A case of glycogen storage disease type 1a mimicking familial chylomicronemia syndrome von Olgac, A, Okur, İ, Biberoğlu, G, Ezgü, FS, Tümer, L

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A 7-year-old boy with hand tremors and a novel mutation for L-2-hydroxyglutaric aciduria von Olgac, A, Tekin, Orgun L, Ezgü, FS, Biberoǧlu, G, Tümer, L

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SRD5A3-CDG: A patient with a novel mutation von Kasapkara, C.S, Tümer, L, Ezgü, F.S, Hasanoğlu, A, Race, V, Matthijs, G, Jaeken, J

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Suspected allergy to lamotrigine von Gücüyener, K, Türktaş, Serdarog lu, A, Ezgü, Fs

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Beneficial Effects of Modified Atkins Diet in Glycogen Storage Disease Type IIIa von Olgac, Asburce, İnci, Aslı, Okur, İlyas, Biberoğlu, Gürsel, Oğuz, Deniz, Ezgü, Fatih Süheyl, Kasapkara, Çiğdem Seher, Aktaş, Emine, Tümer, Leyla

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Phenotype-genotype correlations in patients with Marinesco-Sjögren syndrome von Ezgu, F., Krejci, P., Li, S., de Sousa, C., Graham Jr, J.M., Hansmann, I., He, W., Porpora, K., Wand, D., Wertelecki, W., Schneider, A., Wilcox, W.R.

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Plasma leptin levels of large for gestational age and small for gestational age infants von Cinaz, P, Şen, E, Bideci, A, Ezgü, F Süheyl, Atalay, Y, Koca, E

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P17—Importance of Family Screening in Fabry Disease: Reaching the Bottom of the iceberg von Koca, S, Ezgu, F, Okur, I, Biberoglu, G, Tumer, L, Bakkaloglu, S, Erten, Y, Bahceci, S, Polat, M, Hasanoglu, A

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A case with rare type of congenital disorder of glycosylation: PGM1-CDG von Küçükçongar, A, Tümer, L, Ezgü, F. Süheyl, Kasapkara, Ç. Seher, Jaeken, Jaak, Matthijs, Gert, Rymen, Daisy, Dalgiç, B, Bıdecı, A, Hasanoğlu, A

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Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R von Hasanoglu, Alev, Balwani, Manisha, Kasapkara, Çiğdem S, Ezgü, Fatih S, Okur, İlyas, Tümer, Leyla, Çakmak, Alpay, Nazarenko, Irina, Yu, Chunli, Clavero, Sonia, Bishop, David F, Desnick, Robert J

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Plasma Leptin Levels of Large for Gestational Age and Small for Gestational Age Infants von Cinaz, P, Şen, E, Bideci, A, Ezgü, F Süheyl, Atalay, Y, Koca, E

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Homocysteine, Fibrinogen and Anti-ox-LDL Antibody Levels as Markers of Atherosclerosis in Prepubertal Obese Children von Ezgü, F., Tümer, L., Ozbay, F., Hasanoğlu, A., Biberoğlu, G., Aybay, C.

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Cerebrospinal Fluid and Serum Nitric Oxide Levels in Asphyxiated Newborns von Ergenekon, Ebru, Gücüyener, Kıvılcım, Erbaş, Deniz, Süheyl Ezgü, Fatih, Atalay, Yıldız

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Effect of enteral and parenteral nutrition on growth parameters of hospitalized Turkish children von Ezgu, F S, Tumer, L, Cinasal, G, Hasanoglu, A, Gunduz, M

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Endothelial activation and inflammation in prepubertal obese Turkish children von Süheyl Ezgü, Fatih, Hasanoğlu, Alev, Tümer, Leyla, Özbay, Ferda, Aybay, Cemalettin, Gündüz, Mehmet

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Neuron-Specific Enolase Levels and Neuroimaging in Asphyxiated Term Newborns von Ezgü, Fatih Süheyl, Atalay, Yidiz, Gücüyener, Kivilcim, Tunç, Sükran, Koç, Esin, Ergenekon, Ebru, Tiraş, Ülkü

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Coagulopathy in Gaucher disease von Oztürk, G, Koçak, U, Gürsel, T, Ezgü, F S

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Cholesteryl ester storage disease in a young child presenting as isolated hepatomegaly treated with simvastatin von Dalgiç, Buket, Sari, Sinan, Gündüz, Mehmet, Ezgü, Fatih, Tümer, Leyla, Hasanoğlu, Alev, Akyol, Gülen

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O-32 APHERESIS-INDUCIBLE CYTOKINE PATTERN CHANGE IN CHILDREN WITH HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA von Kucukcongar, A, Yenicesu, I, Tumer, L, Kasapkara, C. Seher, Ezgu, F. Suheyl, Pasaoglu, O, Demirtas, C, Celik, B, Dilsiz, G, Hasanoglu, A

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The co-existence of Fabry and celiac diseases: a case report von Tümer, Leyla, Ezgü, Fatih S, Hasanoğlu, Alev, Dalgiç, Buket, Bakkaloğlu, Sevcan A, Memiş, Leyla, Dursun, Ayşe

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