Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disorders by Berna Şeker Yılmaz, Serdar Ceylaner, Neslihan Önenli Mungan

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A Case Report of a Very Rare Association of Tyrosinemia type I and Pancreatitis Mimicking Neurologic Crisis of Tyrosinemia Type I by Habibe Koç Uçar, Gökhan Tümgör, Deniz Kör, Neslihan Önenli Mungan, Fatih Kardaş

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Blue-colored sweating: four infants with apocrine chromhidrosis by Ahmet Yöntem, Deniz Kör, Bircan Hızlı-Karabacak, Mehmet Karakaş, Neslihan Önenli-Mungan

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p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiency by Berna Şeker-Yılmaz, Deniz Kör, Gökhan Tümgör, Serdar Ceylaner, Neslihan Önenli-Mungan

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Continuous Venovenous Hemodiafiltration in Three Newborn Patients with Hyperammonemia by Hacer Yapicioglu Yildizdas, Dincer Yildizdas, Ferda Ozlu, Kurthan Mert, Neslihan Onenli Mungan

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Glutarik Asidüri Tip 1 de Yeni Bir Mutasyon Tanımlanan Olgu Sunumu by Nilgün Uyduran ÜNAL, Deniz KÖR, Didem YÜCEL, Gülen Gül MERT, Neslihan Önenli MUNGAN

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A Case of Glutaric Aciduria Type I with a Novel Mutation by Nilgun Uyduran Unal, Deniz Kor, Didem Yucel, Gulen Gul Mert, Neslihan Onenli Mungan

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Erratum to `Recommendations on phenylketonuria in Turkey` [Turk J Pediatr 2022; 64: 413-434] by Turgay Coşkun, Mahmut Çoker, Neslihan Önenli Mungan, Hülya Gökmen Özel, H Serap Sivri

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Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor β1 and biotinidase deficiencies by Dilek Doğruel, Fatma Derya Bulut, Mustafa Yılmaz, Neslihan Önenli-Mungan, Derya Ufuk Altıntaş

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Mukopolisakkaridozlu hastalarda vitamin B12 düzeyleri by Deniz Kor, Fatma Derya Bulut, Berna Şeker, Sebile Kılavuz, H. Neslihan Önenli̇ Mungan

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Recommendations on phenylketonuria in Turkey by Turgay Coşkun, Mahmut Çoker, Neslihan Önenli Mungan, Hülya Gökmen Özel, H Serap Sivri

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Type II hyperprolinemia: a case report by Neslihan Onenli-Mungan, Bilgin Yüksel, Mürüvet Elkay, Ali Kemal Topaloğlu, Tolunay Baykal, Güler Ozer

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Comparison of Calcitonin and Pamidronate Treatments in Children with Osteogenesis Imperfecta by Neslihan Onenli Mungan, Fatih Gurbuz, Eda Mengen, Ozden Ozgur, Ali Kemal Topaloglu, Bilgin Yuksel

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Familial thyroxin-binding globulin excess with ichthyosis: a case report by Neslihan Onenli-Mungan, Bilgin Yüksel, Güler Ozer, Gül Denli, Ali Kemal Topaloğlu, Zeliha Teker

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Osteogenezis İmperfekta Olan Çocuklarda İki Farklı Pamidronat Protokolünün Değerlendirilmesi by Neslihan Önenli MUNGAN, Fatih GÜRBÜZ, Eda MENGEN, Özden ÖZGÜR, Ali Kemal TOPALOĞLU, Bilgin YÜKSEL

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Evaluation of Two Different Pamidronate Treatment Protocols in Children with Osteogenesis Imperfecta by Neslihan Onenli Mungan, Fatih Gurbuz, Eda Mengen, Ozden Ozgur, Ali Kemal Topaloglu, Bilgin Yuksel

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Ostegenezis İmperfekta Olan Çocuklarda Pamidronat ve Kalsitonin Tedavilerinin Karşılaştırılması by Neslihan Önenli MUNGAN, Fatih GÜRBÜZ, Eda MENGEN, Özden ÖZGÜR, Ali Kemal TOPALOGLU, Bilgin YÜKSEL

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Hiperkarotenemi by Nefise Hilal Cansever Övetti, Halise Neslihan Önenli Mungan, Berna Şeker Yılmaz, Fatma Derya Bulut

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Low Serum Adiponectin Levels in Children and Adolescents with Diabetic Retinopathy by Eser Tasci, Mehmet Nuri Ozbek, Neslihan Onenli-Mungan, Fatih Temiz, Ali Kemal Topaloglu, Bilgin Yuksel

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Expert opinion on patient journey, diagnosis and clinical monitoring in acid sphingomyelinase deficiency in Turkey: a pediatric metabolic disease specialist's perspective by Nur Arslan, Mahmut Coker, Gulden Fatma Gokcay, Ertugrul Kiykim, Halise Neslihan Onenli Mungan, Fatih Ezgu

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