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pro vyhledávání: '"Loureiro JL"'
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Akademický článek
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Autor:
Hamid Azzedine, Alessandro Filla, Merle Ruberg, Paula Coutinho, Filippo M. Santorelli, Enrico Bertini, Vítor Tedim Cruz, Elodie Martin, N. Elleuch, D. Grid, Jacques Chomilier, Alessandra Tessa, Naima Bouslam, Perrine Charles, Alexandra Durr, Bertrand Fontaine, Eric LeGuern, Paola S. Denora, Christian Confavreux, Giovanni Stevanin, Anne Marie Ouvrard-Hernandez, Alexis Brice, Meriem Tazir, José Leal Loureiro, Alexander Lossos
Publikováno v:
Nature Genetics
Nature Genetics, Nature Publishing Group, 2007, 39 (3), pp.366-72. ⟨10.1038/ng1980⟩
Nature Genetics, Nature Publishing Group, 2007, 39 (3), pp.366-372. ⟨10.1038/ng1980⟩
Nature Genetics, 2007, 39 (3), pp.366-72. ⟨10.1038/ng1980⟩
Nature Genetics, 2007, 39 (3), pp.366-372. ⟨10.1038/ng1980⟩
Nature Genetics, Nature Publishing Group, 2007, 39 (3), pp.366-72. ⟨10.1038/ng1980⟩
Nature Genetics, Nature Publishing Group, 2007, 39 (3), pp.366-372. ⟨10.1038/ng1980⟩
Nature Genetics, 2007, 39 (3), pp.366-72. ⟨10.1038/ng1980⟩
Nature Genetics, 2007, 39 (3), pp.366-372. ⟨10.1038/ng1980⟩
Autosomal recessive hereditary spastic paraplegia (ARHSP) with thin corpus callosum (TCC) is a common and clinically distinct form of familial spastic paraplegia that is linked to the SPG11 locus on chromosome 15 in most affected families. We analyze
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5971eea2644de5b9f7c847d3c403ad5a
https://hal.archives-ouvertes.fr/hal-00281704
https://hal.archives-ouvertes.fr/hal-00281704
Autor:
Giovanni, Stevanin, Giorgia, Montagna, Hamid, Azzedine, Enza Maria Valente, Alexandra, Durr, Valentina, Scarano, Naima, Bouslam, Denise, Cassandrini, Denora, Paola S., Chiara, Criscuolo, Soraya, Belarbi, Antonio, Orlacchio, Philippe, Jonveaux, Gabriella, Silvestri, Anne Marie Ouvrad Hernandez, De Michele, G., Meriem, Tazir, Caterina, Mariotti, Knut, Brockmann, Alessandro, Malandrini, Van Der Knapp, M. S., Marcella, Neri, Hassan, Tonekaboni, Melone, Mariarosa A. B., Alessandra, Tessa, Teresa Dotti, M., Michela, Tosetti, Pauri, Flavia, Antonio, Federico, Casali, Carlo, Cruz, Vitor T., Loureiro, Jose L., Federico, Zara, Sylvie, Forlani, Enrico, Bertini, Paula, Coutinho, Alessandro, Filla, Alexis, Brice, Santorelli, Filippo M., Casali, C.
