المؤلفون: Durmus, Hacer^Aff1, Sticht, Heinrich, Ceylaner, Serdar, Hashemolhosseini, Said, Deymeer, Feza

المصدر: Acta Neurologica Belgica. 121(6):1755-1760

المؤلفون: Angelini, Corrado^Aff2

المساهمون: Angelini, Corrado^Aff1

المصدر: Genetic Neuromuscular Disorders : A Case-Based Approach. :223-226

المؤلفون: Angelini, Corrado^Aff1, Lispi, Ludovico, Salvoro, Cecilia, Mostacciuolo, Maria Luisa, Vazza, Giovanni

المصدر: Neurological Sciences. 40(3):503-507

المؤلفون: Denis Kudryavtsev, Anastasia Isaeva, Daria Barkova, Ekaterina Spirova, Renata Mukhutdinova, Igor Kasheverov, Victor Tsetlin

المصدر: Molecules, Vol 26, Iss 5, p 1278 (2021)

مصطلحات موضوعية: muscle nicotinic receptor, gain-of-function, channelopathy, slow-channel congenital myasthenia, patch-clamp, molecular dynamics, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1420-3049/26/5/1278; https://doaj.org/toc/1420-3049

URL الوصول: https://doaj.org/article/1883d9d82ce144528da8b6cc88ccab2a

المؤلفون: Weizemann, Luana Patricia, Cheffer, Maycon Hoffmann, Capelario, Elenice de Fatima Souza, Almeida, Samira Maria Ferreira de, Silveira , Rodrigo Euripedes da, Formiga, Cristina Maria Oliveira Martins, Costa, Matheus Gomes da, Silva, Nurya Gabrielly Araújo, Arruda , Maria Dhescyca Ingrid Silva, Zanoni, Rodrigo Daniel

المصدر: Research, Society and Development; Vol. 11 No. 17; e31111738640
Research, Society and Development; Vol. 11 Núm. 17; e31111738640
Research, Society and Development; v. 11 n. 17; e31111738640
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI

مصطلحات موضوعية: Congenital Slow Channel Myasthenic Syndrome, Miastenia Gravis, Síndrome miastênica congênita do canal lento, Myasthenia Gravis, índrome miasténico congénito de canal lento, Atividade motora, Motor activity, Actividad del motor

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3056::367d2c47d9f715073b26c186c38f0af0
https://rsdjournal.org/index.php/rsd/article/view/38640

المؤلفون: Angelini, Corrado^Aff2

المساهمون: Angelini, Corrado^Aff1

المصدر: Genetic Neuromuscular Disorders : A Case-Based Approach. :191-194

Degree: MD

المؤلفون: Jia-Ze Tan, Yuan Man, Fei Xiao

المصدر: Chinese Medical Journal, Vol 129, Iss 21, Pp 2596-2602 (2016)

مصطلحات موضوعية: Acetylcholine Receptor Epsilon-subunit Gene, Repetitive-compound Muscle Action Potential, Repetitive Nerve Stimulation, Slow-channel Congenital Myasthenic Syndrome, Medicine

وصف الملف: electronic resource

Relation: http://www.cmj.org/article.asp?issn=0366-6999;year=2016;volume=129;issue=21;spage=2596;epage=2602;aulast=Tan; https://doaj.org/toc/0366-6999

URL الوصول: https://doaj.org/article/4cc5e0a11305440db774323d10c88c87

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المؤلفون: Huan Yang, Kun Huang, Yue-Bei Luo, Fang-Fang Bi

المصدر: Current Neuropharmacology

مصطلحات موضوعية: 0301 basic medicine, Combination therapy, MEDLINE, Cochrane Library, Gene mutation, Bioinformatics, Article, 03 medical and health sciences, 0302 clinical medicine, Medicine, CHRNE, Pharmacology (medical), primary AChR deficiency, fast-channel syndrome, slow-channel syndrome, Acetylcholine receptor, Pharmacology, biology, business.industry, General Medicine, Congenital myasthenic syndrome, medicine.disease, Psychiatry and Mental health, 030104 developmental biology, Neurology, congenital myasthenic syndrome, Meta-analysis, biology.protein, Neurology (clinical), β2-adrenergic receptor agonist, business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a677059da864b8319e9d79baaf5291c6
https://doi.org/10.2174/1570159x18666200729092332

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