Zobrazeno 1 - 10
of 666
pro vyhledávání: '"Sporadic late-onset nemaline myopathy"'
Publikováno v:
BMJ Neurology Open, Vol 6, Iss 2 (2024)
Background Late-onset sporadic nemaline myopathy (SLONM) is a rare, treatable or potentially life-threatening muscle disorder that typically manifests late in life and is characterised by the presence of nemaline rods within muscle fibres, serving as
Externí odkaz:
https://doaj.org/article/0113100040ac4d999895904b64d2ef5e
Autor:
Nandy, Anirban1 (AUTHOR), Tankisi, Hatice2 (AUTHOR), Krøigård, Anne Bruun3 (AUTHOR), Dalager, Maiken Glud4 (AUTHOR), Hvidbjerg, Marie Skov5 (AUTHOR), Schrøder, Henrik Daa3 (AUTHOR), Obál, Izabella1 (AUTHOR) i.obal@rn.dk
Publikováno v:
BMC Neurology. 6/16/2023, Vol. 23 Issue 1, p1-8. 8p.
Akademický článek
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Autor:
Sadeh M; Neurology, Edith Wolfson Medical Center, Holon, Tel Aviv, Israel., Fellig Y; Pathology, Hadassah Medical Center, Jerusalem, Jerusalem, Israel., Dabby R; Neurology, Edith Wolfson Medical Center, Holon, Tel Aviv, Israel.
Publikováno v:
BMJ neurology open [BMJ Neurol Open] 2024 Nov 14; Vol. 6 (2), pp. e000892. Date of Electronic Publication: 2024 Nov 14 (Print Publication: 2024).
Autor:
Matsuura, Eiji1 (AUTHOR) pine@m.kufm.kagoshima-u.ac.jp, Nozuma, Satoshi1 (AUTHOR), Shigehisa, Ayano1 (AUTHOR), Dozono, Mika1 (AUTHOR), Nakamura, Tomonori1 (AUTHOR), Tanaka, Masakazu2 (AUTHOR), Kubota, Ryuji2 (AUTHOR), Hashiguchi, Akihiro1 (AUTHOR), Takashima, Hiroshi1 (AUTHOR)
Publikováno v:
BMC Musculoskeletal Disorders. 5/6/2023, Vol. 24 Issue 1, p1-6. 6p.
Publikováno v:
BMC Pulmonary Medicine, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background Neuromuscular pathologies must be considered when caring for patients with persistent or progressive respiratory failure. Pertinent disease states may involve skeletal muscles of respiration or associated neurologic structures inc
Externí odkaz:
https://doaj.org/article/494a3c82b9d24343a5f1a07a54518c12
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Anirban Nandy, Hatice Tankisi, Anne Bruun Krøigård, Maiken Glud Dalager, Marie Skov Hvidbjerg, Henrik Daa Schrøder, Izabella Obál
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background Sporadic late onset nemaline myopathy is a rare, progressive muscle disease, presenting in adulthood, mainly affecting proximal limb and bulbar muscles. Muscle biopsies show characteristic nemaline rods. The putative mechanism is
Externí odkaz:
https://doaj.org/article/7cfe005e572b416982c8f90526eb0be8
Autor:
Eiji Matsuura, Satoshi Nozuma, Ayano Shigehisa, Mika Dozono, Tomonori Nakamura, Masakazu Tanaka, Ryuji Kubota, Akihiro Hashiguchi, Hiroshi Takashima
Publikováno v:
BMC Musculoskeletal Disorders, Vol 24, Iss 1, Pp 1-6 (2023)
Abstract Background Sporadic late onset nemaline myopathy (SLONM) is a muscle disorder characterized by the presence of nemaline rods in muscle fibers. SLONM has no known genetic cause but has been associated with monoclonal gammopathy of undetermine
Externí odkaz:
https://doaj.org/article/2ee8ec70d7044e4a8e032fcf931c3e95
Publikováno v:
In Neuromuscular Disorders November 2021 31(11):1154-1160