Turner Syndrome and Its Variants

by Semra Gürsoy, Derya Erçal
Published 2017-12-01

Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-of-Function Mutation

by Özlem Nalbantoğlu, Gülçin Arslan, Özge Köprülü, Filiz Hazan, Semra Gürsoy, Behzat Özkan
Published 2019-12-01

Autoimmunity and intestinal colonization by in patients with type 1 diabetes at the time of the diagnosis

by Semra Gürsoy, Tuba Koçkar, Sezen Ugan Atik, Zerrin Önal, Hasan Önal, Erdal Adal
Published 2018-07-01

Spectrum of Clinical Manifestations in Turkish Patients with Williams-Beuren Syndrome: A Monocentric Study

by Semra Gürsoy, Filiz Hazan, Cüneyt Zihni, Sezer Acar, Murat Muhtar Yılmazer, Timur Meşe, Behzat Özkan
Published 2021-09-01

A newborn with monosomy X in association with corpus callosum agenesis

by Duygu Onur Cura, Burcin Iscan, Semra Gursoy, Handan Guleryuz, Tufan Cankaya, Tulay Ozturk, Ozlem Giray Bozkaya
Published 2017-10-01

Detection of <italic>SHOX</italic> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature

by Semra Gürsoy, Filiz Hazan, Ayça Aykut, Özlem Nalbantoğlu, Hüseyin Anıl Korkmaz, Korcan Demir, Behzat Özkan, Özgür Çoğulu
Published 2020-12-01

The effects of epigenetic regulation on phenotypic expressivity in Turkish patients with familial Mediterranean fever

by Eser Dogan, Semra Gursoy, Giray Bozkaya, Secil Arslansoyu Camlar, Ozge Aksel Kilicarslan, Alper Soylu, Ayfer Ulgenalp, Salih Kavukcu, Ozlem Giray Bozkaya
Published 2019-01-01

Brucellosis impairs endothelial functions in chronic symptomatic patients without overt cardiac involvement

by Mustafa Ozan Gürsoy, İrfan Tursun, Mehmet Alpua, Aslı Haykır Solay, Müge Tokat Çobanlı, Hale Demirtaş, Gülten Ercan, Semra Gürsoy, Macit Kalçık, Süleyman Karakoyun, Mehmet Özkan
Published 2015-04-01

Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy

by Semra Gursoy, Esra Ataman, Bahar Toklu Baysal, Berk Özyılmaz, Pınar Gençpınar, Ayşe Semra Hız, Uluç Yiş, Aycan Ünalp, Nihal Olgaç Dündar, Ayfer Ülgenalp, Derya Erçal
Published 2020-01-01

<i>De Novo PORCN</i> and <i>ZIC2</i> Mutations in a Highly Consanguineous Family

by Laura Castilla-Vallmanya, Semra Gürsoy, Özlem Giray-Bozkaya, Aina Prat-Planas, Gemma Bullich, Leslie Matalonga, Mónica Centeno-Pla, Raquel Rabionet, Daniel Grinberg, Susanna Balcells, Roser Urreizti
Published 2021-02-01