Хайлтын үр дүнгүүд - Flávio Moura Rezende Filho

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  1. 1
    Teaching NeuroImage: Mobile Hypopyon as a Clinical Clue for the Diagnosis of Behçet Disease

    Teaching NeuroImage: Mobile Hypopyon as a Clinical Clue for the Diagnosis of Behçet Disease -н Ígor Melo de Almeida, Flávio Moura Rezende Filho, José Luiz Pedroso, Orlando Graziani Póvoas Barsottini

    Хэвлэсэн 2022
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    Artigo
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  2. 2
    Frontal lobes white matter abnormalities mimicking cystic leukodystrophy in Wilson’s disease

    Frontal lobes white matter abnormalities mimicking cystic leukodystrophy in Wilson’s disease -н Flávio Moura Rezende Filho, Eva Rocha, Lívia Almeida Dutra, José Luiz Pedroso, Orlando Graziani Póvoas Barsottini

    Хэвлэсэн 2017
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    Artigo
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  3. 3
    Downbeat nystagmus and progressive ataxia in adults: consider Chiari malformation type 1

    Downbeat nystagmus and progressive ataxia in adults: consider Chiari malformation type 1 -н Breno Kazuo Massuyama, Thiago Cardoso Vale, Flávio Moura Rezende Filho, Orlando Graziani Póvoas Barsottini, José Luiz Pedroso

    Хэвлэсэн 2023
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    Artigo
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  4. 4
    Aniridia as a clue for the diagnosis of Gillespie syndrome

    Aniridia as a clue for the diagnosis of Gillespie syndrome -н Flávio Moura Rezende Filho, José Luiz Pedroso, Júlian Letícia de Freitas, Luiz Fernando Teixeira, Orlando Graziani Póvoas Barsottini

    Хэвлэсэн 2020
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    Editorial
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  5. 5
    Far beyond the motor neuron: the role of glial cells in amyotrophic lateral sclerosis

    Far beyond the motor neuron: the role of glial cells in amyotrophic lateral sclerosis -н Paulo Victor Sgobbi de Souza, Wladimir Bocca Vieira de Rezende Pinto, Flávio Moura Rezende Filho, Acary Souza Bullé Oliveira

    Хэвлэсэн 2016
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    Revisão
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  6. 6
    A clinical approach to hypertrophic pachymeningitis

    A clinical approach to hypertrophic pachymeningitis -н Fabiano Ferreira Abrantes, Marianna Pinheiro Moraes de Moraes, Flávio Moura Rezende Filho, José Luiz Pedroso, Orlando Graziani Póvoas Barsottini

    Хэвлэсэн 2020
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    Artigo
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  7. 7
    <i>PRPS1</i> Gene Mutation Causes Complex X-Linked Adult-Onset Cerebellar Ataxia in Women

    <i>PRPS1</i> Gene Mutation Causes Complex X-Linked Adult-Onset Cerebellar Ataxia in Women -н Flávio Moura Rezende Filho, Mariana Matioli da Palma, José Luiz Pedroso, Orlando Graziani Póvoas Barsottini, Juliana Maria Ferraz Sallum

    Хэвлэсэн 2021
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    Artigo
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  8. 8
    Conus medullaris syndrome in Vogt-Koyanagi-Harada disease: an unusual presentation

    Conus medullaris syndrome in Vogt-Koyanagi-Harada disease: an unusual presentation -н Fabiano Ferreira Abrantes, Marianna Pinheiro Moraes de Moraes, Wardislau Ferreira, Flávio Moura Rezende Filho, José Luiz Pedroso, Orlando Graziani Póvoas Barsottini

    Хэвлэсэн 2022
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    Artigo
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  9. 9
    Retinal degeneration in spinocerebellar ataxia type 7: an overview of the current knowledge

    Retinal degeneration in spinocerebellar ataxia type 7: an overview of the current knowledge -н Bruna Ferraço Marianelli, Flávio Moura Rezende Filho, Mariana Vallim Salles, José Luiz Pedroso, Orlando Graziani Póvoas Barsottini, Juliana Maria Ferraz Sallum

    Хэвлэсэн 2025
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    Revisão
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  10. 10
    Opsoclonus‐Myoclonus: Not Always Paraneoplastic

    Opsoclonus‐Myoclonus: Not Always Paraneoplastic -н Fernanda Lustosa Cabral Gomez, Luiz José Malta Gaia Ferreira Júnior, Sofia Mônaco Gama, Fabiano Moulin de Moraes, Flávio Moura Rezende Filho

