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

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樓主: Grant
41#
發(fā)表于 2025-3-28 17:04:24 | 只看該作者
Thalassemia and Endocrinopathies: Multicenter Study of 3092 PatientsData regarding the prevalence of endocrine dysfunction in patients with β-thalassaemia major are limited [1, 2], We report the results of a collaborative study of endocrine complications in a large series of patients with β-thalassemia major followed in pediatric and hematology departments throughout Italy.
42#
發(fā)表于 2025-3-28 22:03:08 | 只看該作者
978-88-470-2185-3Springer-Verlag Berlin Heidelberg 1995
43#
發(fā)表于 2025-3-29 00:27:13 | 只看該作者
44#
發(fā)表于 2025-3-29 04:05:49 | 只看該作者
45#
發(fā)表于 2025-3-29 08:33:24 | 只看該作者
Joanne Garde-Hansen,Hannah Gristl 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].
46#
發(fā)表于 2025-3-29 12:40:38 | 只看該作者
https://doi.org/10.1007/978-3-030-19511-3reased absorption from the gastrointestinal tract, with deleterious effects on internal organs and tissues [2, 7–9]. With modern treatment and longer survival, endocrine dysfunction assumes greater importance [1, 3–5]. This study was carried out in an attempt to correlate such dysfunction with pathologic findings in major endocrine organs.
47#
發(fā)表于 2025-3-29 18:57:25 | 只看該作者
Plasma Growth Hormone-Binding Protein and Liver Receptor in Thalassemic Patientsulin-like growth factor I (IGF.) activity is markedly reduced [1–5]. Therefore, the cause of the growth defect is likely to be at the GH receptor or post-receptor level: in either case it would lead to impairment of GH-induced generation of IGF..
48#
發(fā)表于 2025-3-29 23:36:29 | 只看該作者
49#
發(fā)表于 2025-3-29 23:53:33 | 只看該作者
50#
發(fā)表于 2025-3-30 07:07:28 | 只看該作者
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