All Relations between Neuromuscular Diseases and spinal cord ventral horn motor neuron alpha

Reference Sentence Publish Date Extraction Date Species
Stephen D Cahalan, Justin D Perkins, Ines Boehm, Ross A Jones, Thomas H Gillingwater, Richard J Pierc. A method to identify, dissect and stain equine neuromuscular junctions for morphological analysis. Journal of anatomy vol issue 2022 36087283 morphological study of the neuromuscular junction (nmj), a specialised peripheral synapse formed between a lower motor neuron and skeletal muscle fibre, has significantly contributed to the understanding of synaptic biology and neuromuscular disease pathogenesis. 2022-09-10 2022-09-14 Not clear
Gloria Cristofano, Martina Fucci, Maria Carmela Oliva, Marta De Rinaldis, Antonio Trabacc. Peripheral circulation disturbances in two consecutive children with spinal muscular atrophy and literature review. Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology vol 41 issue 2 2022 35832505 spinal muscular atrophy is a progressive and severe hereditary (autosomal recessive) neuromuscular disease characterized by lower motor neuron degeneration in the spinal cord and brainstem causing a clinical picture of progressive muscle atrophy and weakness of skeletal and respiratory muscles. 2022-07-14 2022-07-19 Not clear
Mitra Forouhan, Wooi Fang Lim, Laura C Zanetti-Domingues, Christopher J Tynan, Thomas C Roberts, Bilal Malik, Raquel Manzano, Alfina A Speciale, Ruth Ellerington, Antonio Garcia-Guerra, Pietro Fratta, Gianni Sorar\\xc3\\xba, Linda Greensmith, Maria Pennuto, Matthew J A Wood, Carlo Rinald. AR cooperates with SMAD4 to maintain skeletal muscle homeostasis. Acta neuropathologica vol issue 2022 35522298 this adult-onset neuromuscular disease is caused by a polyglutamine expansion (polyq) in ar and is characterized by progressive muscle weakness and atrophy secondary to a combination of lower motor neuron degeneration and primary muscle atrophy. 2022-05-06 2022-05-07 Not clear
Laura M Mattson, Walter O Alomar-Jimenez, Sandra L Hear. An Atypical Presentation of Hirayama Disease With Lower Limb Myelopathic Symptoms Only. American journal of physical medicine & rehabilitation vol 100 issue 12 2021 34267058 hirayama disease is a rare neuromuscular disease, which classically presents as lower motor neuron weakness and atrophy in the upper limbs and specifically the c7-t1 myotomes. 2021-11-25 2022-01-13 Not clear
Mathilde Chivet, Caterina Marchioretti, Marco Pirazzini, Diana Piol, Chiara Scaramuzzino, Maria Jos\\xc3\\xa8 Polanco, Vanina Romanello, Emanuela Zuccaro, Sara Parodi, Maurizio D'Antonio, Carlo Rinaldi, Fabio Sambataro, Elena Pegoraro, Gianni Soraru, Udai Bhan Pandey, Marco Sandri, Manuela Basso, Maria Pennut. Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism. Cells vol 9 issue 2 2021 32019272 polyglutamine (polyq) expansions in the androgen receptor (ar) gene cause spinal and bulbar muscular atrophy (sbma), a neuromuscular disease characterized by lower motor neuron (mn) loss and skeletal muscle atrophy, with an unknown mechanism. 2021-02-10 2022-01-13 Not clear
Hannelore K van der Burgh, Henk-Jan Westeneng, Jil M Meier, Michael A van Es, Jan H Veldink, Jeroen Hendrikse, Martijn P van den Heuvel, Leonard H van den Ber. Cross-sectional and longitudinal assessment of the upper cervical spinal cord in motor neuron disease. NeuroImage. Clinical vol 24 issue 2020 31499409 amyotrophic lateral sclerosis (als) is a progressive neuromuscular disease characterized by both upper and lower motor neuron degeneration. 2020-09-21 2022-01-13 Not clear
Shannon Niedermeyer, Michael Murn, Philip J Cho. Respiratory Failure in Amyotrophic Lateral\\xc2\\xa0Sclerosis. Chest vol 155 issue 2 2019 29990478 amyotrophic lateral sclerosis is a progressive neuromuscular disease characterized by both lower motor neuron and upper motor neuron dysfunction. 2019-11-15 2022-01-13 Not clear
S\\xc3\\xb2nia A\\xc3\\xb1o. Acute lower motor neuron tetraparesis. The Veterinary clinics of North America. Small animal practice vol 44 issue 6 2015 25441630 flaccid nonambulatory tetraparesis or tetraplegia is an infrequent neurologic presentation; it is characteristic of neuromuscular disease (lower motor neuron [lmn] disease) rather than spinal cord disease. 2015-08-04 2022-01-12 Not clear
Ximena Paez-Colasante, Bonnie Seaberg, Tara L Martinez, Lingling Kong, Charlotte J Sumner, Mendell Rime. Improvement of neuromuscular synaptic phenotypes without enhanced survival and motor function in severe spinal muscular atrophy mice selectively rescued in motor neurons. PloS one vol 8 issue 9 2014 24086650 in the inherited childhood neuromuscular disease spinal muscular atrophy (sma), lower motor neuron death and severe muscle weakness result from the reduction of the ubiquitously expressed protein survival of motor neuron (smn). 2014-07-18 2022-01-12 Not clear
Johnny S Salameh, Nazem Atassi, William S Davi. SOD1 (A4V)-mediated ALS presenting with lower motor neuron facial diplegia and unilateral vocal cord paralysis. Muscle & nerve vol 40 issue 5 2009 19618436 amyotrophic lateral sclerosis (als) is a progressive degenerative neuromuscular disease that presents with upper and lower motor neuron signs. 2009-12-01 2022-01-12 Not clear
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