Browsing by Author "Özbek, Mehmet Nuri"
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Lethal very long-chain acyl-coa dehydrogenase deficiency with a novel mutation
Kasapkara, Çiğdem Seher; Nuoffer, Jean Marc; Baysoy, Gökhan; Aldudak, Bedri; Özbek, Mehmet Nuri; Akçaboy, Meltem; Largiader, Carlo. R. (Gazi University, 2019)Very long chain acyl-CoA dehydrogenase deficiency is an autosomal recessive genetic disorder in which the first step in the mitochondrial beta-oxidation of fatty acids for 14-20 carbons is defective. Clinical presentation ... -
Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty
Çetinkaya, Semra; Poyrazoğlu, Şükran; Baş, Firdevs; Ercan, Oya; Yıldız, Metin; Adal, Erdal; Bereket, Abdullah; Abalı, Saygın; Aycan, Zehra; Erdeve, Senay Savaş; Berberoğlu, Merih; Şıklar, Zeynep; Tayfun, Meltem; Darcan, Şükran; Mengen, Eda; Bircan, İffet; Jones, Filiz Mine Çizmecioğlu; Şimşek, Enver; Papatya, Esra Deniz; Özbek, Mehmet Nuri; Bolu, Semih; Abacı, Ayhan; Büyükinan, Muammer; Darendeliler, Feyza (Walter de Gruyter Gmbh, 2018)Background: The aim of the study was to assess the response to growth hormone (GH) treatment in very young patients with GH deficiency (GHD) through a national, multi-center study. Possible factors affecting growth response ...