Search Results - "Barsottini, O."

Neurologic manifestations of antiphospholipid syndrome by Ricarte, I F, Dutra, L A, Abrantes, F F, Toso, F F, Barsottini, O G P, Silva, G S, de Souza, A W S, Andrade, D

“…Neurological involvement in antiphospholipid antibody syndrome (APS) is common, and its occurrence increases morbidity and mortality. Patients may present…”
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MR Imaging Features of Adult-Onset Neuronal Intranuclear Inclusion Disease May Be Indistinguishable from Fragile X-Associated Tremor/Ataxia Syndrome by Padilha, I G, Nunes, R H, Scortegagna, F A, Pedroso, J L, Marussi, V H, Rodrigues Gonçalves, M R, Barsottini, O G P, da Rocha, A J

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Transcranial Doppler findings in antiphospholipid syndrome by Ricarte, I F, Dutra, L A, Barsottini, O G P, Souza, A W S de, Andrade, D C O de, Mangueira, CLP, Silva, G S

“…Introduction Transcranial Doppler is a method that enables the assessment of different cerebral hemodynamic parameters. It also allows for the evaluation of…”
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Kinetic characterisation and inhibitor sensitivity of Candida albicans and Candida auris recombinant AOX expressed in a self-assembled proteoliposome system by Copsey, Alice C., Barsottini, Mario R. O., May, Benjamin, Xu, Fei, Albury, Mary S., Young, Luke, Moore, Anthony L.

“…Candidemia caused by Candida spp. is a serious threat in hospital settings being a major cause of acquired infection and death and a possible contributor to…”
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Anti‐N‐methyl‐D‐aspartate receptor encephalitis and Epstein‐Barr virus: another tale on autoimmunity? by Danieli, D., Moraes, A. C. M., Alves, M. P., Dutra, L. A., Höftberger, R., Barsottini, O. G. P., Masruha, M. R.

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Functional Diversification of Cerato-Platanins in Moniliophthora perniciosa as Seen by Differential Expression and Protein Function Specialization by BARSOTTINI, Mario R. de O, DE OLIVEIRA, Juliana F, ZERI, Ana C. de M, DIAS, Sandra M. G, PEREIRA, Gonçalo A. G, AMBROSIO, Andre L. B, ADAMOSKI, Douglas, TEIXEIRA, Paulo J. P. L, DO PRADO, Paula F. V, TIEZZI, Henrique O, SFORCA, Mauricio L, CASSAGO, Alexandre, PORTUGAL, Rodrigo V, DE OLIVEIRA, Paulo S. L

“…Cerato-platanins (CP) are small, cysteine-rich fungal-secreted proteins involved in the various stages of the host-fungus interaction process, acting as…”
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Comparison of the Kinetic Parameters of Alternative Oxidases From Trypanosoma brucei and Arabidopsis thaliana—A Tale of Two Cavities by Xu, Fei, Copsey, Alice C., Young, Luke, Barsottini, Mario R. O., Albury, Mary S., Moore, Anthony L.

“…The alternative oxidase (AOX) is widespread in plants, fungi, and some protozoa. While the general structure of the AOX remains consistent, its overall…”
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Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness by Kmoch, S., Majewski, J., Ramamurthy, V., Cao, S., Fahiminiya, S., Ren, H., MacDonald, I. M., Lopez, I., Sun, V., Keser, V., Khan, A., Stránecký, V., Hartmannová, H., Přistoupilová, A., Hodaňová, K., Piherová, L., Kuchař, L., Baxová, A., Chen, R., Barsottini, O. G. P., Pyle, A., Griffin, H., Splitt, M., Sallum, J., Tolmie, J. L., Sampson, J. R., Chinnery, P., Banin, E., Sharon, D., Dutta, S., Grebler, R., Helfrich-Foerster, C., Pedroso, J. L., Kretzschmar, D., Cayouette, M., Koenekoop, R. K.

“…Blindness due to retinal degeneration affects millions of people worldwide, but many disease-causing mutations remain unknown. PNPLA6 encodes the patatin-like…”
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Autonomic dysfunction in hereditary spastic paraplegia type 4 by González‐Salazar, C., Takazaki, K. A. G., Martinez, A. R. M., Pimentel‐Silva, L. R., Jacinto‐Scudeiro, L. A., Nakagawa, É. Y., Fujiwara Murakami, C. E., Saute, J. A. M., Pedroso, J. L., Barsottini, O. G. P., Teive, H. A. G., França Jr, M. C.

