Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Melissa R. Mandarakas"'
Publikováno v:
Current Opinion in Neurology. 34:697-705
Purpose of review Rehabilitation for patients with neuromuscular disorders (NMDs) has undisputed health benefits and is potentially therapeutic for targeting impairments, improving quality of life, and enabling activities of daily living. Whilst reha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28b647fca166cd9e75363f7ee43e393b
https://doi.org/10.1097/wco.0000000000000974
https://doi.org/10.1097/wco.0000000000000974
Autor:
Badrul Islam, Kathleen Bateman, Maria Lucia Brito Ferreira, Pieter A. van Doorn, Bart C. Jacobs, Susumu Kusunoki, Eppie M. Yiu, Hugh J. Willison, Ricardo Reisin, Nortina Shahrizaila, Thirugnanam Umapathi, Mario Emilio Dourado, Cristiane Soares, Melissa R Mandarakas, Yuzhong Wang, Francisco de Assis Aquino Gondim, David R. Cornblath, Richard A. C. Hughes, James J. Sejvar, Sonja E. Leonhard, Carlos A. Pardo
Publikováno v:
Revista Neurociências. 29:1-52
A síndrome de Guillain–Barré (SGB) é uma doença imunomediada rara, mas potencialmente fatal, dos nervos periféricos e das raízes nervosas, que é geralmente desencadeada por infecções. A incidência da SGB pode, portanto, aumentar durante s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f8a6b1d6ceab0b200ebf7cea9de63e9
https://doi.org/10.34024/rnc.2021.v29.11725
https://doi.org/10.34024/rnc.2021.v29.11725
Autor:
Sonja E, Leonhard, Melissa R, Mandarakas, Francisco, de Assis Aquino Gondim, Kathleen, Bateman, Maria L, Brito Ferreira, David R, Cornblath, Pieter A, Van Doorn, Mario E, Dourado, Richard A C, Hughes, Badrul, Islam, Susumu, Kusunoki, Carlos A, Pardo, Ricardo, Reisin, James J, Sejvar, Nortina, Shahrizaila, Cristiane, Soares, Thirugnanam, Umapathi, Yuzhong, Wang, Eppie M, Yiu, Hugh J, Willison, Bart C, Jacobs
Publikováno v:
Medicina. 81(5)
Guillain-Barré syndrome (GBS) is a rare, but potentially fatal, immune-mediated disease of the peripheral nerves and nerve roots that is usually triggered by infections. The incidence of GBS can therefore increase during outbreaks of infectious dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0dea2baf5210d1087b9cc5474ebed00f
https://pubmed.ncbi.nlm.nih.gov/34633957
https://pubmed.ncbi.nlm.nih.gov/34633957
Autor:
Badrul Islam, Thirugnanam Umapathi, Mario Emilio Dourado, Melissa R. Mandarakas, Pieter A. van Doorn, James J. Sejvar, Susumu Kusunoki, Carlos A. Pardo, Cristiane Soares, Hugh J. Willison, Ricardo Reisin, Eppie M. Yiu, Francisco de Assis Aquino Gondim, Sonja E. Leonhard, Nortina Shahrizaila, Bart C. Jacobs, Maria Lucia Brito Ferreira, Richard A. C. Hughes, Yuzhong Wang, David R. Cornblath, Kathleen Bateman
Publikováno v:
Nature Reviews. Neurology
Nature Reviews Neurology, 15(11), 671-683. Nature Publishing Group
Nature Reviews Neurology, 15(11), 671-683. Nature Publishing Group
Guillain–Barré syndrome (GBS) is a rare, but potentially fatal, immune-mediated disease of the peripheral nerves and nerve roots that is usually triggered by infections. The incidence of GBS can therefore increase during outbreaks of infectious di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bb71617de0324bbdb7f0dc2e11743d2
http://europepmc.org/articles/PMC6821638
http://europepmc.org/articles/PMC6821638
Autor:
Kristy Rose, Oranee Sanmaneechai, Melissa R Mandarakas, Joshua Burns, Kathryn M. Refshauge, Manoj P. Menezes
Publikováno v:
Journal of the Peripheral Nervous System. 23:99-107
A functional outcome measure for infants (aged 0-3 years) with Charcot-Marie-Tooth (CMT) disease is needed for upcoming disease-modifying trials. A systematic review of outcome measures for infants with neuromuscular disorders was completed to determ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd4b0e2bf02404baad4b4e0f6c24ad41
