المؤلفون: Wang, François-Charles, Gerard, Pascale, Bouquiaux, Olivier

المصدر: Revue Médicale de Liège, 59 Suppl 1, 38-48 (2004); XIV journées francophones d'ENMG, 26-28 mai 2004

مصطلحات موضوعية: Amyotrophic Lateral Sclerosis/pathology, Cell Count/methods, Electrophysiology, Humans, Motor Neurons/pathology, Human health sciences, Neurology, Sciences de la santé humaine, Neurologie

Relation: urn:issn:0370-629X; urn:issn:2566-1566

URL الوصول: https://orbi.uliege.be/handle/2268/114733

المؤلفون: Rothstein, Jeffrey D.

مصطلحات موضوعية: Amyotrophic lateral sclerosis., Nervous system -- Degeneration., Oligodendroglia., Amyotrophic Lateral Sclerosis -- metabolism., Amyotrophic Lateral Sclerosis -- pathology., Lactic Acid -- metabolism., Monocarboxylic Acid Transporters -- metabolism., Motor Neurons -- pathology., Nerve Degeneration -- metabolism., Oligodendroglia -- metabolism.

المؤلفون: Stefanie Schreiber, Jose Bernal, Philipp Arndt, Frank Schreiber, Patrick Müller, Lorena Morton, Rüdiger Christian Braun-Dullaeus, Maria Del Carmen Valdés-Hernández, Roberto Duarte, Joanna Marguerite Wardlaw, Sven Günther Meuth, Grazia Mietzner, Stefan Vielhaber, Ildiko Rita Dunay, Alexander Dityatev, Solveig Jandke, Hendrik Mattern

المصدر: Schreiber, S, Bernal, J, Arndt, P, Schreiber, F, Müller, P, Morton, L, Braun-Dullaeus, R C, Valdés-Hernández, M D C, Duarte, R, Wardlaw, J M, Meuth, S G, Mietzner, G, Vielhaber, S, Dunay, I R, Dityatev, A, Jandke, S & Mattern, H 2023, ' Brain Vascular Health in ALS Is Mediated through Motor Cortex Microvascular Integrity ', Cells, vol. 12, no. 6 . https://doi.org/10.3390/cells12060957
Cells 12(6), 957 (2023). doi:10.3390/cells12060957 special issue: "Amyotrophic Lateral Sclerosis: Understanding the Pathogenetic Mechanisms for the Development of New Therapies"

مصطلحات موضوعية: metabolism [Motor Cortex], Vascular Endothelial Growth Factor A, amyotrophic lateral sclerosis, pathology [Motor Neurons], metabolism [Amyotrophic Lateral Sclerosis], exerkines, Vascular Endothelial Growth Factor A/metabolism, pathology [Blood-Brain Barrier], vascular supply, metabolism [Vascular Endothelial Growth Factor A], Motor Neurons/pathology, General Medicine, pericytes, Motor Cortex/metabolism, motor cortex, ddc:570, Humans, Amyotrophic Lateral Sclerosis/metabolism, Blood-Brain Barrier/pathology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38970d61fb7a93845bd191b92d860f9f
https://doi.org/10.3390/cells12060957

المساهمون: Nakano, Imaharu., Hirano, Asao, 1926-

مصطلحات موضوعية: Motor Neurons -- pathology., Amyotrophic Lateral Sclerosis., Amyotrophic lateral sclerosis -- Congresses., Congresses.

Relation: TMIN International Symposium on "Amyotrophic Lateral Sclerosis" (1995 : Tokyo, Japan)

المؤلفون: Raghavendra Selvan, Ilary Allodi, Ole Kiehn, Roser Montañana-Rosell, Peter Löw

المساهمون: University of St Andrews. School of Psychology and Neuroscience

المصدر: Nature Communications
Allodi, I, Montañana-Rosell, R, Selvan, R, Löw, P & Kiehn, O 2021, ' Locomotor deficits in a mouse model of ALS are paralleled by loss of V1-interneuron connections onto fast motor neurons ', Nature Communications, vol. 12, no. 1, 3251 . https://doi.org/10.1038/s41467-021-23224-7
Nature Communications, Vol 12, Iss 1, Pp 1-18 (2021)

