Dysmorphic Facial Features and Other Clinical Characteristics in Two Patients with PEX1 Gene Mutations

por Gunduz, Mehmet, Unal, Ozlem
Publicado 2016

Theranostic potential of self-luminescent branched polyethyleneimine-coated superparamagnetic iron oxide nanoparticles

por Khodadust, Rouhollah, Unal, Ozlem, Yagci Acar, Havva
Publicado 2022

Glutaric aciduria type 2 presenting with acute respiratory failure in an adult

por Ersoy, Ebru Ortac, Rama, Dorina, Ünal, Özlem, Sivri, Serap, Topeli, Arzu
Publicado 2015

Renal Cell Carcinoma Metastasis to Ipsilateral Parotid and Submandibular Glands: Report of a Case with Sonoelastographic Findings

por Balaban, Mehtap, Dogruyol, Sureyya Vudali, Idilman, Ilkay S., Unal, Ozlem, Ipek, Ali
Publicado 2016

Depression and anxiety among parents of phenylketonuria children

por Gunduz, Mehmet, Arslan, Nur, Unal, Ozlem, Cakar, Sevim, Kuyum, Pınar, Bulbul, Selda F.
Publicado 2015

Early effects of inactivated (CoronaVac) SARS-CoV-2 vaccine on retrobulbar vascular blood flow and retinal vascular density

por Yorgun, Mücella Arıkan, Saritas, Ozge, Ozkan, Erdem, Tascı Yildiz, Yelda, Unal, Ozlem, Toklu, Yasin
Publicado 2023

Treatment of breast cancer with autophagy inhibitory microRNAs carried by AGO2-conjugated nanoparticles

por Unal, Ozlem, Akkoc, Yunus, Kocak, Muhammed, Nalbat, Esra, Dogan-Ekici, Asiye Isin, Yagci Acar, Havva, Gozuacik, Devrim
Publicado 2020

Magnetofection of Green Fluorescent Protein Encoding DNA-Bearing Polyethyleneimine-Coated Superparamagnetic Iron Oxide Nanoparticles to Human Breast Cancer Cells

por Zuvin, Merve, Kuruoglu, Efe, Kaya, Veysel Ogulcan, Unal, Ozlem, Kutlu, Ozlem, Yagci Acar, Havva, Gozuacik, Devrim, Koşar, Ali
Publicado 2019

CAMLG-CDG: a novel congenital disorder of glycosylation linked to defective membrane trafficking

por Wilson, Matthew P, Durin, Zoé, Unal, Özlem, Ng, Bobby G, Marrecau, Thomas, Keldermans, Liesbeth, Souche, Erika, Rymen, Daisy, Gündüz, Mehmet, Köse, Gülşen, Sturiale, Luisa, Garozzo, Domenico, Freeze, Hudson H, Jaeken, Jaak, Foulquier, François, Matthijs, Gert
Publicado 2022

Three-Country Snapshot of Ornithine Transcarbamylase Deficiency

por Seker Yilmaz, Berna, Baruteau, Julien, Arslan, Nur, Aydin, Halil Ibrahim, Barth, Magalie, Bozaci, Ayse Ergul, Brassier, Anais, Canda, Ebru, Cano, Aline, Chronopoulou, Efstathia, Connolly, Grainne M., Damaj, Lena, Dawson, Charlotte, Dobbelaere, Dries, Douillard, Claire, Eminoglu, Fatma Tuba, Erdol, Sahin, Ersoy, Melike, Fang, Sherry, Feillet, François, Gokcay, Gulden, Goksoy, Emine, Gorce, Magali, Inci, Asli, Kadioglu, Banu, Kardas, Fatih, Kasapkara, Cigdem Seher, Kilic Yildirim, Gonca, Kor, Deniz, Kose, Melis, Marelli, Cecilia, Mundy, Helen, O’Sullivan, Siobhan, Ozturk Hismi, Burcu, Ramachandran, Radha, Roubertie, Agathe, Sanlilar, Mehtap, Schiff, Manuel, Sreekantam, Srividya, Stepien, Karolina M., Uzun Unal, Ozlem, Yildiz, Yilmaz, Zubarioglu, Tanyel, Gissen, Paul
Publicado 2022

Progressive deafness–dystonia due to SERAC1 mutations: A study of 67 cases

por Maas, Roeltje R., Iwanicka‐Pronicka, Katarzyna, Kalkan Ucar, Sema, Alhaddad, Bader, AlSayed, Moeenaldeen, Al‐Owain, Mohammed A., Al‐Zaidan, Hamad I., Balasubramaniam, Shanti, Barić, Ivo, Bubshait, Dalal K., Burlina, Alberto, Christodoulou, John, Chung, Wendy K., Colombo, Roberto, Darin, Niklas, Freisinger, Peter, Garcia Silva, Maria Teresa, Grunewald, Stephanie, Haack, Tobias B., van Hasselt, Peter M., Hikmat, Omar, Hörster, Friederike, Isohanni, Pirjo, Ramzan, Khushnooda, Kovacs‐Nagy, Reka, Krumina, Zita, Martin‐Hernandez, Elena, Mayr, Johannes A., McClean, Patricia, De Meirleir, Linda, Naess, Karin, Ngu, Lock H., Pajdowska, Magdalena, Rahman, Shamima, Riordan, Gillian, Riley, Lisa, Roeben, Benjamin, Rutsch, Frank, Santer, Rene, Schiff, Manuel, Seders, Martine, Sequeira, Silvia, Sperl, Wolfgang, Staufner, Christian, Synofzik, Matthis, Taylor, Robert W., Trubicka, Joanna, Tsiakas, Konstantinos, Unal, Ozlem, Wassmer, Evangeline, Wedatilake, Yehani, Wolff, Toni, Prokisch, Holger, Morava, Eva, Pronicka, Ewa, Wevers, Ron A., de Brouwer, Arjan P., Wortmann, Saskia B.
Publicado 2017