000			02130cam a2200349 a 4500
003			EG-GiCUC
005			20250223031129.0
008			150104s2014 ua dh f m 000 0 eng d
040			_aEG-GiCUC _beng _cEG-GiCUC
041	0		_aeng
049			_aDeposite
097			_aM.Sc
099			_aCai01.11.18.M.Sc.2014.Sa.R
100	0		_aSalwa Hassan Ahmed Ali
245	1	0	_aRole of parathormone and altered calcium homeostasis in bone disease in Egyptian adult patients with thalassemia / _cSalwa Hassan Ahmed Ali ; Supervised Alia Abdelaziz Saad , Hala Mahmoud Fahmy , Mohamed Talaat
246	1	5	_aدراسة دور هرمون الغدة الجاردرقية و خلل نسبة الكالسيوم بالجسم على العظام فى مرضى الثلاسيما المصريين البالغين
260			_aCairo : _bSalwa Hassan Ahmed Ali , _c2014
300			_a162 P. : _bcharts , facsimiles ; _c25cm
502			_aThesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Internal Medicine
520			_aBeta Thalassemia is the most common chronic hemolytic anemia in Egypt (85.1%). Iron overload remains the biggest threat to the health of patients with thalassemia. Multi - transfused thalassaemic patients may develop severe endocrine complications due to iron overload. Etiology of bone disease in thalassemic patients is poorly understood. Number of studies has examined the effect of various conditions on the pathogenesis of bone disease including ineffective erythropoiesis, iron overload, vitamin D concentrations, and the influence of endocrinopathies. Hypopara-thyroidism was found in 7.6% of a group of thalassemic patients in Iran but 3.6 {u2013} 7% reported in Italian thalassemic patients
530			_aIssued also as CD
653		4	_aHypoparathyroidim
653		4	_aIron overload
653		4	_aThalassemia
700	0		_aAlia Abdelaziz Saad , _eSupervisor
700	0		_aHala Mahmoud Fahmy , _eSupervisor
700	0		_aMohamed Talaat , _eSupervisor
856			_uhttp://172.23.153.220/th.pdf
905			_aNazla _eRevisor
905			_aSamia _eCataloger
942			_2ddc _cTH
999			_c48994 _d48994