• Performance on the Latin American version of the Face-Name Associative Memory Exam (LAS-FNAME) distinguishes individuals with Mild Cognitive Impairment from age-matched controls in a sample from Argentina. 

  Keller, Greta; Corvalán, Nicolás; Carello, María Agostina; Arruabarrena, Micaela María; Martínez Canyazo, Carlos; De Los Santos, Loana; Spehrs, Julieta; Vila-Castelar, Clara; Allegri, Ricardo Francisco; Quiroz, Yakeel T.; Crivelli, Lucía (Taylor & Francis, 2024-03-06)

  Introduction: The Latin American Spanish version of the Face-Name Associative Memory Exam (LAS-FNAME) has shown promise in identifying cognitive changes in those at risk for Alzheimer's disease (AD). However, its applicability ...
• New Directions in Infection-Associated Ischemic Stroke 

  Jung, Jin-Man; Gruber, András; Heseltine, Peter; Rajamani, Kumar; Ameriso, Sebastián Francisco; Fisher, Mark J. (Korean Neurological Association, 2024-02-05)

  The relationship between infections and stroke has not been fully characterized, probably delaying the development of specific treatments. This narrative review addresses mechanisms of stroke linked to infections, including ...
• Prevalence and Trajectories of Post-COVID-19 Neurological Manifestations: A Systematic Review and Meta-Analysis 

  Giussani, Giorgia; Westenberg, Érica; García Azorin, David; Bianchi, Elisa; Yusof Khan, Abdul Hanif Khan; Allegri, Ricardo Francisco; Atalar, Arife Çimen; Baykan, Betul; Crivelli, Lucía; Fornari, Arianna; Frontera, Jennifer A.; Guekht, Alla; Helbok, Raimund; Kee Hoo, Fan; Kivipelto, Miia; Leonardi, Matilde; López Rocha, Ana Sabsil; Mangialasche, Francesca; Marcassoli, Alessia; Global COVID-19 Neuro Research Coalition (Karger, 2024-01-25)

  Introduction: The aim of this systematic review and meta-analysis was to evaluate the prevalence of thirteen neurological manifestations in people affected by COVID-19 during the acute phase and at 3, 6, 9 and 12-month ...
• Perspectives of People At-Risk on Parkinson's Prevention Research 

  Keavney, Jessi L.; Mathur, Soania; Schroeder, Karlin; Merrell, Ray; Castillo Torres, Sergio Andrés; Gao, Virginia; Crotty, Grace F.; Schwarzschild, Michael A.; Poma, John M. (IOS Press, 2024-03-14)

  The movement toward prevention trials in people at-risk for Parkinson's disease (PD) is rapidly becoming a reality. The authors of this article include a genetically at-risk advocate with the LRRK2 G2019 S variant and two ...
• Comorbidities in multiple sclerosis and their influence on the choice of treatment 

  Barboza, Andrés G.; Sinay, Vladimiro; Alonso, Ricardo; Carnero Contentti, Edgar; Hryb, Javier; Silva, Berenice Anabel; Tavolini, Darío; Ysrraelit, María Célica; Correale, Jorge (Revista de Neurología, 2024-03-16)

  Los estudios clínicos de tratamientos para personas con esclerosis múltiple (pEM) se realizan en poblaciones seleccionadas, que excluyen a pacientes que presenten comorbilidades o medicaciones concomitantes. Sin embargo, ...
• Friends with benefits: Sharing large-scale transcontinental brain MRI databases in LatAM-FINGERS and US POINTER 

  DaGraça Morais Martin, Maria; Landau, Susan M.; Damian, Andres; Vemuri, Prashanthi; Bérgamo, Yanina; Kimie Suemoto, Claudia; Calandri, Ismael Luis; Caramelli, Paulo; Lopera, Francisco; Allegri, Ricardo Francisco; Lovato, Laura; Delgado, Carolina; Nitrini, Ricardo; Dozzi Brucki, Sonia Maria; Duque, Lissette; Charamelo Baieti, Ana; Custodio, Nilton; Crivelli, Lucía; US POINTER; LatAm-FINGERS (Wiley, 2023-12-25)

  Background Multicentric initiatives to study brain cognition in the elderly offers us a unique collection of brain imaging data accompanied by detailed neuroclinical and neuropsychological evaluations. U.S. POINTER and ...
• Clinical and Genotype Characteristics and Symptom Migration in Patients With Mixed Phenotype Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey 

  Gonzalez-Moreno, Juan; Dispenzieri, Angela; Grogan, Martha; Coelho, Teresa; Tournev, Ivailo; Waddington-Cruz, Márcia; Wixner, Jonas; Diemberger, Igor; Garcia-Pavia, Pablo; Chapman, Doug; Gupta, Pritam; Glass, Oliver; Amass, Leslie; THAOS investigators; Barroso, Fabio Adrián (Springer, 2023-12-20)

  Introduction: Transthyretin amyloidosis (ATTR amyloidosis) is primarily associated with a cardiac or neurologic phenotype, but a mixed phenotype is increasingly described. Methods: This study describes the mixed phenotype ...
• Applying the World Stroke Organization roadmap in planning a model for stroke service implementation in Matrouh Governorate-Egypt: a World Stroke Organization young future stroke leaders’ analytical study 

