neurons | Nervous system | Degeneration | Genetic aspects | Diagnosis | Properties | Health aspects | Biological Sciences
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10. Full Text TDP-43 Proteinopathy and Motor Neuron Disease in Chronic Traumatic Encephalopathy
by McKee, Ann C and Gavett, Brandon E and Stern, Robert A and Nowinski, Christopher J and Cantu, Robert C and Kowall, Neil W and Perl, Daniel P and Hedley-Whyte, E. Tessa and Price, Bruce and Sullivan, Chris and Morin, Peter and Lee, Hyo-Soon and Kubilus, Caroline A and Daneshvar, Daniel H and Wulff, Megan and Budson, Andrew E
Journal of Neuropathology and Experimental Neurology, ISSN 0022-3069, 09/2010, Volume 69, Issue 9, pp. 918 - 929
Epidemiological evidence suggests that the incidence of amyotrophic lateral sclerosis is increased in association with head injury. Repetitive head injury is... 
Amyotrophic lateral sclerosis | Chronic brain injury | TDP-43 | Tau proteins | Motor neuron disease | Sports | HEAD-INJURY | ALZHEIMERS-DISEASE | AMYOTROPHIC-LATERAL-SCLEROSIS | PARKINSONISM-DEMENTIA COMPLEX | PATHOLOGY | FRONTOTEMPORAL LOBAR DEGENERATION | PROFESSIONAL FOOTBALL PLAYERS | GULF-WAR VETERANS | LOU-GEHRIGS-DISEASE | NEUROSCIENCES | CLINICAL NEUROLOGY | CIGARETTE-SMOKING | ANTECEDENT EVENTS | Motor Neuron Disease - etiology | Brain - anatomy & histology | Brain Injury, Chronic - pathology | Humans | Middle Aged | Brain Injury, Chronic - complications | Athletes | DNA-Binding Proteins - genetics | TDP-43 Proteinopathies - etiology | Motor Neuron Disease - pathology | Brain - metabolism | DNA-Binding Proteins - metabolism | Brain Injury, Chronic - physiopathology | Athletic Injuries - pathology | Aged, 80 and over | Athletic Injuries - complications | Brain - pathology | Adult | Aged | TDP-43 Proteinopathies - pathology | Motor Neuron Disease - physiopathology | TDP-43 Proteinopathies - physiopathology
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11. Full Text Human endogenous retrovirus-K contributes to motor neuron disease
by Li, Wenxue and Lee, Myoung-Hwa and Henderson, Lisa and Tyagi, Richa and Bachani, Muzna and Steiner, Joseph and Campanac, Emilie and Hoffman, Dax A and Geldern, Gloria Von and Johnson, Kory and Maric, Dragan and Morris, H. Douglas and Lentz, Margaret and Pak, Katherine and Mammen, Andrew and Ostrow, Lyle and Rothstein, Jeffrey and Nath, Avindra
Science Translational Medicine, ISSN 1946-6234, 09/2015, Volume 7, Issue 307, pp. 307ra153 - 307ra153
The role of human endogenous retroviruses (HERVs) in disease pathogenesis is unclear. We show that HERV-K is activated in a subpopulation of patients with... 
MEDICINE, RESEARCH & EXPERIMENTAL | HUMAN TISSUES | PROTEIN | GENE | REVERSE-TRANSCRIPTASE ACTIVITY | ALS | DETERMINANT | SERUM | MICE | EXPRESSION | DEGENERATION | CELL BIOLOGY | Endogenous Retroviruses - physiology | Amyotrophic Lateral Sclerosis - physiopathology | Humans | Brain - virology | Amyotrophic Lateral Sclerosis - virology | Mice, Transgenic | Motor Neurons - pathology | Nerve Degeneration - pathology | Terminal Repeat Sequences - genetics | Motor Neuron Disease - pathology | Behavior, Animal | DNA-Binding Proteins - metabolism | Motor Neuron Disease - virology | Amyotrophic Lateral Sclerosis - pathology | Phenotype | Animals | Brain - pathology | Motor Neurons - virology | Motor Neuron Disease - physiopathology | Binding Sites | Virus Activation
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12. Motor neuron disease
by Talbot, Kevin and Marsden, Rachael
2008, The facts series, ISBN 0199206910
Motor neurons | Motor Neuron Disease | Amyotrophic lateral sclerosis | Diseases
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13. Full Text TDP-43 A315T mutation in familial motor neuron disease
by Gitcho, Michael A and Baloh, Robert H and Chakraverty, Sumi and Mayo, Kevin and Norton, Joanne B and Levitch, Denise and Hatanpaa, Kimmo J and White III, Charles L and Bigio, Eileen H and Caselli, Richard and Baker, Matt and Al-Lozi, Muhammad T and Morris, John C and Pestronk, Alan and Rademakers, Rosa and Goate, Alison M and Cairns, Nigel J
Annals of Neurology, ISSN 0364-5134, 04/2008, Volume 63, Issue 4, pp. 535 - 538
To identify novel causes of familial neurodegenerative diseases, we extended our previous studies of TAR DNA-binding protein 43 (TDP-43) proteinopathies to... 