مصطلحات موضوعية: 0301 basic medicine, Male, Superoxide Dismutase-1/genetics, General Physics and Astronomy, Mice, 0302 clinical medicine, Superoxide Dismutase-1, Potential source, Spinal Cord/cytology, Motor Neurons, Spinal cord, Multidisciplinary, musculoskeletal, neural, and ocular physiology, Phenotype, medicine.anatomical_structure, Locomotion/physiology, Muscle Fibers, Fast-Twitch, Female, Neuromuscular Junction/pathology, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry, Locomotion, Interneuron, Science, Transgene, Neuromuscular Junction, Mice, Transgenic, QH426 Genetics, Biology, Inhibitory postsynaptic potential, Amyotrophic Lateral Sclerosis (ALS)/genetics, General Biochemistry, Genetics and Molecular Biology, Article, 03 medical and health sciences, Superoxide Dismutase/genetics, Interneurons, medicine, Homeodomain Proteins/metabolism, Animals, Humans, Postnatal day, QH426, Muscle Fibers, Fast-Twitch/physiology, MCC, Homeodomain Proteins, Superoxide Dismutase, Disease progression, Amyotrophic Lateral Sclerosis, DAS, General Chemistry, Motor Neurons/pathology, Motor neuron, Disease Models, Animal, 030104 developmental biology, nervous system, RC0321, Interneurons/pathology, Neuroscience, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bccdc89c04a0317bdef7c2aaf98a8855
http://europepmc.org/articles/PMC8166981

المؤلفون: Graffmo, Karin Sixtensdotter

مصطلحات موضوعية: Superoxide dismutase -- genetics, Amyotrophic lateral sclerosis -- genetics, Amyotrophic lateral sclerosis -- enzymology, Mutation, Spinal cord -- pathology, Motor neurons -- pathology

URL الوصول: http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1376

Degree: Diss. (sammanfattning) Umeå : Univ., 2007

المؤلفون: Eric Tamrazian, Rhona Seijffers, Martin K. Selig, Meri Hynynen, Jiangwen Zhang, Jonathan C. Matthews, Adam Chen, Clifford J. Woolf, Olusegun Babaniyi, Robert H. Brown

المصدر: Proceedings of the National Academy of Sciences. 111:1622-1627

مصطلحات موضوعية: Cell Survival, Muscle, Skeletal/*innervation, Biology, Neuromuscular junction, Mice, Atrophy, Superoxide Dismutase/genetics, medicine, Animals, Amyotrophic lateral sclerosis, Axon, Muscle, Skeletal, Motor Neurons/*pathology, Motor Neurons, Denervation, Activating Transcription Factor 3, Multidisciplinary, Superoxide Dismutase, Amyotrophic Lateral Sclerosis, Biological Sciences, Motor neuron, medicine.disease, Muscle atrophy, Disease Models, Animal, Activating Transcription Factor 3/*metabolism, medicine.anatomical_structure, Amyotrophic Lateral Sclerosis/pathology/*physiopathology, nervous system, Soma, medicine.symptom, Neuroscience

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51a98935747575c38597913208e0e020
https://doi.org/10.1073/pnas.1314826111

المؤلفون: Elizabeth O. Johnson, Panagiotis Skandalakis, Maria Piagkou, Theano Demesticha

المصدر: Clinical Anatomy. 24:143-150

مصطلحات موضوعية: Histology, Mandibular Nerve, Mandibular nerve, Lingual Nerve, Lateral pterygoid muscle, Nerve Compression Syndromes/complications/*pathology/physiopathology, Paresis/etiology/*pathology/physiopathology, Muscle Weakness/etiology/*pathology/physiopathology, stomatognathic system, Tongue, medicine, Humans, Paresthesia, Neuralgia/etiology/*pathology/physiopathology, Lingual nerve, Motor Neurons, Muscle Weakness, Paresthesia/etiology/*pathology/physiopathology, business.industry, Nerve Compression Syndromes, Infratemporal fossa, Motor Neurons/pathology, General Medicine, Hypoesthesia, Anatomy, Axons, Paresis, stomatognathic diseases, Axons/pathology, medicine.anatomical_structure, Entrapment Neuropathy, Neuralgia, Mandibular Nerve/anatomy & histology/pathology, Medial pterygoid muscle, Trigeminal Nerve Injuries, Atrophy/etiology/pathology, Atrophy, medicine.symptom, business, Lingual Nerve/anatomy & histology/pathology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91b0faa9cf6c42498f8466b04ca7bbc0
https://doi.org/10.1002/ca.21089

