Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Rivka Sachdev"'
Publikováno v:
Neurology Alert. Mar2024, Vol. 43 Issue 7, p1-8. 8p.
Autor:
Susan Bressman, Nir Giladi, Joan Miravite, Jose Cabassa, Brooke Johannes, Laurie J. Ozelius, Matthew J. Barrett, Roberto A. Ortega, Karen Marder, William C. Nichols, Jeannie Soto-Valencia, Harini Sarva, Rivka Sachdev, William Severt, Rachel Saunders-Pullman, Nancy Doan, Matthew Swan, Vicki Shanker, Sarah Boschung, Andres Deik, Deborah Raymond
Publikováno v:
Journal of the Neurological Sciences. 370:63-69
Mutations in GBA1 are a well-established risk factor for Parkinson disease (PD). GBA-associated PD (GBA-PD) may have a higher burden of nonmotor symptoms than idiopathic PD (IPD). We sought to characterize the relationship between GBA-PD and neuropsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::232082dbd586e66c0fbd12928e40644d
https://doi.org/10.1016/j.jns.2016.08.059
https://doi.org/10.1016/j.jns.2016.08.059
Autor:
Mark Groves, Vicki Shanker, Diana Ruiz, Marta San Luciano, Mali Gana Weisz, Tanya Gurevich, Nir Giladi, Karen Marder, Elan D. Louis, Anat Mirelman, Ming X. Tang, Laurie J. Ozelius, Rivka Sachdev, Naomi Lubarr, Tsvyatko Dorovski, Harini Sarva, Joan Miravite, Ernest Roos, Roberto A. Ortega, Llency Rosado, Helen Mejia Santana, Deborah Raymond, Cheryl Waters, Christina Palmese, Lucien J. Cote, Kira Yasinovsky, Andres Deik, Susan Bressman, Maayan Zalis, Lawrence Severt, Blair Ford, Oren A. Levy, Lorraine N. Clark, Matthew Swan, Jeannie Soto-Valencia, Michael W. Pauciulo, Avi Orr-Urtreger, William C. Nichols, Stanley Fahn, Pietro Mazzoni, Martha Orbe-Reilly, Ann L. Hunt, Roy N. Alcalay, Avner Thaler, Jose Cabassa, Brooke Johannes, Matthew J. Barrett, Anat Bar Shira, Rachel Saunders-Pullman
Publikováno v:
Movement Disorders. 28:1966-1971
The phenotype of Parkinson's disease (PD) in patients with and without leucine-rich repeat kinase 2 (LRRK2) G2019S mutations reportedly is similar; however, large, uniformly evaluated series are lacking. The objective of this study was to characteriz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c539948b419e56a29514350fe3a6c738
https://doi.org/10.1002/mds.25647
https://doi.org/10.1002/mds.25647
Autor:
Roy N, Alcalay, Anat, Mirelman, Rachel, Saunders-Pullman, Ming-X, Tang, Helen, Mejia Santana, Deborah, Raymond, Ernest, Roos, Martha, Orbe-Reilly, Tanya, Gurevich, Anat, Bar Shira, Mali, Gana Weisz, Kira, Yasinovsky, Maayan, Zalis, Avner, Thaler, Andres, Deik, Matthew James, Barrett, Jose, Cabassa, Mark, Groves, Ann L, Hunt, Naomi, Lubarr, Marta, San Luciano, Joan, Miravite, Christina, Palmese, Rivka, Sachdev, Harini, Sarva, Lawrence, Severt, Vicki, Shanker, Matthew Carrington, Swan, Jeannie, Soto-Valencia, Brooke, Johannes, Robert, Ortega, Stanley, Fahn, Lucien, Cote, Cheryl, Waters, Pietro, Mazzoni, Blair, Ford, Elan, Louis, Oren, Levy, Llency, Rosado, Diana, Ruiz, Tsvyatko, Dorovski, Michael, Pauciulo, William, Nichols, Avi, Orr-Urtreger, Laurie, Ozelius, Lorraine, Clark, Nir, Giladi, Susan, Bressman, Karen S, Marder
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 28(14)
The phenotype of Parkinson's disease (PD) in patients with and without leucine-rich repeat kinase 2 (LRRK2) G2019S mutations reportedly is similar; however, large, uniformly evaluated series are lacking. The objective of this study was to characteriz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1aacccd048f7d5a60f7a2ece61f806f0
https://pubmed.ncbi.nlm.nih.gov/24307480
https://pubmed.ncbi.nlm.nih.gov/24307480
Autor:
Ryan J. Uitti, Seth L. Pullman, A. J. Stoessl, Rachel Saunders-Pullman, M. San Luciano, Deborah Raymond, Susan Bressman, Rivka Sachdev, Douglas E. Hobson, Laurie J. Ozelius, Kaili Stanley, Johann Hagenah, D. Lefton, Richard A. Gatti, T. Nakamura, Michael S. Okun
To compare the phenotype of primary-appearing dystonia due to variant ataxia-telangiectasia (A-T) with that of other dystonia ascertained for genetics research.Movement disorder specialists examined 20 Canadian Mennonite adult probands with primary-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4b2e8f4fed392cfc1edab5308dc2893
https://europepmc.org/articles/PMC3689264/
https://europepmc.org/articles/PMC3689264/
Publikováno v:
Neurology Alert. Jun2023, Vol. 42 Issue 10, p1-8. 8p.
Publikováno v:
Neurology Alert. Apr2023, Vol. 42 Issue 8, p1-8. 8p.
Publikováno v:
Neurology Alert. Feb2023, Vol. 42 Issue 6, p1-8. 8p.
Publikováno v:
Internal Medicine Alert. 5/15/2023, Vol. 45 Issue 9, p1-8. 8p.
Publikováno v:
Internal Medicine Alert. 3/15/2023, Vol. 45 Issue 5, p1-8. 8p.