Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Facial Muscle Weakness"'
Autor:
Hongzhu Li, Guangxian Chen, Guoan Lai, Shiyu Lin, Jingchun Zeng, Liming Lu, Yuemei Li, Shuxin Wang
Publikováno v:
Biomolecules & Biomedicine (2024)
Early diagnosis of Bell's palsy is crucial for effective patient management in primary care settings. This study aimed to develop a simplified diagnostic tool to enhance the accuracy of identifying Bell's palsy among patients with facial muscle weakn
Externí odkaz:
https://doaj.org/article/07cf2cc1cd2a453dbe15d01c9aa1bdad
Akademický článek
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Publikováno v:
Trauma Case Reports, Vol 30, Iss , Pp 100370- (2020)
Facial nerve trauma is a common cause of facial paralysis; both blunt and penetrating forces may compromise the facial nerve. A comprehensive primary and secondary survey is essential for diagnosis and treatment of the injury. Here we report on a you
Externí odkaz:
https://doaj.org/article/3e29eefd22cb4582ad3d870f1c4388de
Autor:
Takahiro Haga, Itaru Kawashima, Masaru Idota, Hideki Hiraiwa, Hiroki Oba, Takefumi Sakaguchi, Shiro Imagama, Shinya Ishizuka, Takafumi Mizuno, Kanae Kuriyama, Akinori Kobayakawa
Publikováno v:
Case Reports in Orthopedics
Case Reports in Orthopedics, Vol 2021 (2021)
Case Reports in Orthopedics, Vol 2021 (2021)
The most common cause of medial scapular winging is long thoracic nerve palsy (LTN) and subsequent serratus anterior muscle dysfunction. A 16-year-old right-handed male high-school rugby player developed severe right-sided neck and shoulder pain afte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3551fa982b0e22ba566b6bfc1c73ed5
https://doi.org/10.1155/2021/4511538
https://doi.org/10.1155/2021/4511538
Publikováno v:
Trauma Case Reports, Vol 30, Iss, Pp 100370-(2020)
Trauma Case Reports
Trauma Case Reports
Facial nerve trauma is a common cause of facial paralysis; both blunt and penetrating forces may compromise the facial nerve. A comprehensive primary and secondary survey is essential for diagnosis and treatment of the injury. Here we report on a you
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::435badd69ec49f57b42dfcedb6675188
https://doi.org/10.5167/uzh-193253
https://doi.org/10.5167/uzh-193253
Autor:
Ghada Albuainain
Publikováno v:
The American Journal of Case Reports
Patient: Male, 37-year-old Final Diagnosis: Guillain-Barré syndrome Symptoms: Facial paralysis • paresthesia Medication: — Clinical Procedure: Cerebrospinal fluid analysis • magnetic resonance image • nerve conduction study Specialty: Neurol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fda305346907dee3cf3386c950418b32
https://doi.org/10.12659/ajcr.932757
https://doi.org/10.12659/ajcr.932757
Autor:
Leentje Van Lommel, Ikuya Nonaka, Tsutomu Takahashi, Katsunori Fujii, Masakazu Mimaki, Ichizo Nishino, Michio Inoue, Hirofumi Komaki, Shinichiro Hayashi, Takuya Yoshizawa, Yu-ichi Goto, Satoru Noguchi, Shumpei Uchino, Yukinori Okada, Aritoshi Iida, Eri Takeshita, Frans Schuit
Publikováno v:
Annals of Neurology. 86:193-202
OBJECTIVE Cytochrome c oxidase (COX) deficiency is a major mitochondrial respiratory chain defect that has vast genetic and phenotypic heterogeneity. This study aims to identify novel causative genes of COX deficiency with only striated muscle-specif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a73f05cddbef1ee2471e55140ff531e2
https://doi.org/10.1002/ana.25517
https://doi.org/10.1002/ana.25517
Autor:
Sumie Hiramatsu, Tomoko Noda, Sachiko Kamada, Morinobu Seki, Akinori Uruha, Sachiko Yutani, Hiroshi Yaguchi, Takashi Shiina, Jin Nakahara, Masayuki Ohira, Aiko Isami, Akira Hanazono, Ichizo Nishino, Shunya Nakane, Seiya Noda, Shiro Matsubara, Asako Onda, Shigeaki Suzuki, Masahisa Katsuno, Masaki Takao, Yuko Ohnuki, Makoto Hibino
Publikováno v:
Journal of Autoimmunity. 100:105-113
Objective To characterize the inflammatory myopathy associated with programmed cell death 1 inhibitors (PD-1 myopathy). Methods We studied 19 Japanese patients with PD-1 myopathy (13 men and 6 women, mean age 70 years), who were referred to Keio Univ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::577d25f88d5720e5360e35db5e3cdb34
https://doi.org/10.1016/j.jaut.2019.03.005
https://doi.org/10.1016/j.jaut.2019.03.005
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 61(2)
A 59-year-old woman presented with a 7-year history of facial numbness on the left side, and gradual worsening of symptoms. Over several years, facial muscle weakness, dysarthria, tongue atrophy and fasciculation had progressed. Then, she developed c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa1768f695469177fcee4fad053c29ff
https://pubmed.ncbi.nlm.nih.gov/33504750
https://pubmed.ncbi.nlm.nih.gov/33504750
Akademický článek
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