Hasil Pencarian - Atil Bisgin

Perbaiki Hasil
  1. 1
    Epilepsi ve anlıksal yetiyitimi olan hastalarda moleküler karyotiplemenin klinik yararı

    Epilepsi ve anlıksal yetiyitimi olan hastalarda moleküler karyotiplemenin klinik yararı oleh Atıl BİŞGİN, Sevcan TUĞ BOZDOĞAN

    Diterbitkan 2018-12-01
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  2. 2
    Nadir görülen iki genetik bozukluğun bir arada bulunması: bir çocukta kistik fibroz ve subkortikal kistleri olan megalensefalik lökoensefalopati

    Nadir görülen iki genetik bozukluğun bir arada bulunması: bir çocukta kistik fibroz ve subkortikal kistleri olan megalensefalik lökoensefalopati oleh Faruk INCECİK, Mustafa YILMAZ, Atıl BİŞGİN

    Diterbitkan 2019-12-01
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  3. 3
    Mitochondrial membrane protein–associated neurodegeneration: A case series of six children

    Mitochondrial membrane protein–associated neurodegeneration: A case series of six children oleh Faruk Incecik, Ozlem M Herguner, Atil Bisgin

    Diterbitkan 2020-01-01
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  4. 4
    Tıbbi genetik uygulamalarında altın standart fenomiks: tüm ekzom analizi yapılan 3 nörogenetik hasta örneği

    Tıbbi genetik uygulamalarında altın standart fenomiks: tüm ekzom analizi yapılan 3 nörogenetik hasta örneği oleh Sevcan Tuğ Bozdoğan, Ibrahım Boga, Atıl Bişgin

    Diterbitkan 2021-06-01
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  5. 5
    Identification of a novel homozygous variant in the alkaline phosphate (ALPL) gene associated with hypophosphatasia

    Identification of a novel homozygous variant in the alkaline phosphate (ALPL) gene associated with hypophosphatasia oleh Atil Bisgin, Ibrahim Boga, Cihan Cetin, Selim Buyukkurt

    Diterbitkan 2020-09-01
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  6. 6
    IL-8, IL-10, TGF-β, and GCSF Levels Were Increased in Severe Persistent Allergic Asthma Patients with the Anti-IgE Treatment

    IL-8, IL-10, TGF-β, and GCSF Levels Were Increased in Severe Persistent Allergic Asthma Patients with the Anti-IgE Treatment oleh Arzu D. Yalcin, Atil Bisgin, Reginald M. Gorczynski

    Diterbitkan 2012-01-01
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  7. 7
    The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID)

    The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID) oleh Atil Bisgin, Ozge Sonmezler, Ibrahim Boga, Mustafa Yilmaz

    Diterbitkan 2021-04-01
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  8. 8
    IL7R GEN MUTASYON VE POLİMORFİZMLARİNİN AĞIR KOMBİNE İMMUN YETMEZLİKLİ HASTALARDAKİ SIKLIĞI

    IL7R GEN MUTASYON VE POLİMORFİZMLARİNİN AĞIR KOMBİNE İMMUN YETMEZLİKLİ HASTALARDAKİ SIKLIĞI oleh Derya Ufuk Altıntaş, Mustafa Yılmaz, İbrahim Boğa, Atıl Bişgin

    Diterbitkan 2018-08-01
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  9. 9
    Serum lubricin levels in patients with juvenile idiopathic arthritis

    Serum lubricin levels in patients with juvenile idiopathic arthritis oleh Rabia Miray Kisla Ekinci, Sibel Balcı, Fatma Coban, Atıl Bisgin

    Diterbitkan 2021-12-01
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  10. 10
    Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene

    Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene oleh Olgu Hallioglu Kilinc, Dilek Giray, Atil Bisgin, Sevcan Tug Bozdogan, Derya Karpuz

    Diterbitkan 2017-07-01
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  11. 11
    The contribution of diet preference to the disease course in children with familial Mediterranean fever: a cross-sectional study

    The contribution of diet preference to the disease course in children with familial Mediterranean fever: a cross-sectional study oleh Rabia Miray Kisla Ekinci, Sibel Balcı, Atıl Bisgin, Fatma Cetin, Gokhan Tumgor

