Biomethane generation in an AnSBBR treating effluent from the biohydrogen production from vinasse: Optimization, metabolic pathways modeling and scale-up estimation
Volpini, V., Lovato, G., Albanez, R., Ratusznei, S.M., Rodrigues, J.A.D.
Published in Renewable energy (01.02.2018)
Published in Renewable energy (01.02.2018)
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Physical exercise affects the epigenetic programming of rat brain and modulates the adaptive response evoked by repeated restraint stress
Kashimoto, R.K., Toffoli, L.V., Manfredo, M.H.F., Volpini, V.L., Martins-Pinge, M.C., Pelosi, G.G., Gomes, M.V.
Published in Behavioural brain research (01.01.2016)
Published in Behavioural brain research (01.01.2016)
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Phenotypic spectrum of MFN2 mutations in the Spanish population
Casasnovas, C, Banchs, I, Cassereau, J, Gueguen, N, Chevrollier, A, Martínez-Matos, J A, Bonneau, D, Volpini, V
Published in Journal of medical genetics (01.04.2010)
Published in Journal of medical genetics (01.04.2010)
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Effects of chronic restraint stress on the global DNA methylation profile of rat lung cells: Modulation by physical exercise
Toffoli, L.V., Volpini, V.L., Nascimento, L.M., Silva, W.R., Verissimo, L.F., Estrada, V.B., Pelosi, G.G., Gomes, M.V.
Published in Behavioural brain research (28.07.2017)
Published in Behavioural brain research (28.07.2017)
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Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT
Cassereau, J, Casasnovas, C, Gueguen, N, Malinge, M-C, Guillet, V, Reynier, P, Bonneau, D, Amati-Bonneau, P, Banchs, I, Volpini, V, Procaccio, V, Chevrollier, A
Published in Neurology (26.04.2011)
Published in Neurology (26.04.2011)
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Mosaicism of alpha-synuclein gene rearrangements: Report of two unrelated cases of early-onset parkinsonism
Perandones, C, Giugni, J.C, Calvo, D.S, Raina, G.B, De Jorge Lopez, L, Volpini, V, Zabetian, C.P, Mata, I.F, Caputo, M, Corach, D, Radrizzani, M, Micheli, F.E
Published in Parkinsonism & related disorders (01.05.2014)
Published in Parkinsonism & related disorders (01.05.2014)
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Ancestral Origins of the Machado-Joseph Disease Mutation: A Worldwide Haplotype Study
Gaspar, C., Lopes-Cendes, I., Hayes, S., Goto, J., Arvidsson, K., Dias, A., Silveira, I., Maciel, P., Coutinho, P., Lima, M., Zhou, Y.-X., Soong, B.-W., Watanabe, M., Giunti, P., Stevanin, G., Riess, O., Sasaki, H., Hsieh, M., Nicholson, G.A., Brunt, E., Higgins, J.J., Lauritzen, M., Tranebjaerg, L., Volpini, V., Wood, N., Ranum, L., Tsuji, S., Brice, A., Sequeiros, J., Rouleau, G.A.
Published in American journal of human genetics (01.02.2001)
Published in American journal of human genetics (01.02.2001)
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Spinocerebellar ataxia type 10 is rare in populations other than Mexicans
Matsuura, T, Ranum, L P W, Volpini, V, Pandolfo, M, Sasaki, H, Tashiro, K, Watase, K, Zoghbi, H Y, Ashizawa, T
Published in Neurology (26.03.2002)
Published in Neurology (26.03.2002)
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Spinocerebellar ataxia type 2 (SCA2) with white matter involvement
Armstrong, J., Bonaventura, I., Rojo, A., González, G., Corral, J., Nadal, N., Volpini, V., Ferrer, I.
Published in Neuroscience letters (24.06.2005)
Published in Neuroscience letters (24.06.2005)
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Journal Article
Expanded GAA repeats and clinical variation in Friedreich's ataxia
Mateo, I., Llorca, J., Volpini, V., Corral, J., Berciano, J., Combarros, O.
Published in Acta neurologica Scandinavica (01.01.2004)
Published in Acta neurologica Scandinavica (01.01.2004)
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Journal Article
A kindred with cerebellar ataxia and thermoanalgesia
Genis, D, Ferrer, I, Valls Solé, J, Corral, J, Volpini, V, San Nicolás, H, Gich, J, Ramió-Torrentà, L, Ferrándiz, M, Puig, J, Márquez, F
Published in Journal of neurology, neurosurgery and psychiatry (01.05.2009)
Published in Journal of neurology, neurosurgery and psychiatry (01.05.2009)
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GAA expansion size and age at onset of Friedreich's ataxia
Mateo, I, Llorca, J, Volpini, V, Corral, J, Berciano, J, Combarros, O
Published in Neurology (22.07.2003)
Published in Neurology (22.07.2003)
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Clinical and molecular analysis of X-linked Charcot-Marie-Tooth disease type 1 in Spanish population
Casasnovas, C, Banchs, I, Corral, J, Martínez-Matos, JA, Volpini, V
Published in Clinical genetics (01.12.2006)
Published in Clinical genetics (01.12.2006)
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Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA1) kindred: (CAG)n expansion and early premonitory signs and symptoms
Genis, D, Matilla, T, Volpini, V, Rosell, J, Dávalos, A, Ferrer, I, Molins, A, Estivill, X
Published in Neurology (01.01.1995)
Published in Neurology (01.01.1995)
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