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pro vyhledávání: '"So FL"'
We propose an approach for adapting the DeBERTa model for electronic health record (EHR) tasks using domain adaptation. We pretrain a small DeBERTa model on a dataset consisting of MIMIC-III discharge summaries, clinical notes, radiology reports, and
Externí odkaz:
http://arxiv.org/abs/2303.14920
Publikováno v:
Legal Spirit, Vol 8, Iss 2, Pp 379-390 (2024)
The rapid advancement of technology has facilitated easier access to information but has concurrently heightened the risks associated with the security of personal data. This has raised concerns about individual privacy, prompting the enactment of re
Externí odkaz:
https://doaj.org/article/9eb00c4117284b27afd7c3e66c8f7ab8
Publikováno v:
Nigerian Journal of Paediatrics, Vol 40, Iss 2, Pp 154-157 (2024)
Background: Tetanus is a public health problem in Nigeria. This study examines the demographic and clinical profile of postneonatal tetanus (PNT) seen in University of Maiduguri Teaching Hospital (UMTH), North- eastern Nigeria. Methods: This is a
Externí odkaz:
https://doaj.org/article/c5ed9c6a391e49a2949a21fa5b5dda1f
Publikováno v:
Romanian Neurosurgery, Vol 38, Iss Special Issue (2024)
Introduction Crouzon syndrome is a genetic disorder caused by mutations in the FGFR2 gene, leading to premature fusion of cranial sutures (craniosynostosis) and resulting in distinct craniofacial abnormalities such as a beaked nose, shallow orbits
Externí odkaz:
https://doaj.org/article/5d93b646797640d0aa570f19770e0f04
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S76-S77 (2024)
Introdução: A doença hemolítica aloimune do recém-nascido (DHRN) é rara e deve ser considerada quando há icterícia precoce e anemia no neonato. Relatamos o caso de um recém nascido (RN) gemelar que evoluiu com clínica suspeita e alteraçõe
Externí odkaz:
https://doaj.org/article/3314de39c37f4df8a2ee9accd0f7de63
APLASIA PURA DE SÉRIE VERMELHA POR PARVOVÍRUS B19 EM LEUCEMIA MIELOIDE AGUDA APÓS TERAPIA DE INDUÇÃO
Autor:
TV Lourenço, LPG Gomes, RG Silva, SS Custodio, TG Teixeira, CRC Pires, IF Martins, IGC Silveira, FL Nogueira, ABF Glória
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S143-S144 (2024)
Introdução: Parvovírus B19 é um vírus de DNA fita simples que tem como alvo principal células de alto índice mitótico, principalmente os progenitores eritroides da medula óssea. Sua transmissão ocorre por meio de contato próximo entre pess
Externí odkaz:
https://doaj.org/article/700d47d21c894a6a842202d774c45072
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S168- (2024)
As talassemias são doenças hereditárias, autossômicas recessivas, caracterizadas por mutações nos genes que codificam as cadeias globínicas da hemoglobina (Hb), resultando na redução ou ausência da produção dessas cadeias. A Talassemia Be
Externí odkaz:
https://doaj.org/article/b98888c4b47e4d19b5cf3c182405e985
Autor:
LP Almeida, MMS Silva, NAHL Silva, MJA Sousa, ML Silva, PHFDCL Casas, MB Nunes, FL Nogueira, TS Soares, JMTPD Nascimento
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S231-S232 (2024)
Objetivos: Reportar um caso de difícil diagnóstico em paciente HIV positivo com história de linfoma plasmablástico e manifestações neurológicas. Materiais e métodos: Relato de caso. Resultados: Paciente de 35 anos, masculino, com histórico d
Externí odkaz:
https://doaj.org/article/f4865afa3687451a825a49c3e2573443
Autor:
N Zing, T Fischer, E Miranda, Y Gonzaga, MA Dias, RLR Baptista, G Duffles, R Schaffel, FL Nogueira, D Bortucchi, RSA Silva, SAB Brasil, KZ Cecyn, VLP Figueiredo, NS Castro, YS Rabelo, GFS Barros, A Hallack-Neto, PPG Radtke, MALHM Conhalato, DV Clé, J Pereira, F Barroso, RR Sousa, H Quintero, D Castro, B Beltran, D Enriquez, J Vasquez, C Roche, D Artiles, F Valvert, L Villela, C Oliver, L Korin, C Pena, M Roa, MAT Viera, AV Glasenapp, A Quiroz, CS Figari, R Rios, S Paredes, EE Saul, C Bermack, K Meza, B Valcarcel, CA Souza, L Malpica, CS Chiattone
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S233-S234 (2024)
Introduction: Adult T-cell leukemia/lymphoma (ATLL) is a mature, peripheral T-cell neoplasm caused by HTLV-1 and its lifetime risk is estimated as 4-7% among HTLV-1 carriers. Acute and lymphoma subtypes are highly aggressive diseases, characterized b
Externí odkaz:
https://doaj.org/article/58c3427ca5c4476bba75d1029b8d3a5f
Autor:
T Fischer, E Miranda, J Pereira, G Duffles, JV Tavares, NS Castro, RSA Silva, DLC Farias, SAB Brasil, CCG Macedo, C Colaço, RLR Baptista, KZ Cecyn, D Bortucchi, GFS Barros, S Nabhan, PPG Radtke, R Schaffel, N Zing, FL Nogueira, AD Cunha-Junior, DV Clé, JTDS Filho, VLP Figueiredo, MD Pont, R Gaiolla, N Hamerschlak, EFO Ribeiro, A Hallack-Neto, MA Dias, Y Gonzaga, YS Rabelo, L Teixeira, G Perini, MALHM Conhalato, P Cury, H Idrobo, D Castro, B Beltran, D Enriquez, J Vasquez, C Roche, D Artiles, F Valvert, L Villela, C Oliver, L Korin, C Pena, M Roa, MAT Viera, AV Gasenapp, A Quiroz, CS Figari, R Rios, S Paredes, EE Saul, C Bermack, K Meza, B Valcarcel, CA Souza, L Malpica, CS Chiattone
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S256-S258 (2024)
Introduction: PTCL accounts for 10-15% of all NHL. As previously demonstrated, Latin America has its own epidemiological distribution, with a high frequency of ATLL and ENKT, likely influenced by distinct genetic profiles and viral epidemiology. 3-ye
Externí odkaz:
https://doaj.org/article/5f15d08093f549d3a333ac68a7b006be