Family history of hypertension as an important risk factor for the development of severe preeclampsia PCFM Bezerra, MD Leão, JW Queiroz, EMD Melo, FVM Pereira, ... Acta obstetricia et gynecologica Scandinavica 89 (5), 612-617, 2010 | 104 | 2010 |
Causes of death in patients with Berardinelli-Seip congenital generalized lipodystrophy JG Lima, LHC Nobrega, NN Lima, MCF Dos Santos, PHD Silva, ... PLoS One 13 (6), e0199052, 2018 | 71 | 2018 |
Identifying leprosy and those at risk of developing leprosy by detection of antibodies against LID-1 and LID-NDO FM Amorim, ML Nobre, LC Ferreira, LS Nascimento, AM Miranda, ... PLoS Neglected Tropical Diseases 10 (9), e0004934, 2016 | 54 | 2016 |
The worldwide mutational landscape of Berardinelli-Seip congenital lipodystrophy ASC Sarmento, LC Ferreira, JG Lima, LB de Azevedo Medeiros, ... Mutation Research/Reviews in Mutation Research 781, 30-52, 2019 | 37 | 2019 |
Risk factors of Helicobacter pylori infection in an urban community in Northeast Brazil and the relationship between the infection and gastric diseases ILD Basílio, MFC Catão, JDS Carvalho, FP Freire-Neto, LC Ferreira, ... Revista da Sociedade Brasileira de Medicina Tropical 51 (02), 183-189, 2018 | 36 | 2018 |
Association between ACVR2A and early-onset preeclampsia: replication study in a Northeastern Brazilian population LC Ferreira, CEM Gomes, ACP Araújo, PF Bezerra, P Duggal, ... Placenta 36 (2), 186-190, 2015 | 30 | 2015 |
Genome-wide association studies of COVID-19: Connecting the dots LC Ferreira, CEM Gomes, JF Rodrigues-Neto, SMB Jeronimo Infection, Genetics and Evolution 106, 105379, 2022 | 29 | 2022 |
Normal bone density and trabecular bone score, but high serum sclerostin in congenital generalized lipodystrophy JG Lima, LHC Nobrega, NN Lima, MCF Dos Santos, PB Maria de Fatima, ... Bone 101, 21-25, 2017 | 19 | 2017 |
Polymorphism in Mitochondrial Group I Introns among Cryptococcus neoformans and Cryptococcus gattii Genotypes and Its Association with Drug Susceptibility FEES Gomes, TD Arantes, JAL Fernandes, LC Ferreira, H Romero, ... Frontiers in microbiology 9, 86, 2018 | 17 | 2018 |
Genetic association of ERAP1 and ERAP2 with eclampsia and preeclampsia in northeastern Brazilian women LC Ferreira, CEM Gomes, P Duggal, I De Paula Holanda, AS de Lima, ... Scientific reports 11 (1), 6764, 2021 | 12 | 2021 |
The maternal 14 bp Ins/Del polymorphism in HLA‐G is not associated with preeclampsia risk LC Ferreira, TPB Lopes, TB Guimarães, CEM Gomes, SMB Jeronimo International Journal of Immunogenetics 44 (6), 350-355, 2017 | 11 | 2017 |
No association between FCGR2A and FCGR3A polymorphisms in Guillain-Barré Syndrome in a Brazilian population MED Junior, LC Ferreira, FP Freire-Neto, SMB Jeronimo Journal of neuroimmunology 298, 160-164, 2016 | 10 | 2016 |
Influência do protocolo laboratorial no rendimento in vitro de células-tronco mesenquimais RF de Melo Silveira, LC Ferreira, F Ginani, CAG Barboza Revista de Ciências Médicas e Biológicas 9 (1), 17-21, 2010 | 3 | 2010 |
Impaired signaling pathways on Berardinelli–Seip congenital lipodystrophy macrophages during Leishmania infantum infection VB Nogueira, C de Oliveira Mendes-Aguiar, DG Teixeira, FP Freire-Neto, ... Scientific reports 14 (1), 11236, 2024 | 2 | 2024 |
Plasma angiotensin II levels in women with severe preeclampsia under magnesium sulfate regimen ASD de Lima, IP Holanda, PRP Nascimento, SMB Jeronimo, LC Ferreira Pregnancy Hypertension 23, 56-58, 2021 | 2 | 2021 |
Distribution and Polymorphisms of Group I Introns in Mitochondrial Genes from Cryptococcus neoformans and Cryptococcus gattii RMOS Gomes, KJG da Silva, LC Ferreira, TD Arantes, RC Theodoro Journal of Fungi 9 (6), 629, 2023 | 1 | 2023 |
Report of a Father With Congenital Bilateral Absence of the Vas Deferens Fathering a Child With Beare–Stevenson Syndrome LC Ferreira, JH Dantas Junior Frontiers in Genetics 11, 104, 2020 | 1 | 2020 |
A Experiência do Espaço em Jogos Eletrônicos: Cidades em Skyrim, Sleeping Dogs e Aion L Ferreira Faculdade de Comunicação, 2018 | 1 | 2018 |
Influence of the laboratory protocol on the in yield of bone marrow mesenchymal stem cells. RFM Silveira, LC Ferreira, F Ginani, CAG Barboza | 1 | 2010 |
Whole exome sequencing shows novel COL4A3 and COL4A4 variants as causes of Alport syndrome in Rio Grande do Norte, Brazil WC Araújo, RM Falcão, RAC Uchoa, CA Garcia, AQB Silva, LC Ferreira, ... | | 2023 |