Zobrazeno 1 - 10
of 2 539
pro vyhledávání: '"multifocal motor neuropathy"'
Dose, exposure, and treatment regimen of intravenous immunoglobulin G in multifocal motor neuropathy
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionIntravenous immunoglobulin (IVIG) is the only approved treatment for multifocal motor neuropathy (MMN), a rare, chronic, immune-mediated demyelinating neuropathy. There is a significant gap in understanding of the role of serum immunoglob
Externí odkaz:
https://doaj.org/article/14cb03d93729418393dd4776a8b554e8
Autor:
Taisiya A. Tumilovich, Victoria V. Sinkova, Daria A. Grishina, Natalia A. Suponeva, Sofya N. Morozova, Marina V. Krotenkova, Anna V. Mansurova, Andrey O. Chechetkin
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 18, Iss 1, Pp 20-32 (2024)
Introduction. Similar asymmetric patterns of motor disorders and neurophysiological changes complicate the differential diagnosis between multifocal motor neuropathy (MMN) and multifocal acquired demyelinating sensory and motor neuropathy (MADSAM) as
Externí odkaz:
https://doaj.org/article/492600dfdff543d7a1dae24e62e8a6c7
Autor:
Kevin Budding, Jeroen W. Bos, Kim Dijkxhoorn, Elisabeth de Zeeuw, Lauri M. Bloemenkamp, Eva M. Zekveld, Ewout J.N. Groen, Bart C. Jacobs, Ruth Huizinga, H. Stephan Goedee, Elisabeth A. Cats, Jeanette H.W. Leusen, Leonard H. van den Berg, C. Erik Hack, W. Ludo van der Pol
Publikováno v:
Journal of Neuroinflammation, Vol 21, Iss 1, Pp 1-14 (2024)
Abstract Background Multifocal motor neuropathy (MMN) is a rare, chronic immune-mediated polyneuropathy characterized by asymmetric distal limb weakness. An important feature of MMN is the presence of IgM antibodies against gangliosides, in particula
Externí odkaz:
https://doaj.org/article/6a575bd7333941c8bd8c09e509cbb6f7
Publikováno v:
Нервно-мышечные болезни, Vol 14, Iss 1, Pp 10-24 (2024)
Background. One of the key distinctions between multifocal motor neuropathy (MMN) and multifocal variant of chronic inflammatory demyelinating polyradiculoneuropathy (mCIDP) lies in the presence or absence of sensory deficits. Nevertheless, existing
Externí odkaz:
https://doaj.org/article/defcad143db54ebf82156d6c9fa080c8
Publikováno v:
Неврология, нейропсихиатрия, психосоматика, Vol 16, Iss 1, Pp 42-48 (2024)
Little attention has been paid abroad to the problem of the long-term course of multifocal motor neuropathy (MMN). In our country, catamnestic studies of MMN have not been conducted at all. However, the results of such an analysis are extremely impor
Externí odkaz:
https://doaj.org/article/2010391dbfbc48768a99b9c2a0e9787d
Autor:
Ivan Kmezic, Rasmus Gustafsson, Katharina Fink, Anders Svenningsson, Kristin Samuelsson, Caroline Ingre, Tomas Olsson, Magnus Hansson, Ingrid Kockum, Milena Z. Adzemovic, Rayomand Press
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundBiomarkers for diagnosis of inflammatory neuropathies, assessment of prognosis, and treatment response are lacking.MethodsCSF and EDTA plasma from patients with Guillain-Barré syndrome (GBS), chronic inflammatory demyelinating polyneuropat
Externí odkaz:
https://doaj.org/article/16a4d9f5634040e7bbcc96cfc6c9796a
Publikováno v:
Neurologijos seminarai, Vol 26, Iss 4 (94) (2023)
Multifocal motor neuropathy is a rare motor neuron disease characterised by a progressive, gradual loss of muscle strength, although sensory functions are preserved. The worldwide frequency of this disease is estimated at 1 person per 100,000 people.
Externí odkaz:
https://doaj.org/article/f85ac0c8b44447dbaed92ebd972e57c0
Autor:
Masaaki Yoshikawa, Kenji Sekiguchi, Hirotomo Suehiro, Shunsuke Watanabe, Yoshikatsu Noda, Hideo Hara, Riki Matsumoto
Publikováno v:
Clinical Neurophysiology Practice, Vol 8, Iss , Pp 228-234 (2023)
Objective: We aimed to evaluate differences in ultrasonographic nerve enlargement sites among typical chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), distal CIDP, multifocal CIDP and multifocal motor neuropathy (MMN) in a Japanese p
Externí odkaz:
https://doaj.org/article/b499fdf0aaab4c93a0fa7ea0686cadb1
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