This article traces out part of the history of studies of the genetic bases of thalassemia carried out in Italy. In particular it illustrates the research and discussions that between the late 1920s and the second half of the 1940s led to the description of the genetic basis of beta-thalassemia. The article encountered by Italian research, explaining why, despite the large number of thalassemia cases and data collected for this disease, Italian researchers succeeded in demonstrating its Mendelian transmission only at the same time as the US researchers
The aim of this study was to describe the changing pattern of mutational spectrum of -thalassemia (-...
The paper examines the historical vicissitudes of Genetics and Medical Genetics in the "Mezzogiorno"...
A description of the method used to detect Thalassemia traits is provided with particular reference ...
This article traces out part of the history of studies of the genetic bases of thalassemia carried o...
The essay reconstructs the antithalassemia campaign carried out by means of population screening and...
The essay reconstructs the antithalassemia campaign carried out by means of population screening and...
The β-thalassaemias are a heterogeneous group of inherited disorders of haemoglobin synthesis, all c...
Beta thalassaemia represents one of the most common autosomal recessive disorders worldwide. High pr...
The first demonstration that a specific human disease, malaria, might have a selective role in the e...
La beta thalassemia rappresenta una delle più comuni patologie autosomiche recessive nel mondo. I Pa...
Summary Fifty‐one subjects originating from Southern Italy and affected by Cooley's anaemia have bee...
Mediterranean anemia or beta-thalassemia is a hereditary syndrome characterized by a severe defect i...
After the Second World War, human genetics in Italy had to cover a gap with respect to the Internat...
The paper reconstructs the investigations and the debates on thalassemia intermedia in Italy from 19...
In our paper, we present a brief historical review of the transfusion practice, with a particular em...
The aim of this study was to describe the changing pattern of mutational spectrum of -thalassemia (-...
The paper examines the historical vicissitudes of Genetics and Medical Genetics in the "Mezzogiorno"...
A description of the method used to detect Thalassemia traits is provided with particular reference ...
This article traces out part of the history of studies of the genetic bases of thalassemia carried o...
The essay reconstructs the antithalassemia campaign carried out by means of population screening and...
The essay reconstructs the antithalassemia campaign carried out by means of population screening and...
The β-thalassaemias are a heterogeneous group of inherited disorders of haemoglobin synthesis, all c...
Beta thalassaemia represents one of the most common autosomal recessive disorders worldwide. High pr...
The first demonstration that a specific human disease, malaria, might have a selective role in the e...
La beta thalassemia rappresenta una delle più comuni patologie autosomiche recessive nel mondo. I Pa...
Summary Fifty‐one subjects originating from Southern Italy and affected by Cooley's anaemia have bee...
Mediterranean anemia or beta-thalassemia is a hereditary syndrome characterized by a severe defect i...
After the Second World War, human genetics in Italy had to cover a gap with respect to the Internat...
The paper reconstructs the investigations and the debates on thalassemia intermedia in Italy from 19...
In our paper, we present a brief historical review of the transfusion practice, with a particular em...
The aim of this study was to describe the changing pattern of mutational spectrum of -thalassemia (-...
The paper examines the historical vicissitudes of Genetics and Medical Genetics in the "Mezzogiorno"...
A description of the method used to detect Thalassemia traits is provided with particular reference ...