Titlebook: Endocrine Disorders in Thalassemia; Physiopathological a Sebastiano Andò (Head of Endocrine Physiopathology Book 1995 Springer-Verlag Berli

Grant

書目名稱Endocrine Disorders in Thalassemia影響因子(影響力)




書目名稱Endocrine Disorders in Thalassemia影響因子(影響力)學(xué)科排名




書目名稱Endocrine Disorders in Thalassemia網(wǎng)絡(luò)公開度




書目名稱Endocrine Disorders in Thalassemia網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Endocrine Disorders in Thalassemia被引頻次




書目名稱Endocrine Disorders in Thalassemia被引頻次學(xué)科排名




書目名稱Endocrine Disorders in Thalassemia年度引用




書目名稱Endocrine Disorders in Thalassemia年度引用學(xué)科排名




書目名稱Endocrine Disorders in Thalassemia讀者反饋




書目名稱Endocrine Disorders in Thalassemia讀者反饋學(xué)科排名

Eeg332

Short-term Follow-up Study of Thyroid Function in Polytransfused Thalassemic Patientsinvestigate the evolutive trend of thyroid function with elapsing of time and its relationship with chelation therapy. We have carried out a follow0up study of thyroid function in 45 polytransfused thalassemic patients, investigated in 1988 and again in 1992.

Jejune

Spermatogenesis in Patients with β-Thalassaemia major and intermediahe assurance of greater longevity and with the prospect of future marriage. For these reasons, many new problems are emerging to challenge doctors who care for patients with thalassaemia. The purpose of this study was to evaluate the fertility potential of thalassaemic men who have achieved full sex

擁護(hù)

Long-term Follow-up of Hypothalamic-Pituitary Axis in Thalassaemic Patients with Secondary Amenorrhol data are available on secondary amenorrhoea (SA), which is a common sequela in transfusion-dependent thalassaemic patients, occurring in 15–25% of Italian thalassaemic patients [3, 13]. Similar figures are available for the United Kingdom [8].

babble

報(bào)復(fù)

Bone Mineral Content by Single- and Dual-Photon Absorptiometry in Thalassemic Patientsextramedullary hematopoiesis, hepatosplenomegaly, osteoporosis, cardiac failure, and increased susceptibility to infections contribute to the mortality and morbidity associated with the disease. Hypertransfusion therapy, although it has dramatically increased the duration and quality of life of thal

報(bào)復(fù)

Osteopenia in Thalassemic Patients with Primary and Secondary Amenorrheality of accurately measuring bone density at the level of the lumbar spine and femur has significantly improved the sensitivity of measurements in thalassemic patients with primary and secondary amenorrhea, using double X-ray absorptiometry (DXA), to investigate the incidence of osteopenia and its c

真實(shí)的人

Imaging, Ultrastructural Aspects, and Trace Elements in the Thalassemic Condrodystrophy1], According to anatomopathological standards, the group of bone diseases observed during growth are characterized by cartilaginous lesions due mainly to both premature and asymmetrical fusion of the metaphyseal cartilage, while those observed in adults are expressed by skeleteal lesions [2–4]. In

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