Results 21 to 30 of about 77,175 (212)
International Journal of Nephrology, Volume 2023, Issue 1, 2023., 2023 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
Demetra, 2014 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
Haplotipos de la hemoglobina S: importancia epidemiológica, antropológica y clínica [PDF]
Revista Panamericana de Salud Pública, 1998 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
Orthopaedic Surgery, Volume 14, Issue 11, Page 2987-2994, November 2022., 2022 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
Journal of the American College of Emergency Physicians Open, Volume 2, Issue 4, August 2021., 2021 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
Association of serum selenium with anemia‐related indicators and risk of anemia
Food Science &Nutrition, Volume 9, Issue 6, Page 3039-3047, June 2021., 2021 Higher serum selenium is associated with an increased serum iron level, MCHC, and hemoglobin level and a decreased risk of anemia. Due to the narrow physiological range of selenium, the relationships between selenium‐ and anemia‐related indicators and risk of anemia were nonlinear.
Qing Zhou +4 more
wiley +1 more source
Ocorrência de hemoglobina S no estado de Mato Grosso do Sul, Brasil [PDF]
Jornal Brasileiro de Patologia e Medicina Laboratorial, 2008 INTRODUCAO: As hemoglobinopatias sao as alteracoes geneticas mais comuns no homem, sendo a hemoglobina (Hb) S a mais frequente entre todas. Sua ocorrencia no estado de Mato Grosso do Sul ainda nao foi sistematicamente avaliada. OBJETIVOS: Caracterizar a ocorrencia de Hb S por genotipos, sexo, idade no momento do diagnostico, indice de cobertura e ...
Holsbach, Denise Rodrigues +4 more
openaire +3 more sources
Anemias ferropénicas asociadas a hemoglobinopatías en comunidades afrodescendientes en Colombia
NOVA, 2018 Objetivo. Determinar la presencia de anemias ferropénicas asociadas a hemoglobinopatías en afrodescendientes adultos colombianos habitantes de la ciudad de Tumaco, en el Departamento de Nariño y residentes de la localidad de Engativá, en Bogotá ...
Martha Castillo Bohórquez +2 more
doaj +1 more source
ACOMPANHAMENTO AMBULATORIAL DE PACIENTE COM HEMOGLOBINA VARIANTE KORLE-BU: RELATO DE CASO
Hematology, Transfusion and Cell Therapy, 2023 Introdução: As hemoglobinas (Hb) variantes ocorrem devido às trocas de aminoácidos na sequência genética da globina, levando à alterações físicas e funcionais.
GB Barroso +5 more
doaj +1 more source
Importância dos programas de triagem para o gene da hemoglobina S [PDF]
Revista Brasileira de Hematologia e Hemoterapia, 2007 A anemia falciforme caracteriza-se como quadro hemolitico hereditario que evolui cronicamente causando danos fisicos e emocionais as pessoas acometidas. Ate o presente momento nao se dispoe de tratamento curativo, a nao ser o transplante de medula ossea, que ainda tem sido realizado de maneira experimental.
Bandeira, Flávia M. G. C. +5 more
openaire +3 more sources