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144 results on '"Masruha, Marcelo Rodrigues"'

15. The cerebellar histiocytosis

Author

de Assis Franco, Igor, primary, Aragão, Marcelo de Melo, additional, Braga-Neto, Pedro, additional, Avelino, Marcela Amaral, additional, Pedroso, José Luiz, additional, Marussi, Victor Hugo Rocha, additional, Freitas, Leonardo Furtado, additional, Masruha, Marcelo Rodrigues, additional, and Barsottini, Orlando G.P., additional

Published
2018
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16. Mitochondrial ND5 mutation: neurological improvement after CoQ10 supplementation (P5.122)

Author

Pedroso, Jose Luiz, primary, Gama, Maria Thereza Drumond, additional, Arita, Juliana Harumi, additional, Ravagnani, Felipe Gustavo, additional, Barros, Mário H, additional, Sanches, Livia Rentas, additional, Picosse, Fabíola Rosa, additional, Lopes, Tania Oliveira, additional, de Carvalho Aguiar, Patrícia, additional, Chiaratti, Marcos, additional, Macabelli, Carolina Habermann, additional, Masruha, Marcelo Rodrigues, additional, Barsottini, Orlando, additional, Quinzii, Catarina M, additional, Hirano, Michio, additional, and Barros, Claudia Cristina Ferreiro, additional

Published
2017
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17. Coreia: uma manifestação rara da arterite de Takayasu

Author

Lopes,Anandreia Simões, Clemente,Gleice, Len,Claudio Arnaldo, Masruha,Marcelo Rodrigues, and Terreri,Maria Teresa

Subjects
Arterite de Takayasu, Sintomas neurológicos, Criança, Vasculite, Coreia
Abstract

RESUMO Relatamos um caso de uma menina com coreia recorrente e diagnóstico de arterite de Takayasu. Esta manifestação clínica foi relatada em apenas um paciente com tal vasculite na faixa etária pediátrica.

Published
2015

18. Coreia: uma manifestação rara da arterite de Takayasu

Author

Lopes, Anandreia Simões, Clemente, Gleice, Len, Claudio Arnaldo, Masruha, Marcelo Rodrigues, and Terreri, Maria Teresa

Subjects
Vasculitis, Takayasu's arteritis, Arterite de Takayasu, Sintomas neurológicos, Chorea, Neurologic symptoms, Criança, cardiovascular diseases, skin and connective tissue diseases, Child, Vasculite, Coreia
Abstract

RESUMO Relatamos um caso de uma menina com coreia recorrente e diagnóstico de arterite de Takayasu. Esta manifestação clínica foi relatada em apenas um paciente com tal vasculite na faixa etária pediátrica. ABSTRACT The case of a girl with recurring chorea and a Takayasu's arteritis diagnosis is reported. This clinical manifestation has been reported in only one patient with this vasculitis in the pediatric group.

Published
2015

21. Chin tremor in full-term neonate after hypoxia

Author

Scattolin, Mônica Ayres de Araújo, Marx, Catherine, Guinsburg, Ruth, Masruha, Marcelo Rodrigues, and Vilanova, Luiz Celso Pereira

Subjects
Hipóxia encefálica, Hypoxia, brain, Chin, Neurologia, Neurology, Tremor, Queixo, Recém-nascido, Infant, newborn
Abstract

CONTEXT: Newborns may present a range of motor phenomena that are not epileptic in nature. Chin tremor is an unusual movement disorder that typically starts in early childhood and may be precipitated by stress and emotion. Its pathophysiology has not been fully elucidated. CASE REPORT: We describe a full-term newborn that, immediately after neonatal anoxia, presented body and chin tremors that were unresponsive to anti-epileptic drugs. Subsequent neurological evaluation revealed signs of pyramidal tract damage and chin tremor triggered by percussion and crying. We discuss the hypothesis that the anatomopathological abnormality may lie at the level of the higher cortical centers or midbrain. CONCLUSIONS: Further studies are needed in order to gain greater comprehension of neonatal tremors. Recognition of the various etiological possibilities and consequent management of treatable causes is essential for care optimization. CONTEXTO: O recém-nascido está sujeito a uma gama de fenômenos motores de natureza não epiléptica. O tremor do mento é um distúrbio do movimento incomum que tem início habitual na infância e pode ser precipitado por estresse e emoção. Sua fisiopatologia não foi completamente elucidada. RELATO DE CASO: Descrevemos um recém-nascido no termo, que, após anóxia neonatal, apresentou tremor de corpo e mento não responsivo ao uso de drogas antiepilépticas. A avaliação neurológica posterior revelou sinais de lesão do trato piramidal e tremor de mento desencadeado por choro e percussão. Discutimos a hipótese de que as alterações anatomopatológicas estejam localizadas no mesencéfalo ou centros corticais superiores. CONCLUSÕES: São necessários novos estudos para maior compreensão dos tremores em recém-nascidos. O reconhecimento das diversas possibilidades etiológicas e o decorrente manejo das causas tratáveis são essenciais para a otimização do atendimento.

