000			01975cam a2200349 a 4500
003			EG-GiCUC
005			20250223030808.0
008			130317s2012 ua dh f m 000 0 eng d
040			_aEG-GiCUC _beng _cEG-GiCUC
041	0		_aeng
049			_aDeposite
097			_aM.Sc
099			_aCai01.11.28.M.Sc.2012.Ib.I
100	0		_aIbrahim Mohamed Osama Touny Hegazy
245	1	0	_aInterferon alpha as a diagnostic marker in Egyptian children clinically diagnosed with Aicardi Goutiėres syndrome / _cIbrahim Mohamed Osama Touny Hegazy ; Supervised Sawsan Abdelhady Hassan , Ghada Mohamed Elhossiny Abdelsalam , Marian Yousry Fahmy
246	1	5	_aالانترفيرون ألفا كدلالة تشخيصية فى الأطفال المصريين المشخصين اكلينيكيا بمتلازمة أيكاردى جوتييه
260			_aCairo : _bIbrahim Mohamed Osama Touny Hegazy , _c2012
300			_a181P. : _bcharts , facsimiles ; _c25cm
502			_aThesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics
520			_aaicardi-goutieres syndrome (AGS) is a congenital infection - like syndrome which is recently considered to be due to an underlying interferonopathy (Rice et al. 2007; crow 2011). Historically it was first described in eight children from five families in 1984 who presented with an early onset encephalopathy intracranial calcification and cerebrospinal fluid (CSF) lymphocytosis despite negative serology for infection (Aicardi and Goutiėres 1984)
530			_aIssued also as CD
653		4	_aAicardi Goutiėres syndrome
653		4	_aCongenital infection
653		4	_aIntracranial calcification
700	0		_aGhada Mohamed Elhossiny Abdelsalam , _eSupervisor
700	0		_aMarian Yousry Fahmy , _eSupervisor
700	0		_aSawsan Abdelhady Hassan , _eSupervisor
856			_uhttp://172.23.153.220/th.pdf
905			_aNazla _eRevisor
905			_aSoheir _eCataloger
942			_2ddc _cTH
999			_c42075 _d42075