The current management of thalassemia includes regular transfusion programs and chelation therapy. It is important that physicians be aware that endocrine abnormalities frequently develop mainly in those patients with significant iron overload due to poor compliance to treatment, particularly after the age of 10 years. Since the quality of life of thalassemia patients is a fundamental aim, it is vital to monitor carefully their growth and pubertal development in order to detect abnormalities and to initiate appropriate and early treatment. Abnormalities should be identified and treatment initiated in consultation with a pediatric or an adult endocrinologist and managed accordingly. Appropriate management shall put in consideration many fact...
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...
Abstract: It is estimated that endocrine abnormalities are present in thalasaemic patients. Despite ...
Endocrine dysfunction in Thalassaemia major (TM) is a common and disturbing complication, which requ...
Copyright © 2014 Parijat De et al. This is an open access article distributed under the Creative Com...
Background: Present transfusion protocols have increased the life expectancy of patients with β-thal...
Endocrine complications in patients with thalassemia major in developing countries may be frequent d...
PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studied to determine the e...
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 ...
AbstrAct Thalassemias are the most common genetic disorder on a wordwide basis. β-thalassemia is a s...
β-thalassaemia major (TM) is an inherited disorder of erythropoiesis requiring regular blood transfu...
Aim: Endocrinopathies are common in patients with thalassemia major (TM) and affect their life quali...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
Iron overload in patients with thalassemia major (TM) affects glucose regulation, and is mediated by...
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...
Abstract: It is estimated that endocrine abnormalities are present in thalasaemic patients. Despite ...
Endocrine dysfunction in Thalassaemia major (TM) is a common and disturbing complication, which requ...
Copyright © 2014 Parijat De et al. This is an open access article distributed under the Creative Com...
Background: Present transfusion protocols have increased the life expectancy of patients with β-thal...
Endocrine complications in patients with thalassemia major in developing countries may be frequent d...
PubMed ID: 11866338Thirty-seven patients with thalassemia major (TM) were studied to determine the e...
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 ...
AbstrAct Thalassemias are the most common genetic disorder on a wordwide basis. β-thalassemia is a s...
β-thalassaemia major (TM) is an inherited disorder of erythropoiesis requiring regular blood transfu...
Aim: Endocrinopathies are common in patients with thalassemia major (TM) and affect their life quali...
Beta-thalassemia major (TM) is among prevalent hereditary disorders imposing high expenses on health...
Iron overload in patients with thalassemia major (TM) affects glucose regulation, and is mediated by...
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...
Abstract: It is estimated that endocrine abnormalities are present in thalasaemic patients. Despite ...