Published
2012

23. Prognostic factors predicting a fatal outcome in HIV-negative children with neurotuberculosis

Author

Rodrigues, Murilo Gimenes, Lin, Jaime, Masruha, Marcelo Rodrigues, Vilanova, Luiz Celso Pereira, and Minett, Thais Soares Cianciarullo

Subjects
child, tuberculosis, meningite, prognóstico, tuberculose, meningitis, prognosis, sistema nervoso central, central nervous system, crianças
Abstract

OBJECTIVE: To identify prognostic factors predicting a fatal outcome in HIV-negative children with neurotuberculosis based on clinical, epidemiological, and laboratory findings. METHOD: The clinical records of all in-patients diagnosed with neurotuberculosis from 1982 to 2005 were evaluated retrospectively. The following prognostic parameters were examined: gender, age, close contact with a tuberculosis-infected individual, vaccination for bacillus Calmette-Guérin, purified protein derivative (PPD) of tuberculin results, concomitant miliary tuberculosis, seizures, CSF results, and hydrocephalus. RESULTS: One hundred forty-one patients diagnosed with neurotuberculosis were included. Seventeen percent of the cases resulted in death. The factors that were correlated with a negative outcome included lack of contact with a tuberculosis-infected individual, negative PPD reaction, coma, and longer hospitalisation time. A multiple logistic regression analysis was performed to identify which of these factors most often resulted in death. CONCLUSION: Coma at diagnosis, lack of tuberculosis contact, and a non-reactive PPD were the most important predictors of fatality in patients with neurotuberculosis OBJETIVO: Identificar elementos prognósticos para a letalidade da neurotuberculose na criança, a partir das manifestações clínicas, dados epidemiológicos e laboratoriais. MÉTODO: Registros de pacientes internados durante o período de 1982 a 2005 foram retrospectivamente avaliados. Os elementos prognósticos considerados foram: sexo, idade, história de contato íntimo com indivíduo com tuberculose, vacinação com o bacilo de Calmette-Guérin (BCG), teste tuberculínico (PPD), concomitância de tuberculose miliar, convulsões, resultados da análise do LCR e presença de hidrocefalia. RESULTADOS: 141 pacientes com diagnóstico de neurotuberculose foram incluídos. Dezessete por cento dos pacientes foram a óbito. Os fatores associados ao óbito foram história negativa de contágio, ausência de reatividade ao teste de PPD, coma e tempo de internação prolongado. Análise por regressão logística múltipla foi usada para investigar as relações entre os elementos prognósticos e o desfecho óbito. CONCLUSÃO: Os fatores prognósticos na previsão de óbito nos pacientes com neurotuberculose foram a presença de coma no momento do diagnóstico, a ausência de história de contágio e a ausência de reação ao PPD

Published
2010

27. Virtual rehabilitation via Nintendo Wii® and conventional physical therapy effectively treat post-stroke hemiparetic patients

Author

da Silva Ribeiro, Nildo Manoel, primary, Ferraz, Daniel Dominguez, additional, Pedreira, Érika, additional, Pinheiro, Ígor, additional, da Silva Pinto, Ana Cláudia, additional, Neto, Mansueto Gomes, additional, dos Santos, Luan Rafael Aguiar, additional, Pozzato, Michele Gea Guimarães, additional, Pinho, Ricardo Silva, additional, and Masruha, Marcelo Rodrigues, additional

Published
2015
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30. Primary diffuse leptomeningeal gliomatosis

Author

Gonçalves, André Leite, Masruha, Marcelo Rodrigues, Carrete Jr, Henrique, Stávale, João Norberto, Silva, Nasjla Saba da, and Vilanova, Luiz Celso Pereira

Published
2008

31. Pyridoxine-dependent epilepsy initially responsive to phenobarbital

Author

Lin, Jaime, Lin, Katia, Masruha, Marcelo Rodrigues, and Vilanova, Luiz Celso Pereira

Subjects
neurologic manifestations, piridoxina, epilepsy, epilepsia, pyridoxine, manifestações neurológicas
Abstract

