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Toplam 27797 kayıt

Delayed time of atrial conduction in children with Familial Mediterranean Fever
DOI    Battal, F., Fatih, B., Aylanç, H., Yıldırım, Ş., Kaymaz, N., ÖZDEMİR, Ö. (2021) "Delayed time of atrial conduction in children with Familial Mediterranean Fever", FAMILY PRACTICE AND PALLIATIVE CARE, (0) [TR Dizin] DOI   " data-bs-content-id="YazarBilgi-21361"> Battal, F., Fatih, B., Aylanç, H., Yıldırım, Ş., Kaymaz, N., ÖZDEMİR, Ö. (2021) "Delayed time of atrial conduction in children with Familial Mediterranean Fever", FAMILY PRACTICE AND PALLIATIVE CARE, (0) [TR Dizin] DOI    Battal, F., Fatih, B., Aylanç, H., Yıldırım, Ş., Kaymaz, N., ÖZDEMİR, Ö. (2021) "Delayed time of atrial conduction in children with Familial Mediterranean Fever", FAMILY PRACTICE AND PALLIATIVE CARE, (0) [TR Dizin] DOI   
2021 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
FAMILY PRACTICE AND PALLIATIVE CARE

The comparison of telomere length in cancer patients Plasma, whole blood and tumor tissue
Link DOI    Urfalı, M., Sılan, F., Furkan, U., Atilla, G., ÖZDEMİR, Ö. (2021) "The comparison of telomere length in cancer patients Plasma, whole blood and tumor tissue", Medicine Science, 10 (4) pp. 1117-1121 [TR Dizin] Link DOI   " data-bs-content-id="YazarBilgi-21362"> Urfalı, M., Sılan, F., Furkan, U., Atilla, G., ÖZDEMİR, Ö. (2021) "The comparison of telomere length in cancer patients Plasma, whole blood and tumor tissue", Medicine Science, 10 (4) pp. 1117-1121 [TR Dizin] Link DOI    Urfalı, M., Sılan, F., Furkan, U., Atilla, G., ÖZDEMİR, Ö. (2021) "The comparison of telomere length in cancer patients Plasma, whole blood and tumor tissue", Medicine Science, 10 (4) pp. 1117-1121 [TR Dizin] Link DOI   
2021 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Medicine Science

Prognostic Prediction of BRCA Mutations by <sup>18</sup>F-FDG PET/CT SUV<sub>max</sub> in Breast Cancer
DOI   Özdemir, S., Sılan, F., M.Yılmaz, A., Nilgun, A., Ismail, C., ÖZDEMİR, Ö. (2021) "Prognostic Prediction of BRCA Mutations by <sup>18</sup>F-FDG PET/CT SUV<sub>max</sub> in Breast Cancer", Molecular Imaging and Radionuclide Therapy, 30 (0) [SCI Expanded] DOI  " data-bs-content-id="YazarBilgi-21363"> Özdemir, S., Sılan, F., M.Yılmaz, A., Nilgun, A., Ismail, C., ÖZDEMİR, Ö. (2021) "Prognostic Prediction of BRCA Mutations by <sup>18</sup>F-FDG PET/CT SUV<sub>max</sub> in Breast Cancer", Molecular Imaging and Radionuclide Therapy, 30 (0) [SCI Expanded] DOI   Özdemir, S., Sılan, F., M.Yılmaz, A., Nilgun, A., Ismail, C., ÖZDEMİR, Ö. (2021) "Prognostic Prediction of BRCA Mutations by <sup>18</sup>F-FDG PET/CT SUV<sub>max</sub> in Breast Cancer", Molecular Imaging and Radionuclide Therapy, 30 (0) [SCI Expanded] DOI  
2021 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Molecular Imaging and Radionuclide Therapy

The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients
DOI   Burcu, A., ÖZDEMİR, Ö., Sılan, F. (2021) "The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients", Clinical Neurology and Neurosurgery, 202 (0) [SCI Expanded] DOI  " data-bs-content-id="YazarBilgi-21364"> Burcu, A., ÖZDEMİR, Ö., Sılan, F. (2021) "The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients", Clinical Neurology and Neurosurgery, 202 (0) [SCI Expanded] DOI   Burcu, A., ÖZDEMİR, Ö., Sılan, F. (2021) "The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients", Clinical Neurology and Neurosurgery, 202 (0) [SCI Expanded] DOI  
2021 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Clinical Neurology and Neurosurgery

