Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Bruna K Ferreira"'
Autor:
Yolanda Paes-Colli, Andrey F. L. Aguiar, Alinny Rosendo Isaac, Bruna K. Ferreira, Raquel Maria P. Campos, Priscila Martins Pinheiro Trindade, Ricardo Augusto de Melo Reis, Luzia S. Sampaio
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 16 (2022)
Historically, Cannabis is one of the first plants to be domesticated and used in medicine, though only in the last years the amount of Cannabis-based products or medicines has increased worldwide. Previous preclinical studies and few published clinic
Externí odkaz:
https://doaj.org/article/cb93ab2b5cae4665b68c743a30d6151d
Autor:
Raquel Maria P. Campos, Andrey F. L. Aguiar, Yolanda Paes-Colli, Priscila Martins Pinheiro Trindade, Bruna K. Ferreira, Ricardo A. de Melo Reis, Luzia S. Sampaio
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Despite the importance of pain as a warning physiological system, chronic neuropathic pain is frequently caused by damage in the nervous system, followed by persistence over a long period, even in the absence of dangerous stimuli or after healing of
Externí odkaz:
https://doaj.org/article/03a98ec98f30460d980efc6059e2c121
Autor:
Ernesto A. Macongonde, Naithan L.F. Costa, Bruna K. Ferreira, Mairis S. Biella, Marisa J.S. Frederico, Marcos R. de Oliveira, Silvio Ávila Júnior, Fátima R.M.B. Silva, Gustavo C. Ferreira, Emilio L. Streck, Patrícia F. Schuck
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 87, Iss 2 suppl, Pp 1451-1459 (2015)
Fructose accumulates in tissue and body fluids of patients affected by hereditary fructose intolerance (HFI), a disorder caused by the deficiency of aldolase B. We investigated the effect of acute fructose administration on the biochemical profile an
Externí odkaz:
https://doaj.org/article/0587adb19c9c445bba9818249ebd063a
Autor:
Jade de Oliveira, Patrícia F. Schuck, Gustavo C. Ferreira, Felipe Dal-Pizzol, Maria Luiza Gomes, Milena Carvalho-Silva, Lara M. Gomes, Giselli Scaini, Emilio L. Streck, Bruna K Ferreira
Publikováno v:
Metabolic Brain Disease. 34:1207-1219
Deficiency of hepatic enzyme tyrosine aminotransferase characterizes the innate error of autosomal recessive disease Tyrosinemia Type II. Patients may develop neurological and developmental difficulties due to high levels of the amino acid tyrosine i
Autor:
Mohammad Abdollahi, Dia Advani, Jyoti Ahlawat, Melissa Albino, Josh Allen, Rashmi K. Ambasta, Diana Simona Antal, Nadezda Apostolova, Florina Ardelean, Olivia R.M. Bagshaw, Christopher J. Balardo, Mark A. Birch-Machin, Nicholas A. Bland, Leigh Ann Callahan, Hector J. Caruncho, Karina Ckless, Biswadeep Das, Castanares-Zapatero Diego, Mohammad Hosein Farzaei, Bruna K. Ferreira, Gustavo C. Ferreira, Gerardo García-Rivas, Priyanka Garg, Maria Manuela Gaspar, Sean M. Geary, Rohan Gupta, Paulina Hernández-Fontes, Olusola Idowu, Janjira Intra, Asmita Jaiswal, Lisa E. Kalynchuk, Aditya Kulkarni, Pravir Kumar, Joana Lopes, Omar Lozano, Mariana Matias, Manju Misra, Aditya Nandi, Mahesh Narayan, Harish Padh, Abhay K. Pandey, Akanksha Pandey, Niyati Pardiwalla, Paritosh Patel, Hantson Philippe, Jacinta Oliveira Pinho, Catarina Reis, Jun Ren, Milagros Rocha, Melissa T. Rodrigues, Elizabeth Ruddy, Uracha Ruktanonchai, Aliasger K. Salem, Irene A.J. Samuel, Rajat Sandhir, Phawanan