Zobrazeno 1 - 10
of 60
pro vyhledávání: '"MS Goncalves"'
Autor:
AMJ Oliveira, LM Fiuza, CVB Figueiredo, CC Guarda, RP Santiago, SCMA Yahouédéhou, SP Carvalho, IM Lyra, MS Goncalves
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S79- (2023)
Sickle cell anemia (SCA) is one of the types of sickle cell disease (SCD), which is characterized by hematological events such as hemolysis and endothelial damage that culminate in vaso-occlusion, leading to the appearance of several clinical manifes
Externí odkaz:
https://doaj.org/article/2ad54a6d2f974133bb3fc830911d4f6c
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S77-S78 (2023)
A anemia falciforme (AF) é uma das doenças monogênicas hereditárias mais comum no mundo. Os indivíduos com AF apresentam diversas manifestações clínicas, como síndrome torácica aguda, acidente vascular cerebral, infecção, priapismo e úlc
Externí odkaz:
https://doaj.org/article/e00ff7fb675e41d68b3accdbe03c3a2c
Autor:
SS Santana, SCMA Yahouedehou, CSA Adanho, CG Barbosa, TN Pitanga, IM Lyra, VA Fortuna, MS Goncalves
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S854-S855 (2023)
A COVID-19 é uma doença inflamatória caracterizada por hipóxia, edema pulmonar e tempestade de citocinas. As complicações são mais graves na presença de lesão vascular subjacente, associada a doenças como diabetes, hipertensão e ateroscler
Externí odkaz:
https://doaj.org/article/eeaa81306d804acf8faa4d43cce6a0e3
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S72- (2024)
Background: Sickle cell disease (SCD) is a genetic monogenic disorder with variable clinical manifestations and is characterized by the presence of the variant hemoglobin S. Renal damage is common in patients with SCD, which begins in childhood, prog
Externí odkaz:
https://doaj.org/article/43bd3f29ef184689a1243691a87de27e
Autor:
RS Leal, CCMX Albuquerque, AG Gbadamassi, MO Cunha, MOO Nascimento, SRL Albuquerque, NA Fraiji, MS Gonçalves, R Ramasawmy, JPM Neto
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S86- (2024)
Objectives: Alpha thalassemia (AT) is a hereditary hemoglobinopathy caused by a partial or complete deletion of the synthesis of alpha globin chains. This deletion has been correlated as a prognostic marker which directly contributes to the phenotypi
Externí odkaz:
https://doaj.org/article/ac7fba28cb714217afa002648ee7df15
Autor:
JSV Campelo, FLO Gomes, AP Alcântara, MOO Nascimento, IPC Tavares, JNV Silva, NA Fraiji, SRL Albuquerque, MS Gonçalves, JPM Neto
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S145- (2024)
Objectives: The urokinase-like plasminogen activator receptor (uPAR) interacts with its ligand (uPA) to convert plasminogen into plasmin, which degrades components of the extracellular matrix. Plasminogen activation can influence many normal and path
Externí odkaz:
https://doaj.org/article/1eda2bea524c4c17928ecdf7189c8ab2
Autor:
JSV Campelo, FLO Gomes, ACS Castro, EJS Freitas, LSF Menesca, MO Cunha, NA Fraiji, SRL Albuquerque, MS Gonçalves, JP NETO MOURA
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S144-S145 (2024)
Objectives: Differential diagnosis of hematologic diseases is a huge challenge and advances in genetic studies have made it possible to unravel the many gene interactions in these diseases. In this study, we performed a literature search on the roles
Externí odkaz:
https://doaj.org/article/6e69deb33e6745e888868e3250fe44ff
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S516- (2024)
Objetivo: O presente estudo teve como objetivo realizar uma revisão sistemática visando estimar a influência de μRNAs no prognóstico do Mieloma Múltiplo (MM) e sua correlação com biomarcadores já padronizados ou com biomoléculas já conheci
Externí odkaz:
https://doaj.org/article/503b32ad81da4c209b86253d0bee5b8e
Autor:
CC Guarda, SCMA Yahouedehou, RP Santiago, SPC Valverde, LM Fiuza, CVB Figueiredo, RM Oliveira, VML Nascimento, MM Aleluia, MS Gonçalves
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S642- (2024)
Sickle cell anemia (SCA) is a hemolytic disorder characterized by reduced red blood cell lifespan due to repeated sickling processes. Patients have complications as a consequence of hemolysis, vaso-occlusion, inflammation, and endothelial dysfunction
Externí odkaz:
https://doaj.org/article/1f42c34f7bcd45eeacc4f5af5f760175
Autor:
ACS Castro, MOO Nascimento, MMP Luciano, JNV Silva, EJS Freitas, IPC Tavares, SRL Albuquerque, RS Leal, MS Gonçalves, JPM Neto
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S877- (2024)
Objective: The Rh blood group is one of the most complex blood groups known in humans, being is clinically relevant mainly due to the fact that antigens are highly immunogenic, responsible for a hemolytic transfusion reaction or on fetal RBCs. The RH
Externí odkaz:
https://doaj.org/article/6d0ac096928c4d6e9faa7f9ae0672595