Sickle Cell Anemia as the First in the Hierarchy for Cardiac Alterations, Drives Attention to the Whole Spectrum of Hemolytic Anemias. [PDF]
Arq Bras Cardiol, 2022 Chacra APM, Saldanha ALR, Martinez TLDR.
europepmc +1 more source
Differences between reference intervals of blood counts of Brazilian adults with and without sickle cell trait according to laboratory tests from the National Health Survey. [PDF]
Rev Bras Epidemiol, 2023 Sá ACMGN +4 more
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Sintomas depressivos nos pacientes internados com doença hematológica em hospital geral: prevalência e correlação com variáveis clínicas [PDF]
, 2006 Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde.
Del Moral, Joanita Angela Gonzaga
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Oxigenoterapia domiciliar prolongada em crianças e adolescentes: uma análise do uso clínico e de custos de um programa assistencial [PDF]
, 2010 Objectives: To describe the clinical and laboratory characteristics of patients on long-term home oxygen therapy followed up by the home care program of Hospital das Clinicas, School of Medicine, Universidade de São Paulo, during a period of 8 years, and
Adde, Fabiola V. +5 more
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Can We Perform the Maximal Treadmill Test on Individuals with Sickle Cell Disease? [PDF]
Arq Bras Cardiol, 2022 Ahner MM, Motta SBD, Franzoni L.
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Síndrome talasémico. Revisión Bibliográfica [PDF]
, 2016 Introducción: el síndrome talasémico es una hemoglobinopatía, es decir una alteración en la estructura de la hemoglobina (Hb), molécula proteica presente en los glóbulos rojos o eritrocitos. Esta enfermedad se caracteriza por una producción anormal de la
Peña Olivar, Irene
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Dermatology in black skin [PDF]
, 2008 This study approaches dermatology in dark skinned individuals. First, it discusses the concepts of race and ethnicity, as well as the classification criteria of the Brazilian population, indicating areas where the dark skinned people are concentrated ...
Abreu, Marilda Aparecida Milanez Morgado de +1 more
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Confirmación de variantes estructurales de hemoglobina empleando gel ácido en la tecnología Hydrasys
Medisur, 2013 Fundamento: En el Centro Nacional de Genética Médica se realiza la pesquisa de las principales anormalidades de la hemoglobina de interés clínico (HbS, HbC) a gestantes de la provincia de Artemisa con la tecnología Hydrasys utilizando geles alcalinos de ...
Jacqueline Pérez Rodríguez +4 more
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Revista Brasileira de Hematologia e Hemoterapia, 2009 A woman with homozygous sickle cell disease developed severe iron deficiency due to long-standing uterine bleeding. At this point, the serum lactic dehydrogenase level was normal and the reticulocyte count was only minimally elevated. This suggested that
Oswaldo Castro +4 more
doaj
Hematology, Transfusion and Cell TherapyObjetivo: Avaliar o perfil clínico dos pacientes com doença falciforme em estado crítico atendidos no Hemocentro Regional de Sobral, Ceará, durante os anos de 2023 e 2024, com foco na adesão ao tratamento com hidroxiuréia, a necessidade de transfusões ...
DO Fontinele +9 more
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