“…Background and purpose SPAST mutations are the most common cause of hereditary spastic paraplegia (SPG4‐HSP), which is characterized by progressive lower limb…”
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Video NeuroImages: Head titubation in anti-mGluR1 autoantibody-associated cerebellitis by Pedroso, José Luiz, Dutra, Lívia Almeida, Espay, Alberto J, Höftberger, Romana, Barsottini, O.G.P

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Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil by Gheno, T. C., Furtado, G. V., Saute, J. A. M., Donis, K. C., Fontanari, A. M. V., Emmel, V. E., Pedroso, J. L., Barsottini, O., Godeiro‐Junior, C., Linden, H., Ternes Pereira, E., Cintra, V. P., Marques, W., Castilhos, R. M., Alonso, I., Sequeiros, J., Cornejo‐Olivas, M., Mazzetti, P., Leotti, V. B., Jardim, L. B., Saraiva‐Pereira, M. L.

“…Background and purpose Spinocerebellar ataxia type 10 is a neurodegenerative disorder that is due to an expanded ATTCT repeat tract in the ATXN10 gene. Our aim…”
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Synthesis and testing of novel alternative oxidase (AOX) inhibitors with antifungal activity against Moniliophthora perniciosa (Stahel), the causal agent of witches' broom disease of cocoa, and other phytopathogens by Barsottini, Mario RO, Pires, Bárbara A, Vieira, Maria L, Pereira, José GC, Costa, Paulo CS, Sanitá, Jaqueline, Coradini, Alessandro, Mello, Fellipe, Marschalk, Cidnei, Silva, Eder M, Paschoal, Daniele, Figueira, Antonio, Rodrigues, Fábio HS, Cordeiro, Artur T, Miranda, Paulo CML, Oliveira, Paulo SL, Sforça, Maurício L, Carazzolle, Marcelo F, Rocco, Silvana A, Pereira, Gonçalo AG

“…Background Moniliophthora perniciosa (Stahel) Aime & Phillips‐Mora is the causal agent of witches' broom disease (WBD) of cocoa (Theobroma cacao L.) and a…”
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Cryopyrin associated periodic syndrome with neurological involvement in a 50-year-old patient by Dutra, L. A., Jesus, A. A., Vasconcellos, M., Silva, C. A., Oliveira, J. B., Terreri, M. T., Barsottini, O. G. P., de Souza, A. W. S.

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Huntington disease and Huntington disease-like in a case series from Brazil by Castilhos, R.M., Souza, A.F.D., Furtado, G.V., Gheno, T.C., Silva, A.L., Vargas, F.R., Lima, M.-A.F.D., Barsottini, O., Pedroso, J.L., Godeiro Jr, C., Salarini, D., Pereira, E.T., Lin, K., Toralles, M.-B., Saute, J.A.M., Rieder, C.R., Quintas, M., Sequeiros, J., Alonso, I., Saraiva-Pereira, M.L., Jardim, L.B.

“…The aim of this study was to identify the relative frequency of Huntington's disease (HD) and HD‐like (HDL) disorders HDL1, HDL2, spinocerebellar ataxia type 2…”
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Clinical correlates of olfactory dysfunction in spinocerebellar ataxia type 3 by Braga-Neto, P, Felicio, A.C, Pedroso, J.L, Dutra, L.A, Bertolucci, P.H.F, Gabbai, A.A, Barsottini, O.G.P

“…Abstract Olfactory dysfunction is a very common and early sign in neurodegenerative disorders, but few data are already available in hereditary ataxias. Our…”
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Teaching neuroimages: a prematurely aging patient presenting with severe leukoaraiosis and stroke by Seixas, J C, Pedroso, J L, Fukuda, T G, de Figueiredo, M M, Baiense, R F, Yared, J H, Ferraz, H B, Barsottini, O G P

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Teaching NeuroImages: brucellosis mimicking demyelinating disease by Abrahão, A, de Aquino, C C H, Pedroso, J L, Baiense, R F, Oliveira, R A, Jorge, V M, Barsottini, O G P

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Biochemical characterization and inhibition of the alternative oxidase enzyme from the fungal phytopathogen Moniliophthora perniciosa by Barsottini, Mario R. O., Copsey, Alice, Young, Luke, Baroni, Renata M., Cordeiro, Artur T., Pereira, Gonçalo A. G., Moore, Anthony L.

“…Moniliophthora perniciosa is a fungal pathogen and causal agent of the witches’ broom disease of cocoa, a threat to the chocolate industry and to the economic…”
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Brain SPECT imaging in Sydenham's chorea by Barsottini, O G P, Ferraz, H B, Seviliano, M M, Barbieri, A

“…The objective of the present study was to determine whether brain single-photon emission computed tomography (SPECT) imaging is capable of detecting…”
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Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): typical clinical and neuroimaging features in a Brazilian family by Pedroso, José Luiz, Braga-Neto, Pedro, Abrahão, Agessandro, Rivero, René Leandro Magalhães, Abdalla, Carolina, Abdala, Nitamar, Barsottini, Orlando Graziani Povoas

“…Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a neurodegenerative disorder characterized by late-infantile onset spastic ataxia and…”
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