Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kaili Stanley"'
Autor:
Abdel Douiri, Benjamin Bray, Ajay Bhalla, Kaili Stanley, Martin W James, Anthony Rudd, Walter Muruet, Lizz Paley, Charles D.A. Wolfe
Publikováno v:
Stroke
Supplemental Digital Content is available in the text.
Background and Purpose: The coronavirus disease 2019 (COVID-19) pandemic has potentially caused indirect harm to patients with other conditions via reduced access to health care services. We
Background and Purpose: The coronavirus disease 2019 (COVID-19) pandemic has potentially caused indirect harm to patients with other conditions via reduced access to health care services. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d3d788680ddad81a4713cb92820fee1
https://doi.org/10.1161/strokeaha.120.032253
https://doi.org/10.1161/strokeaha.120.032253
Autor:
Abdel Douiri, Walter Muruet, A Bhalla, Martin James, Lizz Paley, Kaili Stanley, Anthony Rudd, Charles Wolfe, Benjamin Bray, SSNAP Collaboration Group
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc580794fcdd44f52e8416fb64a4ad74
https://doi.org/10.2139/ssrn.3666860
https://doi.org/10.2139/ssrn.3666860
Autor:
David Eidelberg, Kaili Stanley, Shichun Peng, Sb B. Bressman, Karen Marder, Anat Mirelman, Sj J. Gross, Deborah Raymond, Rachel Saunders-Pullman, Andres Deik, Johann Hagenah, Nicole Schreiber-Agus, Lj J. Ozelius, Mj J. Barrett, Vijay Dhawan
Publikováno v:
Parkinsonism & Related Disorders. 19:186-191
Heterozygous glucocerebrosidase (GBA) mutations are the leading genetic risk factor for Parkinson disease, yet imaging correlates, particularly transcranial sonography, have not been extensively described.To determine whether GBA mutation heterozygot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f8c4ac967e30cffd663909743c819d5
https://doi.org/10.1016/j.parkreldis.2012.09.007
https://doi.org/10.1016/j.parkreldis.2012.09.007
Autor:
Lawrence Severt, Cuiling Wang, Laurie J. Ozelius, Deborah Raymond, Susan B. Bressman, Richard B. Lipton, Kaili Stanley, Vicki Shanker, Rachel Saunders-Pullman, Ann L. Hunt, M. San Luciano
Publikováno v:
Neurology. 77:319-324
Olfactory dysfunction is an established nonmotor feature of idiopathic Parkinson disease (PD), which may precede disease onset. Olfaction is likely disturbed in patients with PD with leucine-rich repeat kinase (LRRK2) G2019S mutations, although the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::429f6abd40779fcb6fc65ed171a2dafc
https://doi.org/10.1212/wnl.0b013e318227041c
https://doi.org/10.1212/wnl.0b013e318227041c
Publikováno v:
Gender Medicine. 8:209-217
Background Gender differences in Parkinson's disease may be attributable to biological and environmental factors as well as health care–seeking behaviors and diagnosis bias. Objective The goal of this pilot study was to determine whether there are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91ca7c5c8b29706cdbce8b6bd72272e2
https://doi.org/10.1016/j.genm.2011.05.002
https://doi.org/10.1016/j.genm.2011.05.002
Autor:
Matthew J. Barrett, Rachel Saunders-Pullman, Laurie J. Ozelius, Marta San Luciano, Ann L. Hunt, Kaili Stanley, Lawrence Severt, Deborah Raymond, Susan B. Bressman, Vicki Shanker
Publikováno v:
Movement Disorders. 25:2536-2541
Leucine rich repeat kinase (LRRK2) G2019S mutations are presumed to cause PD through a toxic gain of function of the protein kinase. Small molecule kinase inhibitors have been developed for the treatment of certain cancers, and some antioncogenic age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd556c6331c6e9a7cbf9b54b768e9a32
https://doi.org/10.1002/mds.23314
https://doi.org/10.1002/mds.23314
Autor:
Christina Palmese, Michele Tagliati, Gregory M. Pastores, Kaili Stanley, Norbert Brüggemann, Rachel Saunders-Pullman, AM Roe, Susan B. Bressman, Laurie J. Ozelius, Vijay Dhawan, Christine Klein, Johann Hagenah, Swati Sathe, Ruth Kornreich, Kelly Condefer
Publikováno v:
Movement Disorders. 25:1364-1372
Among the genes implicated for parkinsonism is glucocerebrosidase (GBA), which causes Gaucher disease (GD). Despite a growing literature that GD may present as parkinsonism, neuroimaging, olfaction, and neuropsychological testing have not been extens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46bba5271487c487d34065556b5151f7
https://doi.org/10.1002/mds.23046
https://doi.org/10.1002/mds.23046
Autor:
Monica M. Kurtis, A. G. Floyd, Rachel Saunders-Pullman, Amanda Deligtisch, Kaili Stanley, Qiping Yu, Seth L. Pullman, Susan B. Bressman, Carol A. Derby, Lawrence Severt, Richard B. Lipton
Publikováno v:
Movement Disorders. 23:531-537
Spiral analysis is an objective, easy to administer noninvasive test that has been proposed to measure motor dysfunction in Parkinson disease (PD). We compared overall Unified Parkinson Disease Rating Scale Part III scores to selected indices derived
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a13ad38a6314b2a87d593c92dfc4e86
https://doi.org/10.1002/mds.21874
https://doi.org/10.1002/mds.21874
Autor:
Kaili Stanley, Laurie J. Ozelius, Marta San Luciano, Susan Bressman, Jose Cabassa, Rachel Saunders-Pullman, Deborah Raymond
Publikováno v:
Movement Disorders. 26:1771-1773
We read with interest the article by Shino et al. that reported a higher familial aggregation of Parkinson’s Disease (PD) among Hispanics1. In their evaluation of incident PD cases in Northern California, they propose that there is an increased rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab2a4f5bd4fcc7c4b69f5c368a1570b7
https://doi.org/10.1002/mds.23632
https://doi.org/10.1002/mds.23632
Autor:
Rachel Saunders-Pullman, Naomi Lubarr, Johann Hagenah, Deborah Raymond, Susan B. Bressman, Laurie J. Ozelius, Christine Klein, Norbert Brüggemann, Marta San Luciano, Kaili Stanley, Cuiling Wang
Publikováno v:
Parkinsonism & Related Disorders. 16:420-422
DYT6 dystonia is a form of early onset primary dystonia often associated with brachial onset and spread to involve cranial-cervical sites and leg, although the phenotype also includes focal dystonia, and it may start as late as 49 years [1,2]. The re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be8d2532691932d2d505993749afc82d
https://doi.org/10.1016/j.parkreldis.2010.03.003
https://doi.org/10.1016/j.parkreldis.2010.03.003