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

Volltext

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

Volltext

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

Volltext

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

Volltext

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.

Volltext

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.

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Benign fibrous histiocytoma of the cervical vertebra: A rare case von Ezgu, Mehmet, Cicek, Ali, Yasar, Soner

Volltext