[1]王明秋,肖兴军,朱冬梅.常染色体隐性遗传性肢带型肌营养不良症研究进展[J].卒中与神经疾病杂志,2017,24(05):481-483.[doi:10.3969/j.issn.1007-0478.2017.05.029]
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常染色体隐性遗传性肢带型肌营养不良症研究进展()
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《卒中与神经疾病》杂志[ISSN:1007-0478/CN:42-1402/R]

卷:
第24卷
期数:
2017年05期
页码:
481-483
栏目:
综 述
出版日期:
2017-10-26

文章信息/Info

文章编号:
1007-0478(2017)05-0481-03
作者:
王明秋肖兴军朱冬梅
150081 黑龙江省哈尔滨医科大学附属第二医院神经内科[王明秋 肖兴军(通信作者)]; 中航工业哈尔滨242医院(朱冬梅)
分类号:
R746.2
DOI:
10.3969/j.issn.1007-0478.2017.05.029

参考文献/References:

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[2] Di Fruscio Giuseppina,Garofalo Arcomaria,Mutarelli Margherita,et al.Are all the previously reported genetic variants in limb girdle muscular dystrophy genes pathogenic?[J].Eur J Hum Genet,2016,24(1):73-77.
[3] Nigro V,Savarese M.Genetic basis of limb-girdle muscular dystrophies:the 2014 update[J].Acta Myol,2014,33(1):1-12.
[4] Schindler F,Scotton Chiara,Zhang Jianguo,et al.POPDC1(S201F)causes muscular dystrophy and arrhythmia by affecting protein trafficking[J].J Clin Invest,2016,126(1):239-253.
[5] Rebelo Sandra,Da Cruz E Silva F,Da Cruz E Silva A.Genetic mutations strengthen functional association of LAP1 with DYT1 dystonia and muscular dystrophy[J].Mutation research.Reviews in mutation research,2015,766(4):42-47.
[6] Mahmood A,Jiang Mei.Limb-girdle muscular dystrophies:where next after six decades from the first proposal(Review)[J].Mol Med Rep,2014,9(5):1515-1532.
[7] Mitsuhashi Satomi,Kang B.Update on the genetics of limb girdle muscular dystrophy[J].Semin Pediatr Neurol,2012,19(4):211-218.
[8] Kaplan JC,Hamroun D.The 2014 version of the gene table of monogenic neuromuscular disorders(nuclear genome)[J].Neuromuscul Disord,2013,23(12):1081-1111.
[9] Cotta Ana,Carvalho Elmano,Da-Cunha-Júnior Lopes,et al.Common recessive limb girdle muscular dystrophies differential diagnosis:why and how?[J].Arq Neuropsiquiatr,2014,72(9):721-734.
[10] Michel Y,Hoenderop G,Bindels J.Calpain-3-mediated regulation of the Na+-Ca2+ exchanger isoform 3[J].Pflugers Arch,2016,468(2):243-255.
[11] Al-Zaidy A,Malik Vinod,Kneile Kelley,et al.A slowly progressive form of limb-girdle muscular dystrophy type 2C associated with founder mutation in the SGCG gene in Puerto Rican Hispanics[J].Mol Genet Genomic Med,2015,3(2):92-98.
[12] Semplicini Claudio,Vissing John,Dahlqvist R,et al.Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E[J].Neurology,2015,84(17):1772-1781.
[13] Lerario A,Cogiamanian F,Marchesi C,et al.Effects of rituximab in two patients with dysferlin-deficient muscular dystrophy [J].BMC Musculoskelet Disord,2010,11(1):157.
[14] Bastian Alexandra,Mageriu V,Micu Gianina,et al.The growing family of Limb-Girdle muscular dystrophies:old and newly identified members[J].Rom J Intern Med,2015,53(1):13-24.
[15] Wattjes P,Kley A,Fischer Dirk.Neuromuscular imaging in inherited muscle diseases[J].Eur Radiol,2010,20(10):2447-2460.
[16] Sarkozy Anna,Deschauer Marcus,Carlier Yves,et al.Muscle MRI findings in limb girdle muscular dystrophy type 2L[J].Neuromuscul Disord,2012,22(Suppl 2):S122-S129.

备注/Memo

备注/Memo:
基金项目:黑龙江省科学技术厅资助肢带型肌营养不良相关基因的克隆和功能研究(D2007-24)
更新日期/Last Update: 2017-10-20