Ayça Aykut (Ayca Aykut)

Publication Activity (10 Years)

Years Active: 2016-2023
Publications (10 Years): 10

Top Topics

Juvenile Idiopathic Arthritis

Candida Albicans

Disease Activity

Intellectual Disability

Top Venues

Case reports in immunology

Journal of clinical research in pediatric endocrinology

Clinical case reports

Scandinavian journal of immunology

This page only lists publications with an associated author ORCID identifier.

Publications

Gulcin Aytac, Burcu Guven, Ilyas Aydin, Ezgi Topyildiz, Ayça Aykut, Asude Alpman Durmaz, Neslihan Edeer Karaca, Güzide Aksu, Necil Kütükçüler
An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission. Case reports in immunology 2023 (2023)
Gulcin Aytac, Burcu Guven, Ilyas Aydin, Ezgi Topyildiz, Ayça Aykut, Asude Alpman Durmaz, Neslihan Edeer Karaca, Güzide Aksu, Necil Kütükçüler
An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission. Case reports in immunology 2023 (2023)
Gulcin Aytac, Burcu Guven, Ilyas Aydin, Ezgi Topyildiz, Ayça Aykut, Asude Alpman Durmaz, Neslihan Edeer Karaca, Güzide Aksu, Necil Kütükçüler
An Extraordinary Case of Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED) Syndrome Misdiagnosed as Juvenile Idiopathic Arthritis on Admission. Case reports in immunology 2023 (2023)
Havva Yazıcı, Gunes Ak, Merve Yoldas Çelik, Fehime Erdem, Ayse Yuksel Yanbolu, Esra Er, Ayse Ergul Bozaci, Merve Saka Güvenç, Ayça Aykut, Asude Alpman Durmaz, Ebru Canda, Sema Kalkan Uçar, Mahmut Coker
Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form. Journal of pediatric endocrinology & metabolism : JPEM (2023)
Ayça Aykut, Asude Durmaz, Neslihan Karaca, Nesrin Gulez, Ferah Genel, Fatih Celmeli, Gulyuz Ozturk, Didem Atay, Cigdem Aydogmus, Ayca Kiykim, Guzide Aksu, Necil Kutukculer
Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variants. Scandinavian journal of immunology 95 (6) (2022)
Mehmet Burak Durmaz, Hilmi Bolat, Zehra Cengisiz, Fuat Akercan, Tuba Sözen Türk, Erhan Parıltay, Aslı Ece Solmaz, Mert Kazandi, Emin Karaca, Asude Alpman Durmaz, Ayça Aykut, Sermet Sağol, Haluk Akın, Ferda Özkınay, Ozgur Cogulu
20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey Turkish journal of medical sciences 51 (4) (2021)
Necil Kütükçüler, Ezgi Topyildiz, Afig Berdeli, Burcu Guven, Ayça Aykut, Asude Alpman Durmaz, Ozgur Cogulu, Guzide Aksu, Neslihan Edeer Karaca
Four diseases, PLAID, APLAID, FCAS3 and CVID and one gene (PHOSPHOLIPASE C, GAMMA-2; PLCG2): Striking clinical phenotypic overlap and difference. Clinical case reports 9 (4) (2021)
Asude Alpman Durmaz, Ayça Aykut, Tahir Atik, Samim Özen, Durdugül Ayyıldız Emecen, Aysun Ata, Esra Isik, Ruhsar Damla Gökşen Şimşek, Ozgur Cogulu, Ferda Özkınay
A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Semra Gürsoy, Filiz Hazan, Ayça Aykut, Özlem Nalbantoğlu, Hüseyin Anil Korkmaz, Korcan Demir, Behzat Ozkan, Ozgur Cogulu
Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature Journal of clinical research in pediatric endocrinology 12 (4) (2020)
Biray Erturk, Emin Karaca, Ayça Aykut, Mehmet Burak Durmaz, Ahmet Guler, Baris Buke, Ahmet Ozgur Yeniel, Ahmet Mete Ergenoğlu, Ferda Ozkinay, Mehmet Ozeren, Mert Kazandi, Fuat Akercan, Sermet Sagol, Cumhur Gunduz, Ozgur Cogulu
Prenatal Evaluation of MicroRNA Expressions in Pregnancies with Down Syndrome. BioMed research international 2016 (2016)