1. Shengyao Su, Lin Lei, Zhirong Fan, Shu Zhang, Qi Wen, Jingsi Wang, Yan Lu, Li Di, Min Wang, Hai Chen and Yuwei Da.Clinical Predictors of Relapse in a Cohort of Steroid-Treated Patients With Well-Controlled Myasthenia Gravis.Front Immunol.2022.13.816243.SCI |
2. Li Di, Faxiu Shen, Xinmei Wen, Yan Lu, Wenjia Zhu, Min Wang and Yuwei Da. A Randomized Open-Labeled Trial of Methotrexate as a Steroid-Sparing Agent for Patients With Generalized Myasthenia Gravis.frontiers in immunology.2022.13.1-10.SCI |
3. Lin Lei 1, Zhirong Fan, Shengyao Su, Min Xu, Hai Chen, Wenjia Zhu, Qinrong Luan, Yuwei Da.Involvement of Ocular Muscles in Patients With Myasthenia Gravis With Nonocular Onset.J Neuroophthalmol.2022.42(1).e260-e266.SCI |
4. Qianwen Li , Wenjia Zhu ,Xinmei Wen , Zhenxiang Zang ,Yuwei Da ,Jie Lu.Different sensorimotor mechanism in fast and slow progression amyotrophic lateral sclerosis.Hum Brain Mapp.2022.1(43).1710-1719.SCI |
5. Qianwen Li, Wenjia Zhu, Xinmei Wen, Zhenxiang Zang, Yuwei Da and Jie Lu.Beyond the Motor Cortex: Thalamic Iron Deposition Accounts for Disease Severity in Amyotrophic Lateral Sclerosis.Front Neurol.2022.13.791300. |
6. Lin Lei,Hai Chen,Yan Lu,Wenjia Zhu,Yasheng Ouyang,Jianying Duo,Zhiguo Chen,Yuwei Da*.Unusual electrophysiological findings in a Chinese ALS 4 family with SETX-L389S mutation: a three-year follow-up. J Neurol.2021.268(3).1050-1058.SCI |
7. 雷霖,李尊波,沈发秀,刘晴,张雪萍,范志荣,苏圣尧,卢岩,邸丽,王敏,朵建英,笪宇威*.成人抗低密度脂蛋白受体相关蛋白4抗体阳性重症肌无力患者的临床特点分析.中华神经科杂志.2021.54(2).85-91.核心期刊 |
8. 9. 雷霖,李尊波,沈发秀,刘晴,张雪萍,范志荣,苏圣尧,卢岩,邸丽,王敏,朵建英,笪宇威.成人抗低密度脂蛋白受体相关蛋白4抗体阳性重症肌无力患者的临床特点分析.中华神经科杂志.2021.54(2).85-91.核心期刊 |
9. 6. Zhirong Fan, Deqiang Zheng, Xinmei Wen, Faxiu Shen, Lin Lei, Shengyao Su, Shu Zhang, Qing Liu, Xueping Zhang, Yan Lu, Li Di, Xin-Ming Shen, Yuwei Da.CYP3A5*3 polymorphism and age affect tacrolimus blood trough concentration in myasthenia gravis patients. J Neuroimmunol.2021.355(15).1-6.SCI |
10. Xinmei Wen, Wenjia Zhu, Nan L. Xia, Qianwen Li , Li Di, Shu Zhang, Hai Chen,Yan Lu, Min Wang, Min Xu, Suobin Wang, Xin-Ming Shen, Jie Lu and Yuwei Da.Missense Mutations of Codon 116 in the SOD1 Gene Cause Rapid Progressive Familial ALS and Predict Short Viability With PMA Phenotype.frontiers in genetics.2021.12.1-9.SCI |
11. 5. Lin Lei, Zhirong Fan, Shengyao Su, Min Xu, Hai Chen, Wenjia Zhu, Qinrong Luan, Yuwei Da.Involvement of Ocular Musclers in Patients With Myasthenia Gravis With Nonocular Onset. J Neuroophthalmol.2021.00.1-7.SCI |
12. Di L, Chen H, Lu Y, Selcen D, Engel AG, Da Y*.Determinants of the repetitive-CMAP occurrence and therapy efficacy in slow-channel myasthenia.Neurology.2020. 95(20).e2781- e2793.SCI |
