Abstract. Introduction: It is well known that the older generation of adult TM patients has a higher incidence of morbidities and co-morbidities. At present, little information is available on adult TM patients with multiple endocrine complications (MEC). The main objectives of this longitudinal retrospective survey were: 1) to establish the incidence and progression of MEC (3 or more) in TM patients; 2) to compare the clinical, laboratory and imaging data to a sex and age-matched group of TM patients without MEC; 3) to assess the influence of iron overload represented by serum ferritin (peak and mean annual value at the last endocrine observation). Patients and Methods: The study was started in January 1974 and was completed by the same p...
Endocrine abnormalities are amongst the most common complica-tions of b-thalassaemia major (TM). Thi...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
Background: This study aimed to estimate the prevalence of complications and in β-thalassemia patien...
PubMedID: 30657116In adult thalassemia major (TM) patients, a number of occult and emerging endocrin...
OBJECTIVE Thalassaemia major is a common and serious medical problem, worldwide. However, there are ...
Objective: Despite regular transfusions and iron-chelation therapies, endocrine complications still ...
Abstract Background Beta thalassemia major (TM) is the most common inherited genetic disorder worldw...
Abstract: It is estimated that endocrine abnormalities are present in thalasaemic patients. Despite ...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
Beta- thalassemia major is a type of inherited blood disorder, characterized by impaired synthesis...
Background: Multi-transfused thalassemia major (TM) patients frequently develop severe endocrine com...
PubMed: 24854890The endocrinological complications in ?-thalassemia major patients do affect the lif...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
Endocrine abnormalities are amongst the most common complications of b-thalassaemia major (TM). This...
Background: Multi-transfused thalassemia major (TM) patients frequently develop severe endocrine com...
Endocrine abnormalities are amongst the most common complica-tions of b-thalassaemia major (TM). Thi...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
Background: This study aimed to estimate the prevalence of complications and in β-thalassemia patien...
PubMedID: 30657116In adult thalassemia major (TM) patients, a number of occult and emerging endocrin...
OBJECTIVE Thalassaemia major is a common and serious medical problem, worldwide. However, there are ...
Objective: Despite regular transfusions and iron-chelation therapies, endocrine complications still ...
Abstract Background Beta thalassemia major (TM) is the most common inherited genetic disorder worldw...
Abstract: It is estimated that endocrine abnormalities are present in thalasaemic patients. Despite ...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
Beta- thalassemia major is a type of inherited blood disorder, characterized by impaired synthesis...
Background: Multi-transfused thalassemia major (TM) patients frequently develop severe endocrine com...
PubMed: 24854890The endocrinological complications in ?-thalassemia major patients do affect the lif...
Present chelation protocols have increased the life quality and survival of the patients with β-thal...
Endocrine abnormalities are amongst the most common complications of b-thalassaemia major (TM). This...
Background: Multi-transfused thalassemia major (TM) patients frequently develop severe endocrine com...
Endocrine abnormalities are amongst the most common complica-tions of b-thalassaemia major (TM). Thi...
OBJECTIVE: To determine the major endocrine complications present in patients of Thalassemia major p...
Background: This study aimed to estimate the prevalence of complications and in β-thalassemia patien...