Pyridoxine-dependent epilepsy is a rare autossomal recessive disorder characterized by recurrent seizures that are not controlled by anticonvulsant medications but remits after administration of pyridoxine. We report on a 30 day-old girl who presented with seizures during the first day of life, initially responsive to anticonvulsant therapy, which remitted within two weeks. Seizures were characterized as multifocal myoclonic jerks of upper and lower limbs associated with buccal-lingual oral movements and eyelid blinking. Laboratory and neuroimaging studies were normal. Electroencephalographic record demonstrated a abnormal background activity with high-voltage epileptic discharges and a burst-suppression pattern. The seizures ceased after oral administration of pyridoxine, but recurred after withdrawal, confirming the diagnosis. A epilepsia por dependência de piridoxina é uma doença autossômica recessiva rara caracterizada por crises recorrentes refratárias a tratamento medicamentoso, mas que remitem após a administração de piridoxina. Relatamos o caso de menina de 30 dias de vida que iniciou crises convulsivas desde o primeiro dia de vida, inicialmente responsivas a tratamento com drogas anticonvulsivantes, mas que reiniciaram após a segunda semana de vida. As crises eram caracterizadas por movimentos clônicos erráticos de membros superiores e inferiores associados a movimentos oromandibulares e piscamentos. Exames laboratoriais e de neuroimagem foram normais. O exame eletrencefalográfico evidenciou atividade de base desorganizada com descargas epilépticas de alta voltagem associadas a um padrão de surto-supressão. As crises cessaram após a administração de piridoxina e recorreram após a sua retirada, confirmando o diagnóstico.

Published
2007

36. Detection of Cerebral Vasculopathy by Transcranial Doppler in Children With Neurofibromatosis Type 1.

Author

Paschoal, Joelma Karin Sagica Fernandes, Paschoal, Fernando Mendes, de Lima, Fernanda Teresa, Pinho, Ricardo Silva, Vilanova, Luiz Celso Pereira, Bor-Seng-Shu, Edson, and Masruha, Marcelo Rodrigues

Subjects
NEUROFIBROMATOSIS 1, NEUROFIBROMATOSIS in children, CEREBROVASCULAR disease in children, DIAGNOSIS of brain diseases, TRANSCRANIAL Doppler ultrasonography
Abstract

Neurofibromatosis type 1 is characterized by nerve sheath neurofibromas associated with a number of additional clinical features, including cerebrovascular disease. The aim of this study was to use transcranial Doppler as a screening method for identifying cerebral vasculopathy in children with neurofibromatosis type 1. Forty children with neurofibromatosis type 1, aged 5 to 18 years old, were examined by transcranial Doppler. Patients presenting with hemodynamic features of arterial stenosis/occlusion on transcranial Doppler underwent magnetic resonance angiography to confirm the findings. Magnetic resonance angiography was performed on 4 children who exhibited a transcranial Doppler hemodynamic pattern indicative of cerebral vasculopathy. Among these cases, 2 presented internal carotid artery stenosis/occlusion, 1 had bilateral middle cerebral artery stenosis, and 1 presented a normal magnetic resonance angiography result. Transcranial Doppler can be used routinely in the investigation of cerebrovascular disease in neurofibromatosis type 1 patients, where magnetic resonance angiography can be subsequently applied to confirm the diagnosis, further contributing to the prevention of cerebrovascular events. [ABSTRACT FROM AUTHOR]

Published
2016
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37. Sleep terrors antecedent is common in adolescents with migraine

Author

Fialho, Libânia Melo Nunes, primary, Pinho, Ricardo Silva, additional, Lin, Jaime, additional, Minett, Thais Soares Cianciarullo, additional, Vitalle, Maria Sylvia de Souza, additional, Fisberg, Mauro, additional, Peres, Mario Fernando Prieto, additional, Vilanova, Luiz Celso Pereira, additional, and Masruha, Marcelo Rodrigues, additional

Published
2013
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38. Adolescents with chronic migraine commonly exhibit depressive symptoms

Author

Arita, Juliana Harumi, primary, Lin, Jaime, additional, Pinho, Ricardo Silva, additional, Minett, Thais Soares Cianciarullo, additional, de Souza Vitalle, Maria Sylvia, additional, Fisberg, Mauro, additional, Peres, Mario Fernando Prieto, additional, Vilanova, Luiz Celso Pereira, additional, and Masruha, Marcelo Rodrigues, additional

Published
2012
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40. Pediatric Central Nervous System Tumors

Author

Pinho, Ricardo Silva, primary, Andreoni, Solange, additional, Silva, Nasjla Saba, additional, Cappellano, Andrea Maria, additional, Masruha, Marcelo Rodrigues, additional, Cavalheiro, Sérgio, additional, and Vilanova, Luiz Celso Pereira, additional

Published
2011
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48. Trigger factors in migraine patients

Author

Fukui, Patrícia Timy, primary, Gonçalves, Tessa Rachel Tranquillini, additional, Strabelli, Cintia Giunchetti, additional, Lucchino, Natalia Maria Fernandes, additional, Matos, Fernanda Cunha, additional, Santos, Juliana Pinto Moreira dos, additional, Zukerman, Eliova, additional, Zukerman-Guendler, Vera, additional, Mercante, Juliane Prieto, additional, Masruha, Marcelo Rodrigues, additional, Vieira, Domingos Sávio, additional, and Peres, Mario Fernando Prieto, additional

Published
2008
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