Results 21 to 30 of about 21,321,554 (196)
Investigação bibliográfica sobre a hemoglobina S de 1976 a 2007 [PDF]
OBJETIVO: Buscar na literatura aspectos epidemiológicos explorados sobre a hemoglobina S. MÉTODOS: Trata-se de um levantamento bibliográfico nas bases de dados Medline e Lilacs. Também foi feita uma busca não eletrônica, em publicações de 1976 a 2007. RESULTADOS: Os resultados mostraram que, dos 21 artigos selecionados, 7 (33,3%) foram publicados entre
Holsbach, Denise Rodrigues +4 more
openaire +3 more sources
Hemoglobinas AS/alfa talassemia: importância diagnóstica [PDF]
Portadores de traço falciforme (hemoglobina AS) associados a talassemia alfa apresentam alterações na morfologia dos eritrócitos, normalmente ausentes nos heterozigotos para esta variante de hemoglobina.
Renata Tomé-Alves +6 more
doaj +1 more source
Este estudo teve como objetivo constatar e acompanhar a prevalência das hemoglobinas variantes S e C em doadores de sangue do Hemope Recife entre os anos de 2018 e 2020.
LR Lima +4 more
doaj +1 more source
The survival of childhood leukemia: An 8‐year single‐center experience
Abstract Background The survival of childhood leukemia has improved. We aimed to report the survival rate and the associated factors in children with acute leukemia during an 8‐year follow‐up. Aims This study investigates the 8‐year survival rates of children with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) in Shiraz, the ...
Mohammadreza Bordbar +7 more
wiley +1 more source
We confirmed the reversibility of cognitive impairment and NV decoupling in patients with ESRD after a single hemodialysis session, highlighting the potential value of NV coupling as an objective and physiologic biomarker of brain dysfunction in ESRD.
Peng Li +8 more
wiley +1 more source
Sickle Cell Disease (SCD) is a chronic inherited disorder, characterized by the presence of abnormal erythrocytes containing S hemoglobin (HbS) that leads to diverse clinical complications and special nutritional needs.
Jorginete de Jesus Damião Trevisani +7 more
doaj +1 more source
Zinc supplementation may ameliorate zinc deficiency in maintenance hemodialysis patients; however, no standard protocol has been established. This study aimed to investigate the effects of zinc acetate hydrate (ZAH) and polaprezinc (PPZ) as zinc supplements in hemodialysis patients.
Etsuko Kumagai +6 more
wiley +1 more source
Haplotipos de la hemoglobina S: importancia epidemiológica, antropológica y clínica [PDF]
La relacion entre la drepanocitosis y los diferentes haplotipos del gen que codifica la subunidad betas de la globina ha permitido llegar a entender mejor las manifestaciones clinicas de aquella enfermedad. El uso de mejores tecnicas de laboratorio permite descartar la presencia de otros factores hereditarios capaces de ocultar el verdadero genotipo ...
Walter E. Rodríguez Romero +2 more
openaire +1 more source
A flow chart was shown for the included studies. Abbreviations: PJI: periprosthetic joint infection; THA, total hip arthroplasty; TKA, total knee arthroplasty. Objective C‐reactive protein (CRP), erythrocyte sedimentation rate (ESR), plasma fibrinogen and D‐Dimer are used as diagnostic biomarkers of prosthetic joint infection (PJI) after total joint ...
Yuangang Wu +8 more
wiley +1 more source
Developing an emergency department order set to treat acute pain in sickle cell disease
Abstract Study Objective Patients with sickle cell disease (SCD) have many emergency department visits because of painful vaso‐occlusive episodes (VOE). Guidelines recommend treatment within 30 minutes of triage, but this is rarely achieved in clinical practice.
Yves Duroseau +12 more
wiley +1 more source

