Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Debra Ehrlich"'
Autor:
Esther Yoon, Sarah Ahmed, Ryan Li, Sara Bandres-Ciga, Cornelis Blauwendraat, Irene Dustin, Sonja Scholz, Mark Hallett, Debra Ehrlich
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Deep brain stimulation (DBS) is a well-established treatment option for select patients with Parkinson’s Disease (PD). However, response to DBS varies, therefore, the ability to predict who will have better outcomes can aid pati
Externí odkaz:
https://doaj.org/article/57a6aa8d89fe42aeaa690c5f30bb56b5
Autor:
Felipe Vial, Patrick McGurrin, Thomas Osterholt, Debra Ehrlich, Dietrich Haubenberger, Mark Hallett
Publikováno v:
Clinical Neurophysiology Practice, Vol 5, Iss , Pp 30-34 (2020)
Objective: The electrophysiological classification of tremors can be a key element in the diagnosis and can facilitate treatment of a patient with tremor; however, the ability to conduct electrophysiological studies of tremor is not widely available.
Externí odkaz:
https://doaj.org/article/90ecb0dc563d4346877315a43065747b
Autor:
Michael Farrell, Barbara I. Karp, Panagiotis Kassavetis, William Berrigan, Simge Yonter, Debra Ehrlich, Katharine E. Alter
Publikováno v:
Toxins, Vol 12, Iss 10, p 626 (2020)
Chemodenervation of cervical musculature using botulinum neurotoxin (BoNT) is established as the gold standard or treatment of choice for management of Cervical Dystonia (CD). The success of BoNT procedures is measured by improved symptomology while
Externí odkaz:
https://doaj.org/article/46a1a5670d194441ae2c306dfd07815e
Autor:
William Zhu, Xiaoping Huang, Esther Yoon, Sara Bandres-Ciga, Cornelis Blauwendraat, Kimberly J Billingsley, Joshua H Cade, Beverly P Wu, Victoria H Williams, Alice B Schindler, Janet Brooks, J Raphael Gibbs, Dena G Hernandez, Debra Ehrlich, Andrew B Singleton, Derek P Narendra
Publikováno v:
Brain
PRKN mutations are the most common recessive cause of Parkinson’s disease and are a promising target for gene and cell replacement therapies. Identification of biallelic PRKN patients at the population scale, however, remains a challenge, as roughl
Autor:
Gian Pal, Graziella Mangone, Emily J. Hill, Bichun Ouyang, Yuanqing Liu, Vanessa Lythe, Debra Ehrlich, Rachel Saunders‐Pullman, Vicki Shanker, Susan Bressman, Roy N. Alcalay, Priscilla Garcia, Karen S. Marder, Jan Aasly, M. Maral Mouradian, Samantha Link, Marc Rosenbaum, Sharlet Anderson, Bryan Bernard, Robert Wilson, Glenn Stebbins, William C. Nichols, Marie‐Laure Welter, Sepehr Sani, Mitra Afshari, Leo Verhagen, Rob M.A. Bie, Tom Foltynie, Deborah Hall, Jean‐Christophe Corvol, Christopher G. Goetz
Publikováno v:
Annals of neurology, 91(3), 424-435. John Wiley and Sons Inc.
Objective: This study was undertaken to compare the rate of change in cognition between glucocerebrosidase (GBA) mutation carriers and noncarriers with and without subthalamic nucleus deep brain stimulation (STN-DBS) in Parkinson disease. Methods: Cl
Autor:
Patrick McGurrin, Felipe Vial, Thomas Osterholt, Gina Norato, Imran Khan, Dietrich Haubenberger, Debra Ehrlich, Mark Hallett
Publikováno v:
Mov Disord Clin Pract
BACKGROUND: Essential tremor is a common movement disorder, characterized by 4–12 Hz tremor of the hands and arms that can affect many activities of daily living. It has been reported by patients that when performing tasks bimanually their tremor i
Autor:
Gian Pal, Graziella Mangone, Bichun Ouyang, Debra Ehrlich, Rachel Saunders‐Pullman, Susan Bressman, Roy N. Alcalay, Karen Marder, Jan Aasly, M. Maral Mouradian, Sharlet Anderson, Bryan Bernard, Glenn Stebbins, Sepehr Sani, Mitra Afshari, Leo Verhagen, Rob M.A. de Bie, Tom Foltynie, Deborah Hall, Jean‐Christophe Corvol, Christopher G. Goetz
Publikováno v:
Annals of neurology, 92(2), 345-346. John Wiley and Sons Inc.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6992c3714d050cc9d627398ee0d8105
https://pure.amc.nl/en/publications/reply-to(7dbbbb58-625b-4f06-b64d-668792a10cc4).html
https://pure.amc.nl/en/publications/reply-to(7dbbbb58-625b-4f06-b64d-668792a10cc4).html
Autor:
Anthony R. Soltis, Ziv Gan-Or, Clifton L. Dalgard, Debra Ehrlich, Leonard H, Sara Saez-Atienzar, Cornelis Blauwendraat, Ali Torkamani, J. R. Gibbs, Sonja W. Scholz, Bryan J. Traynor, Clemens R. Scherzer, Jonggeol Jeff Kim, Jinhui Ding, Mark R. Cookson, Juan A. Botía, Matt Bookman, Andrew B. Singleton, Mike A. Nalls, Sara Bandres-Ciga, Monica Diez-Fairen, Hirotaka Iwaki, Lasse Pihlstrøm, Alastair J. Noyce, Dena G. Hernandez, Mina Ryten, Mary B. Makarious, Faraz Faghri
Publikováno v:
Acta Neuropathologica
Polygenic inheritance plays a central role in Parkinson disease (PD). A priority in elucidating PD etiology lies in defining the biological basis of genetic risk. Unraveling how risk leads to disruption will yield disease-modifying therapeutic target
Autor:
Mark Hallett, Thomas Osterholt, Debra Ehrlich, Felipe Vial, Patrick McGurrin, Dietrich Haubenberger
Publikováno v:
Clinical Neurophysiology Practice, Vol 5, Iss, Pp 30-34 (2020)
Clinical Neurophysiology Practice
Clinical Neurophysiology Practice
Highlights • The electrophysiological characterization of tremor is a useful technique. • There has not been much software available for tremor analysis. • We developed a free online platform for tremor analysis.
Objective The electrophysi
Objective The electrophysi
Publikováno v:
Journal of neurology. 269(10)
Several genetic variants are associated with an increased risk for developing Parkinson's Disease (PD) and limited genotype/phenotype correlation. Specifically, mutations in GBA1, the gene coding for the lysosomal enzyme glucocerebrosidase, are assoc