Zinc deficiency in the pediatric age group is common but underevaluated von Vuralli, Dogus, Tumer, Leyla, Hasanoglu, Alev

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Severe renal tubulopathy in a newborn due to BCS1L gene mutation: Effects of different treatment modalities on the clinical course von Ezgu, Fatih, Senaca, Sara, Gunduz, Mehmet, Tumer, Leyla, Hasanoglu, Alev, Tiras, Ulku, Unsal, Rukiye, Bakkaloglu, Sevcan A.

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High incidence of co-existing factors significantly modifying the phenotype in patients with Fabry disease von Koca, Serhat, Tümer, Leyla, Okur, İlyas, Erten, Yasemin, Bakkaloğlu, Sevcan, Biberoğlu, Gürsel, Kasapkara, Çiğdem, Küçükçongar, Aynur, Dalgıç, Buket, Oktar, Suna Özhan, Öner, Yusuf, Atalay, Tuba, Cemri, Mustafa, Çiftçi, Bahattin, Topçu, Burcu, Hasanoğlu, Alev, Ezgü, Fatih

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Serum leptin, oxidized low density lipoprotein and plasma asymmetric dimethylarginine levels and their relationship with dyslipidaemia in adolescent girls with polycystic ovary syn... von Demirel, Fatma, Bideci, Aysun, Cinaz, Peyami, Çamurdan, M. Orhun, Biberoğlu, Gürsel, Yesilkaya, Ediz, Hasanoğlu, Alev

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Frequency of vitamin D insufficiency in healthy children between 1 and 16 years of age in Turkey von Oden Akman, Alkim, Tumer, Leyla, Hasanoglu, Alev, Ilhan, Mustafa, Caycı, Banu

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BCS1L gene mutation causing GRACILE syndrome: case report von Kasapkara, Çi dem Seher, Tümer, Leyla, Ezgü, Fatih Suheyl, Küçükçongar, Aynur, Hasano lu, Alev

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“Double Hit” Homozygous Mutations for Two Different Rare Inborn Errors of Metabolism: A Burden for Countries with High Prevalences of Consangineous Marriages von Olgac, Asburce, Tumer, Leyla, Ceylaner, Serdar, Biberoglu, Gursel, Hasanoglu, Alev

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Home sleep study characteristics in patients with mucopolysaccharidosis von Kasapkara, Çiğdem Seher, Tümer, Leyla, Aslan, Ayşe Tana, Hasanoğlu, Alev, Ezgü, Fatih Süheyl, Küçükçongar, Aynur, Tunca, Zeynep, Köktürk, Oğuz

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Quality of life in children treated with restrictive diet for inherited metabolic disease von Eminoglu, Tuba F., Soysal, Sebnem A., Tumer, Leyla, Okur, Ilyas, Hasanoglu, Alev

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Is oxidative damage in operation in patients with hereditary spastic paraparesis? von Guecueyener, Kivilcim, Pinarli, FGueclue, Erbas, Deniz, Hasanoolu, Alev, Serdaroolu, Ayse, Topaloolu, Haluk

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Diagnosis of glycine encephalopathy in a pediatric patient by detection of a GLDC mutation during initial next generation DNA sequencing von Ezgu, Fatih, Çiftci, Bahattin, Topçu, Burcu, Adıyaman, Gülcan, Gökmenoğlu, Hatice, Küçükçongar, Aynur, Kasapkara, Çiğdem, Biberoğlu, Gürsel, Tümer, Leyla, Hasanoğlu, Alev

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DGUOK‐Related Mitochondrial DNA Depletion Syndrome in a Child With an Early Diagnosis of Glycogen Storage Disease von Kasapkara, Çiğdem S., Tümer, Leyla, Küçükçongar, Aynur, Hasanoğlu, Alev, Seneca, Sara, De Meirleir, Linda

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Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): case report with a new mutation von BARIS, Zeren, EMINOGLU, Tuba, DALGIC, Buket, TÜMER, Leyla, HASANOGLU, Alev

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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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Association Between Soluble CD40 Ligand and Hypercholesterolemia in Children and Adolescents von Küçükçongar Yavaş, Aynur, Eminoğlu, Tuba Fatma, Okur, İlyas, Aral, Arzu, Hasanoğlu, Alev, Tümer, Leyla

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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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Ketone Utilization Disorder and Hypodontia von Alaçam, Alev, Güçlü, Zeynep Aslı, Hasanoğlu, Alev

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Could GSD type I expand the spectrum of disorders with elevated plasma chitotriosidase activity? von Tümer, Leyla, Kasapkara, Çiğdem Seher, Biberoğlu, Gürsel, Ezgü, Fatih, Hasanoğlu, Alev

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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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Asymmetric dimethylarginine (ADMA) and L-arginine levels in children with glycogen storage disease type I von Kasapkara, Çiğdem Seher, Tümer, Leyla, Biberoglu, Gursel, Kasapkara, Ahmet, Hasanoğlu, Alev

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