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	1.	Accuracy of combined quantitative diffusion-weighted MRI and routine contrast-enhanced MRI in discrimination of benign and malignant salivary gland tumors. [electronic resource] by Nada, Ayman Hady, Dina Youssef, Ayda Mahmoud, Esmat Assad, Ramy Edward Producer: 20210315 In: The neuroradiology journal vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Glucosidase acid beta gene mutations in Egyptian children with Gaucher disease and relation to disease phenotypes. [electronic resource] by El-Morsy, Zakarya Khashaba, Mohamed T Soliman, Othman El-Sayed Yahia, Sohier El-Hady, Dina Abd Producer: 20120216 In: World journal of pediatrics : WJP vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Disruptive behavior in Down syndrome children: a cross-sectional comparative study. [electronic resource] by Yahia, Sohier El-Hadidy, Mohamed El-Gilany, Abdel-Hady Amdel-Hady, Dina Wahba, Yahya Al-Haggar, Mohammad Producer: 20151026 In: Annals of Saudi medicine vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Partial expression of ornithine transcarbamylase deficiency in an Egyptian female carrier. [electronic resource] by Al-Haggar, Mohammad Largiadèr, Carlo R Abdel-Hady, Dina Barakat, Tarik Nuoffer, Jean-Marc Al-Refaei, Abdel-Aziz Producer: 20140829 In: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children' Hospital, Mansoura, Egypt. [electronic resource] by Al-Haggar, Mohammad S Yahia, Sohier Abdel-Hady, Dina Al-Saied, Afaf Al-Kenawy, Rasha Abo-El-Kasem, Rabab Producer: 20140624 In: Indian journal of human genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature. [electronic resource] by Al-Haggar, Mohammad Ahmad, Nermin Yahia, Sohier Shams, Amany Hasaneen, Bothina Hassan Hassan, Rasha Wahba, Yahya Salem, Nanees Abdel-Badie Abdel-Hady, Dina Producer: 20130221 In: Case reports in genetics vol. 2013 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family. [electronic resource] by Al-Haggar, Mohammad Bakr, Ashraf Tajima, Toshihiro Fujieda, Kenji Hammad, Ayman Soliman, Othman Darwish, Ahmad Al-Said, Afaf Yahia, Sohier Abdel-Hady, Dina Producer: 20091027 In: Clinical and experimental nephrology vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H-syndrome. [electronic resource] by Al-Haggar, Mohammad Salem, Nanees Wahba, Yahya Ahmad, Nermin Jonard, Laurence Abdel-Hady, Dina El-Hawary, Amany El-Sharkawy, Ashraf Eid, Abdel-Rhman El-Hawary, Amira Producer: 20160217 In: Pediatric diabetes vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)