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congenital slow channel syndrome相关文献:
Treatment of slow-channel congenital myasthenic syndrome in a Thai family with fluoxetine.
Dejthevaporn C, Wetchaphanphesat S, Pulkes T, Rattanasiri S, Engel AG, Witoonpanich R.
J Clin Neurosci. 2022 Feb;96:85-89. doi: 10.1016/j.jocn.2021.12.016. Epub 2022 Jan 6.
PMID:34999496
Slow-Channel Congenital Myasthenic Syndrome Due to the Novel Variant c.1396G_A in CHRNA1 That Responds Favorably to 3,4-Diaminopyridine: A Case Report.
Finsterer J.
Cureus. 2024 Nov 13;16(11):e73601. doi: 10.7759/cureus.73601. eCollection 2024 Nov.
PMID:39677241
Fluoxetine is neuroprotective in slow-channel congenital myasthenic syndrome.
Zhu H, Grajales-Reyes GE, Alicea-Vázquez V, Grajales-Reyes JG, Robinson K, Pytel P, Báez-Pagán CA, Lasalde-Dominicci JA, Gomez CM.
Exp Neurol. 2015 Aug;270:88-94. doi: 10.1016/j.expneurol.2014.10.008. Epub 2014 Oct 23.
PMID:25448156
Congenital myasthenic syndromes.
Beeson D.
Handb Clin Neurol. 2024;203:69-88. doi: 10.1016/B978-0-323-90820-7.00013-6.
PMID:39174255
Slow-Channel Congenital Myasthenic Syndrome Due to CHRND Mutation in South Korea.
Min JH, Sohn SY, Kim SY, Joo IS.
J Clin Neurol. 2025 Sep;21(5):464-466. doi: 10.3988/jcn.2025.0186.
PMID:40878311
[Clinical and genetic analysis of a patient with slow-channel congenital myasthenic syndrome].
Liu Y, Ye S, Zhang H, Zhang K, Lyu Y, Gao M, Gai Z, Liu Y.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 May 10;37(5):551-554. doi: 10.3760/cma.j.issn.1003-9406.2020.05.014.
PMID:32335884
Slow-Channel Congenital Myasthenic Syndrome due to a Novel Mutation in the Acetylcholine Receptor Alpha Subunit in a South Asian: A Case Report.
Gooneratne IK, Nandasiri S, Maxwell S, Webster R, Cossins J, Beeson D, Gunaratne K, Herath L, Senanayake S, Chang T.
J Neuromuscul Dis. 2021;8(1):163-167. doi: 10.3233/JND-200566.
PMID:33216040
Acquired slow-channel syndrome.
Scola RH, Werneck LC, Iwamoto FM, Comerlato EA, Kay CK.
Muscle Nerve. 2000 Oct;23(10):1582-5. doi: 10.1002/1097-4598(200010)23:10<1582::aid-mus16>3.0.co;2-h.
PMID:11003795
Molecular Pathophysiology of Congenital Long QT Syndrome.
Bohnen MS, Peng G, Robey SH, Terrenoire C, Iyer V, Sampson KJ, Kass RS.
Physiol Rev. 2017 Jan;97(1):89-134. doi: 10.1152/physrev.00008.2016.
PMID:27807201
Congenital myasthenic syndromes.
Hantaï D, Richard P, Koenig J, Eymard B.
Curr Opin Neurol. 2004 Oct;17(5):539-51. doi: 10.1097/00019052-200410000-00004.
PMID:15367858
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