E-LIB Suche - Ergebnisse für: Değirmencioğlu, S.

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P.721 Hippocampal apoptosis, neurogenesis suppression, BDNF..:

Golgeli, A. ; Yazgan Özdıraz, K. ; Değirmencioğlu, S....
European Neuropsychopharmacology. 29 (2019) - p. S486-S487 , 2019

Link: https://doi.org/10.1016/..

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Pertuzumab, trastuzumab and taxane-based treatment for visc..:

Turkish Oncology Group ; Esin, Ece ; Oksuzoglu, B....
Cancer Chemotherapy and Pharmacology. 83 (2018) 1 - p. 131-143 , 2018

Link: https://doi.org/10.1007/..

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1090 POSTER The Polymorphism of the IGF-1 Gene in Patients ..:

Yaren, A. ; Turgut, S. ; Ayada, C....
European Journal of Cancer. 47 (2011) - p. S121 , 2011

Link: https://doi.org/10.1016/..

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1091 POSTER Association Between Serum Adipokines Levels and..:

Demiray, G. ; Yaren, A. ; Ozkan, S....
European Journal of Cancer. 47 (2011) - p. S122 , 2011

Link: https://doi.org/10.1016/..

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Expression of Toll-like Receptor 4, Survivin and Caspase 3 ..:

Yapar Taskoylu B ; Arman Karakaya Y ; Gokcen Demiray A...
UHOD - Uluslararasi Hematoloji-Onkoloji Dergisi. , 2022

Link: https://hdl.handle.net/1..

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Ultrasound-guided wire localization biopsy in non-palpable ..:

Degirmencioglu, S ; Aykota, M. R ; Aslan, H. S..
European Review For Medical And Pharmacological Sciences. , 2022

Link: https://hdl.handle.net/1..

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Diagnóstico prenatal del síndrome de Jarcho-Levin ; Prenata..:

Rondón Tapia, Marta ; Reyna Villasmil, Eduardo ; Torres Cepeda, Duly
Demir N, Peker E, Gülşen İ, Ağengin K, Kaba S, Tuncer O. A Single-Center Experience of CNS Anomalies or Neural Tube Defects in Patients With Jarcho-Levin Syndrome. J Child Neurol. 2016;31(4):415-20. doi:10.1177/0883073815596614. 2. Chandra N, Kumar S, Raj V, Vishwakarma PK, Sinha S, Saha RP. Jarcho-Levin Syndrome with Splenic Herniation: A Rare Presentation. Am J Case Rep. 2016;17:745-748. 3. Yurttutan S, Değirmencioğlu H, Oncel MY, Kara S, Sari F, Dilmen U. Jarcho-Levin syndrome presenting with severe hydrocephalus: a report of three cases. Genet Couns. 2013;24(4):361-6. 4. Cornier AS, Staehling-Hampton K, Delventhal KM, Saga Y, Caubet JF, Sasaki N, et al. Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome. Am J Hum Genet. 2008;82(6):1334-41. doi:10.1016/j.ajhg.2008.04.014. 5. Anjankar SD, Subodh R. Spondylocostal dysostosis with lipomyelomeningocele: Case report and review of the literature. J Pediatr Neurosc.... , 2022

Link: https://doi.org/10.31260..

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