OBJECTIVES: To determine whether kidney disease and hemolysis are associated with bone mass density in a population of adult Brazilian patients with sickle cell disease. INTRODUCTION: Bone involvement is a frequent clinical manifestation of sickle cell disease, and it has multiple causes; however, there are few consistent clinical associations between bone involvement and sickle cell disease. METHODS: Patients over 20 years of age with sickle cell disease who were regularly followed at the Hematology and Hemotherapy Center of Campinas, Brazil, were sorted into three groups, including those with normal bone mass density, those with osteopenia, and those with osteoporosis, according to the World Health Organization criteria. The clinical data...
Background: Pathogenetic mechanism as well as laboratory and clinical correlates of osteonecrosis in...
Background: Sickle cell anemia (SCD) is one of many haemoglobinopathic disorders which is probably t...
Female patient with past medical history of anaemia associated with multiple painful crises, charac...
Background Adult patients with sickle-cell disease (SCD) often have multiple bone compactions causin...
Background: Sickle cell anemia is the most common genetic disease in sub-Saharan Africa. It is an in...
Introdução: A doença falciforme (DF) é a hemoglobinopatia mais comum no mundo, e geralmente é assoc...
Objectives (background): Both sickle cell disease and vitamin D deficiency are common among Saudi p...
Sickle bone disease (SBD) is a chronic and invalidating complication of Sickle cell disease (SCD), a...
Texto completo: acesso restrito. p. 2037-2042Summary In sickle cell disease, erythroid hyperplasia c...
Introduction Sickle cell anemia and thalassemia result in impaired bone health in both adults and yo...
Bone mineral density (BMD) was evaluated in the proximal femora (femoral neck, Ward's triangle, and ...
Sickle cell disease (SCD) is a genetic hemoglobinopathy that has grown into a global health concern....
In sickle cell disease, erythroid hyperplasia causes trabecular destruction leading to low bone dens...
Sickle cell disease is an inherited chronic haemolytic anaemia whose clinical manifestations arise f...
Background Bone changes are common in sickle cell disease, but the pathogenesis is not fully underst...
Background: Pathogenetic mechanism as well as laboratory and clinical correlates of osteonecrosis in...
Background: Sickle cell anemia (SCD) is one of many haemoglobinopathic disorders which is probably t...
Female patient with past medical history of anaemia associated with multiple painful crises, charac...
Background Adult patients with sickle-cell disease (SCD) often have multiple bone compactions causin...
Background: Sickle cell anemia is the most common genetic disease in sub-Saharan Africa. It is an in...
Introdução: A doença falciforme (DF) é a hemoglobinopatia mais comum no mundo, e geralmente é assoc...
Objectives (background): Both sickle cell disease and vitamin D deficiency are common among Saudi p...
Sickle bone disease (SBD) is a chronic and invalidating complication of Sickle cell disease (SCD), a...
Texto completo: acesso restrito. p. 2037-2042Summary In sickle cell disease, erythroid hyperplasia c...
Introduction Sickle cell anemia and thalassemia result in impaired bone health in both adults and yo...
Bone mineral density (BMD) was evaluated in the proximal femora (femoral neck, Ward's triangle, and ...
Sickle cell disease (SCD) is a genetic hemoglobinopathy that has grown into a global health concern....
In sickle cell disease, erythroid hyperplasia causes trabecular destruction leading to low bone dens...
Sickle cell disease is an inherited chronic haemolytic anaemia whose clinical manifestations arise f...
Background Bone changes are common in sickle cell disease, but the pathogenesis is not fully underst...
Background: Pathogenetic mechanism as well as laboratory and clinical correlates of osteonecrosis in...
Background: Sickle cell anemia (SCD) is one of many haemoglobinopathic disorders which is probably t...
Female patient with past medical history of anaemia associated with multiple painful crises, charac...