Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Clinical Research Short Report"'
Publikováno v:
Muscle & Nerve
Introduction/Aims The development and persistence of neurological symptoms following severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection is referred to as “long‐haul” syndrome. We aimed to determine whether small fiber ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::867164ed8b194f9b0e46bc4acc32e2b5
https://doi.org/10.1002/mus.27458
https://doi.org/10.1002/mus.27458
Autor:
Hitomi Nishizawa, Akinori Nakamura
Publikováno v:
Muscle & Nerve
Introduction/Aim This retrospective study aimed to quantify the changes in motor function in patients with Duchenne muscular dystrophy (DMD) due to the government‐imposed travel restrictions associated with the coronavirus disease 2019 (COVID‐19)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e2a4d226872e3d436718ac0609a7543
https://doi.org/10.1002/mus.27348
https://doi.org/10.1002/mus.27348
Autor:
Tomoko Narita, Sarosh R. Irani, Leslie Jacobson, Hidenori Matsuo, Patrick Waters, Angela Vincent, Mark Woodhall, Akiko Nagaishi
Publikováno v:
Muscle & Nerve
Introduction The majority of patients with myasthenia gravis (MG) initially present with ocular symptoms, but it is difficult to predict which cases will remain as ocular MG (OMG) or will progress to generalized MG. Herein we evaluated the serologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::912bb0d60b706548f86955d67528f3ab
https://doi.org/10.1002/mus.27103
https://doi.org/10.1002/mus.27103
Publikováno v:
Muscle & Nerve, 62(1), 111-114. WILEY
Muscle & Nerve, 62(1), 111-114. John Wiley & Sons Inc.
Muscle & Nerve
Muscle & Nerve, 62(1), 111-114. John Wiley & Sons Inc.
Muscle & Nerve
Background Increment of compound muscle action potential amplitude is a diagnostic hallmark of Lambert‐Eaton myasthenic syndrome (LEMS). Making a diagnosis can be challenging, therefore, a proper cutoff for abnormal increment is highly relevant for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2fdbecab8e073ea7861f092b514a013
https://doi.org/10.1002/mus.26885
https://doi.org/10.1002/mus.26885
Autor:
Lay Khoon Loo, Di Liang, Ashwin S. Gowda, Brendan Davies, Yusuf A. Rajabally, Salini Sumangala, Omar Salim, Aimee Goel
Publikováno v:
Muscle & Nerve
Introduction/Aims We aimed to determine whether specific severe acute respiratory syndrome coronavirus 2 (SARS‐CoV2) vaccines may be associated with acute‐onset polyradiculoneuropathy and if they may result in particular clinical presentations. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b455698199b7eaf5abe527fc2a8053e
https://publications.aston.ac.uk/id/eprint/43297/1/FINAL_PRE_PUBLISHED_VERSION_Loo_et_al.Muscle_Nerve_2021.pdf
https://publications.aston.ac.uk/id/eprint/43297/1/FINAL_PRE_PUBLISHED_VERSION_Loo_et_al.Muscle_Nerve_2021.pdf
Publikováno v:
Muscle & Nerve
Introduction/Aims The initial surge of the coronavirus disease‐2019 (COVID‐19) pandemic in early 2020 led to widespread cancellation of elective medical procedures in the United States, including nonurgent outpatient and inpatient electrodiagnost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f06118fa1c1f4c3edbf02a392d873915
https://pubmed.ncbi.nlm.nih.gov/34131929
https://pubmed.ncbi.nlm.nih.gov/34131929
Autor:
Enrico Alfonsi, Matteo Gastaldi, Elena Colombo, Sebastiano Arceri, Gloria Vaghi, Elena Ballante, Enrico Marchioni, Paola Bini, Luca Diamanti, Giuseppe Cosentino, Giulia Mallucci, Alfredo Costa, Sabrina Ravaglia, Diego Franciotta, Pietro Businaro
Publikováno v:
Muscle & Nerve
Introduction/Aims Coronavirus disease 2019 (COVID‐19), a disease caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection, has become a global pandemic. Patients with myasthenia gravis (MG), often treated with immunosupp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::261f7af2270e7e620d79f2a33960947b
http://europepmc.org/articles/PMC8242475
http://europepmc.org/articles/PMC8242475
Autor:
Martina Wiedau-Pazos, Shawn Liu, Terry Heiman-Patterson, Wendy Agnese, Erik P. Pioro, Jeffrey Zhang, Stephen Apple, Jeremy M. Shefner
Publikováno v:
Muscle & Nerve
Background In a Phase 3 study, amyotrophic lateral sclerosis (ALS) patients experienced significantly less physical functional decline with 24‐week edaravone vs placebo, followed by open‐label treatment for an additional 24 weeks. Methods Outcome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67cc906295ebcbbb112aa61bfecc68fc
http://europepmc.org/articles/PMC7004197
http://europepmc.org/articles/PMC7004197
Autor:
Allan M. Glanzman, Elena S. Mazzone, Sally Dunaway Young, Eugenio Mercuri, Wildon Farwell, Eugene Schneider, Basil T. Darras, Darryl C. De Vivo, Kathie M. Bishop, C. Frank Bennett, Richard S. Finkel, Jacqueline Montes, Francesco Muntoni, Richard Foster, Amy Pasternak
Publikováno v:
Muscle & Nerve
Introduction Ambulatory individuals with spinal muscular atrophy (SMA) experience muscle weakness, gait impairments, and fatigue that affect their walking ability. Improvements have been observed in motor function in children treated with nusinersen,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac1d596a49ceffccfbb8d0b1cf721eb4
https://doi.org/10.1002/mus.26633
https://doi.org/10.1002/mus.26633
Autor:
Ingrid J.T. Herraets, Jan-Thies H. van Asseldonk, Hessel Franssen, H. Stephan Goedee, W. Ludo van der Pol, Leonard H. van den Berg, Leo H. Visser
Publikováno v:
Muscle & Nerve
Introduction We present a case series of six treatment‐naive patients with clinical phenotypes compatible with chronic inflammatory demyelinating polyneuropathy and multifocal motor neuropathy without electrodiagnostic features of demyelination but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ba0203488d651876078167248e08bcd
https://doi.org/10.1002/mus.26629
https://doi.org/10.1002/mus.26629