Sawangchan, Elizabeth A. Schroder, Patricia F. Schuck, Amit Kumar Sharma, Sudhanshu Sharma, Snehal Shenoy, Amit Kumar Singh, Nitin Singhal, Jeffrey A. Stuart, Jiraphong Suksiriworapong, Rajesh Sunasee, Gerald Supinski, Yasamin Davatgaran Taghipour, Shreya Thakkar, Rahul Tripathi, Suresh K. Verma, Teressa Vezza, Victor M. Victor, Lin Wang, Amaraporn Wongrakpanich, Lin Wu, Yingmei Zhang, Gewei Zhu, Sean L.S. Zoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f1ffd3e2e65a9b3df95406a629e2055
https://doi.org/10.1016/b978-0-323-85666-9.09987-3
https://doi.org/10.1016/b978-0-323-85666-9.09987-3
Autor:
Fátima Regina Mena Barreto Silva, Gustavo C. Ferreira, Naithan Ludian Fernandes Costa, Marisa Jádna Silva Frederico, Emilio L. Streck, Mairis S. Biella, Patrícia F. Schuck, Ernesto António Macongonde, Bruna K Ferreira, Marcos Roberto de Oliveira, Silvio Ávila Júnior
Publikováno v:
Anais da Academia Brasileira de Ciências v.87 n.2 suppl.0 2015
Anais da Academia Brasileira de Ciências
Academia Brasileira de Ciências (ABC)
instacron:ABC
Anais da Academia Brasileira de Ciências, Vol 87, Iss 2 suppl, Pp 1451-1459 (2015)
Anais da Academia Brasileira de Ciências, Volume: 87, Issue: 2 Supplement, Pages: 1451-1459, Published: 25 AUG 2015
Redalyc
Anais da Academia Brasileira de Ciências
Academia Brasileira de Ciências (ABC)
instacron:ABC
Anais da Academia Brasileira de Ciências, Vol 87, Iss 2 suppl, Pp 1451-1459 (2015)
Anais da Academia Brasileira de Ciências, Volume: 87, Issue: 2 Supplement, Pages: 1451-1459, Published: 25 AUG 2015
Redalyc
Fructose accumulates in tissue and body fluids of patients affected by hereditary fructose intolerance (HFI), a disorder caused by the deficiency of aldolase B. We investigated the effect of acute fructose administration on the biochemical profile an
Autor:
Brenda da Silva Andrade, Bruna K Ferreira, Fabiola Diniz, Nathalia Frederico da Cunha, Gustavo C. Ferreira, Nicole Nazareth, Gilda Neves, Luis Eduardo Nunes, Adriana M Marques, Newton G. Castro, Gisely Novaes Borges da Cunha, Thainá Lione
Publikováno v:
IBRO Reports. 6:S447
Evidence of oxidative stress in brain and liver of young rats submitted to experimental galactosemia
Autor:
Marcos Roberto de Oliveira, Emilio L. Streck, Patrícia F. Schuck, Bruna K Ferreira, Lucineia Gainski Danielski, Fabricia Petronilho, Adália E Chipindo, Monique Michels, Márcia B Castro, Gustavo C. Ferreira, José H. Cararo, Marina Lummertz Magenis
Publikováno v:
Metabolic brain disease. 31(6)
Galactosemia is a disorder of galactose metabolism, leading to the accumulation of this carbohydrate. Galactosemic patients present brain and liver damage. For evaluated oxidative stress, 30-day-old males Wistar rats were divided into two groups: gal
Autor:
Giselli Scaini, Silvio Avila, Marcos Roberto de Oliveira, Thais Ceresér Vilela, Emilio L. Streck, Bruna K Ferreira, Cinara L. Gonçalves, Patrícia F. Schuck, Ernesto António Macongonde, Naithan Ludian Fernandes Costa, Gustavo C. Ferreira
Publikováno v:
Disease Markers
Disease Markers, Vol 2015 (2015)
Disease Markers, Vol 2015 (2015)
Hereditary fructose intolerance (HFI) is an autosomal-recessive disorder characterized by fructose and fructose-1-phosphate accumulation in tissues and biological fluids of patients. This disease results from a deficiency of aldolase B, which metabol