Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Brooke Johannes"'
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:
Roy N. Alcalay, Nir Giladi, Laurie J. Ozelius, Roberto A. Ortega, Brooke Johannes, Marta San Luciano, Helen Mejia-Santana, Kira Yasinovsky, Cuiling Wang, Susan Bressman, Karen Marder, Avi Orr-Utreger, Anat Mirelman, Lorraine N. Clark, Amanda Glickman, Nancy Doan, Rachel Saunders-Pullman, Deborah Raymond
Publikováno v:
Movement Disorders. 30:1834-1839
Background Rapid eye movement sleep behavior disorder occurs with idiopathic Parkinson's disease (PD) and often precedes PD. Its frequency in LRRK2-PD and utility as a preclinical marker has not been established. Methods One hundred forty-four idiopa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e89b4f16dc6e03c449ad3cfcc1ff8509
https://doi.org/10.1002/mds.26413
https://doi.org/10.1002/mds.26413
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:
Laurie J. Ozelius, Brooke Johannes, Cuiling Wang, Roberto A. Ortega, Helen Mejia-Santana, Nir Giladi, Avi Orr-Urtreger, Karen Marder, Susan Bressman, Deborah Raymond, Martha Orbe-Reilly, Roy N. Alcalay, Avner Thaler, Anat Mirelman, Rachel Saunders-Pullman
Publikováno v:
JAMA Neurology. 75:312
Importance Few prospective longitudinal studies have evaluated the progression of Parkinson disease (PD) in patients with the leucine-rich repeat kinase 2 ( LRRK2 [OMIM609007]) mutation. Knowledge about such progression will aid clinical trials. Obje
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e11f92224771ac6788f199a0efd235b4
https://doi.org/10.1001/jamaneurol.2017.4019
https://doi.org/10.1001/jamaneurol.2017.4019
Autor:
Rachel, Saunders-Pullman, Roy N, Alcalay, Anat, Mirelman, Cuiling, Wang, Marta San, Luciano, Roberto A, Ortega, Amanda, Glickman, Deborah, Raymond, Helen, Mejia-Santana, Nancy, Doan, Brooke, Johannes, Kira, Yasinovsky, Laurie, Ozelius, Lorraine, Clark, Avi, Orr-Utreger, Karen, Marder, Nir, Giladi, Susan B, Bressman, Ora, Assais
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 30(13)
Rapid eye movement sleep behavior disorder occurs with idiopathic Parkinson's disease (PD) and often precedes PD. Its frequency in LRRK2-PD and utility as a preclinical marker has not been established.One hundred forty-four idiopathic PD, 142 LRRK2 G
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::849560b7f80e0aab9af635fa20f8ba80
https://pubmed.ncbi.nlm.nih.gov/26366513
https://pubmed.ncbi.nlm.nih.gov/26366513
Autor:
Deborah Raymond, Paola Torres, Susan B. Bressman, William C. Nichols, Matthew Swan, Gregory M. Pastores, Roberto A. Ortega, Lawrence Severt, Rachel Saunders-Pullman, Ann L. Hunt, Brooke Johannes, Matthew J. Barrett, Vicki Shanker, Sarah Boschung
Publikováno v:
Journal of Clinical Neuroscience. 28:185-186
Mutations in the glucocerebrosidase (GBA1) gene, the most common genetic contributor to Parkinson’s disease (PD), are associated with an increased risk of PD in heterozygous and homozygous carriers. While glucocerebrosidase enzyme (GCase) activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9013b088cd190c23a4f26354ed8b80bf
https://doi.org/10.1016/j.jocn.2015.12.004
https://doi.org/10.1016/j.jocn.2015.12.004
Autor:
Rachel Saunders-Pullman, E. Deegan, Yuji Kajiwara, Andres Deik, Brooke Johannes, Elena Sánchez, K. Landy, Janet C. Rucker, S. E. Brodie, S. Scelsa, Coro Paisán-Ruiz
PNPLA6 mutations, known to be associated with the development of motor neuron phenotypes, have recently been identified in families with Boucher–Neuhauser syndrome. Boucher–Neuhauser is a rare autosomal recessive syndrome characterized by the co-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::840d80e4b3e132689d13f571714b3cd0
https://europepmc.org/articles/PMC4245359/
https://europepmc.org/articles/PMC4245359/
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