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	1.	A Different SLC2A1 Gene Mutation in Glut 1 Deficiency Syndrome: c.734A>C. [electronic resource] by Çolak, Rüya Alkan Özdemir, Senem Yangın Ergon, Ezgi Kağnıcı, Mehtap Çalkavur, Şebnem Producer: 20180131 In: Balkan medical journal vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A rare vascular lesion of newborn: cutis marmorata telangiectatica congenital. [electronic resource] by Ergon, Ezgi Yangın Çelik, Kıymet Çolak, Rüya Özdemir, Senem Alkan Olukman, Özgür Kundak, Selcen Çalkavur, Şebnem Publication details: Turk pediatri arsivi 2019 In: Turk pediatri arsivi vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Abernethy Malformation Type 2 and Biliary Atresia Coexistence: A Rare Cause of Infantile Liver Transplant. [electronic resource] by Yangın-Ergon, Ezgi Ermis, Nebahat Colak, Ruya Polat, Burak Alkan-Ozdemir, Senem Yıldız, Meral Kulalı, Ferit Omur-Ecevit, Cigden Ergun, Orkan Calkavur, Sebnem Publication details: Euroasian journal of hepato-gastroenterology In: Euroasian journal of hepato-gastroenterology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Challenges in the management of an ignored cause of hyperammonemic encephalopathy: pyruvate carboxylase deficiency. [electronic resource] by Demir Köse, Melis Colak, Ruya Yangin Ergon, Ezgi Kulali, Ferit Yildiz, Meral Alkan, Senem Atilgan, Taner Aslan, Fatma Brown, Ruth Brown, Garry Serdaroğlu, Erkin Çalkavur, Sebnem Producer: 20210305 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)