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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Audiologic findings in children with biotinidase deficiency in Turkey von Genc, G.A, Sivri-Kalkanoğlu, H.S, Dursun, A, Aydın, H.İ, Tokatlı, A, Sennaroglu, L, Belgin, E, Wolf, B, Coşkun, T

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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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The effect of oral L-carnitine supplementation on the lipid profiles of hyperlipidaemic children von GÜNES, B, YALCIN, S. S, KALKANOGLU, H. S, ÖNOL, S, DURSUN, A, COSKUN, T

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Mutation analysis in Turkish patients with hereditary fructose intolerance von Dursun, A., Kalkanoğlu, H. S., Coşkun, T., Tokatli, A., Bittner, R., Koçak, N, Yüce, A., Ozalp, I., Boehme, H.‐J.

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Maple syrup urine disease: Mutation analysis in Turkish patients von Dursun, A., Henneke, M., Özgül, K., Gartner, J., Coşkun, T., Tokatli, A., Kalkanoğlu, H. S., Demirkol, M., Wendel, U., Özalp, İ.

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Molecular basis of mild hyperphenylalaninaemia in Turkey von Yilmaz, E., Cali, F., Romano, V., Özalp, I., Coşkun, T., Tokatli, A., Kalkanoğlu, H. S., ÖzgüÇ, M.

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Evaluation of a fetus at risk for dihydropteridine reductase deficiency by direct mutation analysis using denaturing gradient gel electrophoresis von Serap Kalkanoğlu, H., Romstad, Anne, Coşkun, Turgay, Güttler, Flemming

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Factor V Leiden mutation in Turkish patients with homozygous cystathionine β‐synthase deficiency von Kalkanoğlu, H. S., Coşkun, T., Aydoğdu, S. D., Tokatli, A., Gürgey, A.

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Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE) von ROMSTAD, Anne, KALKANOGLU, H. Serap, COSKUN, Turgay, DEMIRKOL, Mübeccel, TOKATLI, Aysegül, DURSUN, Ali, BAYKAL, Tolunay, ÖZALP, Imran, GULDBERG, Per, GÜTTLER, Flemming

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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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Focal segmental glomerulosclerosis associated with mitochondrial cytopathy: report of two cases with special emphasis on podocytes von Güçer, Safak, Talim, Beril, Aşan, Esin, Korkusuz, Petek, Ozen, Seza, Unal, Sule, Kalkanoğlu, Serap H, Kale, Gülsev, Cağlar, Melda

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Phenylketonuria and cystic fibrosis in the same patient von Kalkanoğlu, H S, Anadol, D, Yilmaz, E, Coşkun, T

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Factor V Leiden mutation in Turkish patients with homozygous cystathionine [beta]-synthase deficiency von Kalkanoglu, H S, Coskun, T, Aydogdu, S D, Tokatli, A, Gurgey, A

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A Boy With Spastic Paraparesis and Dyspnea von Kalkanoglu, H. Serap, Dursun, Ali, Tokatli, Aysegül, Coskun, Turgay, Karasimav, Defne, Topaloglu, Haluk

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Permanent Transfemoral Pacemaker Implantation in a Child with Maroteaux Lamy Syndrome von DILBER, EMBIYA, CELIKER, ALPAY, KARAGÖZ, TEVFIK, KALKANOĞLU, H. SERAP

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Four-Month-Old Infant With Focal Segmental Glomerulosclerosis and Mitochondrial DNA Deletion von Unal, Sule, Serap Kalkanoğlu, H., Kocaefe, Cetin, Gucer, Safak, Ozen, Seza, Turanlt, Guzide, Coskun, Turgay

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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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The effect of oral L-carnitine supplementation on the lipid profiles of hyperlipidaemic children von Güneş, B, Songül Yalçin, S, Kalkanoğlu, HS, Önol, S, Dursun, A, Coşkun, Turgay

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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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