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Akademický článek
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Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S69- (2024)
Background: Sickle cell disease (SCD) is an inherited multisystem blood disorder that produces sickle-shaped erythrocytes that obstruct blood flow, leading to severe clinical complications, including painful vaso-occlusive events (VOE). VOE are often
Externí odkaz:
https://doaj.org/article/37d02237eb5e4a2eb3709321a2df1917
Autor:
JGM Lusvarghi, GC Gonçalves, JAOD Reis, FF Ribeiro, PAS Chagas, LOC Barbosa, PPM Melo, AP Avellar, GBL Oliveira
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S93-S94 (2024)
Objetivo: O objetivo deste relato foi associar a aplasia de medula com hemoglobinúria paroxística noturna, uma desordem clonal adquirida que causa mutações genéticas e pode levar a deficiência global de certas proteínas na superfície de célu
Externí odkaz:
https://doaj.org/article/952af052286348699d716e2d234a625f
Autor:
JGM Lusvarghi, FF Ribeiro, LOC Barbosa, GC Gonçalves, JAOD Reis, GBL Oliveira, PPM Melo, AP Avellar, PAS Chagas
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S209- (2024)
Objetivo: Este relato tem como objetivo evidenciar um caso atípico de Linfoma de Hodgkin (LH) devido ao acometimento inicial de pele em face, com posterior envolvimento de partes moles, osso e orofaringe, levando a piora da qualidade de vida devido
Externí odkaz:
https://doaj.org/article/46ffa6c0c3054432a43953fda9144395
Autor:
JGM Lusvarghi, AP Avellar, PAS Chagas, GC Gonçalves, JAOD Reis, LOC Barbosa, PPM Melo, GBL Oliveira, FF Ribeiro
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S242-S243 (2024)
Objetivo: Visa demonstrar a associação da quimioterapia ao possível diagnóstico de Leucoencefalopatia Multifocal Progressiva (LEMP) em paciente vivendo com o HIV. Relato de caso: Masculino, 31 anos, pessoa vivendo com HIV, em tratamento regular,
Externí odkaz:
https://doaj.org/article/75cff0c88336450480cd1c337651c55d
Autor:
JGM Lusvarghi, JGP Capobiando, GBL Oliveira, PPM Melo, GC Gonçalves, JAOD Reis, LOC Barbosa, FF Ribeiro, AP Avellar, PAS Chagas
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S243- (2024)
Objetivo: O presente relato objetiva a apresentação de um caso de síndrome de Horner como manifestação associada a doença hematológica - linfoma não Hodgkin difuso de grandes células B. Relato de caso: Masculino, 52 anos, com diagnóstico de
Externí odkaz:
https://doaj.org/article/f97cd02977aa4cbbbd331f891dcda0b1
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
D'ANGELO, Ivana, Parajó, Yb, Y. B, Horvth, Ac, A. C, Kéri, Gc, G. C, Rotonda, La, Mia, M. I. A, Alonso
Publikováno v:
Journal of Microencapsulation. 27:57-66
Clinical studies have demonstrated the efficacy of new strategies in cancer therapy, such as chemotherapy and radiotherapy, associated to the administration of tumour vascularization inhibitors. A critical limitation for the clinical application of a
Autor:
DT Gnaoulé, PHD in mdecine, Radiologist, AEB Bravo-Tsri, PHD in mdecine, Radiologist, A Toure, PHD in mdecine, Radiologist, AP Ndja, PHD in mdecine, Radiologist, A Le Dion, PHD in mdecine, NE Fatto, Hospital Intern, AE Zouzou, PHD in mdecine, Radiologist, D Isart, PHD in mdecine, Radiologist, GC Gbazi, PHD in mdecine, Radiologist
Publikováno v:
Radiology Case Reports, Vol 16, Iss 11, Pp 3196-3200 (2021)
Duplication of the inferior vena cava is a rare malformation, normally without clinical impact, explained by abnormal development and regression of certain segments of the venous system during embryonic life. However, its presence and type should be
Externí odkaz:
https://doaj.org/article/a0c37eb1bc08431197321c6966c78d0b