MISSENSE | GENE | INCLUSIONS | TAU | AMYOTROPHIC-LATERAL-SCLEROSIS | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | CLINICAL NEUROLOGY | Amino Acid Sequence | Humans | Middle Aged | Molecular Sequence Data | Male | DNA-Binding Proteins - genetics | Mutation, Missense - genetics | Motor Neuron Disease - pathology | Motor Neuron Disease - metabolism | Alanine - genetics | Genes, Dominant | Motor Neuron Disease - genetics | DNA Mutational Analysis | Pedigree | Threonine - genetics | Aged, 80 and over | Amino Acid Substitution - genetics | Female | Aged
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14. Full Text Mutant dynactin in motor neuron disease
by Floeter, Mary Kay and Bidus, Kimberly and Brown, Robert H and Mann, Eric and Drayna, Dennis and Ludlow, Christy L and LaMonte, Bernadette H and Tokito, Mariko and Jonnakuty, Catherine and Holzbaur, Erika L.F and Fischbeck, Kenneth H and Puls, Imke and Oh, Shin J
Nature Genetics, ISSN 1061-4036, 04/2003, Volume 33, Issue 4, pp. 455 - 456
Impaired axonal transport in motor neurons has been proposed as a mechanism for neuronal degeneration in motor neuron disease. Here we show linkage of a lower... 
CYTOPLASMIC DYNEIN | SWISS-MODEL | COMPLEX | DROSOPHILA-MELANOGASTER | P150(GLUED) COMPONENT | GENETICS & HEREDITY | FAST AXONAL-TRANSPORT | Protein Structure, Tertiary | Microtubule-Associated Proteins - genetics | Protein Structure, Secondary | Drosophila | Humans | Dynactin Complex | Models, Molecular | Mice, Transgenic | Centromere - metabolism | Amino Acid Motifs | Protein Transport | Chromosomes, Human, Pair 2 | Microtubules - metabolism | Animals | Biological Transport | Motor Neuron Disease - genetics | Recombination, Genetic | Cloning, Molecular | Protein Binding | Mice | Models, Genetic | Mutation | Genetic Linkage | Complications and side effects | Gene mutations | Nervous system | Degeneration | Research | Diagnosis | Health aspects | Genetic screening | Methods | Risk factors
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15. WHAT IS HAPPENING TO MOTOR NEURON DISEASE IN NIGERIA?
by Imam, I and Ogunniyi, A
WHAT IS HAPPENING TO MOTOR NEURON DISEASE IN NIGERIA?, 2004
Background: Systematic studies of motor neuron disease were last reported from Ibadan, Nigeria, more than two decades ago. Since then, information about motor... 
Medicine | Motor neuron disease, amyotrophic lateral sclerosis, Nigeria am04001
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16. Drosophila melanogaster models of motor neuron disease
by Cauchi, Ruben J
2013, Neurodegenerative diseases--laboratory and clinical research, ISBN 1626187975
Motor neurons | Amyotrophic lateral sclerosis | Models | Drosophila melanogaster
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17. Full Text Motor Neuron Disease: Pathophysiology, Diagnosis, and Management
by Foster, Laura A and Salajegheh, Mohammad Kian
The American Journal of Medicine, ISSN 0002-9343, 01/2019, Volume 132, Issue 1, pp. 32 - 37
Patients with motor neuron diseases may present to primary care clinic or may be initially encountered in the inpatient setting. Timely diagnosis of these... 
Amyotrophic lateral sclerosis | Poliomyelitis | Motor neuron disease | Kennedy disease | CRITERIA | MEDICINE, GENERAL & INTERNAL | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | GLOBAL EPIDEMIOLOGY | MYELITIS
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18. Full Text Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders
by Novarino, Gaia and Fenstermaker, Ali G and Zaki, Maha S and Hofree, Matan and Silhavy, Jennifer L and Heiberg, Andrew D and Abdellateef, Mostafa and Rosti, Basak and Scott, Eric and Mansour, Lobna and Masri, Amira and Kayserili, Hulya and Al-Aama, Jumana Y and Abdel-Salam, Ghada M. H and Karminejad, Ariana and Kara, Majdi and Kara, Bulent and Bozorgmehri, Bita and Ben-Omran, Tawfeg and Mojahedi, Faezeh and Mahmoud, Iman Gamal El Din and Bouslam, Naima and Bouhouche, Ahmed and Benomar, Ali and Hanein, Sylvain and Raymond, Laure and Forlani, Sylvie and Mascaro, Massimo and Selim, Laila and Shehata, Nabil and Al-Allawi, Nasir and Bindu, P.S and Azam, Matloob and Gunel, Murat and Caglayan, Ahmet and Bilguvar, Kaya and Tolun, Aslihan and Issa, Mahmoud Y and Schroth, Jana and Spencer, Emily G and Rosti, Rasim O and Akizu, Naiara and Vaux, Keith K and Johansen, Anide and Koh, Alice A and Megahed, Hisham and Durr, Alexandra and Brice, Alexis and Stevanin, Giovanni and Gabriel, Stacy B and Ideker, Trey and Gleeson, Joseph G
Science, ISSN 0036-8075, 2014, Volume 343, Issue 6170, pp. 506 - 511
Hereditary spastic paraplegias (HSPs) are neurodegenerative motor neuron diseases characterized by progressive age-dependent loss of corticospinal motor tract... 
PATHWAYS | CYTOKINESIS | TRANSPORT | PROTEIN | HEREDITARY SPASTIC PARAPLEGIA | MULTIDISCIPLINARY SCIENCES | GOLGI-APPARATUS | ARCHITECTURE | ENDOPLASMIC-RETICULUM | MUTATIONS | SUBUNIT | Spastic Paraplegia, Hereditary - genetics | Genetic Association Studies | Synapses - physiology | Humans | Transcriptome | Nucleotides - genetics | Zebrafish | Axons - physiology | Gene Regulatory Networks | Nucleotides - metabolism | Sequence Analysis, DNA | Exome - genetics | Animals | Motor Neuron Disease - genetics | Pyramidal Tracts - metabolism | Biological Transport - genetics | Neurons - metabolism | Mutation | Cohort Studies | Neurogenetics | Physiological aspects | Genetic research | Nervous system | Degeneration | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing | Genetics | Neurons | Neurodegeneration | Neurological disorders
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