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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Continuous glucose monitoring in children with glycogen storage disease type I von Kasapkara, Ç S, Cinasal Demir, G, Hasanoğlu, A, Tümer, L

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P13—A Case of Fabry Disease With Unexplained Abdominal Pain von Küçükçongar, A, Ezgü, F.S, Tümer, L, Dalgıç, B, Hasanoğlu, A

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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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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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378 Vitamin a and Zinc Deficiency in School-Aged Children in a Developing Country, Turkey von Tümer, L, Vuralli, D, Hasanoğlu, A, Biberoğlu, G, Ilhan, M

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Home sleep study characteristics in patients with mucopolysaccharidosis von Aslan, A.T, Kasapkara, C, Tumer, L, Kokturk, O

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

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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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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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Endomysium antibodies in the diagnosis of celiac disease in short-statured children with no gastrointestinal symptoms von Tümer, Leyla, Hasanoglu, Alev, Aybay, Cemalettin

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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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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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Diagnostic dilemma: osteopetrosis with superimposed rickets causing neonatal hypocalcemia von Olgac, A., Tumer, L., Boyuna a, O., K z lkaya, M., Hasano lu, A.

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Pattern of human leukocyte antigens in Turkish children with celiac disease von Tümer, Leyla, Altuntaş, Buket, Hasanoğlu, Alev, Söylemezoğlu, Oğuz, Arinsoy, Turgay

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Investigating for Inborn Errors of Metabolism with Tandem Mass Spectrometry in Ankara Region, Turkey: A 2 Years Evaluation von Tümer, Leyla, Biberoglu, Gürsel, Hasanoglu, Alev, Ezgu, Fatih Suheyl, Atalay, Yildiz

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