| 000 | 01732cam a2200349 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 005 | 20250223031133.0 | ||
| 008 | 150114s2014 ua d 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.G | ||
| 100 | 0 | _aSara Elsayed Abdelghani Anter | |
| 245 | 1 | 0 |
_aGonadal function in adult Egyptian thalassemic patients / _cSara Elsayed Abdelghani Anter ; Supervised Mona Mansour Abdelrahman , Nehad Mohamed Tawfeek , Nahed Mohamed Ibrahim |
| 246 | 1 | 5 | _aوظائف الغدد التناسلية فى مرضى أنيميا البحر المتوسط البالغين فى مصر |
| 260 |
_aCairo : _bSara Elsayed Abdelghani Anter , _c2014 |
||
| 300 |
_a228 P. : _bcharts ; _c25cm |
||
| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Internal Medicine | ||
| 520 | _aThalassemia 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 | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aGonadal function | |
| 653 | 4 | _aThalassemia | |
| 653 | 4 | _aThalassemic patients | |
| 700 | 0 |
_aMona Mansour Abdelrahman , _eSupervisor |
|
| 700 | 0 |
_aNahed Mohamed Ibrahim , _eSupervisor |
|
| 700 | 0 |
_aNehad Mohamed Tawfeek , _eSupervisor |
|
| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aNazla _eRevisor |
||
| 905 |
_aSamia _eCataloger |
||
| 942 |
_2ddc _cTH |
||
| 999 |
_c49133 _d49133 |
||