| 000 | 01667cam a2200349 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 005 | 20250223030649.0 | ||
| 008 | 120905s2012 ua h f m 000 0 eng d | ||
| 040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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| 041 | 0 | _aeng | |
| 049 | _aDeposite | ||
| 097 | _aM.Sc | ||
| 099 | _aCai01.11.28.M.Sc.2012.Am.A | ||
| 100 | 0 | _aAmerah Mohamed Ahmed Elshahawy | |
| 245 | 1 | 0 |
_aAcute hemolytic anemia as an initial presentation of wilson's disease / _cAmerah Mohamed Ahmed Elshahawy ; Supervised Mona Elsaid Elraziky , Mona Mohamed Hamdy , Amal Abdelhamid Ali |
| 246 | 1 | 5 | _aأنيميا إنحلال الدم الحادة كعرض أولى لمرض ويلسون |
| 260 |
_aCairo : _bAmerah Mohamed Ahmed Elshahawy , _c2012 |
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| 300 |
_a123 P. : _bfacsimiles ; _c25cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics | ||
| 520 | _aWilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism resulting in pathological accumulation of copper in many organs and tissues. Hemolytic anemia (HA) in WD occurs in up to 17% of patients at some point in time during the natural course of illness. The aim of current study was to screen for WD among children presenting HA | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aHemolytic anemia | |
| 653 | 4 | _aInitial presentation | |
| 653 | 4 | _aWilson's disease | |
| 700 | 0 |
_aAmal Abdelhamid Ali , _eSupervisor |
|
| 700 | 0 |
_aMona Elsaid Elraziky , _eSupervisor |
|
| 700 | 0 |
_aMona Mohamed Hamdy , _eSupervisor |
|
| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aNazla _eRevisor |
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| 905 |
_aSamia _eCataloger |
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| 942 |
_2ddc _cTH |
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| 999 |
_c39353 _d39353 |
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