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Homozygous PGAP2 mutation cause hyperphosphatasia with mental retardation syndrome-3 (HPMRS3): Genetic and clinical evaluation of the ultra rare inherited glycosylphosphatidylinosi... von Küçükçongar Yavaş, Aynur, Özbey, Sümeyra Zeynep, Ergin, Bora, Ünal, Yasemin, Bilginer Gürbüz, Berrak, Karaatmaca, Betül, Özyürek, Hamit, Oflaz, Ofcan, Basan, Hacer, Kasapkara, Çiğdem Seher

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Coronary flow reserve is impaired in patients with nonalcoholic fatty liver disease: Association with liver fibrosis von Yilmaz, Yusuf, Kurt, Ramazan, Yonal, Oya, Polat, Nihat, Celikel, Cigdem Ataizi, Gurdal, Ahmet, Oflaz, Huseyin, Ozdogan, Osman, Imeryuz, Nese, Kalayci, Cem, Avsar, Erol

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Secondary Hemophagocytosis in Propionic Acidemia von Kasapkara, Cigdem Seher, Kangin, Murat, Oflaz Ozmen, Banu, Ozbek, Mehmet Nuri, Demir, Remezan, Karatas, Mustafa, Tumer, Leyla, Ezgu, Fatih Suhey, Hasanoglu, Alev

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Kadın Sınıf Öğretmenlerinin Mesleki Tükenmişlik Düzeylerinin İncelenmesi von İnanç, Çiğdem, Gezgüç, Kamile, Başal, Murat, Yılmaz, Hülya, Oflaz, Neslihan, Kaya, Büşra

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