Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Tsvyatko, Dorovski"'
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
Comparison of Parkinson risk in Ashkenazi Jewish patients with Gaucher disease and GBA heterozygotes
Autor:
Tsvyatko Dorovski, Huma Q. Rana, Deborah Elstein, Cheryl Waters, Louise Bier, Manisha Balwani, William C. Nichols, Karina Sakanaka, Oren A. Levy, Wendy K. Chung, Tama Dinur, Michael W. Pauciulo, Ari Zimran, Timothy Quinn, Stanley Fahn, Roy N. Alcalay
Publikováno v:
JAMA neurology. 71(6)
Importance Information on age-specific risk for Parkinson disease (PD) in patients with Gaucher disease (GD) and glucocerebrosidase ( GBA ) heterozygotes is important for understanding the pathophysiology of the genetic association and for counseling
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
Autor:
Karen Marder, Karina Sakanaka, Timothy Quinn, Louise Bier, Stanley Fahn, Deborah Elstein, Ari Zimran, Oren A. Levy, Manisha Balwani, Cheryl Waters, Tsvyatko Dorovski, William C. Nichols, Tama Dinur, Michael W. Pauciulo, Roy N. Alcalay, Huma Q. Rana
Publikováno v:
Molecular Genetics and Metabolism. 111:S37-S38
Autor:
San Luciano, Marta, Tanner, Caroline M., Meng, Cheryl, Marras, Connie, Goldman, Samuel M., Lang, Anthony E., Tolosa, Eduardo, Schüle, Birgitt, Langston, J. William, Brice, Alexis, Corvol, Jean‐Christophe, Goldwurm, Stefano, Klein, Christine, Brockman, Simone, Berg, Daniela, Brockmann, Kathrin, Ferreira, Joachim J., Tazir, Meriem, Mellick, George D., Sue, Carolyn M.
Publikováno v:
Movement Disorders; Oct2020, Vol. 35 Issue 10, p1755-1764, 10p
Autor:
Berkovic, Samuel, Epi4K Consortium
Publikováno v:
Brain: A Journal of Neurology; Aug2017, Vol. 140 Issue 8, p2144-2156, 13p
Autor:
Pont‐Sunyer, Claustre, Tolosa, Eduardo, Caspell‐Garcia, Chelsea, Coffey, Christopher, Alcalay, Roy N., Chan, Piu, Duda, John E., Facheris, Maurizio, Fernández‐Santiago, Rubén, Marek, Kenneth, Lomeña, Francisco, Marras, Connie, Mondragon, Elisabet, Saunders‐Pullman, Rachel, Waro, Bjorg, Pont-Sunyer, Claustre, Caspell-Garcia, Chelsea, Fernández-Santiago, Rubén, Lomeña, Francisco, Saunders-Pullman, Rachel
Publikováno v:
Movement Disorders; May2017, Vol. 32 Issue 5, p726-738, 14p
Autor:
Marras, Connie, Alcalay, Roy N., Caspell‐Garcia, Chelsea, Coffey, Christopher, Chan, Piu, Duda, John E., Facheris, Maurizio F., Fernández‐Santiago, Rubén, Ruíz‐Martínez, Javier, Mestre, Tiago, Saunders‐Pullman, Rachel, Pont‐Sunyer, Claustre, Tolosa, Eduardo, Waro, Bjorg
Publikováno v:
Movement Disorders; Aug2016, Vol. 31 Issue 8, p1192-1202, 11p
Autor:
Vilas, Dolores, Shaw, Leslie M., Taylor, Peggy, Berg, Daniela, Brockmann, Kathrin, Aasly, Jan, Marras, Connie, Pont‐Sunyer, Claustre, Ríos, José, Marek, Ken, Tolosa, Eduardo
Publikováno v:
Movement Disorders; Jun2016, Vol. 31 Issue 6, p906-914, 10p
REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers.
Autor:
Saunders‐Pullman, Rachel, Alcalay, Roy N., Mirelman, Anat, Wang, Cuiling, Luciano, Marta San, Ortega, Roberto A., Glickman, Amanda, Raymond, Deborah, Mejia‐Santana, Helen, Doan, Nancy, Johannes, Brooke, Yasinovsky, Kira, Ozelius, Laurie, Clark, Lorraine, Orr‐Utreger, Avi, Marder, Karen, Giladi, Nir, Bressman, Susan B.
Publikováno v:
Movement Disorders; Nov2015, Vol. 30 Issue 13, p1834-1839, 6p