  Roushdy, Tamer; Alet, Matías Javier; Lotlikar, Radhika; Ramage, Emily; Ullberg, Teresa; Mosconi, Maria Giulia; Li, Linxin (Springer, 2023-11-14)

  Background The global incidence of stroke is on the rise, primarily due to an increase in the aging population and the prevalence of vascular risk factors among the elderly. However, stroke is a treatable condition if ...
• Remyelinating effect driven by transferrin-loaded extracellular vesicles 

  Mattera, Vanesa S.; Occhiuzzi, Federico; Correale, Jorge; Pasquini, Juana María (Wiley, 2023-10-20)

  Extracellular vesicles (EVs) are involved in diverse cellular functions, playing a significant role in cell-to-cell communication in both physiological conditions and pathological scenarios. Therefore, EVs represent a ...
• Hipofisitis primaria: diagnóstico y tratamiento. Estudio multicéntrico 

  Tkatch, Julieta; Szuman, Gabriela; Agüero, Mónica; Alfieri, Analía; Ballarino, María Carolina; Bamberger, Elizabeth; Battistone, María Florencia; Boero, Laura; Danilowicz, Karina; Donoso, Marina; Fainstein-Day, Patricia; Furioso, Alejandra; Glerean, Mariela; González Pernas, Mariana Soledad; Guitelman, Mirtha; Katz, Débora Adela; Loto, Mónica; Pignatta, Analía; Slavinsky, Patricia; Sosa, Soledad (Fundación Revista Medicina, 2023-06-06)

  Introducción: La hipofisitis es una enfermedad infrecuente que plantea un desafío en el diagnóstico y tratamiento. El objetivo de este estudio multicéntrico y retrospectivo fue describir: a) características de pacientes ...
• Ataxias espinocerebelosas de herencia autosómica dominante: nueva clasificación clínica y desarrollo de una herramienta informática para la orientación y predicción diagnóstica 

  Rossi, Malco Damián (2016)

  Introducción: Las ataxias espinocerebelosas (SCA) son un grupo de trastornos neurodegenerativos y heterogéneos desde el punto de vista clínico y genético que se caracterizan por la presencia de ataxia progresiva como ...
• Mortality of neuromyelitis optica spectrum disorder patients in an Argentinean population: A study from the RelevarEM registry 

  Carnero Contentti, Edgar; López, Pablo A.; Pettinicchi, Juan Pablo; Criniti, Juan; Pappolla, Agustín; Miguez, Jimena; Cristiano, Edgardo; Patrucco, Liliana; Liwacki, Susana; Tkachuk, Verónica; Balbuena, María E.; Vrech, Carlos; Deri, Norma; Correale, Jorge; Marrodán, Mariano; Ysrraelit, María Célica; Leguizamon, Felisa; Luetic, Geraldine; Menichini, María L.; Tavolini, Darío (Sage, 2023-10-17)

  We aimed to evaluate mortality and causes of death among Argentinean neuromyelitis optica spectrum disorder (NMOSD) patients and identify predictors of death. Retrospective study included 158 NMOSD patients and 11 (7%) ...
• Longitudinal clinical, cognitive and biomarker profiles in dominantly inherited versus sporadic early-onset Alzheimer's disease 

  Llibre Guerra, Jorge J.; Iaccarino, Leonardo; Coble, Dean; Edwards, Lauren; Li, Yan; McDade, Eric; Strom, Amelia; Gordon, Brian; Mundada, Nidhi; Schindler, Suzanne E.; Tsoy, Elena; Ma, Yinjiao; Lu, Ruijin; Fagan, Anne M.; Benzinger, Tammie L. S.; Soleimani-Meigooni, David; Aschenbrenner, Andrew J.; Allegri, Ricardo Francisco; Patricio Alexis, Chrem Méndez; Surace, Ezequiel Ignacio (Oxford University Press, 2023-10-18)

  Approximately 5% of Alzheimer's disease cases have an early age at onset (<65 years), with 5-10% of these cases attributed to dominantly inherited mutations and the remainder considered as sporadic. The extent to which ...
• Persistence of Basal Ganglia Oscillatory Activity During Tremor Attenuation by Movement in Parkinson's Disease Patients 

  Wilken, Miguel; Andres, Daniela S.; Bianchi, Gianfranco; Hallett, Mark; Merello, Marcelo (Wiley, 2024-02-28)

  Background: One of the characteristics of parkinsonian tremor is that its amplitude decreases with movement. Current models suggest an interaction between basal ganglia (BG) and cerebello-thalamo-cortical circuits in ...
• Evaluation and treatment approaches for neurological post-acute sequelae of COVID-19: A consensus statement and scoping review from the global COVID-19 neuro research coalition 

