Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Bruno A. Telles"'
Autor:
Bruna Andrade e Silva, Ricardo C. Cassilhas, Cecília Attux, Quirino Cordeiro, André L. Gadelha, Bruno A. Telles, Rodrigo A. Bressan, Francine N. Ferreira, Paulo H. Rodstein, Claudiane S. Daltio, Sérgio Tufik, Marco T. de Mello
Publikováno v:
Brazilian Journal of Psychiatry, Iss 0, Pp 00-00 (2015)
Objective:To evaluate the effects of 20 weeks of resistance and concurrent training on psychotic and depressive symptoms, quality of life outcomes, and serum IGF-1, IGFBP-3, and brain-derived neurotrophic factor (BDNF) concentrations in patients with
Externí odkaz:
https://doaj.org/article/1fb8913c95a74846b8aabd5e36b6dc78
Autor:
Daniel Almeida do Valle, Mara Lúcia Schmitz Ferreira Santos, Bruno Augusto Telles, Mara L. Cordeiro
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Mucopolysaccharidosis type III (MPS III) or Sanfilippo syndrome is the most common form of MPS, in which neurological involvement in all stages of the disease is prominent. The current study aimed to comprehensively describe the neurological profile
Externí odkaz:
https://doaj.org/article/896f0fcefe2a4396b11db69ced1f2169
Autor:
Vanessa Zanette, Daniel do Valle, Bruno Augusto Telles, Alan J. Robinson, Vaneisse Monteiro, Mara Lucia S. F. Santos, Ricardo Lehtonen R. Souza, Cristiane Benincá
Publikováno v:
Genetics and Molecular Biology, Vol 44, Iss 4 (2021)
Abstract Mitochondrial complex I (CI) deficiency is the most common oxidative phosphorylation disorder described. It shows a wide range of phenotypes with poor correlation within genotypes. Herein we expand the clinics and genetics of CI deficiency i
Externí odkaz:
https://doaj.org/article/e8799b279fc8482c9331a2c67730d109
Autor:
Julio Henrique Muzetti, Daniel Almeida do Valle, Mara L. S. Ferreira Santos, Bruno Augusto Telles, Mara L. Cordeiro
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Glycogen storage diseases (GSD) encompass a group of rare inherited diseases due dysfunction of glycogen metabolism. Hypoglycemia is the most common primary manifestation of GSD, and disturbances in glucose metabolism can cause neurological damage. T
Externí odkaz:
https://doaj.org/article/316741f3cc3142dc9b3eb17b4999753f
Autor:
Alexander J. Whitworth, Julien Prudent, Enrico Baruffini, Anna Yeates, Daniel Almeida do Valle, Alan J. Robinson, Erika Fernandez-Vizarra, Michele Brischigliaro, Aurelio Reyes, Mara Lúcia Schmitz Ferreira Santos, Ricardo L.R. Souza, Mark H. Johnson, Massimo Zeviani, Bruno Augusto Telles, Andrea Degiorgi, Cristiane Benincá, Vanessa Zanette
Publikováno v:
Journal of Medical Genetics. 58:155-167
BackgroundMitochondria provide ATP through the process of oxidative phosphorylation, physically located in the inner mitochondrial membrane (IMM). The mitochondrial contact site and organising system (MICOS) complex is known as the ‘mitoskeleton’
Autor:
Daniel Almeida, do Valle, Mara Lúcia Schmitz Ferreira, Santos, Bruno Augusto, Telles, Mara L, Cordeiro
Mucopolysaccharidosis type III (MPS III) or Sanfilippo syndrome is the most common form of MPS, in which neurological involvement in all stages of the disease is prominent. The current study aimed to comprehensively describe the neurological profile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c4d186d80839a718d84923cdd359854
https://escholarship.org/uc/item/5k007542
https://escholarship.org/uc/item/5k007542
Autor:
Flank Melo De Lima, Joseir Gandra Percy, Diogo Cunha, Emanuel Apoema Sortica, Flávia de Oliveira Lima Falcão, Bruno Fidalgo Telles Rodrigues, Rafael Lopez França, Joao Paulo Teixeira Da Fonseca, Marcos Vinicius Pereira, Sidarta Mocelin
Publikováno v:
Rio Oil and Gas Expo and Conference. 22:280-281
Publikováno v:
Headache Medicine. 11:32-34
Reversible Cerebral Vasoconstriction Syndrome (RCVS) is a clinical and radiological syndrome that is primarily defined by thunderclap headache, with or without further neurological deficits, and segmental intracranial vasoconstriction that resolves w
Publikováno v:
Parasitology International. 89:102585
Pudica trichomysae n. sp. (Trichostrongylina, Heligmosomoidea, Helligmonellidae, Pudicinae) from the small intestine of Trichomys fosteri (Rodentia: Echimydae) from the Pantanal of Mato Grosso do Sul is described by light and scanning electron micros
Autor:
Carolina Prando, Daniel Almeida do Valle, Mônica J Spinosa, Mara Lúcia Schmitz Ferreira Santos, Bruno Augusto Telles, Mara L. Cordeiro
Publikováno v:
Medicine
Medicine, vol 100, iss 23
Medicine, vol 100, iss 23
Rationale: Human parvovirus B19 (B19) infection can produce a spectrum of clinical syndromes, including neurological manifestations, most notably encephalitis. Although symptoms suggestive of autoimmune disease in patients with B19 infection have bee