Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Shiao-lin Lai"'
Autor:
J Raphael Gibbs, Marcel P van der Brug, Dena G Hernandez, Bryan J Traynor, Michael A Nalls, Shiao-Lin Lai, Sampath Arepalli, Allissa Dillman, Ian P Rafferty, Juan Troncoso, Robert Johnson, H Ronald Zielke, Luigi Ferrucci, Dan L Longo, Mark R Cookson, Andrew B Singleton
Publikováno v:
PLoS Genetics, Vol 6, Iss 5, p e1000952 (2010)
A fundamental challenge in the post-genome era is to understand and annotate the consequences of genetic variation, particularly within the context of human tissues. We present a set of integrated experiments that investigate the effects of common ge
Externí odkaz:
https://doaj.org/article/2c6bddb840f5434bb40322ece5b8e839
Publikováno v:
Journal of the Formosan Medical Association, Vol 112, Iss 9, Pp 578-579 (2013)
Externí odkaz:
https://doaj.org/article/a94b7a8a3b6745929436d9b2af0779de
Autor:
Shiao Lin Lai, Chaur Jong Hu, Jen Tsung Yang, Ying Chih Huang, Tsong Hai Lee, Leng Chieh Lin, Hsu-Huei Weng
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 22:e152-e158
Background Understanding hospital costs and length of stay (LOS) can optimize the in-hospital management of acute stroke. We investigated cost and LOS in first-ever and recurrent stroke patients in Taiwan. Methods Data were examined in patients at Ch
Publikováno v:
Journal of Clinical Neuroscience. 13:111-114
Disuse myopathy can be caused by many disorders. However, disuse myopathy with symmetrical weakness of the proximal muscles in the four limbs is rare. Here we report a 45-year-old man who presented with the appearance of myopathy similar to the clini
Neurorehabilitation of congenital mirror movements enhanced by stroke: a case report with fMRI study
Autor:
Yee Hwa Wu, Ying Chih Huang, Kai Hua Chen, Chaur Jong Hu, Yuan Hsiung Tsai, Yi Ching Huang, Shiao Lin Lai, Mei Yu Yeh, Yu Fang Cheng
Publikováno v:
Clinical neurology and neurosurgery. 115(10)
Department of Physical Medicine and Rehabilitation, Chang Gung Memorial Hospital, Chiayi, Taiwan School of Medicine, Chang Gung University, Taoyuan, Taiwan Department of Diagnostic Radiology, Chang Gung Memorial Hospital, Chiayi, Taiwan College of Me
Autor:
Pentti J. Tienari, Maarit Tanskanen, Andrew B. Singleton, John Hardy, Mira Mäkelä, Hannu Kalimo, Shiao-lin Lai, Tuomo Polvikoski, Anders Paetau, Raimo Sulkava, Sampath Arepalli, Terhi Peuralinna, Liisa Myllykangas, Bryan J. Traynor, Dena G. Hernandez
Publikováno v:
Journal of Alzheimer's disease : JAD. 26(2)
Cortical and cerebrovascular amyloid-beta (A-beta) deposition is a hallmark of Alzheimer’s disease (AD), but also occurs in elderly people not affected by dementia. The apolipoprotein E (APOE) epsilon4 is a major genetic modulator of A-beta deposit
Autor:
Amelia Conte, Mario Sabatelli, Maria Rosaria Monsurrò, Travis Dunckley, Ilaria Bartolomei, Yevgeniya Abramzon, Gabriella Restagno, Kalliopi Marinou, Shiao Lin Lai, Patrizia Sola, Gioacchino Tedeschi, Fabio Giannini, Mark R. Cookson, Allissa Dillman, Giovanni Luigi Mancardi, Fabrizio Salvi, Rossella Spataro, Dietrich A. Stephan, Gabriele Mora, Claudia Caponnetto, Adriano Chiò, Bryan J. Traynor, Jessica Mandrioli, Andrea Calvo, Stefania Battistini, Federica Lombardo, Jennifer C. Schymick
Mutations in the FUS gene have recently been described as a cause of familial amyotrophic lateral sclerosis (ALS), but their role in the pathogenesis of sporadic ALS is unclear. We undertook mutational screening of all coding exons of FUS in 228 spor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a65e78eb78b42c62bbc1050de435d8d
http://hdl.handle.net/2318/78239
http://hdl.handle.net/2318/78239
Autor:
Gabriele Mora, Marcel P. van der Brug, Raphael Gibbs, Sampath Arepalli, Janel O. Johnson, Mike A. Nalls, Mark R. Cookson, Cristina Moglia, Shiao Lin Lai, Jennifer C. Schymick, Dena G. Hernandez, Gabriella Restagno, Bryan J. Traynor, Adriano Chiò, Allissa Dillman, Andrea Calvo
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 107(27)
It was recently reported that rs1541160 on chromosome 1q24.2 has a marked effect on survival of amyotrophic lateral sclerosis (ALS) patients by influencing KIFAP3 expression. The cohorts used in that study were collected from ALS specialty clinics. W
Autor:
Cristina Moglia, Maura Brunetti, Irene Ossola, Shiao-lin Lai, Andrea Calvo, Yevgeniya Abramzon, Adriano Chiò, Bryan J. Traynor, Gabriella Restagno, Luca Sbaiz
Publikováno v:
Neurobiology of aging. 32(3)
Mutations in the Cu/Zn superoxide dismutase (SOD1), transactive response (TAR)-DNA binding protein (TARDBP) and fused in sarcoma (FUS) genes account for approximately one third of familial amyotrophic lateral sclerosis (ALS) cases. Mutations in these
Autor:
Shy-Chyi Chin, Shiao-Lin Lai, Chiung-Mei Chen, Yen-Chu Huang, Tsong-Hai Lee, Yi-Chun Chen, Sien-Tsong Chen
Publikováno v:
Journal of the neurological sciences. 253(1-2)
Although hemodynamic change has been identified as the main mechanism of infarcts in intracranial internal carotid artery dissection, no report has utilized computed tomography perfusion study to evaluate the cerebral flow change in such cases. This