This study focused on clinical, hematological, and molecular aspects of sickle cell anemia pediatric patients from two different cites in Brazil. Seventy-one patients from São Paulo and Salvador, aged 3 to 18 years, were evaluated. Hematological analyses, betaS globin gene haplotypes, and alpha2 3.7kb-thalassemia were performed. Numbers of hospitalizations due to vaso-occlusive crises, infections, stroke, and cholelithiasis were investigated. São Paulo had more hospitalizations from vaso-occlusion, cholelithiasis, and stroke than Salvador. The Ben/CAR genotype predominated in both cities. alpha2 3.7kb-thalassemia had a frequency of 28.2% in Salvador, mostly with Ben/CAR genotype (45.0%), while São Paulo had 22.5% with similar frequencies of...
Immigrants from many parts of the world settled in Paraná State in Brazil, contributing to the diver...
Foram analisados 47 pacientes com diagnóstico clínico, laboratorial e molecular de anemia falciforme...
A Hemocromatose Hereditária (HH) é uma doença autossômica recessiva. As mutações C282Y e H63D no gen...
Sickle cell disease is a Public Health problem in Brazil where hemoglobin S has been found in a freq...
This study focused on clinical, hematological, and molecular aspects of sickle cell anemia pediatric...
doença SC é muito prevalente no Brasil, principalmente na Bahia, sendo que os pacientes apresentam a...
Beta S-globin gene (βS-globin) haplotypes, markers for severe sickle cell anemia (SCA), and the alph...
OBJECTIVE: To describe clinical events of sickle cell disease and the correlation with β-globin...
β s haplotypes were studied in 47 non-related patients with sickle-cell anemia from the state of Rio...
p. 621-625Beta S-globin gene (βS-globin) haplotypes, markers for severe sickle cell anemia (SCA), an...
To compare the features of sickle-cell anemia in Brazil with those in other locales, we studied the ...
The beta(S)-globin haplotypes were studied in 78 sickle cell Brazilian patients from Bahia, Northeas...
A anemia falciforme e geneticamente determinada pela homozigose (SS) da hemoglobina S, em consequenc...
Brazil was the country that received the largest number of Africans during the time of colonization,...
Haplotypes linked to the βS gene represent patterns of DNA polymorphisms along chromosome 11 of ind...
Immigrants from many parts of the world settled in Paraná State in Brazil, contributing to the diver...
Foram analisados 47 pacientes com diagnóstico clínico, laboratorial e molecular de anemia falciforme...
A Hemocromatose Hereditária (HH) é uma doença autossômica recessiva. As mutações C282Y e H63D no gen...
Sickle cell disease is a Public Health problem in Brazil where hemoglobin S has been found in a freq...
This study focused on clinical, hematological, and molecular aspects of sickle cell anemia pediatric...
doença SC é muito prevalente no Brasil, principalmente na Bahia, sendo que os pacientes apresentam a...
Beta S-globin gene (βS-globin) haplotypes, markers for severe sickle cell anemia (SCA), and the alph...
OBJECTIVE: To describe clinical events of sickle cell disease and the correlation with β-globin...
β s haplotypes were studied in 47 non-related patients with sickle-cell anemia from the state of Rio...
p. 621-625Beta S-globin gene (βS-globin) haplotypes, markers for severe sickle cell anemia (SCA), an...
To compare the features of sickle-cell anemia in Brazil with those in other locales, we studied the ...
The beta(S)-globin haplotypes were studied in 78 sickle cell Brazilian patients from Bahia, Northeas...
A anemia falciforme e geneticamente determinada pela homozigose (SS) da hemoglobina S, em consequenc...
Brazil was the country that received the largest number of Africans during the time of colonization,...
Haplotypes linked to the βS gene represent patterns of DNA polymorphisms along chromosome 11 of ind...
Immigrants from many parts of the world settled in Paraná State in Brazil, contributing to the diver...
Foram analisados 47 pacientes com diagnóstico clínico, laboratorial e molecular de anemia falciforme...
A Hemocromatose Hereditária (HH) é uma doença autossômica recessiva. As mutações C282Y e H63D no gen...