| 000 | 01802cam a2200349 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 005 | 20250223030828.0 | ||
| 008 | 130427s2012 ua dh 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.He.P | ||
| 100 | 0 | _aHeba Mohamed Esmail Ahmed | |
| 245 | 1 | 0 |
_aPulmonary function assessment in pediatric patients with lysosomal storage diseases / _cHeba Mohamed Esmail Ahmed ; Supervised Mona Moustafa Elfalaki , Marian Yousry Fahmy , Aliaa Adel Ali |
| 246 | 1 | 5 | _aدراسة تقييم وظائف الرئة فى الاطفال المصابين بأمراض الاختزان الليسوسومى |
| 260 |
_aCairo : _bHeba Mohamed Esmail Ahmed , _c2012 |
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| 300 |
_a248P. : _bcharts , facsimiles ; _c25cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics | ||
| 520 | _aRespiratory problems are frequently encountered by patients with mucopolysaccharidosis due to progressive accumulation of glycoaminglycans is the airways and lungs contributing to premature mortality seen in individuals with the disease . The aim of the study is to identify the pattern of pulmonary functions in different lysosomal storage diseases and to assess the severity of lung involvement in these diseases | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _ainfant lung function tests - IOS | |
| 653 | 4 | _aLysosomal storage diseases | |
| 653 | 4 | _aMucopolysaccharidosis | |
| 700 | 0 |
_aAliaa Adel Ali , _eSupervisor |
|
| 700 | 0 |
_aMarian Yousry Fahmy , _eSupervisor |
|
| 700 | 0 |
_aMona Moustafa Elfalaki , _eSupervisor |
|
| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aNazla _eRevisor |
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| 905 |
_aSoheir _eCataloger |
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| 942 |
_2ddc _cTH |
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| 999 |
_c42784 _d42784 |
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