13. 沈发秀,李尊波,雷霖,范志荣,卢岩,王敏, 邸丽,徐敏,陈海,王锁彬,笪宇威*.MuSK 抗体阳性重症肌无力10 例临床分析.Chin J Nerv Ment Dis.2020.46(1).24-28.核心期刊 |
14. Zhirong Fan, Zunbo Li, Faxiu Shen, Xueping Zhang, Lin Lei, Shengyao Su, Yan Lu, Li Di, Min Wang, Min Xu, Yuwei Da*.Favorable effects of tacrolimus monotherapy on myasthenia gravis patients.Frontiers in neurology.2020.11.594152.SCI |
15. 沈发秀,笪宇威*.甲氨蝶呤治疗重症肌无力临床.Chin J Nerv Ment Dis.2020.46(5).308-310.核心期刊 |
16. 沈发秀,笪宇威*,陈海.皮质受累CLIPPERS综合征一例.中国现代神经疾病杂志.2019.19(4).286-289.核心期刊 |
17. Sun Y, Chen H, Lu Y, Duo J, Lei L, OuYang Y, Hao Y, Da Y*, Shen XM. Limb girdle muscular dystrophy D3 HNRNPDL related in a Chinese family with distal muscle weakness caused by a mutation in the prion-like domain.J Neurol.2019.266(2).498-506.SCI |
18. Lin Lei , Xin-Ming Shen , Shu-Yan Wang , Yan Lu , Suo-Bin Wang , Hai Chen, Zheng Liu, Ya-Sheng Ouyang , Jian-Ying Duo , Yu-Wei Da*, Zhi-Guo Chen..Presence of antibodies against low-density lipoprotein receptor-related protein 4 and impairment of neuromuscular junction in a Chinese cohort of amyotrophic lateral sclerosis.Chinese Medical Journal.2019.132(12).1487-89.SCI |
19. 翁映虹,笪宇威*,徐敏,卢岩,徐佳丽,邱占东,贾宇,赵红梅.伴锥体束损害及眼震快速进展型重症肌无力一例临床分析.中国全科医学.2019.22(30).3757-3761.核心期刊 |
20. 梁宝毅,杨坚炜,陈海*,笪宇威.脊髓亚急性联合变性75例临床分析.中国现代神经疾病杂志.2019.19(4).277-280.核心期刊 |
21. 孙亚楠,笪宇威*.我国肢带型肌营养不良患者中发现HNRNPDL基因类朊蛋白域突变.中华神经科杂志.2019.10(52).872.核心期刊 |
22. 刘晴,陈海 ,雷霖, 朱文佳, 邸丽, 卢岩, 王敏, 王锁彬,笪宇威*.以臂丛神经损害为首发症状的遗传性压力易感性周围神经病一例临床表型及基因突变分析.中国现代神经疾病杂志.2018.18(2).123-127.核心期刊 |
23. 苏牟潇,笪宇威*,朵建英.散发性眼咽远端型肌病的临床、肌肉影像与电生理特点.中国神经精神疾病杂志.2018.44(5).261-265.核心期刊 |
24. Di L, Guan Y, Shen XM, Da Y*.A unique case of dysferlinopathy with a large-segment duplication mutation who experienced rapid deterioration after small-dosage corticosteroid treatment. . J Neurol Sci.2017.376.35-37.SCI |
25. Wang M, Lei L, Chen H, Di L, Pang M, Lu Y, Lu L, Shen XM, Da Y*.Monoclonal gammopathy with both nemaline myopathy and amyloid myopathy..Neuromuscul Disord..2017.27.942-946.SCI |
26. 雷霖, 邸丽, 朵建英, 庞咪, 笪宇威*.以肌肉损害为首发表现的淀粉样神经肌病一例.中华神经科杂志.2017.50(4).304-305.核心期刊 |
27. 雷霖,笪宇威*.难治性重症肌无力治疗的研究进展.中华神经医学杂志.2016.15(03).319-321.核心期刊 |
28. 雷霖,笪宇威*.中国家族性肌萎缩侧索硬化患者中发现囊泡相关膜蛋白相关蛋白B基因突变.中华神经科杂志.2016.49(8).664.核心期刊 |
29. Di L, Chen H, Da Y, Wang S, Shen XM.. Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutation.J Neurol.2016.263(2).263-8.SCI |
30. Da Y*, Lei L, Jurkat-Rott K, Lehmann-Horn F*.Successful treatment of periodic paralysis with coenzyme Q10: two case reports.Acta Myol.2016.2(2).107-108.SCI |
