Sarah Falcão Brasileiro Henriques
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Sarah Falcão Brasileiro Henriques has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Alexandra Prufer de Queiroz Campos Araújo
Universidade Federal do Rio de Janeiro, Faculdade de Medicina, Departamento de Pediatria, Rio de Janeiro RJ, Brazil
2 shared publications - Flávia Nardes
Universidade Federal do Rio de Janeiro, Brazil
2 shared publications - Ana Gabriela Vianna de Moura1 shared publication
- Clarisse Pereira Dias Drumond Fortes
Universidade Federal do Rio de Janeiro, Instituto de Puericultura e Pediatria Martagão Gesteira, Rio de Janeiro RJ, Brazil
1 shared publication - Jaqueline de Jesus Pereira
Universidade de São Paulo, Brazil
1 shared publication - Larissa Dos Santos Borges Soares1 shared publication
Latest Publications
- Open Access
- 31 March 2026
- Published by Revista Brasileira de Neurologia in Revista Brasileira de Neurologia
- Vol. 62 (1)
Neuromuscular assessment form (NAF): pediatric outpatient follow-up experience from a single Brazilian center
Background: Neuromuscular disorders are a heterogeneous group of genetic or acquired diseases affecting the anterior horn, peripheral nerves, neuromuscular junctions, or muscles. Given their multisystemic complexity, comprehensive care and standardized evaluation tools are essential. Objective: To describe the development, implementation, and utility of the Neuromuscular Assessment Form (NAF) as a tool for integrated clinical evaluation in patients with NMDs at a Brazilian reference center. Methods: A descriptive observational study was conducted using retrospective data from patients followed over the past thirty years at a reference center. The NAF was designed based on literature review, national therapeutic guidelines, and consultations with multidisciplinary specialists in pediatric neurology, physiotherapy, speech therapy, and other support areas. Results: The NAF enabled the systematic documentation of motor and multisystemic data, including cardiac, respiratory, nutritional, orthopedic, and neuropsychiatric functions. It facilitated interdisciplinary interventions and ensured continuity of care. Background: Neuromuscular disorders are a heterogeneous group of genetic or acquired diseases affecting the anterior horn, peripheral nerves, neuromuscular junctions, or muscles. Given their multisystemic complexity, comprehensive care and standardized evaluation tools are essential. Objective: To describe the development, implementation, and utility of the Neuromuscular Assessment Form (NAF) as a tool for integrated clinical evaluation in patients with NMDs at a Brazilian reference center. Methods: A descriptive observational study was conducted using retrospective data from patients followed over the past thirty years at a reference center. The NAF was designed based on literature review, national therapeutic guidelines, and consultations with multidisciplinary specialists in pediatric neurology, physiotherapy, speech therapy, and other support areas. Results: The NAF enabled the systematic documentation of motor and multisystemic data, including cardiac, respiratory, nutritional, orthopedic, and neuropsychiatric functions. It facilitated interdisciplinary interventions and ensured continuity of care. Conclusion: The NAF is a practical and effective tool for standardized clinical evaluation and longitudinal follow-up of patients with NMDs. It has the potential to promote equitable care and enhance research across different regions, especially in resource-limited settings. Future validation and integration into electronic health systems may further improve its applicability and impact.
- 31 March 2026
- Published by Revista Brasileira de Neurologia in Revista Brasileira de Neurologia
- Vol. 62 (1)
Open AccessNeuromuscular assessment form (NAF): pediatric outpatient follow-up experience from a single Brazilian center
Background: Neuromuscular disorders are a heterogeneous group of genetic or acquired diseases affecting the anterior horn, peripheral nerves, neuromuscular junctions, or muscles. Given their multisystemic complexity, comprehensive care and standardized evaluation tools are essential. Objective: To describe the development, implementation, and utility of the Neuromuscular Assessment Form (NAF) as a tool for integrated clinical evaluation in patients with NMDs at a Brazilian reference center. Methods: A descriptive observational study was conducted using retrospective data from patients followed over the past thirty years at a reference center. The NAF was designed based on literature review, national therapeutic guidelines, and consultations with multidisciplinary specialists in pediatric neurology, physiotherapy, speech therapy, and other support areas. Results: The NAF enabled the systematic documentation of motor and multisystemic data, including cardiac, respiratory, nutritional, orthopedic, and neuropsychiatric functions. It facilitated interdisciplinary interventions and ensured continuity of care. Background: Neuromuscular disorders are a heterogeneous group of genetic or acquired diseases affecting the anterior horn, peripheral nerves, neuromuscular junctions, or muscles. Given their multisystemic complexity, comprehensive care and standardized evaluation tools are essential. Objective: To describe the development, implementation, and utility of the Neuromuscular Assessment Form (NAF) as a tool for integrated clinical evaluation in patients with NMDs at a Brazilian reference center. Methods: A descriptive observational study was conducted using retrospective data from patients followed over the past thirty years at a reference center. The NAF was designed based on literature review, national therapeutic guidelines, and consultations with multidisciplinary specialists in pediatric neurology, physiotherapy, speech therapy, and other support areas. Results: The NAF enabled the systematic documentation of motor and multisystemic data, including cardiac, respiratory, nutritional, orthopedic, and neuropsychiatric functions. It facilitated interdisciplinary interventions and ensured continuity of care. Conclusion: The NAF is a practical and effective tool for standardized clinical evaluation and longitudinal follow-up of patients with NMDs. It has the potential to promote equitable care and enhance research across different regions, especially in resource-limited settings. Future validation and integration into electronic health systems may further improve its applicability and impact.
- 12 October 2024
- Published by Elsevier in European Journal of Paediatric Neurology
- Vol. 53, 117-122
Similar disease progression in nonsense Duchenne muscular dystrophy boys as general natural history: Single Brazilian center 15 years registry view
- 12 October 2024
- Published by Elsevier in European Journal of Paediatric Neurology
- Vol. 53, 117-122
Similar disease progression in nonsense Duchenne muscular dystrophy boys as general natural history: Single Brazilian center 15 years registry view