Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus (2015)
- Autores:
- Autores USP: SILVA, CLOVIS ARTUR ALMEIDA DA - FM ; SAMPAIO, MAGDA MARIA SALES CARNEIRO - FM ; ROCHA, MANOEL DE SOUZA - FM ; CARRILHO, FLAIR JOSÉ - FM ; ALVES, VENANCIO AVANCINI FERREIRA - FM
- Unidade: FM
- DOI: 10.6061/clinics/2015(03)12
- Assuntos: LÚPUS ERITEMATOSO SISTÊMICO; MUTAÇÃO GENÉTICA; MUTAÇÃO PUNTUAL; BRASIL
- Idioma: Inglês
- Imprenta:
- Fonte:
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by-nc
-
ABNT
LIPHAUS, Bernadete L. et al. Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus. Clinics, v. 70, n. 3, p. 220-227, 2015Tradução . . Disponível em: https://doi.org/10.6061/clinics/2015(03)12. Acesso em: 19 abr. 2024. -
APA
Liphaus, B. L., Umetsu, N., Jesus, A. A., Bando, S. Y., Silva, C. A., & Carneiro-Sampaio, M. (2015). Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus. Clinics, 70( 3), 220-227. doi:10.6061/clinics/2015(03)12 -
NLM
Liphaus BL, Umetsu N, Jesus AA, Bando SY, Silva CA, Carneiro-Sampaio M. Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus [Internet]. Clinics. 2015 ; 70( 3): 220-227.[citado 2024 abr. 19 ] Available from: https://doi.org/10.6061/clinics/2015(03)12 -
Vancouver
Liphaus BL, Umetsu N, Jesus AA, Bando SY, Silva CA, Carneiro-Sampaio M. Molecular characterization of the complement C1q, C2 and C4 genes in Brazilian patients with juvenile systemic lupus erythematosus [Internet]. Clinics. 2015 ; 70( 3): 220-227.[citado 2024 abr. 19 ] Available from: https://doi.org/10.6061/clinics/2015(03)12 - Hepatocellular carcinoma related to Schistosoma mansoni Infection: case series and literature review
- Circulating sTREM-1 as a predictive biomarker of pediatric multisystemic inflammatory syndrome (MIS-C)
- Why is SARS-CoV-2 infection milder among children? [Editorial]
- LRBA deficiency: a new genetic cause of monogenic lupus
- Increased sMer, but not sAxl, sTyro3, and Gas6 relate with active disease in juvenile systemic lupus erythematosus
- Combined hepato-cholangiocarcinoma arising in a gallbladder intracystic papillary neoplasm: A new view on so-called “hepatoid adenocarcinoma of the gallbladder”
- Codon 249 mutation in TP53 is frequency found in bigger and poorly and poorly differentiated hepatocellular carcinoma in Brazil
- Increased hepatic expression of miRNA-122 in patients infected with HCV genotype 3
- 249 TP53 mutation has high prevalence and is correlated with larger and poorly differentiated HCC in Brazilian patients
- A phenotypical map of disseminated hepatocellular carcinoma suggests clonal constraints in metastatic sites
Informações sobre o DOI: 10.6061/clinics/2015(03)12 (Fonte: oaDOI API)
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas