Works by Atik, Tahir

Results: 88
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    Evaluation of the effects of miRNAs in familial Mediterranean fever.

    Published in:
    Clinical Rheumatology, 2019, v. 38, n. 3, p. 635, doi. 10.1007/s10067-017-3914-0
    By:
    • Hortu, Hacer Orsdemir;
    • Karaca, Emin;
    • Sozeri, Betul;
    • Gulez, Nesrin;
    • Makay, Balahan;
    • Gunduz, Cumhur;
    • Atik, Tahir;
    • Tekin, Ismihan Merve;
    • Unsal, Sevket Erbil;
    • Cogulu, Ozgur
    Publication type:
    Article
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    O-09 A rare cause of acute pancreatitis: Werner Syndrome.

    Published in:
    JCEM Case Reports, 2024, v. 2, p. 1, doi. 10.1210/jcemcr/luad146.026
    By:
    • Şakar, Kenan;
    • Akıncı, Barış;
    • Yıldırım Şimşir, Ilgın;
    • Atik, Tahir;
    • Bozkurt Doğan, Ece Dilan;
    • Duman, Hatice;
    • Akbaba, Gülhan;
    • Çınar, Neşe
    Publication type:
    Article
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    Editorial.

    Published in:
    Journal of Pediatric Research, 2020, v. 7, n. 1, p. VIII
    By:
    • Atik, Tahir
    Publication type:
    Article
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    Editorial.

    Published in:
    Journal of Pediatric Research, 2019, v. 6, n. 2, p. A-IX
    By:
    • Atik, Tahir
    Publication type:
    Article
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    Editorial.

    Published in:
    Journal of Pediatric Research, 2018, v. 5, n. 2, p. 1
    By:
    • Atik, Tahir
    Publication type:
    Article
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    A cohort analysis of familial partial lipodystrophy from two Mediterranean countries.

    Published in:
    Diabetes, Obesity & Metabolism, 2024, v. 26, n. 11, p. 4875, doi. 10.1111/dom.15882
    By:
    • Fernández‐Pombo, Antía;
    • Yildirim Simsir, Ilgin;
    • Sánchez‐Iglesias, Sofía;
    • Ozen, Samim;
    • Castro, Ana I.;
    • Atik, Tahir;
    • Loidi, Lourdes;
    • Onay, Huseyin;
    • Prado‐Moraña, Teresa;
    • Adiyaman, Cem;
    • Díaz‐López, Everardo Josué;
    • Altay, Canan;
    • Ginzo‐Villamayor, Maria José;
    • Akinci, Baris;
    • Araújo‐Vilar, David
    Publication type:
    Article
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    A New Unc45a 5'utr Variant In Patients With Aagenaes Syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2025, v. 197, n. 6, p. 1, doi. 10.1002/ajmg.a.64004
    By:
    • Tan, Turkan Turkut;
    • Dogan, Yusuf Can;
    • Yilmaz, Zehra Burcu;
    • Avci Durmusalioglu, Enise;
    • Oguz, Ezgi;
    • Ayyildiz, Durdugul Emecen;
    • Isik, Esra;
    • Aydogdu, Sema;
    • Cogulu, Ozgur;
    • Atik, Tahir
    Publication type:
    Article
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    Featured Cover.

    Published in:
    Clinical Genetics, 2025, v. 107, n. 2, p. 1, doi. 10.1111/cge.14700
    By:
    • Mutlu, Mehmet Burak;
    • Karakaya, Taner;
    • Çelebi, Hamide Betül Gerik;
    • Duymuş, Fahrettin;
    • Seyhan, Serhat;
    • Yılmaz, Sanem;
    • Yiş, Uluç;
    • Atik, Tahir;
    • Yetkin, Mehmet Fatih;
    • Gümüş, Hakan
    Publication type:
    Article
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    Utility of Optical Genome Mapping in Repeat Disorders.

    Published in:
    Clinical Genetics, 2025, v. 107, n. 2, p. 188, doi. 10.1111/cge.14633
    By:
    • Mutlu, Mehmet Burak;
    • Karakaya, Taner;
    • Çelebi, Hamide Betül Gerik;
    • Duymuş, Fahrettin;
    • Seyhan, Serhat;
    • Yılmaz, Sanem;
    • Yiş, Uluç;
    • Atik, Tahir;
    • Yetkin, Mehmet Fatih;
    • Gümüş, Hakan
    Publication type:
    Article
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    Renal complications of lipodystrophy: A closer look at the natural history of kidney disease.

