Browsing by Author Ayter, Şükriye
Showing results 1 to 11 of 11
| Issue Date | Title | Author(s) |
|---|---|---|
| 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 |
| 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 |
| 2016 | Determination of Properties of Bone Marrow and Tissue-Derived Mesenchymal Stromal/Stem Cell Population in Neurofibromatosis Type 1 Patients | Soycan, I. Akar; Karaosmanoğlu, B.; Çetinkaya, D. Uçkan; Ayter, S. ; Taşkıran, E.; Çetin, M.; Anlar, B. |
| 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 |
| 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 |
| 2019 | Lösemiler ve Nf1 ile İlişkili Tümörlerde Evı2a ve Evı2b Genlerinin Rolü | Ayter, Şükriye ; Sharafi, Parisa ; Anlar, Banu; Varan, Ali; Çetin, Mualla |
| May-2017 | Nf1 Gene Mutations Are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome | Sharafi, Parisa ; Anlar, Banu; Ayter, Şükriye |
| 2024 | Nörofibromatozis Tip 1: Multidisipliner Yaklaşım | Akdoğan, Neslihan; Aksoy, M. Cemalettin; Anlar, Banu; Ayter, Şükriye ; Duygulu, Serap |
| Oct-2013 | Phacomatosis | Ayter, Şükriye |
| 3-Apr-2018 | Possible Modifier Genes in the Variation of Neurofibromatosis Type 1 Clinical Phenotypes | Sharafi, Parisa ; Ayter, Şükriye |
| 2020 | Yapay Zekâ ve Genetik | Ayter, Şükriye ; Sharafi, Parisa |