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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Influence of solidification rate and alloying elements on structure, mechanical and electrical properties of Al-Cu-X alloys von Kalkanoglu, A., Kaya, H., Buyuk, U., Cadırlı, E.

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Music Teachers’ Views on the Use of Digital Stories in Musical Literacy von Kalkanoglu, Burcu

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Music Teachers' Opinions on Block (Visual) Based Coding in Digital Literacy von Kalkanoglu, Burcu

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Increased ocular wall thickness and decreased globe volume in children with mucopolysaccharidosis type VI von Yavuz, Ozlem Ozkale, Ayaz, Ercan, Yildiz, Yilmaz, Karaosmanoglu, Ayca Akgoz, Bulut, Elif, Sivri, H. Serap Kalkanoglu, Oguz, Kader K

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Viral Shedding and Immune Responses to Respiratory Syncytial Virus Infection in Older Adults von Walsh, Edward E., Peterson, Derick R., Kalkanoglu, Aja E., Lee, Frances Eun-Hyung, Falsey, Ann R.

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Vanishing White Matter With Hepatomegaly and Hypertriglyceridemia Attacks von Unal, Ozlem, Ozgen, Burce, Orhan, Diclehan, Tokatli, Aysegul, Hismi, Burcu Ozturk, Dursun, Ali, Coskun, Turgay, Kalkanoglu-Sivri, H. Serap

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Natural history, outcome, and treatment efficacy in children and adults with glutaryl-Coa dehydrogenase deficiency von KÖLKER, Stefan, GARBADE, Sven F, TRONCOSO, Monica, WILLIAMS, Monique, WALTER, John H, CAMPISTOL, Jaume, MARTI-HERRERO, Milagros, CASWILL, Melissa, BURLINA, Alberto B, LAGLER, Florian, MAIER, Esther M, SCHWAHN, Bernd, GREENBERG, Cheryl R, TOKATLI, Aysegul, DURSUN, Ali, COSKUN, Turgay, CHALMERS, Ronald A, KOELLER, David M, ZSCHOCKE, Johannes, CHRISTENSEN, Ernst, BURGARD, Peter, HOFFMANN, Georg F, LEONARD, James V, SAUDUBRAY, Jean-Marie, RIBES, Antonia, KALKANOGLU, H. Serap, LUND, Allan M, MERINERO, Begona, WAJNER, Moacir

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A Patient With Pyruvate Carboxylase Deficiency and Nemaline Rods on Muscle Biopsy von Unal, Ozlem, Orhan, Diclehan, Ostergaard, Elsebet, Tokatli, Aysegul, Dursun, Ali, Ozturk-Hismi, Burcu, Coskun, Turgay, Wibrand, Flemming, Kalkanoglu-Sivri, H. Serap

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Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency von Ostergaard, E., Moller, L. Birk, Kalkanoglu-Sivri, H. Serap, Dursun, A., Kibaek, M., Thelle, T., Christensen, E., Duno, M., Wibrand, F.

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Does maternal knowledge impact blood phenylalanine concentration in Turkish children with phenylketonuria? von Gokmen Ozel, H., Kucukkasap, T., Koksal, G., Kalkanoglu Sivri, H. S., Dursun, A., Tokatli, A., Coskun, T.

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Student Views on Literacy in Music Education in Theatre DepartmentsBurcu von Kalkanoğlu, Burcu

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The inability of vaccinia virus A33R protein to form intermolecular disulfide-bonded homodimers does not affect the production of infectious extracellular virus von Chan, Winnie M, Kalkanoglu, Aja E, Ward, Brian M

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A late-diagnosed phenylketonuria case presenting with autism spectrum disorder in early childhood von Mazlum, Betül, Anlar, Banu, Kalkanoğlu-Sivri, H Serap, Karlı-Oğuz, Kader, Özusta, Şeniz, Ünal, Fatih

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Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients von Gao, Hong-Zhi, Kobayashi, Keiko, Tabata, Ayako, Tsuge, Hideaki, Iijima, Mikio, Yasuda, Tomotsugu, Kalkanoglu, H. Serap, Dursun, Ali, Tokatli, Aysegul, Coskun, Turgay, Trefz, Friedrich K., Skladal, Daniela, Mandel, Hanna, Seidel, Joerg, Kodama, Soichi, Shirane, Seiko, Ichida, Takafumi, Makino, Shigeru, Yoshino, Makoto, Kang, Jong-Hon, Mizuguchi, Masashi, Barshop, Bruce A., Fuchinoue, Shohei, Seneca, Sara, Zeesman, Susan, Knerr, Ina, Rodés, Margarita, Wasant, Pornswan, Yoshida, Ichiro, De Meirleir, Linda, Abdul Jalil, Md, Begum, Laila, Horiuchi, Masahisa, Katunuma, Nobuhiko, Nakagawa, Shiro, Saheki, Takeyori

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Haematological findings in children with inborn errors of metabolism von Tavil, Betul, Sivri, Hatice Serapl Kalkanoglu, Coskun, Turgay, Gurgey, Aytemiz, Ozyurek, Emel, Dursun, Ali, Tokatlı, Aysegul, Altay, Cigdem, Gumruk, Fatma

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Neonatal non‐ketotic hyperglycinemia: Report of five cases von Demirel, Nihal, Bas, Ahmet Yagmur, Zenciroglu, Aysegul, Aydemir, Cumhur, Kalkanoglu, Serap, Coskun, Turgay

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The molecular basis of familial hypercholesterolaemia in Turkish patients von Sözen, M. Mert, Whittall, Ros, Öner, Cihan, Tokatlı, Ayşegül, Kalkanoğlu, H. Serap, Dursun, Ali, Coşkun, Turgay, Öner, Reyhan, Humphries, Steve E.

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High cystine in platelets from patients with nephropathic cystinosis: a chemical, ultrastructural, and functional evaluation von Olcay, L, Erdemli, E, Kesimer, M, Büyükaşık, Y, Okur, H, Kalkanoğlu, H S, Coşkun, T, Altay, Ç

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Molecular genetics of maple syrup urine disease in the Turkish population von Gorzelany, Kerstin, Dursun, Ali, Coşkun, Turgay, Kalkanoğlu-Sivri, Serap H, Gökçay, Gülden Fatma, Demirkol, Mübeccel, Feyen, Oliver, Wendel, Udo

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