31. Bednarz M#, Da Y#, Lehmann-Horn F , Fan C , Schallner J, Jurkat-Rott K* .Skeletal Muscle Calcium Channel Mutation R528G: Enhanced Channel Inactivation And Omega-current At Hyperpolarization Contribute To Hypokalemic Periodic Paralysis..Journal Of Neurological Research And Therapy.2016. 1(3).20-30. |
32. 庞咪,笪宇威*.脂质沉积性肌病分子生物学研究进展.卒中与神经疾病.2015.22(5).311-313.核心期刊 |
33. 王旭敏,笪宇威*.表现为肌纤维颤搐的汞中毒一例 .中华神经科 .2014.47(12).1-2.核心期刊 |
34. 陈海,笪宇威*,王敏,卢岩,邸丽.非肿瘤相关的Lambert-Eaton肌无力综合征研究进展.脑与神经疾病杂志 .2014.22(1).78-80.核心期刊 |
35. 陆慧,笪宇威*.典型内因子抗体阳性的亚急性联合变性一例.中国医药.2014.9(9).1400-1401.核心期刊 |
36. 李韵,笪宇威*.腓骨肌萎缩症X型临床、电生理及Connexin 32新突变一例.脑与神经疾病杂志.2013.21(3).218-221.核心期刊 |
37. 邸丽,陈海,卢岩,王敏,笪宇威*.多发性肌炎/皮肌炎85例患者影响预后的因素分析.中华临床医师杂志.2013.7(7).5806-09.核心期刊 |
38. Yuwei Da*, Xuxiang Zhang, Fang Li, Xiaoping Yang, Xinqing Zhang, Jianping Jia..Posterior reversible encephalopathy syndrome in a Leber’s hereditary optic neuropathy patient with mtDNA 11778G>A point mutation.. J Neuro-ophthalmol.2013.0(1).1-3.SCI |
39. 笪宇威*, 李韵, 张新卿, 贾建平.一例成人起病的Krabbe病临床、影像学特点和基因突变分析.中华医学遗传学杂志 .2013.30(5).585-587.核心期刊 |
40. 李韵,笪宇威*.强直性肌营养不良1型三核苷酸重复序列的检测.中华医学遗传学杂志.2012.29(1).16-18. |
41. 笪宇威*, 王敏, 洪道俊, 卢岩, 李韵.常染色体隐性遗传肌原纤维肌病的临床和病理学特点:附1例报告.临床神经病学杂志.2011.24(3).206-208.核心期刊 |
42. Herrmann DN*, O’Connor AB, Schwild S, Da Y, Goodman AD, Rafferty J, Donahue S, Dworkin RH.Broadening the spectrum of controls for skin biopsy in painful neuropathies.Muscle & Nerve.2010.42(3).436-438.SCI |
43. 李韵,笪宇威*.强直性肌营养不良I型的临床与分子生物学研究进展.卒中与神经疾病.2010.17(5).316-318.核心期刊 |
44. 笪宇威*,王敏,卢岩,刘璐.常染色体显性遗传的中央轴空病临床病理特点.卒中与神经疾病.2009.16(6).335-337.核心期刊 |
45. 笪宇威*,卢岩,朴月善,刘爱华,卢德宏,王玉平,王敏,徐敏,刘璐,贾建平.经皮肤活体检查确诊的Lafora病五例.中华神经科杂志.2008.41(7).468-470.核心期刊 |
46. 卢岩,笪宇威*,王敏,刘璐,贾建平.杆状体肌病2例并文献复习.中国神经免疫学和神经病学杂志.2008.15(4).236-238.核心期刊 |
47. 笪宇威*,贾建平,李彦,王敏.原发性肉碱缺陷所致脂质沉积性肌病的临床和病理特点.临床神经病学杂志.2007.20(7).191-193.核心期刊 |
48. Yuwei Da, Jianping Jia*.Study of Antibodies to PMP22, IL-6 and TNF-concentrations in Serum in a Leu89Pro CMTX1 family.Neuroscience Letters.2007.424.73-77.SCI |
49. 笪宇威*,李彦,徐敏,刘尖尖,贾建平.伴有周围神经损害的强直性肌营养不良.卒中与神经疾病.2006.13(6).345-347.核心期刊 |
50. 笪宇威*,贾建平.Charcot-Marie-Tooth病血清PMP22抗体、IL-6和TNF水平的研究.中国神经免疫学和神经病学杂志.2006.13(4).223-226.核心期刊 |
51. 笪宇威*,贾建平,蔡彦宁.实时荧光定量PCR检测腓骨肌萎缩症基因重复.中华神经科杂志.2006.39(8).562-564.核心期刊 |
52. 笪宇威*,贾建平,杨静芳,董秀敏.腓骨肌萎缩症CMTX1型临床,电生理和Connexin32基因突变研究.中国神经精神疾病杂志.2005.31(6).121-123.核心期刊 |
53. 笪宇威*,贾建平,叶静.腓骨肌萎缩症CMTX1型Connexin32基因突变检测 .中华神经科杂志.2005.38(11).435-437.核心期刊 |
54. 笪宇威*,贾建平,王敏,卫华,刘路,李越星,孙异临.线粒体脑肌病合并脂质沉积性肌病一例报告.中华神经科杂志.2005.38(5).344-344.核心期刊 |
55. 笪宇威*,沈定国,苏凤霞,刘淑贤.基因重复的进行性腓骨肌萎缩症1A型临床和电生理研究.中华神经科杂志.2001.21(7).4-6.核心期刊 |
56. 笪宇威*,沈定国.中国人中发现一例Charcot-Marie-Tooth病.中华医学遗传学杂志 .2000.17(5).316-318.核心期刊 |
57. 笪宇威*,沈定国.腓骨肌萎缩症1A 型基因重复的检测.中华神经科杂志.2000.33(4).238-240.核心期刊 |