Zobrazeno 1 - 10
of 951
pro vyhledávání: '"Gezdirici A"'
Publikováno v:
2022 30th Signal Processing and Communications Applications Conference (SIU).
In this study dog walkers were separated into clusters according to walkers' walk habits. Due to the fact that the distributions were non-normal, normalization algorithms were applied before the onset of clustering. After normalizing, K Means algorit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3570::b18d110d5a3ff96e6a5c87642c9057c8
https://hdl.handle.net/20.500.11779/1906
https://hdl.handle.net/20.500.11779/1906
Autor:
Naiboğlu, Sezin1 sezin_ctnol@hotmail.com, Gezdirici, Alper2, Ulaş, Selami1, Turan, Işılay1, Çeliksoy, Mehmet Halil1, Aydoğmuş, Çiğdem1
Publikováno v:
Iranian Journal of Allergy, Asthma & Immunology. Aug2024, Vol. 23 Issue 4, p452-456. 5p.
Conference
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Publikováno v:
Haseki Tıp Bülteni, Vol 62, Iss 2, Pp 92-96 (2024)
Aim: Some recent studies on PD have focused on the WNT-2 and TGF-β1 gene loci, but its genetic basis is still not clearly known. In this context, we aimed to evaluate the presence of WNT-2 and TGF-β1 gene expression and genetic similarity between p
Externí odkaz:
https://doaj.org/article/959fea890c59419fbd94344a78614fa4
Autor:
Sadık Etka Bayramoğlu, Nihat Sayın, Mehmet Erdoğan, Sümeyra Doğan, Alper Gezdirici, Merih Çetinkaya
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 53, Iss 6, Pp 386-389 (2023)
A female infant born with a gestational age of 35 weeks and birth weight of 2500 g was referred for ophthalmic examination on the second postnatal day. Bilateral venous dilatation and arterial tortuosity, severe extraretinal fibrovascular proliferati
Externí odkaz:
https://doaj.org/article/82dec6b0b8ec4258bdfeb805a527f39d
Autor:
Burak Anıl Tuğci, Alper Gezdirici, Can Berk Aşaroğlu, Ercan Atasoy, İbrahim Sayın, Zahide Mine Yazıcı
Publikováno v:
Turkish Archives of Otorhinolaryngology, Vol 61, Iss 4, Pp 192-200 (2023)
In this article, we aim to present details of the cochlear implantation procedure performed in a patient with Primrose syndrome, which is a rare genetic condition characterized by physical deformities, sensorineural hearing loss, and metabolic disord
Externí odkaz:
https://doaj.org/article/a6c695bc0eee40638187472a333d094e
Autor:
Tuğci, Burak Anıl1 b_anl_5@hotmail.com, Gezdirici, Alper2, Aşaroğlu, Can Berk1, Atasoy, Ercan1, Sayın, İbrahim1, Yazıcı, Zahide Mine1
Publikováno v:
Turkish Archives of Otolaryngology / Türk Otolarengoloji Arsivi. Dec2023, Vol. 61 Issue 4, p192-200. 9p.
Autor:
Tüysüz, Beyhan, Kasap, Büşra, Uludağ Alkaya, Dilek, Alp Ünkar, Zeynep, Köseoğlu, Pınar, Geyik, Filiz, Özer, Emre, Önal, Hasan, Gezdirici, Alper, Ercan, Oya
Publikováno v:
In European Journal of Medical Genetics November 2023 66(11)
Akademický článek
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