| 000 | 02021cam a2200361 a 4500 | ||
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| 003 | EG-GiCUC | ||
| 005 | 20250223030153.0 | ||
| 008 | 101601s2009 ua d f m 000 0 eng d | ||
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_aEG-GiCUC _beng _cEG-GiCUC |
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| 041 | 0 | _aeng | |
| 049 | _aDeposite | ||
| 097 | _aPh.D | ||
| 099 | _aCai01.12.04.Ph.D.2009.Az.I | ||
| 100 | 0 | _aAzza Mahamoud Abdellatef Deghaidy | |
| 245 | 1 | 0 |
_aIdentification of some different types of mucopolysaecharidoses disease in affected children in Egyptian population by biophysical and biochemical methods / _cAzza Mahamoud Abdellatef Deghaidy ; Supervised Azza Orabi , Waffaa Ahmed Khalil , Salwa Mohamed Youssef |
| 246 | 1 | 5 | _aالتعرف على بعض الانواع المختلفة لأمراض السكريات المتعددة المخاطبة فى الأطفال المصابين فى التجمعات السكانية المصرية بواسطة الطرق الفيزيائية الحيوية و الكيميائية الحيوية |
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_aCairo : _bAzza Mahamoud Abdellatef Deghaidy , _c2009 |
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_a176 Leaves : _bcharts ; _c30cm |
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| 502 | _aThesis (Ph.D.) - Cairo University - Faculty of Science - Department of Biophysics | ||
| 520 | _aMPS are inheritable disorders caused by deficiency of lysosomal enzymes. The most commonly detected clinical manifestation were coarse facies and mental retardation in all cases followed by hepatosplenomegaly, skeletal deformity, cataracts umblical hemia, heart affection and hearing affection. Our study detected increase in the activity of hyaluronidase in leukocytes in MPS patients | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aHuman-hyaluronidases sulfite oxidase | |
| 653 | 4 | _aLysosomal enzymes | |
| 653 | 4 | _aMPS | |
| 700 | 0 |
_aAzza Orabi , _eSupervisor |
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| 700 | 0 |
_aSalwa Mohamed Youssef , _eSupervisor |
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| 700 | 0 |
_aWaffaa Ahmed Khalil , _eSupervisor |
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| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 902 | _a1 | ||
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_aMustafa _eRevisor |
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| 905 |
_aSamia _eCataloger |
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| 942 |
_2ddc _cTH |
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_c29084 _d29084 |
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