    Published in:
    Clinical Endocrinology, 2018, v. 89, n. 1, p. 65, doi. 10.1111/cen.13732
    By:
    • Akinci, Baris;
    • Unlu, Sadiye Mehtat;
    • Celik, Ali;
    • Simsir, Ilgin Yildirim;
    • Sen, Sait;
    • Nur, Banu;
    • Keskin, Fatma Ela;
    • Ozgen Saydam, Basak;
    • Kutbay Ozdemir, Nilufer;
    • Sarer Yurekli, Banu;
    • Ergur, Bekir Ugur;
    • Sonmez, Melda;
    • Atik, Tahir;
    • Arslan, Atakan;
    • Demir, Tevfik;
    • Altay, Canan;
    • Tunc, Ulku Aybuke;
    • Arkan, Tugba;
    • Gen, Ramazan;
    • Eren, Erdal
    Publication type:
    Article
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    Clinical and molecular spectrum along with genotype–phenotype correlation of 25 patients diagnosed with 3 M syndrome: a study from Turkey.

    Published in:
    European Journal of Pediatrics, 2025, v. 184, n. 1, p. 1, doi. 10.1007/s00431-024-05855-2
    By:
    • Akalın, Akçahan;
    • Özalkak, Şervan;
    • Yıldırım, Ruken;
    • Karakaya, Amine Aktar;
    • Kolbaşı, Barış;
    • Durmuşalioğlu, Enise Avcı;
    • Kökali, Funda;
    • Ürel-Demir, Gizem;
    • Öz, Veysel;
    • Ünal, Edip;
    • Atik, Tahir;
    • Şimşek-Kiper, Pelin Özlem;
    • Elcioglu, Nursel H.
    Publication type:
    Article
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    Biliary atresia in Turkish children.

    Published in:
    Pediatrics International, 2004, v. 46, n. 2, p. 158, doi. 10.1046/j.1442-200x.2004.01875.x
    By:
    • Aydogdu, Sema;
    • Özgenç, Funda;
    • Atik, Tahir;
    • Ünal, Fatih;
    • Tokat, Yaman;
    • Yagci, Rasit Vural
    Publication type:
    Article
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    Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome.

    Published in:
    2015
    By:
    • Atik, Tahir;
    • Koparir, Asuman;
    • Bademci, Guney;
    • Foster II, Joseph;
    • Altunoglu, Umut;
    • Mutlu, Gül Yesiltepe;
    • Bowdin, Sarah;
    • Elcioglu, Nursel;
    • Tayfun, Gulsen A.;
    • Atik, Sevinc Sahin;
    • Ozen, Mustafa;
    • Ozkinay, Ferda;
    • Alanay, Yasemin;
    • Kayserili, Hulya;
    • Thiel, Steffen;
    • Tekin, Mustafa;
    • Foster, Joseph 2nd
    Publication type:
    journal article
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    Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and their Genotype-phenotype Correlation.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2024, v. 16, n. 4, p. 431, doi. 10.4274/jcrpe.galenos.2024.2022-12-8
    By:
    • Özen, Samim;
    • Gökşen, Damla;
    • Evin, Ferda;
    • Işık, Esra;
    • Onay, Hüseyin;
    • Akgün, Bilçağ;
    • Ata, Aysun;
    • Atik, Tahir;
    • Düzcan, Füsun;
    • Özkınay, Ferda;
    • Darcan, Şükran;
    • Çoğulu, Özgür
    Publication type:
    Article
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    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.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2021, v. 13, n. 1, p. 52, doi. 10.4274/jcrpe.galenos.2020.2020.0101
    By:
    • Durmaz, Asude;
    • Aykut, Ayça;
    • Atik, Tahir;
    • Özen, Samim;
    • Emecen, Durdugül Ayyıldız;
    • Ata, Aysun;
    • Işık, Esra;
    • Gökşen, Damla;
    • Çoğulu, Özgür;
    • Özkınay, Ferda
    Publication type:
    Article
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