Publications by authors named "Roberto Weiser"

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Neuromyelitis optica spectrum disorder in Latin America: a global data share initiative.
Juan I Rojas, Liliana Patrucco, Edgardo Cristiano, José I Gortari, Paola A Ortiz Salas, Roberto Weiser

Mult Scler Relat Disord· June 2025

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Multiple sclerosis in Central America and Caribbean countries: frequency and clinical characterization of an emergent disease.
Fernando Gracia, Deyanira A Ramírez Navarro, Nicia E Ramírez Sánchez, Roberto Weiser, Alexander Parajeles-Vindas

Front Epidemiol· June 2024

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Neuromyelitis Optica Spectrum Disorder in Central America and the Caribbean: A Multinational Clinical Characterization Study.
Fernando Gracia, Deyanira Ramírez, Alexander Parajeles-Vindas, Alejandro Díaz, Amado Díaz de la Fé, Roberto Weiser

Neurol Int· March 2022

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Status of the neuromyelitis optica spectrum disorder in Latin America.
Victor M Rivera, Fernando Hamuy, Veronica Rivas, Fernando Gracia, Juan Ignacio Rojas, Roberto Weiser

Mult Scler Relat Disord· August 2021

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COVID-19 in multiple sclerosis and neuromyelitis optica spectrum disorder patients in Latin America: COVID-19 in MS and NMOSD patients in LATAM.
Ricardo Alonso, Berenice Silva, Orlando Garcea, Patricio E Correa Diaz, Giordani Rodrigues Dos Passos, Roberto Weiser

Mult Scler Relat Disord· June 2021

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Care of patients with Huntington's disease in South America: a survey.
Ricardo Oliveira Horta Maciel, Francisco Eduardo Costa Cardoso, Pedro Chaná-Cuevas, Carlos Cosentino, William Fernández, Roberto Weiser

Arq Neuropsiquiatr· June 2013

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Américo Negrette and Huntington's disease.
Mariana Moscovich, Renato P Munhoz, Nilson Becker, Egberto Reis Barbosa, Alberto J Espay, Roberto Weiser

Arq Neuropsiquiatr· August 2011

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Glucocerebrosidase mutations are also found in subjects with early-onset parkinsonism from Venezuela.
Michael J Eblan, Joann Nguyen, Shira G Ziegler, Alicia Lwin, Melissa Hanson, Roberto Weiser

Mov Disord· February 2006

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Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease.
Javier Simon-Sanchez, Melissa Hanson, Amanda Singleton, Dena Hernandez, Aideen McInerney, Roberto Weiser

Neurosci Lett· July 2005

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Mutation at the SCA17 locus is not a common cause of parkinsonism.
Dena Hernandez, Melissa Hanson, Amanda Singleton, Katrina Gwinn-Hardy, Jason Freeman, Roberto Weiser

Parkinsonism Relat Disord· August 2003

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Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.
Stephen Hague, Ekaterina Rogaeva, Dena Hernandez, Cindy Gulick, Amanda Singleton, Roberto Weiser

Ann Neurol· August 2003

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