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LEONARDO C FERREIRA
LEONARDO C FERREIRA
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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
1042010
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
712018
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
542016
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
372019
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
362018
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
302015
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
292022
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
192017
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
172018
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
122021
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
112017
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
102016
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
32010
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
22024
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
22021
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
12023
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
12020
A Experiência do Espaço em Jogos Eletrônicos: Cidades em Skyrim, Sleeping Dogs e Aion
L Ferreira
Faculdade de Comunicação, 2018
12018
Influence of the laboratory protocol on the in yield of bone marrow mesenchymal stem cells.
RFM Silveira, LC Ferreira, F Ginani, CAG Barboza
12010
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
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