Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Sporadic late-onset nemaline myopathy"'
Publikováno v:
BMC Rheumatology, Vol 6, Iss 1, Pp 1-5 (2022)
Abstract Background Nemaline myopathies are congenital or acquired muscle disorders that typically present in childhood but can occasionally occur in adults with underlying malignant, infectious or autoimmune disorders. There is a great genetic heter
Externí odkaz:
https://doaj.org/article/469ba3e61bab4ede909afba399eceade
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
Autor:
Erina Ono, Akira Ishii, Yoshiaki Higashi, Natsuko Koita, Takashi Ayaki, Katsuya Tanigaki, Shunsuke Takayanagi, Naoya Kondo, Kaoru Sakai, Shuichiro Endo, Hideki Yokoi, Takeshi Matsubara, Sachiko Minamiguchi, Ichizo Nishino, Ryosuke Takahashi, Motoko Yanagita
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-8 (2021)
Abstract Background Lately, monoclonal gammopathy of renal significance (MGRS) has been defined as a group of renal disorders that are strongly associated with monoclonal protein, including amyloid immunoglobulin light chain (AL) amyloidosis. Amyloid
Externí odkaz:
https://doaj.org/article/3494f0f0d62b4d5bafcbe09b66373f12
Publikováno v:
Clinical Case Reports, Vol 9, Iss 7, Pp n/a-n/a (2021)
Abstract Monoclonal gammopathy of undetermined significance (MGUS) may be associated with pathologies with severe neuromuscular manifestations such as sporadic late‐onset nemaline myopathy (SLONM). We describe a difficult to diagnose case of SLNOM
Externí odkaz:
https://doaj.org/article/3f871f9f1d3b46fca3a70b1eb1df173a
Autor:
Matthias Türk, Armin M. Nagel, Frank Roemer, Ursula Schlötzer-Schrehardt, Christian T. Thiel, Martin Winterholler, Rolf Schröder
Publikováno v:
BMC Musculoskeletal Disorders, Vol 20, Iss 1, Pp 1-4 (2019)
Abstract Background Camptocormia has been reported in a plethora of diseases comprising disorders of the central nervous system, the peripheral nervous system, and the neuromuscular junction as well as hereditary and acquired myopathies. In sporadic
Externí odkaz:
https://doaj.org/article/d88cb575e39a49c49a27a4e24fc8c85a
Akademický článek
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Autor:
André Truffert, Ruxandra Iancu Ferfoglia, Johannes Alexander Lobrinus, Kaveh Samii, André Kohler
Publikováno v:
European Journal of Translational Myology (2020)
Monoclonal gammopathy of undetermined significance (MGUS) associated to sporadic late onset nemaline myopathy (SLONM) is a rare and severely disabling condition of quickly progressive limb girdle acquired myopathy. It is believed by some authors to b
Externí odkaz:
https://doaj.org/article/68779f81851747d48b67d3b4d3b92a7a
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Ando, Takashi, Sato, Takahiko, Kurahashi, Shingo, Kawaguchi, Yuka, Kagaya, Yusuke, Ozawa, Yukiyasu, Hirano, Satoko, Goto, Yoji, Mano, Kazuo, Yokoi, Satoshi, Nakamura, Tomohiko, Murakami, Ayuka, Noda, Seiya, Kimura, Seigo, Sone, Jun, Kuru, Satoshi, Sobue, Gen, Katsuno, Masahisa
Publikováno v:
Nagoya Journal of Medical Science. 83(3):641-647
A 47-year-old woman presented with progressive limb weakness. A neurological examination revealed proximal dominant symmetrical muscle weakness in her limbs, and electromyography revealed complex repetitive discharges and short motor unit potentials
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::ff01c6cbeb03e4030e87ab95689508ce
https://nagoya.repo.nii.ac.jp/records/2001452
https://nagoya.repo.nii.ac.jp/records/2001452
Autor:
Naoya Kondo, Natsuko Koita, Shuichiro Endo, Erina Ono, Takeshi Matsubara, Shunsuke Takayanagi, Ryosuke Takahashi, Katsuya Tanigaki, Ichizo Nishino, Takashi Ayaki, Motoko Yanagita, Hideki Yokoi, Kaoru Sakai, Yoshiaki Higashi, Akira Ishii, Sachiko Minamiguchi
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-8 (2021)
BMC Nephrology
BMC Nephrology
Background Lately, monoclonal gammopathy of renal significance (MGRS) has been defined as a group of renal disorders that are strongly associated with monoclonal protein, including amyloid immunoglobulin light chain (AL) amyloidosis. Amyloid myopathy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fc56192eb7f5288131599965a605969
https://doaj.org/article/3494f0f0d62b4d5bafcbe09b66373f12
https://doaj.org/article/3494f0f0d62b4d5bafcbe09b66373f12