    Diterbitkan 2020-04-01
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  12. 12
    The cumulative effects of MEFV gene polymorphisms and mutations in patients with inflammatory bowel diseases

    The cumulative effects of MEFV gene polymorphisms and mutations in patients with inflammatory bowel diseases oleh Mehmet Agin, Atil Bisgin, Mustafa Yilmaz, Aylin Kont Ozhan, Ferid Mammadov, Gokhan Tumgor

    Diterbitkan 2020-10-01
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  13. 13
    Konjenital glukoz galaktoz malabsorbsiyonu sendromunda yeni bir mutasyon

    Konjenital glukoz galaktoz malabsorbsiyonu sendromunda yeni bir mutasyon oleh Mehmet Satar, Mustafa Akçalı, Hacer Yapıcıoğlu Yıldızdaş, Ferda Özlü, Mehmet Ağın, Gökhan Tümgör, Atıl Bişgin

    Diterbitkan 2018-12-01
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  14. 14
    Different clinical manifestations of three prime repair exonuclease 1 mutation: A case series

    Different clinical manifestations of three prime repair exonuclease 1 mutation: A case series oleh Faruk Incecik, Sibel Balci, Rabia Miray Kisla Ekinci, Ozlem M Herguner, Atil Bisgin, Mustafa Yilmaz

    Diterbitkan 2020-01-01
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  15. 15
    Autosomal Dominant Polycystic Disease is Associated with Depressed Levels of Soluble Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand

    Autosomal Dominant Polycystic Disease is Associated with Depressed Levels of Soluble Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand oleh Funda Sarı, Arzu Didem Yalçın, Gizem Esra Genç, Metin Sarıkaya, Atıl Bisgin, Ramazan Çetinkaya, Saadet Gümüşlü

    Diterbitkan 2016-10-01
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  16. 16
    Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey

    Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey oleh Rabia Miray Kışla Ekinci, Fatih Gürbüz, Sibel Balcı, Atıl Bişgin, Mehmet Taştan, Bilgin Yüksel, Mustafa Yılmaz

    Diterbitkan 2019-03-01
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  17. 17
    Henoch Schönlein Purpurası tanılı çocuklarda Kompleman C2 gen polimorfizmleri

    Henoch Schönlein Purpurası tanılı çocuklarda Kompleman C2 gen polimorfizmleri oleh Rabia Miray KİSLA EKİNCİ, Sibel BALCİ, Bahriye ATMİS, Aysun KARABAY BAYAZİT, Dilek DOGRUEL, Derya Ufuk ALTİNTAS, Atil BİSGİN

    Diterbitkan 2020-03-01
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  18. 18
    An Updated Review on the Role of Nanoformulated Phytochemicals in Colorectal Cancer

    An Updated Review on the Role of Nanoformulated Phytochemicals in Colorectal Cancer oleh Alakesh Das, Suman Adhikari, Dikshita Deka, Nabajyoti Baildya, Padmavati Sahare, Antara Banerjee, Sujay Paul, Atil Bisgin, Surajit Pathak

    Diterbitkan 2023-03-01
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  19. 19
    Gender Identity and Assignment Recommendations in Disorders of Sex Development Patients: 20 Years’ Experience and Challenges

    Gender Identity and Assignment Recommendations in Disorders of Sex Development Patients: 20 Years’ Experience and Challenges oleh Fatih Gürbüz, Murat Alkan, Gonca Çelik, Atıl Bişgin, Necmi Çekin, İlker Ünal, Ali Kemal Topaloğlu, Ünal Zorludemir, Ayşe Avcı, Bilgin Yüksel

    Diterbitkan 2020-12-01
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  20. 20
    Morquio A syndrome and effect of enzyme replacement therapy in different age groups of Turkish patients: a case series

    Morquio A syndrome and effect of enzyme replacement therapy in different age groups of Turkish patients: a case series oleh Sebile Kılavuz, Sibel Basaran, Deniz Kor, Fatma Derya Bulut, Sevcan Erdem, Hüseyin Tuğsan Ballı, Muhammed Dağkıran, Atil Bisgin, Halise Neslihan Önenli Mungan

    Diterbitkan 2021-03-01
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