Title, Hemoglobinopatias e talassemias. Author, Paulo César Naoum. Publisher, SARVIER, ISBN, , Length, pages. Download scientific diagram | Distribuição de hemoglobinopatias (talassemias e anemia falciforme). from publication: Análise crítica do programa de triagem. Hemoglobinopatias E Talassemias (Em Portuguese do Brasil): Paulo Cesar Naoum: Books –

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Rapid detection oh the hemoglobin C mutation by allele-specific polymerase chain reaction. Acid agar electrophoresis of human hemoglobin. The ovalbumin gene- sequence of putative control regions. Hereditary hemoglobinopathies in a population from Southeast Brazil.

Hb F levels, longevity of homozygotes and clinical course of sickle cell anemia in Brazil. hemoglobinopatuas

Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine. Stains for Inclusion Bodies. Memorandum from a W. Bonini-Domingos 1 Regina A. Entre os companheiros analisados, todos apresentaram hemoglobinas normais.


Tipos de hemoglobinas em escolares da cidade de Natal, RN. Appropriated counseling and management requires definitive diagnosis. Stains for inclusions bodies. Hereditary haemoglobin desorders in Brazil.

Beta Talassemia

The population genetics of the haemoglobinopathies. Bootstrap methods and their applications.

The cytological evaluation evidenced the presence of alpha Thalassemia. Of the total of pregnant women analysed, All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License.

Hemoglobinopathies: a study in pregnancy

The interaction of alpha- thalassemia and homozigous sickle cell disease. Hemogolbinopatias electrophoresis and quantiation of hemoglobin on cellulose acetate. Howard University Mc Graw Hill, p. Genetics services for hemoglobinopathies in Latin-America. Genetics and public healt: Estimation of small percentages of foetal haemoglobin.

Rio de Janeiro, Estimation of small percentages of foetal haemoglobin. Mortality and mobility in Jamaican adults with sickle-cell trait and with normal hemoglobin followed up for twelve years.

The clinical follow-up of the homozygotes and the hemoglobinpoatias of the heterozygotes and especially the couples at risk represent a more effective mode of acting to avoid the birth of children who are carriers of a genetic disease, that is frequently lethal. Thus, the detection of carriers of the genetic alterations is important for public health, since they represent sources of new heterozygotes and possible homozygotes.


Hereditary hemoglobins disorders in a brazilian population. Molecular basis of beta-thalassemia in Brazil. Prentice HallNew Jersey, Abnormal hemoglobins studied and counseling in Brazil. For the laboratorial diagnosis the blood samples were submitted to electrophoretic procedures in alkaline and acid pH and cytological evaluation of hemoglobin H.

The variable expression of sickle cell disease is genetically determined.