Movimientos Anormales.artículos: Envíos recientes

  • Rossi, Malco Damián; Stephen, Christopher D.; Damásio, Joana; Pedroso, José Luiz; Kuo, Sheng-Han; Lin, Chi-Ying R.; Ojo, Oluwadamilola; El-Jaafary, Shaimaa; Lee, Woong-Woo; Madoev, Harutyun; Barsottini, Orlando G.; Srivastava, Achal Kumar; Klein, Christine; Van de Warrenburg, Bart (Wiley, 2025-07-18)
    The landscape of genetic ataxias is influenced by migration, population genetics, consanguinity, and founder effects, resulting in significant regional variation. Within the expanding domain of genetic ataxias, knowledge ...
  • Marín-Medina, Daniel S.; Miño Zambrano, Joselyn; Espay, Alberto J.; Merello, Marcelo (Springer-Verlag, 2026-04-08)
    Background: Misdiagnosis of functional movement disorders (FMD) remains a concern for clinicians. We sought to review the phenomenology and clinical features associated with FMD misdiagnosis. Methods: We conducted a ...
  • Rossi, Malco Damián; Castillo Torres, Sergio Andrés; Merello, Marcelo (Elsevier, 2022-09-15)
    Background: Mutations in the glucocerebrosidase (GBA) gene represent the most common genetic risk factor for Parkinson's Disease (PD) and are associated with a more aggressive motor phenotype at late stages. However, the ...
  • Varani, Andrés Pablo; Bagliani, María Camila; Rossi, Malco Damián (Elsevier, 2025-12-11)
    Parkinson's disease is characterized by a variety of motor and non-motor symptoms that arise from different regions of the central nervous system. Growing evidence indicates that pathological alterations in Parkinson's ...
  • Chaparro-Solano, Henry Mauricio; Teixeira-Dos-Santos, Daniel; Waldo, Emily; Leal, Thiago P.; Inca-Martinez, Miguel; Alcauter, Sarael; Medina-Rivera, Alejandra; Ruiz-Contreras, Alejandra E.; Cornejo Olivas, Mario; Mejia-Rojas, Koni; Armas, Cintia; Chaná Cuevas, Pedro; Rojas, Natalia; Orozco, Jorge L.; Muñoz Ospina, Beatriz; Aguillón, David; Buritica, Omar; Moreno Masmela, Sonia; Merello, Marcelo (IOS Press, 2026-04-17)
    BackgroundAlthough levodopa is the gold standard treatment for Parkinson's disease (PD), its chronic use is associated with levodopa-induced dyskinesia (LID), a motor complication that impacts prognosis, quality of life, ...
  • Medina Escobar, Alex; Rossi, Malco Damián; Richer, Maxime; Gautreau, Sylvia; Lang, Anthony E. (Wiley, 2025-05-11)
    Background: Corticobasal syndrome (CBS) is a rare, clinically heterogeneous form of atypical Parkinsonism. Hyperkinetic movements, aside from myoclonus and dystonia, have rarely been reported in CBS. Cases: We present ...
  • Wilken, Miguel; Granda, Luna; Cruz, Ivonne; Rossi, Malco Damián; Cerquetti, Daniel; Merello, Marcelo (Wiley, 2025-10-11)
    Background: Levodopa-induced dyskinesias (LIDs) are an important burden for patients with Parkinson's disease (PD), yet their mechanisms remain incompletely understood. Objective: The objective of this study was to ...
  • Castillo Torres, Sergio Andrés; Cruz, Ivonne; Rossi, Malco Damián; Wilken, Miguel; Cerquetti, Daniel; Merello, Marcelo (Wiley, 2025-06-22)
    Background: MDS-UPDRS Severity Levels (SLs), derived from clinician- and patient-rated scales, remain underused to evaluate response to subthalamic deep brain stimulation (STN-DBS) in patients with Parkinson's disease ...
  • Marín-Medina, Daniel S.; Lopez, Gala; Rossi, Malco Damián; Merello, Marcelo (Elsevier, 2025-09-22)
    Introduction: Functional Movement Disorders (FMD) exhibit a variable course over time. Understanding FMD phenotype trajectories may improve knowledge of its natural history and prognosis. Methods: Retrospective study ...
