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1دورية أكاديمية
المؤلفون: Merih Ozgen, Didem Turgut Cosan, Fulya Doganer, Ahu Soyocak, Onur Armagan, Hasan Veysi Gunes, Irfan Degirmenci, Gulsah Ogutler Ozkara, Fezan Sahin Mutlu
المصدر: Clinics, Vol 67, Iss 11, Pp 1299-1302 (2012)
مصطلحات موضوعية: Osteoporosis, Polymorphism, Plasminogen Activator Inhibitor Type-1 (PAI-1) Gene, Bone Mineral Density, Turkish Women, Medicine (General), R5-920
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Toksoz, Fatma, Acikgoz, Ayfer, Mutlu, Fezan Sahin, Sayik, Dilek
المصدر: In Journal of Pediatric Nursing November-December 2023 73:e509-e515
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3دورية أكاديمية
المؤلفون: Akay, Olga Meltem, Aras, Beyhan Durak, Isiksoy, Serap, Toprak, Cigdem, Mutlu, Fezan Sahin, Artan, Sevilhan, Oner, Ulku, Gulbas, Zafer
المصدر: In Cancer Genetics March 2014 207(3):87-93
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4دورية أكاديمية
المصدر: In Transfusion and Apheresis Science June 2013 48(3):387-390
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5دورية أكاديمية
المؤلفون: Ozgen, Merih, Cosan, Didem Turgut, Doganer, Fulya, Soyocak, Ahu, Armagan, Onur, Gunes, Hasan Veysi, Degirmenci, Irfan, Ozkara, Gulsah Ogutler, Mutlu, Fezan Sahin
المصدر: Clinics. November 2012 67(11)
مصطلحات موضوعية: Osteoporosis, Polymorphism, Plasminogen Activator Inhibitor Type-1 (PAI-1) Gene, Bone Mineral Density, Turkish Women
وصف الملف: text/html
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المؤلفون: Ferdi Köşger, Fezan Sahin, Didem Turgut Coşan, Altan Eşsizoğlu, Gülcan Güleç, Melis Danışman Sonkurt, İbrahim Uğur Çaliş
المصدر: Turk psikiyatri dergisi = Turkish journal of psychiatry. 32(3)
مصطلحات موضوعية: medicine.medical_specialty, Turkish population, Polymorphism, Genetic, Turkey, Genotype, business.industry, Smoking, Neurexin, Nerve Tissue Proteins, General Medicine, Neurological disorder, Tobacco Use Disorder, medicine.disease, Nicotine, Psychiatry and Mental health, Polymorphism (computer science), Internal medicine, medicine, Humans, Allele, business, Association (psychology), medicine.drug
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::354d1b0fedca8a9aeac338c9ca382451
https://pubmed.ncbi.nlm.nih.gov/34647286 -
7
المؤلفون: Yavuz Pehlivan, M. Cinar, Emel Gönüllü, Dilek Solmaz, Bunyamin Kisacik, Umut Kalyoncu, Müge Aydın Tufan, Fezan Sahin, Sibel Yilmaz Oner, Eren Erken, Cemal Bes, Haner Direskeneli, Veli Yazisiz, Duygu Ersozlu Bozkirli, Ismail Sari, Gozde Yildirim Cetin, Mehmet Sayarlioglu, Levent Kilic, Şule Yaşar Bilge, Timuçin Kaşifoğlu, Fatih Yildiz, Servet Akar, Sedat Yilmaz, Soner Senel, Kenan Aksu, Hakan Emmungil, Şükran Erten, Sema Yilmaz
المساهمون: Çukurova Üniversitesi, Selçuk Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Yılmaz, Sema, Ege Üniversitesi, Bilge, Sule Yasar, Solmaz, Dilek, Senel, Soner, Emmungil, Hakan, Kilic, Levent, Oner, Sibel Yilmaz, Yidiz, Fatih, Yilmaz, Sedat, Bozkirli, Duygu Ersozlu, Tufan, Muge Aydin, Yilmaz, Sema, Yazisiz, Veli, Pehlivan, Yavuz, Bes, Cemal, Cetin, Gozde Yildirim, Erten, Sukran, Gonullu, Emel, Sahin, Fezan, Akar, Servet, Aksu, Kenan, Kalyoncu, Umut, Direskeneli, Haner, Erken, Eren, Kisacik, Bunyamin, Sayarlioglu, Mehmet, Cinar, Muhammed, Kasifoglu, Timucin, Sari, Ismail
المصدر: European Journal of Rheumatology
European Journal of Rheumatology, Vol 6, Iss 1, Pp 34-37 (2019)مصطلحات موضوعية: lcsh:Immunologic diseases. Allergy, 0301 basic medicine, medicine.medical_specialty, Familial Mediterranean fever, E148Q, medicine.disease_cause, FREQUENCY, M694V, REGION, 03 medical and health sciences, Exon, 0302 clinical medicine, exon 2, familial Mediterranean fever, Internal medicine, medicine, Family history, 030203 arthritis & rheumatology, Mutation, business.industry, MEFV MUTATIONS, Amyloidosis, medicine.disease, MEFV, Rheumatology, 030104 developmental biology, Population study, Original Article, lcsh:RC581-607, business, GENE-MUTATIONS, exon 10
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::128f656a19135f4328c48682fa865652
http://europepmc.org/articles/PMC6459332 -
8دورية أكاديمية
المصدر: Medical Oncology. September 2009 26(3):358-364
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9دورية أكاديمية
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10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.