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941por Clarke, Benjamin E., Gil, Rebecca San, Yip, Jing, Kalmar, Bernadett, Greensmith, Linda“…Preferential neuronal vulnerability is characteristic of several neurodegenerative diseases including the motor neuron disease amyotrophic lateral sclerosis (ALS). …”
Publicado 2019
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942“…Perampanel (PER) is a selective blocker of AMPA receptors showing efficacy in treating various epileptic disorders including brain tumor-related epilepsy and also potential in treating motor neuron disease. However, besides its inhibition of AMPA-induced currents, whether PER has any other direct ionic effects in different types of neurons remains largely unknown. …”
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943“…Parkinson’s disease, motor neuron disease, cerebral palsy, and stroke) and is defined as excessive saliva accumulation leading to unintentional loss of saliva from the mouth. …”
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944por Bond, Leila, Bowen, Gloria, Mertens, Benjamin, Denson, Keelie, Jordan, Kathleen, Vidakovic, Branislav, Mitchell, Cassie S.“…Associations of modulators of quality of life (QoL) and survival duration are assessed in the fatal motor neuron disease, Amyotrophic Lateral Sclerosis. Major categories include clinical impression of mood (CIM); physical health; patient social support; and usage of interventions, pharmaceuticals, and supplements. …”
Publicado 2020
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945“…Spinal muscular atrophy (SMA) is a motor neuron disease. Nusinersen, a splice-switching antisense oligonucleotide (ASO), was the first approved drug to treat SMA. …”
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946por Ruiz-Soto, María, Riancho, Javier, Tapia, Olga, Lafarga, Miguel, Berciano, María T.“…Conclusions: SGCs emerge as a primary pathophysiological target in the SOD1 transgenic murine model of ALS, clearly reinforcing the pathogenic role of glial cells in motor neuron disease. Presymptomatic alterations of SGCs, might not only be responsible of sensory disturbances in ALS, but due to spinal cord sensory-motor circuits could also contribute to anterior horn motor disturbances.…”
Publicado 2020
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947“…There are also changes in NMJ structure and function in motor neuron disease, spinal muscle atrophy and sarcopenia that are likely to be secondary but might provide treatment targets. …”
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948por Müller, Hans-Peter, Lulé, Dorothée, Roselli, Francesco, Behler, Anna, Ludolph, Albert C., Kassubek, Jan“…CONCLUSION: The tract-of-interest-based analysis showed a microstructural callosal involvement pattern in C9orf72-associated ALS that included the motor segment III together with frontal callosal connections, as an imaging signature of the C9orf72-associated overlap of motor neuron disease and frontotemporal pathology.…”
Publicado 2021
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949por Stipancic, Kaila L., Yunusova, Yana, Campbell, Thomas F., Wang, Jun, Berry, James D., Green, Jordan R.“…Objective: Understanding clinical variants of motor neuron diseases such as amyotrophic lateral sclerosis (ALS) is critical for discovering disease mechanisms and across-patient differences in therapeutic response. …”
Publicado 2021
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950por Kimizu, Tomokazu, Ida, Shinobu, Okamoto, Kentaro, Awano, Hiroyuki, Niba, Emma Tabe Eko, Wijaya, Yogik Onky Silvana, Okazaki, Shin, Shimomura, Hideki, Lee, Tomoko, Tominaga, Koji, Nabatame, Shin, Saito, Toshio, Hamazaki, Takashi, Sakai, Norio, Saito, Kayoko, Shintaku, Haruo, Nozu, Kandai, Takeshima, Yasuhiro, Iijima, Kazumoto, Nishio, Hisahide, Shinohara, Masakazu“…A total of 515 patients suspected of having SMA or another lower motor neuron disease were tested. Among these patients, 228 were diagnosed as having SMA with survival motor neuron 1 (SMN1) deletion. …”
Publicado 2021
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951por Zeng, Xiaoke, MacLeod, Jill, Berriault, Colin, DeBono, Nathan L, Arrandale, Victoria H, Harris, Anne M, Demers, Paul A“…Outcomes included Alzheimer’s disease, Alzheimer’s with other dementias, Parkinson’s disease, parkinsonism, and motor neuron disease. METHODS: The cohort was created by linking a database of mining workers’ work history to healthcare records. …”
Publicado 2021
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952“…Given that the generated NPCs can be differentiated into the majority of excitatory and inhibitory neurons, but hardly MNs, we thus further differentiate NPCs towards MNs by overexpressing refined sets of transcription factors, especially by adding human SOX11, whilst improving a series of differentiation conditions to yield mature MNs for good modeling of motor neuron diseases. We thus refined a detailed step-by-step strategy for inducing hPSCs towards long-term preservable NPCs, and further specified MNs based on the NPC platform.…”
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953“…The neurotoxic effects of MAM administered to rats during cortical brain development (specifically, gestation day 17) are used to model the histological, neurophysiological and behavioral deficits of human schizophrenia, a condition that may precede or follow clinical onset of motor neuron disease in subjects with sporadic ALS and ALS/PDC. …”
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954por Antoniadi, Anna Markella, Galvin, Miriam, Heverin, Mark, Wei, Lan, Hardiman, Orla, Mooney, Catherine“…Amyotrophic Lateral Sclerosis (ALS), also known as Motor Neuron Disease (MND), is a rare and fatal neurodegenerative disease. …”
Publicado 2022
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955por Gaja-Capdevila, Núria, Hernández, Neus, Yeste, Sandra, Reinoso, Raquel F., Burgueño, Javier, Montero, Ana, Merlos, Manuel, Vela, José M., Herrando-Grabulosa, Mireia, Navarro, Xavier“…Motor neuron diseases (MNDs) include sporadic and hereditary neurological disorders characterized by progressive degeneration of motor neurons (MNs). …”
Publicado 2022
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956“…Lathyriasis or lathyrism is a form of upper motor neuron disease caused by the dietary intake of grass pea (Lathyrus sativus). …”
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957por Kapoor, Tarun, Mehan, Sidharth, Suri, Manisha, Sharma, Nidhi, Kumar, Nitish, Narula, Acharan S., Alshammari, Abdulrahman, Alasmari, Abdullah F., Alharbi, Metab, Assiri, Mohammed A., Kalfin, Reni“…Therefore, the results of these studies contribute to a better understanding of the possible role that natural phytochemicals FSK could have in preventing motor neuron diseases, such as multiple sclerosis.…”
Publicado 2022
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958“…Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease. Since there are no pathognomonic tests for ALS prognoses; clinical diagnoses of the disease take time and are usually difficult. …”
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959“…ALS Forum (alsforums.com) is an online support group for those who have motor neuron disease or amyotrophic lateral sclerosis (ALS). …”
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960por Yap, Kah Hui, Azmin, Shahrul, Makpol, Suzana, Damanhuri, Hanafi Ahmad, Mustapha, Muzaimi, Hamzah, Jemaima Che, Ibrahim, Norlinah Mohamed“…This systematic review summarizes the effects of trehalose on its underlying mechanisms in animal models of selected neurodegenerative disorders (tau pathology, synucleinopathy, polyglutamine tract, and motor neuron diseases). All animal studies on neurodegenerative diseases treated with trehalose published in Medline (accessed via EBSCOhost) and Scopus were considered. …”
Publicado 2022
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