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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
Published 2018-02-01Get full text
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Assessing fatigue and related factors in adolescents with familial Mediterranean fever (FMF): psychometric properties of the PedsQL Multidimensional Fatigue Scale by Devrim Can Saraç, Ece Pastutmaz, Sena Kongur, Cennet Hanım Karakurt, İdil Akar, İsrafil İnanç, Özge Altuğ Gücenmez, Belde Kasap Demir, Serkan Metin, Deniz Bayraktar
Published 2023-08-01Get full text
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The outcomes of renin-angiotensin-aldosterone system inhibition and immunosuppressive therapy in children with X-linked Alport syndrome by Gülşah Özdemir, Fehime Kara Eroğlu, Belde Kasap Demir, Selçuk Yüksel, Yılmaz Tabel, Ayşe Ağbaş, Ali Düzova, Mutlu Hayran, Fatih Özaltın, Aysun Karabay Bayazıt, Alev Yılmaz, Oğuz Söylemezoğlu, Bora Gülhan, Eda Didem Kurt-Şükür, Emine Atayar, Raziye Atan, İsmail Dursun, Zeynep Birsin Özçakar, Seha Saygılı, Alper Soylu, Rezan Topaloğlu
Published 2023-06-01Get full text
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