Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Artur F. Schumacher-Schuh"'
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-4 (2022)
Abstract Full sequencing of the GBA1 gene in patients with Parkinson’s disease provides a wide screening of pathogenic variants, but less developed regions of the world, like Latin America, may have difficulties in performing full sequencing. We pe
Externí odkaz:
https://doaj.org/article/8f76d2e610624ca0844055085699bd1d
Autor:
Bruno Lopes SANTOS-LOBATO, Artur F. SCHUMACHER-SCHUH, Carlos R. M. RIEDER, Mara H. HUTZ, Vanderci BORGES, Henrique Ballalai FERRAZ, Ignacio F. MATA, Cyrus P. ZABETIAN, Vitor TUMAS
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 78, Iss 4, Pp 206-216 (2020)
Abstract Background: There are currently no methods to predict the development of levodopa-induced dyskinesia (LID), a frequent complication of Parkinson's disease (PD) treatment. Clinical predictors and single nucleotide polymorphisms (SNP) have bee
Externí odkaz:
https://doaj.org/article/10036ac6d8fe44818d45df98b52e80a9
Autor:
Carlos Roberto de Melo Rieder, Artur F. Schumacher-Schuh, Márcio Schneider Medeiros, Carlos Eduardo Aliatti Mantese
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 78, Iss 10, Pp 624-628 (2020)
Arquivos de Neuro-Psiquiatria, Issue: ahead, Published: 14 SEP 2020
Arquivos de Neuro-Psiquiatria v.78 n.10 2020
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Issue: ahead, Published: 14 SEP 2020
Arquivos de Neuro-Psiquiatria v.78 n.10 2020
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Background: The treatment of Parkinson disease with dopaminergic therapy improves functionality and quality of life. However, as the disease progresses, the wearing-off phenomenon develops. To improve the recognition of this phenomenon, the 19-item w
Autor:
Artur F. Schumacher-Schuh, Andrei Bieger, Olaitan Okunoye, Kin Mok, Shen-Yang Lim, Soraya Bardien, Azlina Ahmad Annuar, Bruno Lopes-Santos, Matheus Zschornack Strelow, Mohamed Salama, Shilpa C Rao, Yared Zenebe Zewde, Saiesha Dindayal, Jihan Azar, LK Prashanth, Roopa Rajan, Alastair J Noyce, Njideka Okubadejo, Mie Rizig, Suzanne Lesage, Ignacio Mata
Human genetics research lacks diversity; over 80% of genome-wide association studies (GWAS) have been conducted on individuals of European ancestry. In addition to limiting insights regarding disease mechanisms, disproportionate representation can cr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::126215e2995f1d3498616508fdeb180c
https://doi.org/10.1101/2021.12.07.21266995
https://doi.org/10.1101/2021.12.07.21266995
Autor:
Carlos E. Arboleda-Bustos, Douglas Loesch, Paul Cannon, Francisco Lopera, Carlos Cosentino, Andrea Rivera-Valdivia, Carlos Velez-Pardo, Cyrus P. Zabetian, Mario Cornejo-Olivas, Ignacio F. Mata, Sonia Moreno, Karl Heilbron, Carlos Roberto de Mello Rieder, Miguel Inca-Martinez, Andrea R. V. R. Horimoto, Pilar Mazzetti, Luis Torres, Vanderci Borges, Dora Yearout, Elison Sarapura-Castro, Gonzalo Arboleda, Timothy D. O’Connor, Artur F. Schumacher-Schuh, Elif Irem Sarihan, Bruno Lopes Santos-Lobato, Vitor Tumas, Marlene Jimenez-Del-Rio, Pedro Chana-Cuevas, William Fernandez, Emily Mason, Andres G. Lescano, Humberto Arboleda, Elena Dieguez, Henrique Ballalai Ferraz, Angel C. Medina, Timothy A. Thornton, Víctor Raggio
Publikováno v:
Ann Neurol
OBJECTIVE This work was undertaken in order to identify Parkinson's disease (PD) risk variants in a Latino cohort, to describe the overlap in the genetic architecture of PD in Latinos compared to European-ancestry subjects, and to increase the divers
Autor:
Marina Coutinho Augustin, Marcia Lorena Fagundes Chaves, Lorenzo Casagrande Reggiani, Artur F. Schumacher-Schuh, Renato Gorga Bandeira-de-Mello, Wyllians Vendramini Borelli, Raphael Machado de Castilhos, Paola Bell Felix de Oliveira
Publikováno v:
Journal of Alzheimer's disease : JAD. 80(4)
Background: The social isolation imposed by COVID-19 pandemic can have a major impact on the mental health of dementia patients and their caregivers. Objective: We aim to evaluate the neurological decline of patients with dementia and the caregivers
