Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Chen Liang"'
Autor:
Cheng-Chang Lu, Wen-Chen Liang, Zi-Miao Liu, Shih-Hsiang Chou, Po-Chih Shen, Yin-Chun Tien, Yen-Mou Lu, Chia-Lung Shih, Yuh-Jyh Jong
Publikováno v:
Clinical Spine Surgery
Study Design: This was a single-center, retrospective study. Objective: The objective of this study was to assess the risk factors for deformity progression after scoliosis correction surgery in spinal muscular atrophy (SMA) patients. Summary of Back
Publikováno v:
World neurosurgery. 134
Although research shows that the ossified masses of ossification of the posterior longitudinal ligament (OPLL) continue to grow postoperatively, information regarding thoracic OPLL (T-OPLL) is lacking. To date, no study has investigated the progressi
Publikováno v:
World neurosurgery. 107
Background Congenital or early-onset brain structural lesions often cause contralateral hemiparesis, cognitive deficits, developmental delays, and seizures. Seizure is the most debilitating condition, as it greatly impairs quality of life in both the
Autor:
Y. C. Chen, S. N. Yang, Yuh-Jyh Jong, Jan-Gowth Chang, Y. C. Wu, S. M. Wu, Yi-Hsin Yang, Tai-Heng Chen, Yining Huang, H. H. Mai, Haiyan Wang, Wen-Chen Liang
Publikováno v:
Neurology. 75:2190-2197
Objective: The purpose of this study was to evaluate the safety and efficacy of hydroxyurea (HU) in spinal muscular atrophy (SMA) in a randomized, double-blind, placebo-controlled trial. Methods: Twenty-eight patients with type 2 SMA and 29 patients
Autor:
Chin Wen Lin, Yuh-Jyh Jong, Kanako Goto, Ichizo Nishino, Pei Lun Lee, Tai-Heng Chen, Yukiko K. Hayashi, Chao Ching Huang, Wen Fu Wang, Hsiang Hung Shih, Wen-Chen Liang, Jong Hau Hsu, Yu Hung Lai
Publikováno v:
Neuromuscular disorders : NMD. 23(4)
Contrary to the classical form, infantile facioscapulohumeral muscular dystrophy (FSHD) usually denotes a severe phenotype and is frequently associated with extramuscular involvements. To elucidate the genotype-phenotype correlation in this severe su
Daily or alternative, that is the question: steroid therapy for Duchenne muscular dystrophy patients
Autor:
Wen-Chen Liang, Ichizo Nishino
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 84:591-591
Duchenne muscular dystrophy (DMD) is an X-linked muscular dystrophy known to affect one in 3600 live male births and leads to progressive proximal muscle weakness in the first years, and orthopaedic, respiratory and cardiac complications in the teens
Autor:
Delphine Issard, Nicola De Stefano, Mark S. Freedman, Marlieke de Vos, Giancarlo Comi, Liang Chen, Bernard M. J. Uitdehaag, Kurt Marhardt, Ludwig Kappos, Frederik Barkhof
Publikováno v:
Comi, G, Stefano, N D, Freedman, M S, Barkhof, F, Uitdehaag, B M J, de Vos, M, Marhardt, K, Chen, L, Issard, D & Kappos, L 2017, ' Subcutaneous interferon ß-1a in the treatment of clinically isolated syndromes : 3-year and 5-year results of the phase III dosing frequency-blind multicentre REFLEXION study ', Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, no. 4, pp. 285–294 . https://doi.org/10.1136/jnnp-2016-314843
Journal of Neurology, Neurosurgery and Psychiatry, 88(4). BMJ Publishing Group
Journal of Neurology, Neurosurgery and Psychiatry, 88(4). BMJ Publishing Group
Objective Early treatment following a first clinical demyelinating event (FCDE) delays further disease activity in patients with multiple sclerosis (MS). This study determined the effects of early versus delayed treatment (DT) with subcutaneous inter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76f3117ba7558557231fea0dde464731
https://research.vumc.nl/en/publications/0bdedeb3-f38e-47d3-8574-5d995962c0ae
https://research.vumc.nl/en/publications/0bdedeb3-f38e-47d3-8574-5d995962c0ae