https://doi.org/10.1111/jns.12258
https://doi.org/10.1111/jns.12258
Autor:
Davide Pareyson, Joshua Burns, Emanuela Pagliano, Isabella Moroni, Michael E. Shy, Maria Foscan, Kathryn M. Refshauge, Oranee Sanmaneechai, Hugo Sampaio, Rachel A. Kennedy, Gyula Acsadi, Karen Herbert, Sabrina W. Yum, David N. Herrmann, Paula Bray, Kristy Rose, Eppie M. Yiu, Michelle A. Farrar, Manoj P. Menezes, T Estilow, Kate Eichinger, Monique M. Ryan, R Shy, Melissa R Mandarakas
Publikováno v:
Brain : a journal of neurology. 142(4)
Many genetic subtypes of Charcot-Marie-Tooth disease (CMT) show signs of symptomatic disease during the earliest years of life. This might be the ideal time to intervene before progression of clinical sequelae due to demyelination and axonal loss. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa92003ba05b6671414d0d956b3a3561
https://pubmed.ncbi.nlm.nih.gov/30476010
https://pubmed.ncbi.nlm.nih.gov/30476010
Autor:
Sabrina W. Yum, Michelle A. Farrar, Gyula Acsadi, Karen Herbert, T Estilow, Michael E. Shy, Manoj P. Menezes, Paula Bray, Joshua Burns, Kristy Rose, Emanuela Pagliano, Melissa R Mandarakas, Kate Eichinger, Oranee Sanmaneechai, Rachel A. Kennedy, R Shy, Eppie M. Yiu, Hugo Sampaio, Kathryn M. Refshauge, David N. Herrmann, Isabella Moroni, Monique M. Ryan, Maria Foscan, Davide Pareyson
Publikováno v:
Brain : a journal of neurology. 141(12)
Many genetic subtypes of Charcot-Marie-Tooth disease (CMT) show signs of symptomatic disease during the earliest years of life. This might be the ideal time to intervene before progression of clinical sequelae due to demyelination and axonal loss. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8934fa5e3bfe960e5192883a6d93b109
https://pubmed.ncbi.nlm.nih.gov/30649217
https://pubmed.ncbi.nlm.nih.gov/30649217
Autor:
Joshua Burns, Amy D Sman, Kayla M D Cornett, Elizabeth Wojciechowski, Terri Walker, Manoj P Menezes, Melissa R Mandarakas, Kristy J Rose, Paula Bray, Hugo Sampaio, Michelle Farrar, Kathryn M Refshauge, Jacqueline Raymond, Jennifer Baldwin, Marnee J McKay, Anita Mudge, Leanne Purcell, Clare Miller, Kelly Gray, Meghan Harman, Natalie Gabrael, Robert A Ouvrier
Publikováno v:
The Lancet. Childadolescent health. 1(2)
Summary Background Exercise is potentially therapeutic for neuromuscular disorders, but a risk of harm exists due to overwork weakness. We aimed to assess the safety and efficacy of progressive resistance exercise for foot dorsiflexion weakness in ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9ab1046ff4c833ed0ea1d0bab362e36
https://pubmed.ncbi.nlm.nih.gov/29289585
https://pubmed.ncbi.nlm.nih.gov/29289585
Publikováno v:
Journal of child neurology. 28(11)
Children with Charcot-Marie-Tooth disease frequently suffer ankle sprain and experience chronic ankle instability; however, no pediatric self-reported measures of chronic ankle instability exist. The aim was to modify and validate the most reliable m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88c40d676e797255a4216f099877879b
https://pubmed.ncbi.nlm.nih.gov/23696628
https://pubmed.ncbi.nlm.nih.gov/23696628
Publikováno v:
Neuromuscular Disorders. 24:910
Children with Charcot-Marie-Tooth disease (CMT) often experience ankle sprains and associated trips or falls. No research has investigated ankle instability in children with CMT and its relationship with overall disability. Thirty-seven children (46%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2a0664829e9bf1883c920862755417a
https://doi.org/10.1016/j.nmd.2014.06.385
https://doi.org/10.1016/j.nmd.2014.06.385