المؤلفون: Paul N. Hoffman, Mohamed H. Farah, Sylvain Lengacher, Ping Wu Zhang, Pierre J. Magistretti, Brett M. Morrison, Akivaga Tsingalia, Lin Jin, Yiting Liu, Youngjin Lee, Yun Li, Luc Pellerin, Jeffrey D. Rothstein

المصدر: Nature
Nature, vol. 487, no. 7408, pp. 443-448

مصطلحات موضوعية: Glutamate Uptake, Neuronal-Activity, Mice, 0302 clinical medicine, Superoxide Dismutase-1, Premovement neuronal activity, Axon, RNA, Small Interfering, Myelin Sheath, Motor Neurons, 0303 health sciences, Multidisciplinary, biology, Symporters, Neurodegeneration, Amyotrophic-Lateral-Sclerosis, Cell biology, Oligodendroglia, Protein Transport, medicine.anatomical_structure, Monocarboxylate transporter 1, Biochemistry, In-Vivo, Genetically modified mouse, Monocarboxylic Acid Transporters, Heterozygote, Cell Survival, Central nervous system, Down-Regulation, Mice, Transgenic, Central-Nervous-System, Article, Transgenic Mice, Cell Line, 03 medical and health sciences, medicine, Animals, Humans, Mouse-Brain, Lactic Acid, 030304 developmental biology, Superoxide Dismutase, Adult Brain, fungi, Amyotrophic Lateral Sclerosis, Spinal-Cord, Transporter, medicine.disease, Axons, Monocarboxylate Transporter Mct1, Disease Models, Animal, nervous system, Symporter, Nerve Degeneration, biology.protein, Amyotrophic Lateral Sclerosis/genetics, Amyotrophic Lateral Sclerosis/metabolism, Axons/metabolism, Axons/pathology, Lactic Acid/metabolism, Monocarboxylic Acid Transporters/deficiency, Monocarboxylic Acid Transporters/genetics, Motor Neurons/metabolism, Motor Neurons/pathology, Myelin Sheath/metabolism, Nerve Degeneration/metabolism, Oligodendroglia/metabolism, Superoxide Dismutase/genetics, Superoxide Dismutase/metabolism, Symporters/deficiency, Symporters/genetics, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::198e443f1de65b536bc9b5c7ab2d083b
https://pubmed.ncbi.nlm.nih.gov/23166928

المؤلفون: Muller, H. D., Mugler, M., RAMAEKERS, Vincent, Schroder, J. M.

المصدر: Hereditary motor and sensory neuropathy with absence of large myelinated fibers due to absence of large neurons in dorsal root ganglia and anterior horns, clinically associated with deafness, mental retardation, and epilepsy (HMSN-ADM). Journal of the peripheral nervous system : JPNS, 5(3), 147-57., United States. (2000).

مصطلحات موضوعية: Anterior Horn Cells/pathology, Cerebellar Nuclei/pathology, Child, Preschool, Deafness/pathology, Epilepsy/pathology, Fatal Outcome, Female, Ganglia, Spinal/pathology, Hereditary Sensory and Motor Neuropathy/pathology, Humans, Infant, Intellectual Disability/pathology, Motor Neurons/pathology, Nerve Fibers, Myelinated/pathology, Neurons, Afferent/pathology, Human health sciences :: Pediatrics, Sciences de la santé humaine :: Pédiatrie, Human health sciences :: Neurology, Sciences de la santé humaine :: Neurologie

URL الوصول: https://orbi.uliege.be/handle/2268/168847