Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rodrigo Mariano Ribeiro"'
Autor:
David Augusto Batista Sá Araújo¹, Rodrigo Mariano Ribeiro, Pedro Lucas Grangeiro Sá Barreto Lima, Dánton Campos de Queiroz, Milena Sales Pitombeira, Bernardo Martins, Pablo Picasso Araújo Coimbra, Cleto Dantas Nogueira, Pedro Braga-Neto, Guilherme Diogo Silva, Paulo Ribeiro Nóbrega
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background To report a case of IgG4-related pachymeningitis presenting with cystic lesions mimicking neurocysticercosis. Case presentation A 40-year-old female patient with tetraparesis, dysphagia and dysphonia was evaluated with clinical ex
Externí odkaz:
https://doaj.org/article/660b8ab7acb646f3a7078347e74ad8e1
Autor:
Carla Marineli Saraiva do Amaral, Samuel Brito de Almeida, Renata Parente de Almeida, Simony Lira do Nascimento, Rodrigo Mariano Ribeiro, Pedro Braga-Neto
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Introduction Postural balance impairment can affect the quality of life of patients with Parkinson’s disease. Previous studies have described connections of the vestibular system with postural functions, suggesting a potential participatio
Externí odkaz:
https://doaj.org/article/6ce10953bcc8444485444e238289b508
Autor:
Paulo Ribeiro Nóbrega, Anderson Moura Bernardes, Rodrigo Mariano Ribeiro, Sophia Costa Vasconcelos, David Augusto Batista Sá Araújo, Vitor Carneiro de Vasconcelos Gama, Helena Fussiger, Carolina de Figueiredo Santos, Daniel Aguiar Dias, André Luíz Santos Pessoa, Wladimir Bocca Vieira de Rezende Pinto, Jonas Alex Morales Saute, Paulo Victor Sgobbi de Souza, Pedro Braga-Neto
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Cerebrotendinous Xanthomatosis represents a rare and underdiagnosed inherited neurometabolic disorder due to homozygous or compound heterozygous variants involving the CYP27A1 gene. This bile acid metabolism disorder represents a key potentially trea
Externí odkaz:
https://doaj.org/article/0efb18fac58149eaa7184750e1d73b5b
Autor:
Rodrigo Mariano Ribeiro, Sophia Costa Vasconcelos, Pedro Lucas Grangeiro de Sá Barreto Lima, Emanuel Ferreira Coelho, Anna Melissa Noronha Oliveira, Emanuel de Assis Bertulino Martins Gomes, Luciano de Albuquerque Mota, Lucas Soares Radtke, Matheus dos Santos Carvalho, David Augusto Batista Sá Araújo, Maria Suelly Nogueira Pinheiro, Vitor Carneiro de Vasconcelos Gama, Renan Magalhães Montenegro Júnior, Pedro Braga Neto, Paulo Ribeiro Nóbrega
Publikováno v:
Brain Sciences, Vol 13, Iss 7, p 979 (2023)
Cerebrotendinous xanthomatosis (CTX) is an autosomal recessive disorder caused by pathogenic variants in CYP27A1, leading to a deficiency in sterol 27-hydroxylase. This defect results in the accumulation of cholestanol and bile alcohols in various ti
Externí odkaz:
https://doaj.org/article/5f3faf1df17b4838a82fcd0324680dd7