Zobrazeno 1 - 10
of 208
pro vyhledávání: '"Jin Hong Shin"'
Autor:
Jaeseob Yun, Sung Hwan Jang, Huiran Cho, Myung Jun Lee, Na-Yeon Jung, Jae-Hyeok Lee, Jin-Hong Shin, Young Min Lee, Jin A Yoon, Kyoungjune Pak, Junkyeung Ko, Jae Meen Lee, Chungsu Hwang, Jae Woo Ahn, Suk Sung, Kyung-Un Choi, Gi Yeong Huh, Eun-Joo Kim
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Butane is an aliphatic hydrocarbon used in various commercial products. While numerous reports of sudden cardiac-related deaths from butane inhalation have been described, butane-associated acute encephalopathy has rarely been rep
Externí odkaz:
https://doaj.org/article/1b84c70e50a44e92a58b0878fda5c37b
Autor:
Kwangsub Song, Sangui Choi, Jin-Hong Shin, Woo-Hyeon Son, Hyuntae Park, Hooman Lee, Nam-Jong Paik
Publikováno v:
IEEE Transactions on Neural Systems and Rehabilitation Engineering, Vol 31, Pp 1867-1877 (2023)
We propose a digital biomarker related to muscle strength and muscle endurance (DB/MS and DB/ME) for the diagnosis of muscle disorders based on a multi-layer perceptron (MLP) using stimulated muscle contraction. When muscle mass is reduced in patient
Externí odkaz:
https://doaj.org/article/5568cd215040410ba455da93c0987a87
Autor:
Jae-Hyeok Lee, Jin-Hong Shin
Publikováno v:
Journal of Movement Disorders, Vol 15, Iss 2, Pp 171-174 (2022)
Mutations in the manganese transporter gene SLC39A14 lead to inherited disorders of manganese metabolism. Chelation therapy with edetate calcium disodium (SLC39A14 deficiencyTA) is known to effectively reduce manganese deposition. We describe the fir
Externí odkaz:
https://doaj.org/article/7ac9bee8c089481d882675096c5aa88e
Autor:
Jae-Yong Nam, Tae Yong Lee, Kwijoo Kim, Sehwan Chun, Min Sung Kim, Jin-Hong Shin, Jung-Joon Sung, Byoung Joon Kim, Byung-Jo Kim, Ki-Wook Oh, Kyung Suk Kim, Seung Hyun Kim
Publikováno v:
Trials, Vol 23, Iss 1, Pp 1-15 (2022)
Abstract Background A single cycle (two repeated treatments) with intrathecal autologous bone marrow-derived mesenchymal stem cells (BM-MSCs, 26-day interval) showed safety and provided therapeutic benefit lasting 6 months in patients with ALS but di
Externí odkaz:
https://doaj.org/article/32d0808cc0c04903a7ee541739ee974f
Publikováno v:
Kosin Medical Journal, Vol 36, Iss 2, Pp 206-210 (2021)
A 49-year-old man developed recurrent myalgia and hyperCKemia during acute attacks of neuromyelitis optica. Muscle biopsy was performed, and the pathological findings were analyzed. Predominant myofibrillar pathology was observed, which constitutes a
Externí odkaz:
https://doaj.org/article/fd9b52e06a294b3a8ad5bf1d8b7a5605
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 21, Iss , Pp 702-709 (2021)
Biallelic mutations in the dysferlin gene cause limb-girdle muscular dystrophy 2B or Miyoshi distal myopathy. We found that nonsense mutations are the most common mutation type among Korean patients with dysferlinopathy; more than half of the patient
Externí odkaz:
https://doaj.org/article/87e50244305244609d0ee95ebfdd6edf
Autor:
Sung-Ho Ahn, Jieun Roh, Kyoung-Nam Woo, Hyun-Sung Kim, Min-Gyu Park, Kyung-Pil Park, Seung-Kug Baik, Jin-Hong Shin
Publikováno v:
Journal of Neurocritical Care, Vol 14, Iss 1, Pp 46-51 (2021)
Background Brainstem encephalitis is a rare, severe, and potentially life-threatening inflammation of the central nervous system, exhibiting various treatment responses and outcomes owing to multiple etiologies. Case Report We describe the favorable
Externí odkaz:
https://doaj.org/article/d699c5a0fb27466288bc91f0dae3a349
Autor:
SunYoung Park, Ji-Hwan Park, Un-Beom Kang, Seong-Kyoon Choi, Ahmed Elfadl, H. M. Arif Ullah, Myung-Jin Chung, Ji-Yoon Son, Hyun Ho Yun, Jae-Min Park, Jae-hyuk Yim, Seung-Jun Jung, Sang-Hyup Kim, Young-Chul Choi, Dae-Seong Kim, Jin-Hong Shin, Jin-Sung Park, Keun Hur, Sang-Han Lee, Eun-Joo Lee, Daehee Hwang, Kyu-Shik Jeong
Publikováno v:
Cell Death Discovery, Vol 7, Iss 1, Pp 1-18 (2021)
Abstract Among the three isoforms encoded by Rtn4, Nogo-A has been intensely investigated as a central nervous system inhibitor. Although Nogo-A expression is increased in muscles of patients with amyotrophic lateral sclerosis, its role in muscle hom
Externí odkaz:
https://doaj.org/article/263d1736b2f14ee082622c348ea84fb6
rAAV8 and rAAV9-Mediated Long-Term Muscle Transduction with Tacrolimus (FK506) in Non-Human Primates
Autor:
Akiko Ishii, Hironori Okada, Hiromi Hayashita-Kinoh, Jin-Hong Shin, Akira Tamaoka, Takashi Okada, Shin’ichi Takeda
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 18, Iss , Pp 44-49 (2020)
To establish an efficient, safe immunosuppressive regimen of adeno-associated vector (AAV)-mediated gene therapy for Duchenne muscular dystrophy (DMD), we evaluated the effect of tacrolimus (FK506) on skeletal muscle transduction with AAV8 and AAV9 v
Externí odkaz:
https://doaj.org/article/a58c999022b54f3a9aef2884be3963e7
Autor:
Na-Yeon Jung, Hyang-Sook Kim, Eun Soo Kim, Sumin Jeon, Myung Jun Lee, Kyoungjune Pak, Jae-Hyeok Lee, Young Min Lee, Kangyoon Lee, Jin-Hong Shin, Jun Kyeung Ko, Jae Meen Lee, Jin A Yoon, Chungsu Hwang, Kyung-Un Choi, Gi Yeong Huh, Young-Eun Kim, Eun-Joo Kim
Publikováno v:
PLoS ONE, Vol 17, Iss 1, p e0261007 (2022)
Low serum progranulin (PGRN) is known to be associated with granulin (GRN) gene mutation and T alleles of GRN rs5848 polymorphism. However, there have been only a few Asian studies exploring these. We investigated the serum PGRN levels, rs5848 genoty
Externí odkaz:
https://doaj.org/article/f5b1c6d1e9c44756908867b2cfffe9c8