Publikováno v:
neurogenetics
neurogenetics, 2006, 7 (3), pp.149-56. ⟨10.1007/s10048-006-0044-2⟩
Neurogenetics, 7(3), 149-156. Springer Verlag
neurogenetics, Springer Verlag, 2006, 7 (3), pp.149-56. ⟨10.1007/s10048-006-0044-2⟩
Stevanin, G, Montagna, G, Azzedine, H, Valente, E M, Durr, A, Scarano, V, Bouslam, N, Cassandrini, D, Denora, P S, Criscuolo, C, Belarbi, S, Orlacchio, A, Jonveaux, P, Silvestri, G, Hernandez, A M O, De Michele, G, Tazir, M, Mariotti, C, Brockmann, K, Malandrini, A, Van Der Knapp, M S, Neri, M, Tonekaboni, H, Melone, M A B, Tessa, A, Dotti, M T, Tosetti, M, Pauri, F, Federico, A, Casali, C, Cruz, V T, Loureiro, J L, Zara, F, Forlani, S, Bertini, E, Coutinho, P, Filla, A, Brice, A & Santorelli, F M 2006, ' Spastic paraplegia with thin corpus callosum : Description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity ', Neurogenetics, vol. 7, no. 3, pp. 149-156 . https://doi.org/10.1007/s10048-006-0044-2
neurogenetics, 2006, 7 (3), pp.149-56. ⟨10.1007/s10048-006-0044-2⟩
Neurogenetics, 7(3), 149-156. Springer Verlag
neurogenetics, Springer Verlag, 2006, 7 (3), pp.149-56. ⟨10.1007/s10048-006-0044-2⟩
Stevanin, G, Montagna, G, Azzedine, H, Valente, E M, Durr, A, Scarano, V, Bouslam, N, Cassandrini, D, Denora, P S, Criscuolo, C, Belarbi, S, Orlacchio, A, Jonveaux, P, Silvestri, G, Hernandez, A M O, De Michele, G, Tazir, M, Mariotti, C, Brockmann, K, Malandrini, A, Van Der Knapp, M S, Neri, M, Tonekaboni, H, Melone, M A B, Tessa, A, Dotti, M T, Tosetti, M, Pauri, F, Federico, A, Casali, C, Cruz, V T, Loureiro, J L, Zara, F, Forlani, S, Bertini, E, Coutinho, P, Filla, A, Brice, A & Santorelli, F M 2006, ' Spastic paraplegia with thin corpus callosum : Description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity ', Neurogenetics, vol. 7, no. 3, pp. 149-156 . https://doi.org/10.1007/s10048-006-0044-2
We studied 20 Mediterranean families (40 patients) with autosomal recessive hereditary spastic paraplegia and thin corpus callosum (ARHSP-TCC, MIM 604360) to characterize their clinical and genetic features. In six families (17 patients) of Algerian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebf7945c57ed1d41b6e14833120c532f
http://hdl.handle.net/11365/23934
http://hdl.handle.net/11365/23934
Autor:
de Alencar Morais Lima W; Laboratory of Galenic Pharmacy, Department of Pharmacy, Federal University of Rio Grande Do Norte, Natal, 59012-570, Brazil., de Souza JG; InovAI Lab, nPITI/IMD, Federal University of Rio Grande Do Norte, Natal, RN, 59078-970, Brazil., García-Villén F; Department of Pharmacy and Pharmaceutical Technology, School of Pharmacy, University of Granada, Campus of Cartuja, 18071, Granada, Spain. fgarvillen@ugr.es., Loureiro JL; Laboratory of Galenic Pharmacy, Department of Pharmacy, Federal University of Rio Grande Do Norte, Natal, 59012-570, Brazil., Raffin FN; Laboratory of Galenic Pharmacy, Department of Pharmacy, Federal University of Rio Grande Do Norte, Natal, 59012-570, Brazil., Fernandes MAC; InovAI Lab, nPITI/IMD, Federal University of Rio Grande Do Norte, Natal, RN, 59078-970, Brazil.; Department of Computer Engineering and Automation, Federal University of Rio Grande Do Norte, Natal, RN, 59078-970, Brazil., Souto EB; Laboratory of Pharmaceutical Technology, Faculty of Pharmacy, University of Porto, Rua Jorge de Viterbo Ferreira, 228, 4050-313, Porto, Portugal., Severino P; Industrial Biotechnology Program, University of Tiradentes (UNIT), Aracaju, Sergipe, 49032-490, Brazil., Barbosa RM; Department of Pharmacy and Pharmaceutical Technology, School of Pharmacy, University of Seville, C/Professor García González, 2, 41012, Seville, Spain. rdemelo@us.es.
Publikováno v:
World journal of pediatrics : WJP [World J Pediatr] 2024 Aug 28. Date of Electronic Publication: 2024 Aug 28.
Autor:
Diaz JL; Department of Cardiac Rehabilitation, Heart Hospital, Hamad Medical Corporation, Doha, Qatar., Surendran PJ; Department of Cardiac Rehabilitation, Heart Hospital, Hamad Medical Corporation, Doha, Qatar., Jacob P; Department of Cardiac Rehabilitation, Heart Hospital, Hamad Medical Corporation, Doha, Qatar., Chbib S; Department of Pharmacy, Heart Hospital, Hamad Medical Corporation, Doha, Qatar., Foster LD; Department of Cardiac Rehabilitation, Cardiff and Vale University Health Board, Cardiff, UK., Abuenjelh AMA; Department of Cardiac Rehabilitation, Heart Hospital, Hamad Medical Corporation, Doha, Qatar., Ibrahim O; Department of Cardiac Rehabilitation, Heart Hospital, Hamad Medical Corporation, Doha, Qatar.
