Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Flavia Nardes"'
Autor:
Alexandra Prufer de Queiroz Campos Araújo, Clarisse Pereira Dias Drumond Fortes, Flavia Nardes, Eduardo Jorge, Salmo Raskin
Publikováno v:
Residência Pediátrica, Vol 13, Iss 4 (2023)
OBJECTIVE: Help the pediatrician in the suspicion of neuromuscular diseases when the child has complaints or altered findings in neuropsychomotor development, presenting one review on the topic. METHODOLOGY: Non-systematic literature review using ar
Externí odkaz:
https://doaj.org/article/8c4369fa587443caadf7b77348b23a9e
Autor:
Alexandra Prufer de Queiroz Campos Araujo, Jonas Alex Morales Saute, Clarisse Pereira Dias Drumond Fortes, Marcondes Cavalcante França Jr, Jaqueline Almeida Pereira, Marco Antonio Veloso de Albuquerque, Alzira Alves de Siqueira Carvalho, Eduardo Boiteux Uchôa Cavalcanti, Anna Paula Paranhos Miranda Covaleski, Simone Chaves Fagondes, Juliana Gurgel-Giannetti, Marcus Vinicius Magno Gonçalves, Alberto Rolim Muro Martinez, Antônio Rodrigues Coimbra Neto, Flavio Reis Neves, Anamarli Nucci, Ana Paula Cassetta dos Santos Nucera, Andre Luis Santos Pessoa, Marcos Ferreira Rebel, Flavia Nardes dos Santos, Rosana Herminia Scola, Cláudia Ferreira da Rosa Sobreira
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 01, Pp 081-094 (2023)
In the last few decades, there have been considerable improvements in the diagnosis and care of Duchenne muscular dystrophy (DMD), the most common childhood muscular dystrophy. International guidelines have been published and recently reviewed. A gro
Externí odkaz:
https://doaj.org/article/e7394276d1634927a5b0e0cfebf906de
Autor:
Alexandra P. Q. C. Araujo, Flavia Nardes, Clarisse P. D. D. Fortes, Jaqueline A. Pereira, Marcos F. Rebel, Cristina M. Dias, Rita de Cassia G. A. Barbosa, Mauro V. R. Lopes, Ana Lucia Langer, Flavio R. Neves, Edna Fátima Reis
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 76, Iss 7, Pp 481-489
ABSTRACT Significant advances in the understanding and management of Duchenne muscular dystrophy (DMD) have occurred since the publication of international guidelines for DMD care in 2010. Our objective was to provide an evidence-based national conse
Externí odkaz:
https://doaj.org/article/d2d35671c4e5479b907d9eb5f5e567d3
Autor:
Brenda Klemm Arci Mattos de Freitas Alves, Alexandra Prufer de Queiroz Campos Araujo, Flávia Nardes dos Santos, Márcia Gonçalves Ribeiro
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 11, Pp 001-008 (2024)
Background Spinal muscular atrophy (SMA-5q) is a neurodegenerative disease characterized by progressive muscle atrophy, hypotonia, and weakness, with SMA 1 presenting symptoms within the first 6 months of life. Disease-modifying therapies have been a
Externí odkaz:
https://doaj.org/article/8f790992c0564e26b1b2e0b680522196
Autor:
Michele Michelin Becker, Flávia Nardes, Tamara Dangouloff, Laurent Servais, Alexandra Prufer de Queiroz Campos Araujo, Juliana Gurgel-Giannetti
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 10, Pp 001-009 (2024)
Spinal muscular atrophy (SMA) is a genetic neuromuscular progressive disorder that is currently treatable. The sooner the disease-modifying therapies are started, the better the prognosis. Newborn screening for SMA, which is already performed in many
Externí odkaz:
https://doaj.org/article/579c5df870ed412bacbd30390a2a1a21
Akademický článek
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Akademický článek
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Autor:
Giuseppe Pastura, Flavia Nardes
Publikováno v:
Residência Pediátrica. 11
OBJECTIVES: To review the main topics that constitute the medical history in pediatric consultations. METHODS: Non-systematic review of the scientific literature, covering 280 databases of the area of health sciences linked to the portal of CAPES Jou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d49c54dd80c955ae3586a240f16a7ec0
https://doi.org/10.25060/residpediatr-2021.v11n1-113
https://doi.org/10.25060/residpediatr-2021.v11n1-113
Autor:
Edmar Zanoteli, Alexandra Prufer de Queiróz Campos Araujo, Michele Michelin Becker, Clarisse Pereira Dias Drumond Fortes, Marcondes Cavalcante França, Marcela Camara Machado-Costa, Wilson Marques, Ciro Matsui Jr, Rodrigo Holanda Mendonça, Flávia Nardes, Acary Souza Bulle Oliveira, Andre Luis Santos Pessoa, Jonas Alex Morales Saute, Paulo Sgobbi, Hélio Van der Linden, Juliana Gurgel-Giannetti
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 82, Iss 01, Pp 001-018 (2024)
Spinal muscular atrophy linked to chromosome 5 (SMA-5q) is an autosomal recessive genetic disease caused by mutations in the SMN1. SMA-5q is characterized by progressive degeneration of the spinal cord and bulbar motor neurons, causing severe motor a
Externí odkaz:
https://doaj.org/article/d5abdbdbc3fe4b4b985d20f677267041
Publikováno v:
Residência Pediátrica, Vol 13, Iss 2 (2023)
INTRODUCTION: Heterozygous mutations in the SCN1A gene are linked to a wide spectrum of epileptic disorders, ranging from self-limited conditions to epileptic encephalopathies, such as Dravet Syndrome. Seizure control is important to prevent both sud
Externí odkaz:
https://doaj.org/article/fbc467de8928476da43ae4b9fb8c6d3a