Publikováno v:
Journal of Personalized Medicine
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Journal of Personalized Medicine, Vol 11, Iss 169, p 169 (2021)
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Journal of Personalized Medicine, Vol 11, Iss 169, p 169 (2021)
Parkinson’s disease (PD) is a condition with heterogeneous clinical manifestations that vary in age at onset, rate of progression, disease course, severity, motor and non-motor symptoms, and a variable response to antiparkinsonian drugs. It is cons
Autor:
Andrea Rivera-Valdivia, Carlos Roberto de Mello Rieder, Víctor Raggio, Emily Mason, Miguel Inca-Martinez, William Fernandez, Angel C. Medina, Paul Cannon, Henrique Ballalai Ferraz, Andres G. Lescano, Pilar Mazzetti, Karl Heilbron, Sonia Moreno, Gonzalo Arboleda, Humberto Arboleda, Timothy D. O’Connor, Carlos E. Arboleda-Bustos, Vanderci Borges, Timothy A. Thornton, Ignacio F. Mata, Bruno Lopes Santos-Lobato, Pedro Chana-Cuevas, Carlos Velez-Pardo, Vitor Tumas, Elena Dieguez, Cyrus P. Zabetian, Douglas Loesch, Francisco Lopera, Marlene Jimenez-Del-Rio, Luis Torres, Dora Yearout, Mario Cornejo-Olivas, Elif Irem Sarihan, Carlos Cosentino, Andrea R. V. R. Horimoto, Elison Sarapura-Castro, Artur F. Schumacher-Schuh
To date, over 90 Parkinson’s disease (PD) risk variants have been reported from genome-wide association studies (GWAS). However, these GWAS efforts have been limited to individuals of European and East Asian ancestry. We performed the first GWAS of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::474c573306004b2a7bda8c26bacfcc29
https://doi.org/10.1101/2020.11.09.20227124
https://doi.org/10.1101/2020.11.09.20227124
Autor:
Artur F. Schumacher-Schuh, Dora Yearout, Sonia Moreno, Andrea Rivera-Valdivia, Gonzalo Arboleda, Elena Dieguez, Vanderci Borges, Elison Sarapura-Castro, Lisa-Marie Niestroj, Carlos Roberto de Mello Rieder, Víctor Raggio, Timothy A. Thornton, Pilar Mazzetti, Carlos Velez-Pardo, Cyrus P. Zabetian, Humberto Arboleda, Pedro Chana-Cuevas, Miguel Inca-Martinez, Henrique Ballalai Ferraz, Eduardo Pérez-Palma, Ignacio F. Mata, Timothy D. O’Connor, William Fernandez, Vitor Tumas, Andres G. Lescano, Bruno Lopes Santos-Lobato, Carlos Cosentino, Marlene Jimenez-Del-Rio, Dennis Lal, Carlos E. Arboleda-Bustos, Douglas Loesch, Francisco Lopera, Luis Torres, Elif Irem Sarihan, Mario Cornejo-Olivas, Andrea R. V. R. Horimoto
Background: Parkinson's disease is the second most common neurodegenerative disorder and affects people from all ethnic backgrounds, yet little is known about the genetics of Parkinson's disease in non-European populations. In addition, the overall i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e785beb1f79e87790b58a3384fd80968
https://doi.org/10.1101/2020.05.29.20100859
https://doi.org/10.1101/2020.05.29.20100859
Autor:
Artur F. Schumacher-Schuh, Henrique Ballalai Ferraz, Carlos Roberto de Mello Rieder, Vanderci Borges, Mara H. Hutz, Ignacio F. Mata, Cyrus P. Zabetian, Bruno Lopes Santos-Lobato, Vitor Tumas
Publikováno v:
Arquivos de Neuro-Psiquiatria, Issue: ahead, Published: 09 APR 2020
Arquivos de Neuro-Psiquiatria, Vol 78, Iss 4, Pp 206-216 (2020)
Arquivos de Neuro-Psiquiatria, Volume: 78, Issue: 4, Pages: 206-216, Published: 09 APR 2020
Arquivos de Neuro-Psiquiatria v.78 n.4 2020
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Arquivos de Neuro-Psiquiatria, Vol 78, Iss 4, Pp 206-216 (2020)
Arquivos de Neuro-Psiquiatria, Volume: 78, Issue: 4, Pages: 206-216, Published: 09 APR 2020
Arquivos de Neuro-Psiquiatria v.78 n.4 2020
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Background: There are currently no methods to predict the development of levodopa-induced dyskinesia (LID), a frequent complication of Parkinson's disease (PD) treatment. Clinical predictors and single nucleotide polymorphisms (SNP) have been associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d577e20f2198fb25765080a5b8087a6d
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2020005008206&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2020005008206&lng=en&tlng=en