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Artigo de periodico
Higher interferon score and normal complement levels may identify a distinct clinical subset in children with systemic lupus erythematosus (2020)
Tesser, Alessandra; Carvalho, Luciana Martins de ; Sandrin-Garcia, Paula; Pin, Alessia; Pastore, Serena; Taddio, Andrea; Roberti, Luciana Rodrigues; Queiroz, Rosane Gomes de Paula; Ferriani, Virgínia Paes Leme ; Crovella, Sergio; Tommasini, Alberto
Source: Arthritis Research & Therapy. Unidade: FMRP
Subjects: LÚPUS ERITEMATOSO SISTÊMICO, INTERFERONS, AUTOIMUNIDADE, CRIANÇAS, INTERFERON TIPO I, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TESSER, Alessandra et al. Higher interferon score and normal complement levels may identify a distinct clinical subset in children with systemic lupus erythematosus. Arthritis Research & Therapy, v. 22, p. 1-12, 2020Tradução . . Disponível em: https://doi.org/10.1186/s13075-020-02161-8. Acesso em: 14 nov. 2024.
APA
Tesser, A., Carvalho, L. M. de, Sandrin-Garcia, P., Pin, A., Pastore, S., Taddio, A., et al. (2020). Higher interferon score and normal complement levels may identify a distinct clinical subset in children with systemic lupus erythematosus. Arthritis Research & Therapy, 22, 1-12. doi:10.1186/s13075-020-02161-8
NLM
Tesser A, Carvalho LM de, Sandrin-Garcia P, Pin A, Pastore S, Taddio A, Roberti LR, Queiroz RG de P, Ferriani VPL, Crovella S, Tommasini A. Higher interferon score and normal complement levels may identify a distinct clinical subset in children with systemic lupus erythematosus [Internet]. Arthritis Research & Therapy. 2020 ; 22 1-12.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1186/s13075-020-02161-8
Vancouver
Tesser A, Carvalho LM de, Sandrin-Garcia P, Pin A, Pastore S, Taddio A, Roberti LR, Queiroz RG de P, Ferriani VPL, Crovella S, Tommasini A. Higher interferon score and normal complement levels may identify a distinct clinical subset in children with systemic lupus erythematosus [Internet]. Arthritis Research & Therapy. 2020 ; 22 1-12.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1186/s13075-020-02161-8
Artigo de periodico
A past and present overview of macrophage metabolism and functional outcomes (2017)
Curi, Rui ; Mendes, Renata de Siqueira; Crispin, Luiz Aurélio de Campos ; Norata, Giuseppe Danilo ; Sampaio, Sandra Coccuzzo ; Newsholme, Philip
Source: Clinical Science. Unidade: ICB
Subjects: FISIOLOGIA, MACRÓFAGOS, METABOLISMO ENERGÉTICO, ÁCIDOS GRAXOS, GLICOSE, GLUTAMINA, INSULINA, HORMÔNIOS TIREOIDIANOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CURI, Rui et al. A past and present overview of macrophage metabolism and functional outcomes. Clinical Science, v. 131, n. 12, p. 1329-1342, 2017Tradução . . Disponível em: https://doi.org/10.1042/CS20170220. Acesso em: 14 nov. 2024.
APA
Curi, R., Mendes, R. de S., Crispin, L. A. de C., Norata, G. D., Sampaio, S. C., & Newsholme, P. (2017). A past and present overview of macrophage metabolism and functional outcomes. Clinical Science, 131( 12), 1329-1342. doi:10.1042/CS20170220
NLM
Curi R, Mendes R de S, Crispin LA de C, Norata GD, Sampaio SC, Newsholme P. A past and present overview of macrophage metabolism and functional outcomes [Internet]. Clinical Science. 2017 ; 131( 12): 1329-1342.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1042/CS20170220
Vancouver
Curi R, Mendes R de S, Crispin LA de C, Norata GD, Sampaio SC, Newsholme P. A past and present overview of macrophage metabolism and functional outcomes [Internet]. Clinical Science. 2017 ; 131( 12): 1329-1342.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1042/CS20170220
Artigo de periodico
Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff Disease: functional characterization of 9 novel sequence variants (2012)
Zampieri, Stefania; Cattarossi, Silvia; Oller Ramirez, Ana Maria; Rosano, Camillo; Lourenço, Charles Marques; Passon, Nadia; Moroni, Isabella; Uziel, Graziella; Pettinari, Antonella; Stanzial, Franco; Kremer, Raquel Dodelson de; Azar, Nydia Beatriz; Hazan, Filiz; Filocamo, Mirella; Bembi, Bruno; Dardis, Andrea
Source: PLOS ONE. Unidade: FMRP
Subjects: TRANSFECÇÃO, REAÇÃO EM CADEIA POR POLIMERASE, DELEÇÃO DE GENES, MUTAÇÃO GENÉTICA, LISOSSOMOS, DOENÇAS NEURODEGENERATIVAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZAMPIERI, Stefania et al. Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff Disease: functional characterization of 9 novel sequence variants. PLOS ONE, v. 7, n. 7, p. 1-10, 2012Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0041516. Acesso em: 14 nov. 2024.
APA
Zampieri, S., Cattarossi, S., Oller Ramirez, A. M., Rosano, C., Lourenço, C. M., Passon, N., et al. (2012). Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff Disease: functional characterization of 9 novel sequence variants. PLOS ONE, 7( 7), 1-10. doi:10.1371/journal.pone.0041516
NLM
Zampieri S, Cattarossi S, Oller Ramirez AM, Rosano C, Lourenço CM, Passon N, Moroni I, Uziel G, Pettinari A, Stanzial F, Kremer RD de, Azar NB, Hazan F, Filocamo M, Bembi B, Dardis A. Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff Disease: functional characterization of 9 novel sequence variants [Internet]. PLOS ONE. 2012 ; 7( 7): 1-10.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1371/journal.pone.0041516
Vancouver
Zampieri S, Cattarossi S, Oller Ramirez AM, Rosano C, Lourenço CM, Passon N, Moroni I, Uziel G, Pettinari A, Stanzial F, Kremer RD de, Azar NB, Hazan F, Filocamo M, Bembi B, Dardis A. Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff Disease: functional characterization of 9 novel sequence variants [Internet]. PLOS ONE. 2012 ; 7( 7): 1-10.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1371/journal.pone.0041516

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