    Хэвлэсэн 2025
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    Artigo
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  11. 11
    Septo-optic dysplasia with late-onset seizure: MRI and ophthalmological features

    Septo-optic dysplasia with late-onset seizure: MRI and ophthalmological features -н Júlian Letícia de Freitas, Flávio Moura Rezende Filho, Leandro Tavares Lucato, Juliana Maria Ferraz Sallum, José Luiz Pedroso, Orlando Graziani Póvoas Barsottini

    Хэвлэсэн 2019
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    Artigo
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  12. 12
    Malignant cerebral edema: an unusual neurological manifestation of systemic lupus erythematosus

    Malignant cerebral edema: an unusual neurological manifestation of systemic lupus erythematosus -н Marianna Pinheiro Moraes de Moraes, Bárbara Trapp, Flávio Moura Rezende Filho, Victor Hugo Rocha Marussi, Orlando Graziani Póvoas Barsottini, José Luiz Pedroso

    Хэвлэсэн 2020
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    Artigo
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  13. 13
    <scp><i>ATP8A2</i></scp>‐Related Disorder: Beyond Cerebellar Ataxia

    <scp><i>ATP8A2</i></scp>‐Related Disorder: Beyond Cerebellar Ataxia -н Luíza Alves Corazza, Vinícius Lopes Braga, Thiago Yoshinaga Tonholo Silva, Flávio Moura Rezende Filho, Juliana Maria Ferraz Sallum, Orlando Graziani Póvoas Barsottini, José Luiz Pedroso

    Хэвлэсэн 2023
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    Artigo
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  14. 14
    Nystagmus may be the first neurological sign in early stages of spinocerebellar ataxia type 3

    Nystagmus may be the first neurological sign in early stages of spinocerebellar ataxia type 3 -н Maria Thereza Drumond Gama, Flávio Moura Rezende Filho, Thiago Junqueira Ribeiro de Rezende, Pedro Braga‐Neto, Marcondes C. França, José Luiz Pedroso, Orlando Graziani Póvoas Barsottini

    Хэвлэсэн 2021
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    Artigo
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  15. 15
    Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS

    Clinical, ophthalmological, imaging and genetic features in Brazilian patients with ARSACS -н Flávio Moura Rezende Filho, Michael Parkinson, José Luiz Pedroso, Roy Poh, Ingrid Faber, Charles Marques Lourenço, Wilson Marques, Marcondes C. França, Fernando Kok, Juliana Maria Ferraz Sallum, Paola Giunti, Orlando Graziani Póvoas Barsottini

    Хэвлэсэн 2018
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    Artigo
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  16. 16
    Cross-cultural adaptation and validation of the International Cooperative Ataxia Rating Scale (ICARS) to Brazilian Portuguese

    Cross-cultural adaptation and validation of the International Cooperative Ataxia Rating Scale (ICARS) to Brazilian Portuguese -н Fernanda Aparecida Maggi, Pedro Braga‐Neto, Hsin Fen Chien, Maria Thereza Drumond Gama, Flávio Moura Rezende Filho, Maria Luiza Saraiva Pereira, Laura Bannach Jardim, Mariana Callil Voos, José Luiz Pedroso, Orlando Graziani Póvoas Barsottini

    Хэвлэсэн 2018
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    Artigo
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  17. 17
    Biallelic Loss‐of‐Function <scp><i>NDUFA12</i></scp> Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy

    Biallelic Loss‐of‐Function <scp><i>NDUFA12</i></scp> Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy -н Francesca Magrinelli, Elisa Calì, Vinícius Lopes Braga, Uluç Yiş, Hoda Tomoum, Hanan E. Shamseldin, Julian Raiman, Christoph Kernstock, Flávio Moura Rezende Filho, Orlando Graziani Póvoas Barsottini, Robert W. Taylor, Elsebet Østergaard, Abdullah Tamim, Karin Schäferhoff, Juliana Maria Ferraz Sallum, Maha S. Zaki, Fernando Kok, Kailash P. Bhatia, Bernd Wissinger, Kate Sergeant, Tobias B. Haack, Rita Horváth, Semra Hız, Fowzan S. Alkuraya, Henry Houlden, José Luiz Pedroso, Reza Maroofian

    Хэвлэсэн 2021
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    Artigo
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