Publikováno v:
Heart views : the official journal of the Gulf Heart Association [Heart Views] 2024 Jan-Mar; Vol. 25 (1), pp. 21-29. Date of Electronic Publication: 2024 Apr 12.
Human adenovirus associated with severe cold agglutinin syndrome: a rare complication in Pediatrics.
Autor:
Sion JL; Universidade de São Paulo, São Paulo, Brazil., Flores ALH; Universidade de São Paulo, São Paulo, Brazil., Cardoso RA; Universidade de São Paulo, São Paulo, Brazil., Garanito MP; Universidade de São Paulo, São Paulo, Brazil.
Publikováno v:
Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo [Rev Paul Pediatr] 2023 Jul 10; Vol. 42, pp. e2022174. Date of Electronic Publication: 2023 Jul 10 (Print Publication: 2023).
Autor:
Gaudencio JL; Pontifícia Universidade Católica de Campinas, Campinas, SP, Brazil. Electronic address: julia.lg4@puccampinas.edu.br., Fortunato PN; Hospital Municipal Dr. Mário Gatti, Campinas, SP, Brazil., Junior HMDS; Pontifícia Universidade Católica de Campinas, Campinas, SP, Brazil.
Publikováno v:
Thrombosis research [Thromb Res] 2022 May; Vol. 213, pp. 125-127. Date of Electronic Publication: 2022 Mar 26.
Autor:
Rodrigues R; Neurology Department, Centro Hospitalar de Entre o Douro e Vouga, Santa Maria da Feira, 4520-211, Portugal., Rocha R; Neurology Department, Hospital Pedro Hispano, Unidade Local de Saúde de Matosinhos, Matosinhos, 4450-021, Portugal., Bonifácio G; Neurology Department, Centro Hospitalar de Setúbal, Setúbal 2910-446, Portugal., Ferro D; Neurology Department, Centro Hospitalar Universitário de São João, Porto 4200-319, Portugal; Department of Clinical Neurosciences and Mental Health, Faculty of Medicine of Porto University, Porto 4200-319, Portugal., Sabença F; Neurology Department, Centro Hospitalar Vila Nova de Gaia/Espinho, Vila Nova de Gaia 4400-129, Portugal., Gonçalves AI; Neurology Department, Hospital Beatriz Ângelo, Loures, 2674-514, Portugal., Correia F; Neurology Department, Hospital Pedro Hispano, Unidade Local de Saúde de Matosinhos, Matosinhos, 4450-021, Portugal., Pinheiro J; Neurology Department, Centro Hospitalar Vila Nova de Gaia/Espinho, Vila Nova de Gaia 4400-129, Portugal., Loureiro JL; Neurology Department, Centro Hospitalar de Entre o Douro e Vouga, Santa Maria da Feira, 4520-211, Portugal; Institute for Molecular and Cell Biology, I3S, Porto 4200-135, Portugal., Guerreiro RP; Neurology Department, Centro Hospitalar de Setúbal, Setúbal 2910-446, Portugal., Vale J; Neurology Department, Hospital Beatriz Ângelo, Loures, 2674-514, Portugal., Sá MJ; Neurology Department, Centro Hospitalar Universitário de São João, Porto 4200-319, Portugal; Faculdade de Ciências da Saúde, Universidade Fernando Pessoa, Porto 4249-004, Portugal., Costa A; Neurology Department, Centro Hospitalar Universitário de São João, Porto 4200-319, Portugal; Department of Clinical Neurosciences and Mental Health, Faculty of Medicine of Porto University, Porto 4200-319, Portugal. Electronic address: andreiafgcosta@gmail.com.
Publikováno v:
Multiple sclerosis and related disorders [Mult Scler Relat Disord] 2021 Oct; Vol. 55, pp. 103176. Date of Electronic Publication: 2021 Jul 27.