OBJECTIVE Thalassaemia major is a common and serious medical problem, worldwide. However, there are few data concerning the various endocrine disorders which occur in this condition. We have surveyed 25 Italian centres in order to establish the prevalences and times of onset of endocrine disorders in patients with beta-thalasaemia major. PROJECT AND PATIENTS A questionnaire specifically designed to investigate the prevalences of endocrinopathies was sent to 25 paediatric and haematology departments. The following data were recorded in the questionnaire: sex, age, height and weight, pubertal status according to Tanner's classification, history of secondary amenorrhoea, type of endocrinopathy and hormone levels at diagnosis, associated compli...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
Endocrine abnormalities are amongst the most common complica-tions of b-thalassaemia major (TM). Thi...
The current management of thalassemia includes regular transfusion programs and chelation therapy. I...
OBJECTIVE Thalassaemia major is a common and serious medical problem, worldwide. However, there are ...
Abstract. Introduction: It is well known that the older generation of adult TM patients has a higher...
PubMed: 24854890The endocrinological complications in ?-thalassemia major patients do affect the lif...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
PubMedID: 30657116In adult thalassemia major (TM) patients, a number of occult and emerging endocrin...
Abstract Background Beta thalassemia major (TM) is the most common inherited genetic disorder worldw...
Aim: Endocrinopathies are common in patients with thalassemia major (TM) and affect their life quali...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Endocrine complications in patients with thalassemia major in developing countries may be frequent d...
WOS: 000174189100011PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studie...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studied to determine the e...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
Endocrine abnormalities are amongst the most common complica-tions of b-thalassaemia major (TM). Thi...
The current management of thalassemia includes regular transfusion programs and chelation therapy. I...
OBJECTIVE Thalassaemia major is a common and serious medical problem, worldwide. However, there are ...
Abstract. Introduction: It is well known that the older generation of adult TM patients has a higher...
PubMed: 24854890The endocrinological complications in ?-thalassemia major patients do affect the lif...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
PubMedID: 30657116In adult thalassemia major (TM) patients, a number of occult and emerging endocrin...
Abstract Background Beta thalassemia major (TM) is the most common inherited genetic disorder worldw...
Aim: Endocrinopathies are common in patients with thalassemia major (TM) and affect their life quali...
Abstract Background The combination of transfusion and chelation therapy has dramatically extended t...
Endocrine complications in patients with thalassemia major in developing countries may be frequent d...
WOS: 000174189100011PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studie...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studied to determine the e...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
Endocrine abnormalities are amongst the most common complica-tions of b-thalassaemia major (TM). Thi...
The current management of thalassemia includes regular transfusion programs and chelation therapy. I...