Publications by authors named "Rodrigo H Mendonca"

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Thrombotic microangiopathy following gene therapy for 5q-spinal muscular atrophy.
Clara Gontijo Camelo, Rodrigo Holanda Mendonça, Cristiane Araújo Martins Moreno, Juliana Caires Oliveira Achili Ferreira, Adriana Banzzatto Ortega

Gene Ther· December 2025

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Safety and tolerability of onasemnogene abeparvovec for patients with spinal muscular atrophy weighing ≤17 kg and ≤24 months old from OFELIA, a phase 4, open-label, multicenter, non-randomised, interventional study.
Jonas Alex Saute, Javier Muntadas, Juliana Gurgel-Giannetti, Soledad Monges, Paula Aliberti

Lancet Reg Health Am· September 2025

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Clinical and molecular spectrum of TK2-deficiency: a large Brazilian cohort.
Cristiane Araujo Martins Moreno, Mariana Cunha Artilheiro, Alulin Tacio Quadros Santos Monteiro Fonseca, André Macedo Serafim da Silva, Tatiana Ribeiro Fernandes

Sci Rep· March 2025

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Brazilian Portuguese version of the revised upper-limb module: cross-cultural adaptation and validation.
Mariana Cunha Artilheiro, Juliana Rodrigues Iannicelli, Graziela Jorge Polido, Tatiana Ribeiro Fernandes, Leandro Augusto de Almeida

Arq Neuropsiquiatr· March 2025

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A self-reported Brazilian registry of 5q-spinal muscular atrophy: data on natural history, genetic characteristics, and multidisciplinary care.
Rodrigo Holanda Mendonça, Juliane Suellen Arndt de Godoi, Edmar Zanoteli

Arq Neuropsiquiatr· December 2024

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Teaching NeuroImage: Superficial Siderosis in Marfan Syndrome.
João Cláudio Urbano, Adalberto Studart-Neto, Rodrigo H Mendonça, Eduardo G Mutarelli, Cristiana Borges Pereira

Neurology· November 2024

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Gene replacement therapy for spinal muscular atrophy: safety and preliminary efficacy in a Brazilian cohort.
Rodrigo Holanda Mendonça, Adriana Banzzatto Ortega, Ciro Matsui, Vanessa van der Linden, Marcelo Kerstenetzky

Gene Ther· July 2024

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Integrated Approaches and Practical Recommendations in Patient Care Identified with 5q Spinal Muscular Atrophy through Newborn Screening.
Vanessa L Romanelli Tavares, Rodrigo Holanda Mendonça, Maytê S Toledo, Sônia M Hadachi, Carmela M Grindler

Genes (Basel)· June 2024

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Consensus from the Brazilian Academy of Neurology for the diagnosis, genetic counseling, and use of disease-modifying therapies in 5q spinal muscular atrophy.
Edmar Zanoteli, Alexandra Prufer de Queiróz Campos Araujo, Michele Michelin Becker, Clarisse Pereira Dias Drumond Fortes, Marcondes Cavalcante França

Arq Neuropsiquiatr· January 2024

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Muscle Ultrasound Changes Correlate With Functional Impairment in Spinal Muscular Atrophy.
Ana Lucila Moreira, Rodrigo Holanda Mendonça, Graziela Jorge Polido, Marcos Castello Barbosa Oliveira, André Macedo Serafim Silva

Ultrasound Med Biol· July 2023

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Guillain-Barré syndrome spectrum as manifestation of HIV-related immune reconstitution inflammatory syndrome: case report and literature review.
José E Vidal, Bruno F Guedes, Hélio R Gomes, Rodrigo Holanda Mendonça

Braz J Infect Dis· June 2022

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Effect of the COVID-19 pandemic on patients with inherited neuromuscular disorders.
Cristiane Araujo Martins Moreno, Clara Gontijo Camelo, Pedro Henrique Marte de Arruda Sampaio, Alulin Tácio Quadros Santos Monteiro Fonseca, Eduardo de Paula Estephan

Arq Neuropsiquiatr· June 2022

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Gene therapy in neuromuscular disorders.
Rodrigo Holanda Mendonça, Edmar Zanoteli

Arq Neuropsiquiatr· May 2022

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Real-World Data from Nusinersen Treatment for Patients with Later-Onset Spinal Muscular Atrophy: A Single Center Experience.
Rodrigo H Mendonça, Graziela J Polido, Ciro Matsui, André M S Silva, Davi J F Solla

J Neuromuscul Dis· October 2021

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Motor unit number index (MUNIX) in children and adults with 5q-spinal muscular atrophy: Variability and clinical correlations.
Rodrigo Holanda Mendonça, Ligia Maria Sotero Machado, Carlos Otto Heise, Graziela Jorge Polido, Ciro Matsui

Neuromuscul Disord· June 2021

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Myasthenia Gravis and COVID-19: Clinical Characteristics and Outcomes.
Antonio E Camelo-Filho, André M S Silva, Eduardo P Estephan, Antônio A Zambon, Rodrigo H Mendonça

Front Neurol· September 2020

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Neurological consultations and diagnoses in a large, dedicated COVID-19 university hospital.
Adalberto Studart-Neto, Bruno Fukelmann Guedes, Raphael de Luca E Tuma, Antonio Edvan Camelo Filho, Gabriel Taricani Kubota

Arq Neuropsiquiatr· August 2020

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Reply to "Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0".
Rodrigo H Mendonça, Antônio J Rocha, Andres Lozano-Arango, Astry B Diaz, Claudia Castiglioni

Ann Neurol· November 2019

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Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy.
Pablo B Winckler, André M S da Silva, Antônio R Coimbra-Neto, Elmano Carvalho, Eduardo B U Cavalcanti

Clin Genet· October 2019

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Severe brain involvement in 5q spinal muscular atrophy type 0.
Rodrigo H Mendonça, Antônio J Rocha, Andres Lozano-Arango, Astry B Diaz, Claudia Castiglioni

Ann Neurol· September 2019

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Pearls & Oy-sters: A curable myopathy manifesting as exercise intolerance and respiratory failure.
André M S Silva, Rodrigo H Mendonça, Diogo C Soares, Dagoberto Callegaro, Vitor M Caldas

Neurology· July 2018

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A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome.
Eduardo de Paula Estephan, Cláudia Ferreira da Rosa Sobreira, André Clériston José Dos Santos, Pedro José Tomaselli, Wilson Marques

J Neurol· March 2018

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Clinical, histological and radiological responses to methylprednisolone in HIV-associated rod myopathy.
André M S Silva, Rodrigo H Mendonça, Cristiane A M Moreno, Eduardo P Estephan, Paulo V P Helito

Neuromuscul Disord· August 2017

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