يعرض 1 - 8 نتائج من 8 نتيجة بحث عن '"Ceylaner, Serdar"', وقت الاستعلام: 1.38s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency?

    المؤلفون: Öztürk, Gökcan, Haskoloğlu, Şule, Deveci, Nazlı, Erkmen, Hasret, Çelik, Nur Ayça, Sucak, Gülsan, Ceylaner, Serdar, İkincioğulları, Aydan, Doğu, Figen

    المصدر: Turkish Archives of Pediatrics; Jan2024, Vol. 59 Issue 1, p106-108, 3p

    مصطلحات موضوعية: DIGEORGE syndrome, PRIMARY immunodeficiency diseases, SEQUENCE analysis, DIFFERENTIAL diagnosis, REINFECTION, DEVELOPMENTAL disabilities, THROMBOPENIC purpura, BODY dysmorphic disorder, SPLEEN diseases, FLUORESCENCE in situ hybridization

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  2. 2
    دورية أكاديمية
    Maturity-onset diabetes of the young (MODY)-related genetic variants in a Turkish patient cohort with early-onset diabetes: a cross-sectional study.

    المؤلفون: Gökçay Canpolat, Asena, Keskin, Çağlar, Aydoğan, Berna İmge, Güllü, Sevim, Demir, Özgür, Şahin, Mustafa, Emral, Rıfat, Erdoğan, Murat Faik, Tonyukuk Gedik, Vedia, Çorapçıoğlu, Demet, Ceylaner, Gülay, Ceylaner, Serdar, Başkal, Nilgün

    المصدر: International Journal of Diabetes in Developing Countries; Apr2023, Vol. 43 Issue 2, p244-251, 8p

    مصطلحات موضوعية: MATURITY onset diabetes of the young, GLYCOSYLATED hemoglobin, SEQUENCE analysis, MOLECULAR diagnosis, CROSS-sectional method, GENETIC variation, GENETIC testing, AGE factors in disease, GENETIC counseling, LONGITUDINAL method, C-peptide

    مصطلحات جغرافية: TURKEY

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  3. 3
    دورية أكاديمية
    Hb Andrew-Minneapolis Variant in a Turkish Family.

    Alternate Title: Bir Türk Ailesinde Hb Andrew-Minneapolis Varyantı. (Turkish)

    المؤلفون: Sümter, Hamza, Mızrak, Soycan, Ceylaner, Serdar, Canatan, Duran

    المصدر: Turkish Journal of Hematology; 2023, Vol. 40 Issue 3, p234-235, 2p

    مصطلحات موضوعية: HEMOGLOBINS, OXYGEN, SEQUENCE analysis, BLOOD testing, RARE diseases

    مصطلحات جغرافية: TURKEY

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  4. 4
    دورية أكاديمية
    Analysis of TP53 gene in uterine myomas: No mutations but P72R polymorphism is associated with myoma development.

    المؤلفون: Altinkaya, S. Ozlem, Avcioglu, Sumeyra N., Sezer, Selda D., Ceylaner, Serdar

    المصدر: Journal of Obstetrics & Gynaecology Research; Oct2019, Vol. 45 Issue 10, p2088-2094, 7p, 3 Charts

    مصطلحات موضوعية: BLOOD collection, COMPARATIVE studies, CONFIDENCE intervals, GENETIC polymorphisms, GENOMES, HISTOLOGICAL techniques, GENETIC mutation, ONCOGENES, POPULATION geography, RISK assessment, UTERINE fibroids, UTERINE tumors, WOMEN'S health, DESCRIPTIVE statistics, SEQUENCE analysis, ODDS ratio, GENOTYPES, DISEASE risk factors

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  5. 5
    دورية أكاديمية
    A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans.

    المؤلفون: Tuhan, Hale, Ceylaner, Serdar, Nalbantoğlu, Özlem, Acar, Sezer, Abacı, Ayhan, Böber, Ece, Demir, Korcan

    المصدر: Journal of Clinical Research in Pediatric Endocrinology; Dec2017, Vol. 9 Issue 4, p371-374, 4p

    مصطلحات موضوعية: CELL receptors, HAIR, INSULIN resistance, MELANOSIS, GENETIC mutation, PHYSICAL diagnosis, PREDIABETIC state, SEVERITY of illness index, SEQUENCE analysis

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  6. 6
    دورية أكاديمية
    A 6-Month-Old Boy with Reddish, Scaly Skin: Netherton Syndrome.

    المؤلفون: Bulut, Fatma Derya, Kör, Deniz, Yılmaz, Berna Şeker, Yılmaz, Mustafa, Altıntaş, Derya Ufuk, Ceylaner, Serdar, Kılavuz, Sebile, Mungan, Neslihan Önenli

    المصدر: Journal of Pediatric Research; 2018Supplement1, Vol. 5, p54-56, 3p

    مصطلحات موضوعية: ALLERGIES, GENOMES, ICHTHYOSIS, SEQUENCE analysis, CONGENITAL ichthyosiform erythroderma

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  7. 7
    دورية أكاديمية
    Importance of DNA Sequencing for Abnormal Hemoglobins Detected by HPLC Screening.

    Alternate Title: HPLC ile Tanımlanan Anormal Hemoglobinler için DNA Dizilemenin Önemi Duran Canatan, Abdullah Çim, Serpil Delibaş, Emel Altunsoy, Serdar Ceylaner. (Turkish)

    المؤلفون: Canatan, Duran, Çim, Abdullah, Delibaş, Serpil, Altunsoy, Emel, Ceylaner, Serdar

    المصدر: Turkish Journal of Hematology; 2020, Vol. 37 Issue 2, p134-135, 2p

    مصطلحات موضوعية: HEMOGLOBINOPATHY diagnosis, BLOOD testing, HEMOGLOBINS, HIGH performance liquid chromatography, MOLECULAR diagnosis, SEQUENCE analysis

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  8. 8
    Sendromik olmayan mandibular retrognati olgularında ıgf-1 gen mutasyonu ve polimorfizmlerinin kodlandığı bölgelerin ve intron-ekzon birleşim bölgelerinin dizi analizi ile araştırılması

    المؤلفون: Öztürk, Duygu

    المساهمون: Kale Varlık, Selin, Ceylaner, Serdar, Ortodonti Anabilim Dalı

    مصطلحات موضوعية: Diş Hekimliği, Genes, Retrognathism, Dentistry, Dentists, Mutation, Sequence analysis, Mandible, Polymorphism-genetic, Insulin like growth factor I

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_____10208::b71a5002f9c4a0560d15f02522927ed5
    https://acikbilim.yok.gov.tr/handle/20.500.12812/350097

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