Gonadal function in adult Egyptian thalassemic patients / Sara Elsayed Abdelghani Anter ; Supervised Mona Mansour Abdelrahman , Nehad Mohamed Tawfeek , Nahed Mohamed Ibrahim
Material type:
TextLanguage: English Publication details: Cairo :  Sara Elsayed Abdelghani Anter ,  2014Description: 228 P. :  charts ;  25cmOther title: - وظائف الغدد التناسلية فى مرضى أنيميا البحر المتوسط البالغين فى مصر [Added title page title]
 
- Issued also as CD
 
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                        قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.18.M.Sc.2014.Sa.G (Browse shelf(Opens below)) | Not for loan | 01010110064392000 | ||
                            
                                
                                     
                                
                            
                            CD - Rom
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                        مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.18.M.Sc.2014.Sa.G (Browse shelf(Opens below)) | 64392.CD | Not for loan | 01020110064392000 | 
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| Cai01.11.18.M.Sc.2014.Re.E Effects of supplementation with ergocalciferol on vitamin D level in hemodialysis patients / | Cai01.11.18.M.Sc.2014.Re.E Effects of supplementation with ergocalciferol on vitamin D level in hemodialysis patients / | Cai01.11.18.M.Sc.2014.Sa.G Gonadal function in adult Egyptian thalassemic patients / | Cai01.11.18.M.Sc.2014.Sa.G Gonadal function in adult Egyptian thalassemic patients / | Cai01.11.18.M.Sc.2014.Sa.R Role of parathormone and altered calcium homeostasis in bone disease in Egyptian adult patients with thalassemia / | Cai01.11.18.M.Sc.2014.Sa.R Role of parathormone and altered calcium homeostasis in bone disease in Egyptian adult patients with thalassemia / | Cai01.11.18.M.Sc.2014.Sa.S Study of the relation between subclinical hypothyroidism and diabetic microvascular complications / | 
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Internal Medicine
Thalassemia is an inherited autosomal recessive blood disorder. Early and regular blood transfusion therapy in patients with homozygous Ý- thalassemia decreases the complications of sever anemia and prolongs suvival but the beneficial effects of trausfusion are limited by organ damage from iron overload. Well chelated patients are fertile. Non chelated patients suffer from hypogonadism
Issued also as CD
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