  • Marín-Medina, Daniel S.; Lopez, Gala; Rossi, Malco Damián; Merello, Marcelo (Wiley, 2025-09-03)
    Background: Awareness and major external events can contribute to the number of FMD cases. Objective: To analyze trends in new Functional Movement Disorders (FMD) consultations and the impact of the COVID-19 ...
  • Pinheiro Camurugy da Hora, Raphael; Rossi, Malco Damián; Rebelo Procaci, Victor; Yoshinaga Tonholo Silva, Thiago; Alves Corazza, Luiza; Novis, Luiz Eduardo; Barsottini, Orlando G.; Pedroso, José Luiz (Elsevier, 2025-07-21)
    Nucleotide repeat expansions are a key genetic mechanism underlying various neurological disorders, especially in movement disorders. While many expansion-related conditions are caused by variants in coding regions, an ...
  • Di Luca, Daniel G.; Prasad, Shweta; Kirby, Alana; Merello, Marcelo; Bhatia, Kailash P.; Goetz, Christopher (Wiley, 2025-05-05)
  • Ángel, María José; Mizraji, Gabril F.; Gómez-Arévalo, Gonzalo; Garcia, Silvia; González-Toledo, María Eugenia; Avale, Elena; Paez-Paz, Indiana; Falzone, Tomás; Holubiec, Mariana; Peralta, María C.; Castano, Federico; Sevlever, Gustavo Emilio; Mezmezian, Mónica Beatriz; Marras, Connie; Gershanik, Oscar; Chade, Anabel; Pardo, Carolina; Rellan, Florencia; Campastri, Ana; Couto, Blas (Elsevier, 2025-05-15)
    Background: Progressive supranuclear palsy (PSP) and corticobasal syndrome (CBS) are neurodegenerative disorders with disabling postural instability, falls and cognitive impairment associated with 4-repeat tau protein ...
  • Rossi, Malco Damián; Merello, Marcelo (Springer, 2025-04-08)
    Hereditary or genetic ataxias are hundreds of disorders characterized by large phenotypic, genetic, and epidemiological heterogeneity. In Argentina, 35 genetic ataxias have been identified, with SCA1 (ATX-ATXN1), SCA2 ...
  • Fung, Victor S.C.; Bhatia, Kailash P.; Burn, David J.; Goetz, Christopher G.; Hallett, Mark; Jankovic, Joseph; Kieburtz, Karl; Klein, Christine; Kordower, Jeffrey H.; Lang, Anthony E.; Merello, Marcelo; Stern, Matthew B.; Stoessl, A. Jon; Thompson, Philip D. (Wiley, 2025-02-13)
    Resumen no disponible
  • Latorre, Anna; van der Veen, S.; Pena, Ashley; Truong, Daniel; Erro, Roberto; Frucht, Steven; Ganos, Christos; Hallett, Mark; Perez-Duenas, Belen; Rossi, Malco Damián; Roze, Emmanuel; Vidailhet, Marie; Aj de Koning-Tijssen, Marina; Caviness, John N. (Elsevier, 2025-02-20)
    Introduction: Recent new advances in myoclonus characterization and etiology justify an update of the 40-year-old respected classification of myoclonus proposed by Marsden, Hallett, and Fahn. New advances include genetic ...
  • Medina Escobar, Alex; Munoz, Daniela; Gautreau, Sylvia; Rossi, Malco Damián; Pringsheim, Tamara (Wiley, 2025-02-22)
    Background: Primary tic disorders (TD) are common movement disorders in childhood. However, it is unclear if international guidelines are applied in Latin America. Objectives: To investigate the applicability of TD ...
  • Rossi, Malco Damián; Schaake, Susen; Usnich, Tatiana; Boehm, Josephine; Steffen, Nina; Schell, Nathalie; Krüger, Clara; Gül-Demirkale, Tuğçe; Bahr, Natascha; Kleinz, Teresa; Madoev, Harutyun; Laabs, Björn-Hergen; Gan-Or, Ziv; Alcalay, Roy N.; Lohmann, Katja; Klein, Christine (Wiley, 2025-02-10)
    Depending on zygosity and the specific change, different variants in the GBA1 gene can cause Parkinson's disease (PD, PARK-GBA1) with reduced penetrance, act as genetic risk factors for PD or parkinsonism, and/or lead to ...

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