1. Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late‐onset multiple acyl‐CoA dehydrogenase deficiency. Issue 3 (20th December 2013) Authors: Xi, Jianying; Wen, Bing; Lin, Jie; Zhu, Wenhua; Luo, Sushan; Zhao, Chongbo; Li, Duoling; Lin, Pengfei; Lu, Jiahong; Yan, Chuanzhu Journal: Journal of inherited metabolic disease Issue: Volume 37:Issue 3(2014) Page Start: 399 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical features and long exercise test in Chinese patients with Andersen‐Tawil syndrome. Issue 6 (11th October 2016) Authors: Song, Jie; Luo, Sushan; Cheng, Xin; Yue, Dongyue; Zhu, Wenhua; Lin, Jie; Huang, Jun; Lu, Jiahong; Zhao, Chongbo; Qiao, Kai Journal: Muscle & nerve Issue: Volume 54:Issue 6(2016) Page Start: 1059 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Congenital myasthenia syndrome in a Chinese family with mutations in MUSK: A hotspot mutation and literature review. (June 2020) Authors: Liu, Yiqi; Qiao, Kai; Yan, Chong; Song, Jie; Huan, Xiao; Luo, Sushan; Lu, Jiahong; Zhao, Chongbo; Xi, Jianying Journal: Journal of clinical neuroscience Issue: Volume 76(2020) Page Start: 161 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Electromyographic Features in a Chinese Cohort With Hereditary Skeletal Muscle Channelopathies. Issue 3 (May 2020) Authors: Sun, Jian; Luo, Sushan; Song, Jie; Huang, Jun; Cai, Shuang; Zhu, Wenhua; Zhou, Lei; Xi, Jianying; Lin, Jie; Lu, Jiahong; Xu, Minjie; Dou, Tonghai; Zhao, Chongbo; Qiao, Kai Journal: Journal of clinical neurophysiology Issue: Volume 37:Issue 3(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Fatty infiltration evaluation and selective pattern characterization of lower limbs in limb‐girdle muscular dystrophy type 2A by muscle magnetic resonance imaging. Issue 4 (3rd September 2018) Authors: Feng, Xuelin; Luo, Sushan; Li, Jing; Yue, Dongyue; Xi, Jianying; Zhu, Wenhua; Gao, Xinfang; Guan, Xueni; Lu, Jiahong; Liang, Zonghui; Zhao, Chongbo Journal: Muscle & nerve Issue: Volume 58:Issue 4(2018) Page Start: 536 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genotype–phenotype correlations in valosin-containing protein disease: a retrospective muticentre study. Issue 10 (27th July 2022) Authors: Schiava, Marianela; Ikenaga, Chiseko; Villar-Quiles, Rocío Nur; Caballero-Ávila, Marta; Topf, Ana; Nishino, Ichizo; Kimonis, Virginia; Udd, Bjarne; Schoser, Benedikt; Zanoteli, Edmar; Souza, Paulo Victor Sgobbi; Tasca, Giorgio; Lloyd, Thomas; Lopez-de Munain, Adolfo; Paradas, Carmen; Pegoraro, El... Other Names: author non-byline.; Munain Adolfo López de author non-byline.; Ramos-Fransi Alba author non-byline.; Nadaj-Pakleza Aleksandra author non-byline.; Alonso-Jiménez Alicia author non-byline.; Martinez-Piñeiro Alicia author non-byline.; Töpf Ana author non-byline.; Oldfors Anders author non-byline.; ... Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 93:Issue 10(2022) Page Start: 1099 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. In‐depth peripheral CD4+ T profile correlates with myasthenic crisis. Issue 4 (22nd February 2021) Authors: Huan, Xiao; Luo, Sushan; Zhong, Huahua; Zheng, Xueying; Song, Jie; Zhou, Lei; Lu, Jun; Wang, Ying; Xu, Yafang; Xi, Jianying; Zou, Zhangyu; Chen, Sheng; Zhao, Chongbo Journal: Annals of clinical and translational neurology Issue: Volume 8:Issue 4(2021) Page Start: 749 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Molecular landscape of CAPN3 mutations in limb-girdle muscular dystrophy type R1: from a Chinese multicentre analysis to a worldwide perspective. Issue 11 (29th September 2020) Authors: Zhong, Huahua; Zheng, Yiming; Zhao, Zhe; Lin, Pengfei; Xi, Jianying; Zhu, Wenhua; Lin, Jie; Lu, Jun; Yu, Meng; Zhang, Wei; Lv, He; Yan, Chuanzhu; Hu, Jing; Wang, Zhaoxia; Lu, Jiahong; Zhao, Chongbo; Yuan, Yun; Luo, Sushan Journal: Journal of medical genetics Issue: Volume 58:Issue 11(2021) Page Start: 729 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Molecular landscape of DYSF mutations in dysferlinopathy: From a Chinese multicenter analysis to a worldwide perspective. Issue 12 (11th October 2021) Authors: Zhong, Huahua; Yu, Meng; Lin, Pengfei; Zhao, Zhe; Zheng, Xueying; Xi, Jianying; Zhu, Wenhua; Zheng, Yiming; Zhang, Wei; Lv, He; Yan, Chuanzhu; Hu, Jing; Wang, Zhaoxia; Lu, Jiahong; Zhao, Chongbo; Luo, Sushan; Yuan, Yun Journal: Human mutation Issue: Volume 42:Issue 12(2021) Page Start: 1615 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Multiple deep white matter lesions mimic multiple sclerosis as an unusual complication of left atrial myxoma. (January 2015) Authors: Quan, Chao; ZhangBao, Jingzi; Luo, Sushan; Fang, Kun; Xi, Jianying; Du, Zunguo; Zhao, Chongbo; Lu, Jiahong Journal: Multiple sclerosis Issue: Volume 21:Number 1(2015) Page Start: 108 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