晚发型庞贝病的低频酶替代疗法 - Suppr

Low-frequency enzyme replacement therapy in late-onset Pompe disease.

作者信息

Lin Dar-Shong, Chiang Ming-Fu, Ho Che-Sheng, Hsiao Chung-Der, Lin Chang-Yi, Wang Nien-Lu, Chuang Chih-Kuang, Huang Yu-Wen, Chang Po-Chun, Liu Hsuan-Liang

出版信息

Muscle Nerve. 2013 Apr;47(4):612-3. doi: 10.1002/mus.23658. Epub 2013 Jan 16.

DOI:10.1002/mus.23658

PMID:23322609

Abstract

摘要

相似文献

Low-frequency enzyme replacement therapy in late-onset Pompe disease.晚发型庞贝病的低频酶替代疗法

Muscle Nerve. 2013 Apr;47(4):612-3. doi: 10.1002/mus.23658. Epub 2013 Jan 16.

Long-term enzyme-replacement therapy (ERT) with alglucosidase alfa: Evolution of two siblings with juvenile late-onset Pompe disease.用阿糖苷酶α进行长期酶替代疗法（ERT）：两名青少年晚发型庞贝病患者的病情演变

J Neurol Sci. 2015 Nov 15;358(1-2):459-60. doi: 10.1016/j.jns.2015.08.007. Epub 2015 Aug 7.

Improvement of bilateral ptosis on higher dose enzyme replacement therapy in Pompe disease.庞贝病中高剂量酶替代疗法对双侧上睑下垂的改善作用。

J Neuroophthalmol. 2010 Jun;30(2):165-6. doi: 10.1097/WNO.0b013e3181ce162a.

Infantile Pompe disease: clinical and genetic characteristics with an experience of enzyme replacement therapy.婴儿型庞贝病：酶替代治疗经验下的临床和遗传特征

J Child Neurol. 2012 Mar;27(3):319-24. doi: 10.1177/0883073811420295. Epub 2011 Sep 22.

Ptosis in Pompe disease: common genetic background in infantile and adult series.庞贝病中的上睑下垂：婴儿型和成人型系列的共同遗传背景。

J Neuroophthalmol. 2010 Dec;30(4):389-90. doi: 10.1097/WNO.0b013e3181f9a923.

Quantitative computed tomography for enzyme replacement therapy in Pompe disease.用于庞贝病酶替代疗法的定量计算机断层扫描

Brain Dev. 2012 Nov;34(10):834-9. doi: 10.1016/j.braindev.2012.01.013. Epub 2012 Apr 21.

Prognostic factors for late-onset Pompe disease with enzyme replacement therapy: The two sides of low BMI.酶替代疗法治疗晚发型庞贝病的预后因素：低体重指数的两面性。

Mol Genet Metab. 2010 Aug;100(4):388. doi: 10.1016/j.ymgme.2010.04.005. Epub 2010 Apr 20.

Immune modulation in Pompe disease treated with enzyme replacement therapy.采用酶替代疗法治疗庞贝病的免疫调节

Expert Rev Clin Immunol. 2012 Aug;8(6):497-9. doi: 10.1586/eci.12.40.

Efficient therapy of Pompe disease by an acid α-glucosidase conjugate.通过酸性α-葡萄糖苷酶缀合物对庞贝病进行有效治疗。

J Control Release. 2018 Jan 10;269:441-442. doi: 10.1016/j.jconrel.2017.12.010.

24-months results in two adults with Pompe disease on enzyme replacement therapy.两名接受酶替代疗法的庞贝病成年患者的24个月治疗结果。

Clin Neurol Neurosurg. 2011 Jun;113(5):350-7. doi: 10.1016/j.clineuro.2010.09.016. Epub 2011 Apr 7.

引用本文的文献

Are Anti-rhGAA Antibodies a Determinant of Treatment Outcome in Adults with Late-Onset Pompe Disease? A Systematic Review.抗 rhGAA 抗体是否是晚期庞贝病成人治疗效果的决定因素？系统评价。

Biomolecules. 2023 Sep 19;13(9):1414. doi: 10.3390/biom13091414.

36-Months follow-up assessment after cessation and resuming of enzyme replacement therapy in late onset Pompe disease: data from the Swiss Pompe Registry.36 个月随访评估：晚发性庞贝病停止和重新开始酶替代治疗后的结果：来自瑞士庞贝病登记处的数据。

J Neurol. 2018 Dec;265(12):2783-2788. doi: 10.1007/s00415-018-9065-7. Epub 2018 Sep 19.

Cessation and resuming of alglucosidase alfa in Pompe disease: a retrospective analysis.庞贝病中阿糖苷酶α的停药与恢复用药：一项回顾性分析

J Neurol. 2014 Sep;261(9):1684-90. doi: 10.1007/s00415-014-7402-z. Epub 2014 Jun 13.

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Low-frequency enzyme replacement therapy in late-onset Pompe disease.

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