A novel OCRL1 gene mutation in a Turkish child with Lowe syndrome by Ali Kanık, Belde Kasap-Demir, Rüya Ateşli, Kayı Eliaçık, Onder Yavaşcan, Mehmet Helvacı

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A Childhood Inflammatory Myopathy with Cytochrome Oxidase Deficiency: Which Came First, the Chicken or the Egg? by Gülden Diniz, Önder Yavaşcan, Ümit Başak Şarkış, Zübeyde Yıldırım, Caner Alparslan, Can Öztürk, Afig Berdeli

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Recurrent debilitating calf pain associated with fasciitis in Familial Mediterranean fever and response to canacinumab by Belde Kasap Demir, Demet Alaygut, Caner Alparslan, Eren Soyaltın, Fatma Mutlubaş, Seçil Arslansoyu Çamlar, Önder Yavaşcan

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A partial response to abatacept in a patient with steroid resistant focal segmental glomerulosclerosis by Eren Soyaltın, Belde Kasap Demir, Caner Alparslan, Seçil Arslansoyu Çamlar, Demet Alaygut, Önder Yavaşcan, Fatma Mutlubaş

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Henoch-Schönlein purpura in children from western Turkey: a retrospective analysis of 430 cases by Murat Anil, Nejat Aksu, Orhan Deniz Kara, Alkan Bal, Ayşe Berna Anil, Onder Yavaşcan, Binnur Un

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A rare cause of neonatal hypertension: Congenital mesoblastic nephroma by Eren Soyaltın, Demet Alaygut, Caner Alparslan, Tunç Özdemir, Seçil Arslansoyu- Çamlar, Fatma Mutlubaş, Belde Kasap-Demir, Önder Yavaşcan

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A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings by Caner Alparslan, Elif Perihan Öncel, Sinem Akbay, Demet Alaygut, Fatma Mutlubaş, Mansur Tatlı, Martin Konrad, Önder Yavaşcan, Belde Kasap-Demir

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Toilet training age and influencing factors: a multicenter study by Hüseyin Tarhan, Yusuf Özlem İlbey, Özlem Özkarakaş, Feyza Koç, Selma Cun, Fatma Mutlubaş Özsan, Önder Yavaşcan, Nejat Aksu, Mehmet Helvacı, Derya Uzelli, Sıtkı Ün, Rahmi Gökhan Ekin, İlker Akarken, Özgür Çakmak, Ferruh Zorlu

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