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Artigo de periodico
A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects (2021)
Palagano, Eleonora; Gordon, Christopher T; Uva, Paolo ; Strina, Dario ; Dimartino, Clémantine; Villa, Anna; Amiel, Jeanne; Guion-Almeida, Maria Leine; Pittoli, Siulan Vendramini Paulovich ; Nakata, Nancy Mizue Kokitsu ; Zechi-Ceide, Roseli Maria ; Sobacchi, Cristina
Fonte: Bone. Unidade: HRAC
Assuntos: DISOSTOSE MANDIBULOFACIAL, MUTAÇÃO GENÉTICA, FENÓTIPOS, CONVULSÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PALAGANO, Eleonora et al. A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects. Bone, v. 153, p. 7 , 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bone.2021.116152. Acesso em: 02 ago. 2024.
APA
Palagano, E., Gordon, C. T., Uva, P., Strina, D., Dimartino, C., Villa, A., et al. (2021). A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects. Bone, 153, 7 . doi:10.1016/j.bone.2021.116152
NLM
Palagano E, Gordon CT, Uva P, Strina D, Dimartino C, Villa A, Amiel J, Guion-Almeida ML, Pittoli SVP, Nakata NMK, Zechi-Ceide RM, Sobacchi C. A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects [Internet]. Bone. 2021 ; 153 7 .[citado 2024 ago. 02 ] Available from: https://doi.org/10.1016/j.bone.2021.116152
Vancouver
Palagano E, Gordon CT, Uva P, Strina D, Dimartino C, Villa A, Amiel J, Guion-Almeida ML, Pittoli SVP, Nakata NMK, Zechi-Ceide RM, Sobacchi C. A novel intronic variant in PIGB in acrofrontofacionasal dysostosis type 1 patients expands the spectrum of phenotypes associated with GPI biosynthesis defects [Internet]. Bone. 2021 ; 153 7 .[citado 2024 ago. 02 ] Available from: https://doi.org/10.1016/j.bone.2021.116152
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
Fonte: Arthritis Research & Therapy. Unidade: FMRP
Assuntos: 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: 02 ago. 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 ago. 02 ] 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 ago. 02 ] 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
Fonte: Clinical Science. Unidade: ICB
Assuntos: 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: 02 ago. 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 ago. 02 ] 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 ago. 02 ] Available from: https://doi.org/10.1042/CS20170220

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