Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Cynthia C. Jones"'
Autor:
Mitzi J. Williams, Lilyana Amezcua, Annette Okai, Darin T. Okuda, Stanley Cohan, Ray Su, Becky Parks, Jason P. Mendoza, James B. Lewin, Cynthia C. Jones
Publikováno v:
Neurology and Therapy, Vol 9, Iss 2, Pp 483-493 (2020)
Abstract Introduction Black or African American (black/AA) patients with multiple sclerosis (MS) are reported to exhibit greater disease severity compared with non-black or non-AA patients. Whether differences exist in response to MS disease-modifyin
Externí odkaz:
https://doaj.org/article/85d7a4d0f6eb4477bc4ce8aec51e644c
Autor:
Angel Chinea, Lilyana Amezcua, Wendy Vargas, Annette Okai, Mitzi J. Williams, Ray Su, Becky Parks, Jason P. Mendoza, James B. Lewin, Cynthia C. Jones
Publikováno v:
Neurology and Therapy, Vol 9, Iss 2, Pp 495-504 (2020)
Abstract Introduction Compared with the non-Hispanic/non-Latino population, Hispanic/Latino patients with multiple sclerosis (MS) are reported to exhibit greater disease severity. Geographical location and genetics play a role in differences observed
Externí odkaz:
https://doaj.org/article/628eae7e81094885992adf0e786a8a07
Autor:
Ingrid E. C. Verhaart, Agata Robertson, Ian J. Wilson, Annemieke Aartsma-Rus, Shona Cameron, Cynthia C. Jones, Suzanne F. Cook, Hanns Lochmüller
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-15 (2017)
Abstract Spinal muscular atrophy linked to chromosome 5q (SMA) is a recessive, progressive, neuromuscular disorder caused by bi-allelic mutations in the SMN1 gene, resulting in motor neuron degeneration and variable presentation in relation to onset
Externí odkaz:
https://doaj.org/article/408e38e2af034b6784ac8c8b34bfabea
Autor:
Rosangel Cruz, Susan A. Hall, Angela D. Paradis, Jill Jarecki, Mary K. Schroth, Colleen McCarthy O’Toole, Nicole B. Johnson, Shannon O’Brien, Sandra P. Reyna, Lisa Belter, Cynthia C. Jones
Publikováno v:
Journal of Neuromuscular Diseases
Background: Cure SMA maintains the largest patient-reported database for people affected with spinal muscular atrophy (SMA). In 2017, Cure SMA initiated annual surveys with their membership to collect demographic and disease characteristics, healthca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fbf2c3cc8796c1b736d25b757f6faa2
http://europepmc.org/articles/PMC7902958
http://europepmc.org/articles/PMC7902958
Autor:
Becky Parks, Darin T. Okuda, James B. Lewin, Jason P. Mendoza, Stanley Cohan, Lilyana Amezcua, Mitzi J. Williams, Ray Su, Cynthia C. Jones, Annette Okai
Publikováno v:
Neurology and Therapy, Vol 9, Iss 2, Pp 483-493 (2020)
Neurology and Therapy
Neurology and Therapy
Introduction Black or African American (black/AA) patients with multiple sclerosis (MS) are reported to exhibit greater disease severity compared with non-black or non-AA patients. Whether differences exist in response to MS disease-modifying therapi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97ac439d11db8f7b0391021f6c8eb2e8
https://doi.org/10.1007/s40120-020-00193-5
https://doi.org/10.1007/s40120-020-00193-5
Autor:
Becky Parks, Wendy Vargas, Cynthia C. Jones, Jason P. Mendoza, James B. Lewin, Lilyana Amezcua, Ray Su, Annette Okai, Angel Chinea, Mitzi J. Williams
Publikováno v:
Neurology and Therapy, Vol 9, Iss 2, Pp 495-504 (2020)
Neurology and Therapy
Neurology and Therapy
Introduction Compared with the non-Hispanic/non-Latino population, Hispanic/Latino patients with multiple sclerosis (MS) are reported to exhibit greater disease severity. Geographical location and genetics play a role in differences observed across H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fce062e837c35dd35c82142fb794cf9
https://doaj.org/article/628eae7e81094885992adf0e786a8a07
https://doaj.org/article/628eae7e81094885992adf0e786a8a07
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 93:A5.2-A5
IntroductionThe delayed-release dimethyl fumarate (DMF) label recommends use during pregnancy only if potential benefit justifies the potential risk. Given limited pregnancy data, United Kingdom (UK) and Ireland are enrolling DMF-exposed pregnant wom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68fda64beceb20614304e6684ff8a261
https://doi.org/10.1136/jnnp-2022-abn.14
https://doi.org/10.1136/jnnp-2022-abn.14
Publikováno v:
Braindevelopment. 43(1)
Introduction Spinal muscular atrophy (SMA) is caused by a defect in the survival motor neuron 1 (SMN1) gene. The Cooperative Study of the natural history of SMA Type I in Taiwan is a retrospective, longitudinal, observational study that helps in furt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a52ca1275ea5ec6ff5ad6cb3a8543263
https://pubmed.ncbi.nlm.nih.gov/32878721
https://pubmed.ncbi.nlm.nih.gov/32878721
Autor:
Mcguigan Christopher, Xiaomei Peng, Cynthia C. Jones, Filipe Branco, Kerstin Hellwig, Oksana Mokliatchouk, David Rog
Publikováno v:
Revue Neurologique. 177:S113-S114
Introduction DMF a montre un profil benefice–risque favorable dans les essais et en pharmacovigilance. DMF est recommande chez les femmes enceintes que si le benefice justifie le risque pour le fœtus. Objectifs Fournir les issues de grossesses et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23922159482f6a6db4889c9405ac4dfb
https://doi.org/10.1016/j.neurol.2021.02.342
https://doi.org/10.1016/j.neurol.2021.02.342
Autor:
Cynthia C. Jones, Cathy Lally, W. Dana Flanders, Sandra P. Reyna, Wildon Farwell, Suzanne F. Cook
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-6 (2017)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Spinal muscular atrophy (SMA) is a progressive, devastating disease and a leading inherited cause of infant mortality. The limited population-based literature is confined to small regional studies. Estimates of prevalence are needed to cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39d025d5f52c9a2a34bac673f8d56d71
http://link.springer.com/article/10.1186/s13023-017-0724-z
http://link.springer.com/article/10.1186/s13023-017-0724-z