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1

Blue-colored sweating: four infants with apocrine chromhidrosis by Ahmet Yöntem, Deniz Kör, Bircan Hızlı-Karabacak, Mehmet Karakaş, Neslihan Önenli-Mungan

Published 2015-06-01

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2

p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency by Berna Şeker-Yılmaz, Deniz Kör, Gökhan Tümgör, Serdar Ceylaner, Neslihan Önenli-Mungan

Published 2017-06-01

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3

X-linked adrenoleukodystrophy in a 6-year-old boy initially presenting with psychiatric symptoms by Faruk İncecik, M Özlem Hergüner, Gülen Mert, Neslihan Önenli-Mungan, Serdar Ceylaner, Deniz Kör, Şakir Altunbaşak

Published 2014-12-01

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4

Clinical features of 27 Turkish Propionic acidemia patients with 12 novel mutations by Deniz Kör, Berna Şeker-Yılmaz, Fatma Derya Bulut, Sebile Kılavuz, Murat Öktem, Serdar Ceylaner, Dinçer Yıldızdaş, Neslihan Önenli-Mungan

Published 2019-06-01

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5

Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations by Berna Şeker-Yılmaz, Deniz Kör, Fatma Derya Bulut, Bilgin Yüksel, Aysun Karabay-Bayazıt, Ali Kemal Topaloğlu, Gülay Ceylaner, Neslihan Önenli-Mungan

Published 2017-08-01

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6

Genotypic and phenotypic features of the cystinosis patients from the South Eastern part of Turkey by Neslihan Önenli-Mungan, Bilgin Yüksel, Ali Kemal Topaloğlu, Berna Şeker-Yılmaz, Gülay Ceylaner, Aytül Noyan, Sevgi Yavuz, Nurcan Cengiz, Aysun Karabay-Bayazıt, Deniz Kör, Ali Anarat

Published 2016-08-01

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