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SURVIVING WITH THALASSEMIA MAJOR: The Italian Experience
Pediatric Hematology and Oncology, 2007Until not long ago, the diagnosis of thalassemia major was a tragic event. Everybody in Italy knew that having the Mediterranean anemia meant living a short and unhappy life.
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Growth and puberty in thalassemia major.
Journal of pediatric endocrinology & metabolism : JPEM, 2003Present transfusional regimen protocols increase the life expectancy of patients with beta-thalassemia major, but cause a progressive iron overload that can be prevented or limited only by appropriate iron chelation. Siderosis is responsible for the clinical complications of the disease. Short stature and hypogonadism are extremely frequent in patients
RAIOLA G +7 more
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ENDOCRINE FUNCTION IN THALASSEMIA MAJOR
Annals of the New York Academy of Sciences, 1974V C, Canale +3 more
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Peripheral Neuropathy in Thalassemia Major
The Indian Journal of Pediatrics, 2018Jaya Shankar, Kaushik +5 more
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ENDOCRINE EVALUATION IN THALASSEMIA MAJOR*
Annals of the New York Academy of Sciences, 1974M N, Lassman +6 more
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Clinical Classification, Screening and Diagnosis for Thalassemia
Hematology/Oncology Clinics of North America, 2018Vip Viprakasit, Supachai Ekwattanakit
exaly
Concomitant inheritance of α-thalassemia in β°-thalassemia/hb e disease
American Journal of Hematology, 1985Pranee Winichagoon +2 more
exaly