  Frontera, Jennifer; Guekht, Alla; Allegri, Ricardo Francisco; Ashraf, Mariam; Baykan, Betül; Crivelli, Lucía; Easton, Ava; Garcia-Azorin, David; Helbok, Raimund; Joshi, Jatin; Koehn, Julia; Koralnik, Igor; Netravathi, M.; Benedict, Michael; Nilo, Annacarmen; Özge, Aynur; Padda, Karanbir; Pellitteri, Gaia; Prasad, Kameshwar; Romozzi, Marina (Elsevier, 2023-11-15)

  Post-acute neurological sequelae of COVID-19 affect millions of people worldwide, yet little data is available to guide treatment strategies for the most common symptoms. We conducted a scoping review of PubMed/Medline ...
• Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project 

  Vollstedt, Eva-Juliane; Madoev, Harutyun; Aasly, Anna; Ahmad-Annuar, Azlina; Al-Mubarak, Bashayer; Alcalay, Roy N.; Alvarez, Victoria; Amorin, Ignacio; Annesi, Grazia; Arkadir, David; Bardien, Soraya; Barker, Roger A.; Barkhuizen, Melinda; Basak, A. Nazli; Bonifati, Vincenzo; Boon, Agnita; Brighina, Laura; Brockmann, Kathrin; Belin, Andrea Carmine; Merello, Marcelo (Public Library of Science, 2023-10-03)

  Parkinson's disease (PD) is the fastest-growing neurodegenerative disorder, currently affecting ~7 million people worldwide. PD is clinically and genetically heterogeneous, with at least 10% of all cases explained by a ...
• Predictors and Pathophysiology of Axial Postural Abnormalities in Parkinsonism: A Scoping Review 

  Artusi, Carlo Alberto; Geroin, Christian; Nonnekes, Jorik; Aquino, Camila; Garg, Divyani; Dale, Marian L.; Schlosser, Darbe; Lai, Yijie; Al-Wardat, Mohammad; Salari, Mehri; Wolke, Robin; Tsinda Labou, Valery; Imbalzano, Gabriele; Camozzi, Serena; Merello, Marcelo; Bloem, Bastiaan R.; Capato, Tamine; Djaldetti, Ruth; Doherty, Karen; International Parkinson and Movement Disorders Society Task Force on Postural Abnormalities (Wiley, 2023-09-06)

  Background: Postural abnormalities involving the trunk are referred to as axial postural abnormalities and can be observed in over 20% of patients with Parkinson's disease (PD) and in atypical parkinsonism. These symptoms ...
• Migraine in older adults 

  Hugger, Sarah Sonja; Do, Thien Phu; Ashina, Håkan; Goicochea, María Teresa; Jenkins, Bronwyn; Sacco, Simona; Lee, Mi Ji; Brennan, K. C.; Amin, Faisal Mohammad; Steiner, Timothy J.; Ashina, Messoud (Elsevier, 2023-09-20)

  Migraine is an evolving, and sometimes lifelong disorder. The prevalence of episodic migraine peaks among individuals aged in their late 30s, implying a tendency for the disorder to remit with increasing age thereafter, ...
• Presenilin-1 mutation position influences amyloidosis, small vessel disease, and dementia with disease stage 

  Joseph-Mathurin, Nelly; Feldman, Rebecca L.; Lu, Ruijin; Shirzadi, Zahra; Toomer, Carmen; Saint Clair, Junie R.; Ma, Yinjiao; McKay, Nicole S.; Strain, Jeremy F.; Kilgore, Collin; Friedrichsen, Karl A.; Chen, Charles D.; Gordon, Brian A.; Chen, Gengsheng; Hornbeck, Russ C.; Massoumzadeh, Parinaz; McCullough, Austin A.; Wang, Qing; Li, Yan; Allegri, Ricardo Francisco; Dominantly Inherited Alzheimer Network (John Wiley & Sons, 2024-02-21)

  Introduction: Amyloidosis, including cerebral amyloid angiopathy, and markers of small vessel disease (SVD) vary across dominantly inherited Alzheimer's disease (DIAD) presenilin-1 (PSEN1) mutation carriers. We investigated ...
• Alzheimer's polygenic risk scores are associated with cognitive phenotypes in Down syndrome 

  Gorijala, Priyanka; Aslam, M. Muaaz; Dang, Lam-Ha T.; Xicota, L.; Fernández, María V.; Sung, Yun Ju; Fan, Kang-Hsien; Feingold, Eleanor; Surace, Ezequiel Ignacio; Chhatwal, Jasmeer P.; Hom, Christy L.; Dominantly Inherited Alzheimer Network (DIAN), the Alzheimer's Disease Neuroimaging Initiative (ADNI); NIA-LOAD family study, for the Alzheimer's Biomarkers Consortium-Down Syndrome (ABC-DS) Investigators; Hartley, Sigan L.; Hassenstab, Jason; Perrin, Richard J.; Mapstone, Mark; Zaman, Shahid H.; Ances, Beau M.; Kamboh, M. Ilyas; Lee, Joseph H.; Cruchaga, Carlos (John Wiley & Sons, 2023-10-19)

  Introduction: This study aimed to investigate the influence of the overall Alzheimer's disease (AD) genetic architecture on Down syndrome (DS) status, cognitive measures, and cerebrospinal fluid (CSF) biomarkers. Methods: ...

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