03. School of Medicine
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Issue Date | Title | Author(s) | |
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1 | Feb-2018 | Clinical findings and mutation analysis of NF1 patients in Turkey | Terzi, Yunus Kasım; Balcı, Sibel Oğuzkan; Anlar, Banu; Varan, Ali; Evans, Sibel Ersoy; Sharafi, Parisa ; Ayter, Şükriye |
2 | 2023 | Clinical signs and genetic evaluation of patients with neurofibromatosis type 1 with and without optic pathway gliomas in a center in Turkey | Sharafi, Parisa ; Varan, Ali; Ersoy-Evans, Sibel; Ayter, Şükriye |
3 | 1-Jul-2018 | The effect of parental age on NF1 patients in Turkey | Ersoy, Evans Sibel; Sharafi, Parisa ; Anlar, Banu; Varan, Ali; Yılmaz, Ömer Faruk; Turan, Mustafa ; Ayter, Şükriye |
4 | 2018 | Factors influencing the success of cord blood collection: A tertiary perinatal medicine center’s experience | Tanaçan, Atakan; Yurdakul, Pınar ; Aktoz, Fatih; Örgül, Gökçen; Beksaç, Mehmet Sinan |
5 | Nov-2017 | Flow Cytometric Aldehyde Dehydrogenase (ALDH) Assay Enables a Fast and Accurate Human Umblical Cord Blood Hematopoietic Stem Cell Assessment. | Gencer, Emine Begüm; Yurdakul, Pınar ; Dalva, Klara; Beksaç, Meral |
6 | 1-May-2018 | Heightened CXCR4 and CXCL12 expression in NF1-associated neurofibromas | Karaosmanoğlu, Beren; Kocaefe, Çetin Y.; Söylemezoğlu, Figen; Anlar, Banu; Varan, Ali; Vargel, İbrahim; Ayter, Şükriye |
7 | 2019 | Lösemiler ve NF1 ile İlişkili Tümörlerde EVI2A ve EVI2B Genlerinin Rolü | Ayter, Şükriye ; Sharafi, Parisa ; Anlar, Banu; Varan, Ali; Çetin, Mualla |
8 | May-2017 | NF1 Gene Mutations are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome | Sharafi, Parisa ; Anlar, Banu; Ayter, Şükriye |
9 | 2024 | Nörofibromatozis Tip 1: Multidisipliner Yaklaşım | Akdoğan, Neslihan; Aksoy, M. Cemalettin; Anlar, Banu; Ayter, Şükriye ; Duygulu, Serap |
10 | Oct-2013 | Phacomatosis | Ayter, Şükriye |
11 | 3-Apr-2018 | Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypes | Sharafi, Parisa ; Ayter, Şükriye |
12 | 2020 | Yapay Zekâ ve Genetik | Ayter, Şükriye ; Sharafi, Parisa |