title Blau syndrome with a rare mutation in exon 9 of iNOD2/i gene/title
Link DOI   Velıckovıc, J., Sılan, F., Bir, F.D., Sılan, C., Albuz, B., ÖZDEMİR, Ö. (2019) "title Blau syndrome with a rare mutation in exon 9 of iNOD2/i gene/title", Autoimmunity, (0) pp. 1-8 [SCI] Link DOI  " data-bs-content-id="YazarBilgi-21367"> Velıckovıc, J., Sılan, F., Bir, F.D., Sılan, C., Albuz, B., ÖZDEMİR, Ö. (2019) "title Blau syndrome with a rare mutation in exon 9 of iNOD2/i gene/title", Autoimmunity, (0) pp. 1-8 [SCI] Link DOI   Velıckovıc, J., Sılan, F., Bir, F.D., Sılan, C., Albuz, B., ÖZDEMİR, Ö. (2019) "title Blau syndrome with a rare mutation in exon 9 of iNOD2/i gene/title", Autoimmunity, (0) pp. 1-8 [SCI] Link DOI  
2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Autoimmunity

The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas
Link DOI   Kurtulgan, H.K., Altuntas, E.E., Yıldırım, M.E., ÖZDEMİR, Ö., Bağcı, B., Sezgin, İ. (2019) "The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas", The Journal of International Advanced Otology, 15 (3) pp. 373-378 [SCI Expanded] Link DOI  " data-bs-content-id="YazarBilgi-21368"> Kurtulgan, H.K., Altuntas, E.E., Yıldırım, M.E., ÖZDEMİR, Ö., Bağcı, B., Sezgin, İ. (2019) "The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas", The Journal of International Advanced Otology, 15 (3) pp. 373-378 [SCI Expanded] Link DOI   Kurtulgan, H.K., Altuntas, E.E., Yıldırım, M.E., ÖZDEMİR, Ö., Bağcı, B., Sezgin, İ. (2019) "The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas", The Journal of International Advanced Otology, 15 (3) pp. 373-378 [SCI Expanded] Link DOI  
2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
The Journal of International Advanced Otology

Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in CentralAnatolia
DOI   Yıldırım, M.E., Kurtulgan, H.K., ÖZDEMİR, Ö., Kılıçgün, H., Aydemir, D.S., Başer, B., Sezgin, İ. (2019) "Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in CentralAnatolia", ANNALS OF SAUDI MEDICINE, 39 (6) pp. 382-387 [SCI Expanded] DOI  " data-bs-content-id="YazarBilgi-21369"> Yıldırım, M.E., Kurtulgan, H.K., ÖZDEMİR, Ö., Kılıçgün, H., Aydemir, D.S., Başer, B., Sezgin, İ. (2019) "Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in CentralAnatolia", ANNALS OF SAUDI MEDICINE, 39 (6) pp. 382-387 [SCI Expanded] DOI   Yıldırım, M.E., Kurtulgan, H.K., ÖZDEMİR, Ö., Kılıçgün, H., Aydemir, D.S., Başer, B., Sezgin, İ. (2019) "Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in CentralAnatolia", ANNALS OF SAUDI MEDICINE, 39 (6) pp. 382-387 [SCI Expanded] DOI  
2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
ANNALS OF SAUDI MEDICINE

Is BCL11B a potential candidate gene for the diffuse cutaneous mastocytosis: A case report
DOI   Sılan, F., Albuz, B., Bourouba, R., Öztürk, M., Yıldız, O., ÖZDEMİR, Ö. (2020) "Is BCL11B a potential candidate gene for the diffuse cutaneous mastocytosis: A case report", Cumhuriyet Medical Journal, (3) pp. 396-402 [TR Dizin] DOI  " data-bs-content-id="YazarBilgi-21370"> Sılan, F., Albuz, B., Bourouba, R., Öztürk, M., Yıldız, O., ÖZDEMİR, Ö. (2020) "Is BCL11B a potential candidate gene for the diffuse cutaneous mastocytosis: A case report", Cumhuriyet Medical Journal, (3) pp. 396-402 [TR Dizin] DOI   Sılan, F., Albuz, B., Bourouba, R., Öztürk, M., Yıldız, O., ÖZDEMİR, Ö. (2020) "Is BCL11B a potential candidate gene for the diffuse cutaneous mastocytosis: A case report", Cumhuriyet Medical Journal, (3) pp. 396-402 [TR Dizin] DOI  
2020 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Cumhuriyet Medical Journal

Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers
Link DOI   ÖZDEMİR, Ö., Sezgin, İ., Kurtulgan, H.K., Candan, F., Binnur, K., Sümer, E.H., İçağasıoğlu, D.F., Uslu, A., Yıldız, F., Arslan, S., Öztemur, Z., Çetinkaya, S., Kayataş, M. (2011) "Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers", Molecular Biology Reports, 38 (5) pp. 3195-3200 [SSCI] Link DOI  " data-bs-content-id="YazarBilgi-21371"> ÖZDEMİR, Ö., Sezgin, İ., Kurtulgan, H.K., Candan, F., Binnur, K., Sümer, E.H., İçağasıoğlu, D.F., Uslu, A., Yıldız, F., Arslan, S., Öztemur, Z., Çetinkaya, S., Kayataş, M. (2011) "Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers", Molecular Biology Reports, 38 (5) pp. 3195-3200 [SSCI] Link DOI   ÖZDEMİR, Ö., Sezgin, İ., Kurtulgan, H.K., Candan, F., Binnur, K., Sümer, E.H., İçağasıoğlu, D.F., Uslu, A., Yıldız, F., Arslan, S., Öztemur, Z., Çetinkaya, S., Kayataş, M. (2011) "Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers", Molecular Biology Reports, 38 (5) pp. 3195-3200 [SSCI] Link DOI  
2011 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Molecular Biology Reports

The Diagnostic Accuracy of Non-invasive Fetal RhD Genotyping by Using Cell-free Fetal DNA in Maternal Plasma
Link DOI    Akurut, Ç., Sılan, F., Yalçıntepe, S., ÖZDEMİR, Ö. (2019) "The Diagnostic Accuracy of Non-invasive Fetal RhD Genotyping by Using Cell-free Fetal DNA in Maternal Plasma", Family Practice and Palliative Care, 4 (1) pp. 1-6 [TR Dizin] Link DOI   " data-bs-content-id="YazarBilgi-21372"> Akurut, Ç., Sılan, F., Yalçıntepe, S., ÖZDEMİR, Ö. (2019) "The Diagnostic Accuracy of Non-invasive Fetal RhD Genotyping by Using Cell-free Fetal DNA in Maternal Plasma", Family Practice and Palliative Care, 4 (1) pp. 1-6 [TR Dizin] Link DOI    Akurut, Ç., Sılan, F., Yalçıntepe, S., ÖZDEMİR, Ö. (2019) "The Diagnostic Accuracy of Non-invasive Fetal RhD Genotyping by Using Cell-free Fetal DNA in Maternal Plasma", Family Practice and Palliative Care, 4 (1) pp. 1-6 [TR Dizin] Link DOI   
2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Family Practice and Palliative Care

Tedaviyi Etkileyen Tarama Testleri
Karakaya, T., Sılan, F., ÖZDEMİR, Ö. (2020) "Tedaviyi Etkileyen Tarama Testleri", Türkiye Klinikleri Sağlık Bilimleri Dergisi, (0) pp. 16-24 [TR Dizin]   Karakaya, T., Sılan, F., ÖZDEMİR, Ö. (2020) "Tedaviyi Etkileyen Tarama Testleri", Türkiye Klinikleri Sağlık Bilimleri Dergisi, (0) pp. 16-24 [TR Dizin]  
2020 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Türkiye Klinikleri Sağlık Bilimleri Dergisi

Diagnostic outcomes for genetic testing of 54 genes in pregnancy loss using array CGH method: A two-year retrospective study Gebelik kayıplarında 54 genin array CGH methoduyla yapılan tanısal sonuçları: İki yıllık retrospektif çalışma
DOI   Paksoy, B., Sılan, F., ÖZDEMİR, Ö. (2020) "Diagnostic outcomes for genetic testing of 54 genes in pregnancy loss using array CGH method: A two-year retrospective study Gebelik kayıplarında 54 genin array CGH methoduyla yapılan tanısal sonuçları: İki yıllık retrospektif çalışma", Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi, 17 (4) pp. 599-609 [TR Dizin] DOI  " data-bs-content-id="YazarBilgi-21374"> Paksoy, B., Sılan, F., ÖZDEMİR, Ö. (2020) "Diagnostic outcomes for genetic testing of 54 genes in pregnancy loss using array CGH method: A two-year retrospective study Gebelik kayıplarında 54 genin array CGH methoduyla yapılan tanısal sonuçları: İki yıllık retrospektif çalışma", Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi, 17 (4) pp. 599-609 [TR Dizin] DOI   Paksoy, B., Sılan, F., ÖZDEMİR, Ö. (2020) "Diagnostic outcomes for genetic testing of 54 genes in pregnancy loss using array CGH method: A two-year retrospective study Gebelik kayıplarında 54 genin array CGH methoduyla yapılan tanısal sonuçları: İki yıllık retrospektif çalışma", Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi, 17 (4) pp. 599-609 [TR Dizin] DOI  
2020 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi

