A Patient with a Novel RARS2 Variant Exhibiting Liver Involvement as a New Clinical Feature and Review of the Literature von Sevinç, Selin, İnci, Aslı, Ezgü, Fatih S., Eminoğlu, Fatma T.

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Galactosialidosis in a newborn with a novel mutation in the CTSA gene presenting with transient hyperparathyroidism von Okulu, E, Tunc, G, Eminoglu, T, Erdeve, O, Atasay, B, Arsan, S

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Computation of Stability Delay Margin of Time-Delayed Generator Excitation Control System with a Stabilizing Transformer von Ayasun, Saffet, Eminoğlu, Ulaş, Sönmez, Şahin

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MLP01 3-Methylcrotonyl-CoA carboxylase deficiency: phenotypic variability in a family von Aktürk, A, Arhan, E, Eminoğlu, T, Biberoğlu, G, Serdaroğlu, A, Tümer, L, Hasanoğlu, A, Demir, E, Gücüyener, K

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Co-Occurring Atypical Galactosemia and Wilson Disease von Doğulu, Neslihan, Kose, Engin, Tuna Kirsaçlioğlu, Ceyda, Ezgü, Fatih S., Kuloğlu, Zarife, Kansu, Aydan, Eminoglu, Fatma T.

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Multisystem involvement in a patient due to accumulation of amylopectin-like material with diminished branching enzyme activity von Eminoglu, T. F., Tumer, L., Okur, I., Olgunturk, R., Hasanoglu, A., Gonul, I. I., Dalgic, B.

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Gaucher disease type 3: Variability in phenotype among siblings with same mutation von Eminoglu, Fatma T., Öncül, Ummühan

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Undiagnosed Phenylketonuria Can Exist Everywhere: Results From an International Survey von van Wegberg, Annemiek M.J., Trefz, Friedrich, Gizewska, Maria, Ahmed, Sibtain, Chabraoui, Layachi, van Spronsen, Francjan J., Al Mutairi, F., Arnoux, J.B., Ballhausen, D., Baruteau, J., Bernstein, L., Bijarnia-Mahay, S., Bordugo, A., Brodosi, L., Brooks, S., Chew, H.B., Chyz, K., Coker, M., Collingwood, C., Cornejo, V., Cozens, A., Das, A.M., de las Heras Montero, J., Debray, F.G., Dercksen, M., Descartes, M., Eminoglu, F.T., Enns, G.M., Ford, S., Freisinger, P., Grafakou, O., Gramer, G., Gray, S., Groselj, U., Grünert, S.C., Haas, D., Handoom, B., Harte, T.B., Hendriksz, C., Hoi-Yee Wu, T., Jamuar, S.S., Jonsson, J.J., Jovanovic, A., Kern, I., Kilavuz, S., Knerr, I., Korycinska-Chaaban, D., Kreile, M., Kumru, B., Lanpher, B., Lapatto, R., Leao-Teles, E., Leuzzi, V., Longo, N., Lopez-Uriarte, A., Lubout, C.M.A., MacDonald, A., Mitchell, J., Mochel, F., Morris, A., Moura de Souza, C.F., Munoz, T., Oscarson, M., Õunap, K., Paci, S., Pastores, G.M., Pearl, P.L., Pitt, J., Poon, G., Presner, N., Rabaty, A.A., Reinson, K., Reismann, P., Rink, T., Rocha, J.C., Rodrigues, E., Saini, A.G., Sander, J., Schwartz, I.V.D., Sharma, R., Siriwardena, K., Sirrs, S., Sjarif, D.R., Sondheimer, N., Sparkes, R., Specola, N., Stepien, K.M., Szatmari, I., Tchan, M., Valle, M.G., Vela-Amieva, M., Verdaguer, M.L., Vergano, S.A., Vermeersch, P., Wagenmakers, M.A.E.M., Weinhold, N., Wilson, W.G., Zafeiriou, D., Zhang, H., Ziagaki, A.

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Case presentation: A girl with cholesterol ester storage disease von Eminoglu, Fatma T., Bolkent, Musa Gökalp, Kuloglu, Zarife, Kansu, Aydan

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A Patient with a Novel RARS2 Variant Exhibiting Liver Involvement as a New Clinical Feature and Review of the Literature von Sevinç, Selin, İnci, Aslı, Ezgü, Fatih S, Eminoğlu, Fatma T

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Three-Country Snapshot of Ornithine Transcarbamylase Deficiency von 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

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Mucolipidosis type II (I-cell disease) with pulmonary hypertension and difficult airway von Eminoglu, Fatma T., Yaman, Ayhan, Kendirli, Tanıl, Odek, Caglar, Ucar, Tayfun

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Management of phenylketonuria in Europe: Survey results from 19 countries von Blau, Nenad, Bélanger-Quintana, Amaya, Demirkol, Mübeccel, Feillet, François, Giovannini, Marcello, MacDonald, Anita, Trefz, Friedrich K., Spronsen, Francjan van

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Association Between Soluble CD40 Ligand and Hypercholesterolemia in Children and Adolescent von Eminoglu FT, Kucukcongar A

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Co-Occurring Atypical Galactosemia and Wilson Disease von Doğulu, Neslihan, Kose, Engin, Tuna Kirsaçlioğlu, Ceyda, Ezgü, Fatih S, Kuloğlu, Zarife, Kansu, Aydan, Eminoglu, Fatma T

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FACTORS RELATED TO NON‐ALCOHOLIC FATTY LIVER DISEASE IN OBESE CHILDREN von Dalgiç, B, Çamurdan, MO, Eminoglu, FT, Oktar, SÖ, Özer, Ç, Gülbahar, Ö

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THE IMPACT OF STARTER CULTURES ON QUARK TYPE CHEESE PRODUCTION von Eminoğlu, Gökçe

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Intragastric Balloon as a Noninvasive Method for Obesity Treatment: A Single-Center Retrospective Study von Eminoğlu, Levent

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UNDERSTANDING THE NEW WAR IN THE MODERN AGE: AN ASSESSMENT ON THE RUSSIA – UKRAINE WAR von Özdemir, Şennur, Eminoğlu, Ayça

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2018 İngilizce Dersi 8. Sınıf Öğretim Programının CIPP Modeli Kullanılarak Değerlendirilmesi von Kerimoğlu, Esra, Eminoğlu Küçüktepe, Seval

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