Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Alexandra Prüfer de Queiroz Campos Araújo"'
Autor:
Giuseppe Pastura, Tadeu Takao Almodovar Kubo, Maria Angélica Regalla, Cíntia Machado Mesquita, Gabriel Coutinho, Emerson Leandro Gasparetto, Otávio Figueiredo, Paulo Mattos, Alexandra Prüfer de Queiroz Campos Araújo
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 74, Iss 10, Pp 785-790
ABSTRACT Objective To perform a pilot study to investigate the association between working memory and cortical thickness in a sample of attention deficit/hyperactivity disorder (ADHD) children. Methods Seventeen children aged 7-10 years diagnosed wit
Externí odkaz:
https://doaj.org/article/bd2ccb9e2c86459cb5e4811108a61a11
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
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
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
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 96, Iss 4, Pp 503-510 (2020)
Objective: Duchenne muscular dystrophy, an X-linked genetic disease, leads to progressive muscle weakness mainly in the lower limbs. Motor function tests help to monitor disease progression. Can low-cost, simple assessments help in the diagnostic sus
Externí odkaz:
https://doaj.org/article/68f62b78026a4008b2fb9d540dcbfb9b
Publikováno v:
Jornal de Pediatria, Vol 96, Iss 4, Pp 503-510 (2020)
Objective: Duchenne muscular dystrophy, an X-linked genetic disease, leads to progressive muscle weakness mainly in the lower limbs. Motor function tests help to monitor disease progression. Can low-cost, simple assessments help in the diagnostic sus
Externí odkaz:
https://doaj.org/article/9c1180650b8e40dba91e8fb42c8fe7f0
Autor:
Flávia Nardes, Alexandra Prufer de Queiroz Campos Araújo, Márcia Gonçalves Ribeiro, Maíta Bittar, Hanid Fontes Gomes
Publikováno v:
Annals of Child Neurology, Vol 28, Iss 2, Pp 57-65 (2020)
Purpose Given that intellectual disability affects 15% to 63% of boys with Duchenne muscular dystrophy (DMD), it is relevant to evaluate if the Mini-Mental State Examination (MMSE) is a reliable test for screening in these cognitively impaired boys.
Externí odkaz:
https://doaj.org/article/8eef774d01474ec19367ade02f9ceb0c
Publikováno v:
Cadernos de Saúde Coletiva, Vol 27, Iss 2, Pp 202-209 (2019)
Resumo Introdução Questionários de avaliação são ferramentas habituais nas diferentes áreas de saúde. Frequentemente são desenvolvidos na língua inglesa e muitas vezes utilizados em populações diferentes daquelas para as quais foram origi
Externí odkaz:
https://doaj.org/article/e1caf517e3f54030aac8d8ebcc3ad73e