Detection of genotoxic effect of potassium permanganate by using in vitro micronucleus assay
DOI   Gençer, E.G., Özdemir, L., ÖZDEMİR, Ö. (2020) "Detection of genotoxic effect of potassium permanganate by using in vitro micronucleus assay", Cumhuriyet Medical Journal, 42 (1) pp. 79-85 [TR Dizin] DOI  " data-bs-content-id="YazarBilgi-21375"> Gençer, E.G., Özdemir, L., ÖZDEMİR, Ö. (2020) "Detection of genotoxic effect of potassium permanganate by using in vitro micronucleus assay", Cumhuriyet Medical Journal, 42 (1) pp. 79-85 [TR Dizin] DOI   Gençer, E.G., Özdemir, L., ÖZDEMİR, Ö. (2020) "Detection of genotoxic effect of potassium permanganate by using in vitro micronucleus assay", Cumhuriyet Medical Journal, 42 (1) pp. 79-85 [TR Dizin] DOI  
2020 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Cumhuriyet Medical Journal

Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population
DOI   Kılıç, S., ÖZDEMİR, Ö., Sılan, F., Işık, S., Yıldız, O., Karaağaçlı, D., Sılan, C., Öğretmen, Z. (2017) "Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population", Clinical and Experimental Dermatology, 42 (1) pp. 8-13 [SCI Expanded] DOI  " data-bs-content-id="YazarBilgi-21376"> Kılıç, S., ÖZDEMİR, Ö., Sılan, F., Işık, S., Yıldız, O., Karaağaçlı, D., Sılan, C., Öğretmen, Z. (2017) "Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population", Clinical and Experimental Dermatology, 42 (1) pp. 8-13 [SCI Expanded] DOI   Kılıç, S., ÖZDEMİR, Ö., Sılan, F., Işık, S., Yıldız, O., Karaağaçlı, D., Sılan, C., Öğretmen, Z. (2017) "Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population", Clinical and Experimental Dermatology, 42 (1) pp. 8-13 [SCI Expanded] DOI  
2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Clinical and Experimental Dermatology

Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations
Link DOI   ÖZDEMİR, Ö., Yenicesu, G.İ., Sılan, F., Köksal, B., Atik, S., Özen, F., Göl, M., Çetin, A. (2012) "Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations", Genetic Testing and Molecular Biomarkers, 16 (4) pp. 279-286 [SCI Expanded] Link DOI  " data-bs-content-id="YazarBilgi-21378"> ÖZDEMİR, Ö., Yenicesu, G.İ., Sılan, F., Köksal, B., Atik, S., Özen, F., Göl, M., Çetin, A. (2012) "Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations", Genetic Testing and Molecular Biomarkers, 16 (4) pp. 279-286 [SCI Expanded] Link DOI   ÖZDEMİR, Ö., Yenicesu, G.İ., Sılan, F., Köksal, B., Atik, S., Özen, F., Göl, M., Çetin, A. (2012) "Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations", Genetic Testing and Molecular Biomarkers, 16 (4) pp. 279-286 [SCI Expanded] Link DOI  
2012 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Genetic Testing and Molecular Biomarkers

Akciğer Kanserli Derin Ven Trombozu Olgularında Protrombotik Gen Polimorfizmi Farklılıkları
ERDİŞ, E., KARAHAN, O., MANDUZ, Ş., ÖZDEMİR, Ö. (2010) "Akciğer Kanserli Derin Ven Trombozu Olgularında Protrombotik Gen Polimorfizmi Farklılıkları", Turkiye Klinikleri Cardiovascular Sciences, 22 (1) pp. 54-60 [SSCI]   ERDİŞ, E., KARAHAN, O., MANDUZ, Ş., ÖZDEMİR, Ö. (2010) "Akciğer Kanserli Derin Ven Trombozu Olgularında Protrombotik Gen Polimorfizmi Farklılıkları", Turkiye Klinikleri Cardiovascular Sciences, 22 (1) pp. 54-60 [SSCI]  
2010 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Turkiye Klinikleri Cardiovascular Sciences

Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G Variations in Breast Carcinoma
Link DOI   Özen, F., Erdiş, E., Şık, E., Silan, F., Uludağ, A., ÖZDEMİR, Ö. (2013) "Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G Variations in Breast Carcinoma", Asian Pacific Journal of Cancer Prevention, 14 (5) pp. 2903-2908 [SCI Expanded] Link DOI  " data-bs-content-id="YazarBilgi-21380"> Özen, F., Erdiş, E., Şık, E., Silan, F., Uludağ, A., ÖZDEMİR, Ö. (2013) "Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G Variations in Breast Carcinoma", Asian Pacific Journal of Cancer Prevention, 14 (5) pp. 2903-2908 [SCI Expanded] Link DOI   Özen, F., Erdiş, E., Şık, E., Silan, F., Uludağ, A., ÖZDEMİR, Ö. (2013) "Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G Variations in Breast Carcinoma", Asian Pacific Journal of Cancer Prevention, 14 (5) pp. 2903-2908 [SCI Expanded] Link DOI  
2013 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Asian Pacific Journal of Cancer Prevention

Warfarin Resistance: A Case Report
DOI    Gönlügür, U., Gönlügür, T., ÖZDEMİR, Ö., Sılan, F. (2019) "Warfarin Resistance: A Case Report", EURASIAN JOURNAL OF EMERGENCY MEDICINE, 18 (1) pp. 61-63 [SSCI] DOI   " data-bs-content-id="YazarBilgi-21381"> Gönlügür, U., Gönlügür, T., ÖZDEMİR, Ö., Sılan, F. (2019) "Warfarin Resistance: A Case Report", EURASIAN JOURNAL OF EMERGENCY MEDICINE, 18 (1) pp. 61-63 [SSCI] DOI    Gönlügür, U., Gönlügür, T., ÖZDEMİR, Ö., Sılan, F. (2019) "Warfarin Resistance: A Case Report", EURASIAN JOURNAL OF EMERGENCY MEDICINE, 18 (1) pp. 61-63 [SSCI] DOI   
2019 Diğer (Teknik, not, yorum, vaka takdimi, editöre mektup, özet, kitap krıtiği, araştırma notu, bilirkişi raporu ve benzeri) SCI/SSCI/AHCI ESCI Scopus
EURASIAN JOURNAL OF EMERGENCY MEDICINE

MEME KANSERLİ HASTALAR VE BİRİNCİ DERECEYAKINLARINDA PERİFERAL TRANSKRİPTOMPROFİLLERİNİN ARAŞTIRILMASI
DOI    Erdiş, E., Yücel, B., ÖZDEMİR, Ö. (2019) "MEME KANSERLİ HASTALAR VE BİRİNCİ DERECEYAKINLARINDA PERİFERAL TRANSKRİPTOMPROFİLLERİNİN ARAŞTIRILMASI", Bozok Tıp Derg, 9 (4) pp. 27-31 [TR Dizin] DOI   " data-bs-content-id="YazarBilgi-21382"> Erdiş, E., Yücel, B., ÖZDEMİR, Ö. (2019) "MEME KANSERLİ HASTALAR VE BİRİNCİ DERECEYAKINLARINDA PERİFERAL TRANSKRİPTOMPROFİLLERİNİN ARAŞTIRILMASI", Bozok Tıp Derg, 9 (4) pp. 27-31 [TR Dizin] DOI    Erdiş, E., Yücel, B., ÖZDEMİR, Ö. (2019) "MEME KANSERLİ HASTALAR VE BİRİNCİ DERECEYAKINLARINDA PERİFERAL TRANSKRİPTOMPROFİLLERİNİN ARAŞTIRILMASI", Bozok Tıp Derg, 9 (4) pp. 27-31 [TR Dizin] DOI   
2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Bozok Tıp Derg

Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation
Link DOI   Battal, F., Aylanç, H., Yıldırım, Ş., Yeliz, E., Sılan, F., ÖZDEMİR, Ö. (2017) "Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation", Family Practice and Palliative Care, (0) pp. 23-28 Link DOI  " data-bs-content-id="YazarBilgi-21384"> Battal, F., Aylanç, H., Yıldırım, Ş., Yeliz, E., Sılan, F., ÖZDEMİR, Ö. (2017) "Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation", Family Practice and Palliative Care, (0) pp. 23-28 Link DOI   Battal, F., Aylanç, H., Yıldırım, Ş., Yeliz, E., Sılan, F., ÖZDEMİR, Ö. (2017) "Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation", Family Practice and Palliative Care, (0) pp. 23-28 Link DOI  
2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Family Practice and Palliative Care