Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Kathleen M. McEvoy"'
Publikováno v:
Neuro-Ophthalmology. 42:117-121
A 33-year-old female presented with bilateral papilloedema and constricted visual fields from autoimmune retinopathy. She then developed a painful peripheral neuropathy that led to further work-up and the diagnosis of systemic lupus erythematosus. Pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feeb30f1ef1c1955c7e67c5084dd0449
https://doi.org/10.1080/01658107.2017.1355395
https://doi.org/10.1080/01658107.2017.1355395
Autor:
Mohamed Kazamel, Lyell K. Jones, Eric J. Sorenson, Margherita Milone, Kathleen M. McEvoy, Andrea N. Leep-Hunderfund, Michelle L. Mauermann
Publikováno v:
Muscle & Nerve. 54:94-99
Introduction Valosin containing protein (VCP) mutations cause a rare disorder characterized by hereditary inclusion body myopathy, Paget disease of bone (PDB), and frontotemporal dementia (FTD) with variable penetrance. VCP mutations have also been l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c87fd6778175fa9bf74e7d172c3f4b2e
https://doi.org/10.1002/mus.24980
https://doi.org/10.1002/mus.24980
Autor:
Lourdes P. Dale, Jolanta W. Borto, Michelle A. Couto, Kathleen McDonald, Kathleen M. McEvoy, Jordana Klein, Anne E. Pidano, Heather Olson, James DiLoreto
Publikováno v:
Psychology of Popular Media Culture. 2:134-149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a44bb1818580b287a09f564c7113540
https://doi.org/10.1037/a0030555
https://doi.org/10.1037/a0030555
Publikováno v:
Muscle & Nerve. 45:897-900
Introduction: Caveolin-3 is a major component of the caveolae in skeletal and cardiac muscle.Mutations in the caveolin-3 gene (CAV3) lead to a spectrum of clinical phenotypes including limb-girdle muscular dystrophy 1C, distal myopathy, rippling musc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e348fc6bce797bce85ca295f6293ec8
https://doi.org/10.1002/mus.23270
https://doi.org/10.1002/mus.23270
Publikováno v:
Training and Education in Professional Psychology. 4:121-127
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d4adfbd70a766aedbb9a66ba31f4d27
https://doi.org/10.1037/a0017589
https://doi.org/10.1037/a0017589
Publikováno v:
Neurology. 72:1607-1613
A patient reported fatigue and imbalance for “most of her life.” As a child, she walked more slowly than others and had difficulty ice skating. She noted definite gait impairment about 16 years before presentation and this was more noticeable to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e4325ce710d64eb76885bc74b60c272
https://doi.org/10.1212/wnl.0b013e3181a413fe
https://doi.org/10.1212/wnl.0b013e3181a413fe
Publikováno v:
Neuromuscular Disorders. 25:S186-S187
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::026602bd52a030364b115e10cbd0a33b
https://doi.org/10.1016/j.nmd.2015.06.015
https://doi.org/10.1016/j.nmd.2015.06.015
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 20(11)
Sporadic inclusion body myositis (sIBM) is a slowly progressive idiopathic inflammatory myopathy. The characteristic early quadriceps and finger flexor muscle weakness often leads to the diagnosis of sIBM, especially when all canonical pathological f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d95296e394de7dc9952d456f2efc341f
https://pubmed.ncbi.nlm.nih.gov/24055211
https://pubmed.ncbi.nlm.nih.gov/24055211
Autor:
Josep Dalmau, Robert J. Harvey, Kathleen M. McEvoy, Andrew McKeon, Sean J. Pittock, Vanda A. Lennon, Joseph Y. Matsumoto, Eugenia Martinez-Hernandez, Eric Lancaster
Publikováno v:
JAMA Neurology
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Objectives: To determine whether glycine receptor alpha 1 subunit-specific autoantibodies (GlyR alpha 1-IgG) occur in a broader spectrum of brainstem and spinal hyperexcitability disorders than the progressive encephalomyelitis with rigidity and myoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47dbbd06feaed2458547766e85ec853e
https://pubmed.ncbi.nlm.nih.gov/23318510
https://pubmed.ncbi.nlm.nih.gov/23318510
Publikováno v:
Musclenerve. 45(6)
Caveolin-3 is a major component of the caveolae in skeletal and cardiac muscle. Mutations in the caveolin-3 gene (CAV3) lead to a spectrum of clinical phenotypes including limb-girdle muscular dystrophy 1C, distal myopathy, rippling muscle disease, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b9690777403e59188bd0b9623f7b4f25
https://pubmed.ncbi.nlm.nih.gov/22581547
https://pubmed.ncbi.nlm.nih.gov/22581547