Fetal Outcomes of Anti-epileptic Drug Use in Pregnancy: Teratologic Approach
Kalaycı Yiğin, Aysel, Alay, Mustafa Tarık, Seven, Mehmet
Published in Türk nöroloji dergisi (01.03.2021)
Published in Türk nöroloji dergisi (01.03.2021)
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Journal Article
Ameliorative effects of garlic oil on FNDC5 and irisin sensitivity in liver of streptozotocin-induced diabetic rats
Eser, Nadire, Yoldas, Atila, Turk, Ahmet, Kalaycı Yigin, Aysel, Yalcin, Alper, Cicek, Mustafa
Published in Journal of pharmacy and pharmacology (27.04.2021)
Published in Journal of pharmacy and pharmacology (27.04.2021)
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Journal Article
Should chromosomal analysis be performed routinely during the baseline evaluation of the gender affirmation process? The outcomes of a large cohort of gender dysphoric individuals
Kalaycı Yigin, Aysel, Turan, Şenol, Alay, Mustafa Tarık, Kavla, Yasin, Demirel, Öznur, Seven, Mehmet
Published in International journal of impotence research (01.08.2023)
Published in International journal of impotence research (01.08.2023)
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Journal Article
A Novel Homozygous ACBD5 Variant in an Emerging Peroxisomal Disorder Presenting with Retinal Dystrophy and a Review of the Literature
Hasturk, Berfin Ayla, Cinar, Çisem, Zubarioglu, Tanyel, Tiryaki-Demir, Semra, Cansever, Mehmet Serif, Kiykim, Ertugrul, Kalaycı Yigin, Aysel, Yalcinkaya, Cengiz, Aktuglu-Zeybek, Cigdem
Published in Molecular syndromology (01.06.2024)
Published in Molecular syndromology (01.06.2024)
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Journal Article
Rare Findings in Cleidocranial Dysplasia Caused by RUNX Mutation
Kalayci Yigin, Aysel, Duz, Mehmet Bugrahan, Seven, Mehmet
Published in Global medical genetics (01.03.2022)
Published in Global medical genetics (01.03.2022)
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Journal Article
The Effect of PAI-1 Gene Variants and PAI-1 Plasma Levels on Development of Thrombophilia in Patients With Klinefelter Syndrome
Erkal, Burcin, Kalayci Yigin, Aysel, Palanduz, Sukru, Dasdemir, Selcuk, Seven, Mehmet
Published in American journal of men's health (01.11.2018)
Published in American journal of men's health (01.11.2018)
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Journal Article
Three novel mutations in 20 patients with hereditary spastic paraparesis
Duz, Mehmet Bugrahan, Dasdemir, Selcuk, Kalayci Yigin, Aysel, Akalin, Mehmet Ali, Seven, Mehmet
Published in Neurological sciences (01.09.2018)
Published in Neurological sciences (01.09.2018)
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Journal Article
Evaluation of the Effect of Delivery Mode on Methylation Changes in the Global DNA and the PTEN Gene
USLU YUVACI, Hilal, KALAYCI YİĞİN, Aysel, ASLAN, Mehmet Musa, ÖZDEMİR, Filiz, ÖZEL, Ayşegül, CEVRİOĞLU, Arif Serhan, SEVEN, Mehmet
Published in Journal of clinical obstetrics & gynecology (2023)
Published in Journal of clinical obstetrics & gynecology (2023)
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Journal Article
5 Alfa Redüktaz Tip 2 Enzim Eksikliği Olan Hastalarda SRD5A2 Geni Metilasyon Değişikliklerinin Araştırılması
Kirat, Emre, Yiğin, Aysel Kalayci, Özdemir, Filiz, Seven, Mehmet
Published in Türkiye klinikleri. Türkiye klinikeri journal of medical sciences. Tıp bilimleri dergisi (01.01.2020)
Published in Türkiye klinikleri. Türkiye klinikeri journal of medical sciences. Tıp bilimleri dergisi (01.01.2020)
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Journal Article
Anti-inflammatory effects of nobiletin on TLR4/TRIF/IRF3 and TLR9/IRF7 signaling pathways in prostate cancer cells
Deveci Ozkan, Asuman, Kaleli, Suleyman, Onen, Hacer Ilke, Sarihan, Mehmet, Guney Eskiler, Gamze, Kalayci Yigin, Aysel, Akdogan, Mehmet
Published in Immunopharmacology and immunotoxicology (03.03.2020)
Published in Immunopharmacology and immunotoxicology (03.03.2020)
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Journal Article
Co-existing bipolar disease and 17q12 deletion: a rare case report
Bulu, Ersel, Kalayci Yigin, Aysel, Agirbasli, Deniz, Demirel, Omer Faruk, Aksoy Poyraz, Cana, Seven, Mehmet
Published in Psychiatric genetics (01.02.2022)
Published in Psychiatric genetics (01.02.2022)
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Journal Article
Bilateral plaque like macular atrophy and pigmentary retinopathy in an infant with a missense mutation in the MFF gene
Kılıçarslan, Oğuzhan, Batu Oto, Bilge, Yetik, Hüseyin, Ağırbaşlı, Deniz, Kalaycı Yiğin, Aysel, Çelik, Gökhan
Published in Ophthalmic genetics (03.09.2023)
Published in Ophthalmic genetics (03.09.2023)
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Journal Article
A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature
Koca, Oguzhan, Alay, Mustafa Tarık, Murt, Ahmet, Kalayci Yigin, Aysel, Seven, Mehmet, Bavunoglu, Isil
Published in CEN case reports (03.02.2024)
Published in CEN case reports (03.02.2024)
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Journal Article
Frequency of Y chromosome Microdeletions in Turkish Infertile Men: Single Center Experience
AĞIRBAŞLI, Deniz, ERDOĞAN ERDUR, Gizem, SEVEN, Mehmet, KALAYCI YİĞİN, Aysel
Published in Genel tip dergisi (31.12.2022)
Published in Genel tip dergisi (31.12.2022)
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Journal Article
Pigmentary retinopathy with perivascular sparing in a SOFT syndrome patient with a novel homozygous splicing variant in POC1A gene
Batu Oto, Bilge, Ağırbaşlı, Deniz, Kılıçarslan, Oğuzhan, Celik, Gökhan, Kalayci Yigin, Aysel, Seven, Mehmet, Yetik, Hüseyin
Published in Ophthalmic genetics (01.02.2023)
Published in Ophthalmic genetics (01.02.2023)
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Journal Article