The essay reconstructs the antithalassemia campaign carried out by means of population screening and pre-marriage counseling for about twenty years in Italy, immediately after the relationship between microcythemia and Cooley's anemia had been established, as well as its genetic bases. We examine the Italian contributions to the understanding of the genetics and of the clinical treatment of thalassemic disorders, and analyze the approaches to prevention as well as the results obtained by the first campaign against a genetic disease, conceived and largely implemented in Italy by Ezio Silvestroni and Ida Bianco. We discuss the resistances met by the antithalassemia campaign due to the cultural and organizational backwardness of the Italian me...
Initially focused above all on the cases of Great Britain, the United States and Germany, the histor...
The articles collected in this special section of «Popolazione e Storia» take stock of the results o...
To reduce the incidence of β-thalassaemia major and other severe haemoglobin-related disorders by th...
The essay reconstructs the antithalassemia campaign carried out by means of population screening and...
Mediterranean anemia or beta-thalassemia is a hereditary syndrome characterized by a severe defect i...
This article traces out part of the history of studies of the genetic bases of thalassemia carried o...
This article traces out part of the history of studies of the genetic bases of thalassemia carried o...
The thalassemias are among the most common inherited diseases worldwide, affecting individuals origi...
The incidence of β-thalassemia in Sardinia is high and β-39 is the most common mutation. The prevent...
International audienceThe role of natural selection in maintaining the thalassemia polymorphism is e...
Recent developements of molecular biology and genetic of thalassemia syndromes are discussed with s...
Beta thalassaemia represents one of the most common autosomal recessive disorders worldwide. High pr...
The paper reconstructs the investigations and the debates on thalassemia intermedia in Italy from 19...
The role of natural selection in maintaining the thalassemia polymorphism is examined in a southern ...
La beta thalassemia rappresenta una delle più comuni patologie autosomiche recessive nel mondo. I Pa...
Initially focused above all on the cases of Great Britain, the United States and Germany, the histor...
The articles collected in this special section of «Popolazione e Storia» take stock of the results o...
To reduce the incidence of β-thalassaemia major and other severe haemoglobin-related disorders by th...
The essay reconstructs the antithalassemia campaign carried out by means of population screening and...
Mediterranean anemia or beta-thalassemia is a hereditary syndrome characterized by a severe defect i...
This article traces out part of the history of studies of the genetic bases of thalassemia carried o...
This article traces out part of the history of studies of the genetic bases of thalassemia carried o...
The thalassemias are among the most common inherited diseases worldwide, affecting individuals origi...
The incidence of β-thalassemia in Sardinia is high and β-39 is the most common mutation. The prevent...
International audienceThe role of natural selection in maintaining the thalassemia polymorphism is e...
Recent developements of molecular biology and genetic of thalassemia syndromes are discussed with s...
Beta thalassaemia represents one of the most common autosomal recessive disorders worldwide. High pr...
The paper reconstructs the investigations and the debates on thalassemia intermedia in Italy from 19...
The role of natural selection in maintaining the thalassemia polymorphism is examined in a southern ...
La beta thalassemia rappresenta una delle più comuni patologie autosomiche recessive nel mondo. I Pa...
Initially focused above all on the cases of Great Britain, the United States and Germany, the histor...
The articles collected in this special section of «Popolazione e Storia» take stock of the results o...
To reduce the incidence of β-thalassaemia major and other severe haemoglobin-related disorders by th...