Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Yu-Wei Da"'
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 19, Iss 4, Pp 277-280 (2019)
Objective To summarize the clinical manifestations, laboratory, electrophysiological and imaging features, treatment and prognosis of subacute combined degeneration of the spinal cord (SCD). Methods and Results The clinical data of 75 SCD patients fr
Externí odkaz:
https://doaj.org/article/47c9e1803bc4481caa9b0a7efb735db0
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 19, Iss 4, Pp 286-289 (2019)
DOI: 10.3969/j.issn.1672-6731.2019.04.013
Externí odkaz:
https://doaj.org/article/ecb209243c9840e0a6a2232344822768
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 18, Iss 2, Pp 123-127 (2018)
Objective To summarize the features of clinical phenotype and genetic mutation of hereditary neuropathy with liability to pressure palsies (HNPP) presenting brachial plexus injury as the first manifestation. Methods and Results A 46-year-old male pat
Externí odkaz:
https://doaj.org/article/849938f8b99d4afb9addac5b06959f53
Autor:
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, Yuan-Yuan Ji
Publikováno v:
Chinese Medical Journal, Vol 132, Iss 12, Pp 1487-1489 (2019)
Externí odkaz:
https://doaj.org/article/b24dcf67de3c4b199bb9b8440c26c27c
Publikováno v:
Frontiers in Neuroscience, Vol 12 (2018)
Externí odkaz:
https://doaj.org/article/c2674f1623b24506a3004a78f377e256
Publikováno v:
Frontiers in Neuroscience, Vol 12 (2018)
Hereditary Inclusion Body Myopathy (HIBM) is a rare autosomal dominant or recessive adult onset muscle disease which affects one to three individuals per million worldwide. This disease is autosomal dominant or recessive and occurs in adulthood. Our
Externí odkaz:
https://doaj.org/article/607ae1e5327c4f56a38377e78d2754ab
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 13, Iss 6, Pp 538-543 (2013)
Objective To investigate the onset pattern, clinical manifestations, laboratory findings and imaging features of 17 Chinese patients with steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT). Methods The clinical data of 1
Externí odkaz:
https://doaj.org/article/1e76653794414c259ef3476f431d262f
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 29, Iss 3, Pp 172-175 (2013)
We report an unusual case involving a patient with myotonia. A 57-year-old man had multisystemic symptoms including skeletal muscle weakness, atrophy and percussion myotonia, cataract, heart involved, gastrointestinal tract symptoms, and urinary inco
Externí odkaz:
https://doaj.org/article/c388283a1dc54f9d9f68f1e114fcfc8e
Publikováno v:
In Journal of Manufacturing Processes 15 March 2024 113:238-250
Autor:
Yu, Wei-da, Jing, Yu-an, He, Xu-zhe, Yang, Yin-ning, Zhang, Meng-fei, Cheng, Shuai, Li, Wan-ming
Publikováno v:
In Journal of Manufacturing Processes December 2022 84:1428-1437