Characteristics of continuous venovenous hemodiafiltration in the acute treatment of inherited metabolic disorders von Eminoğlu, Fatma Tuba, Öncül, Ümmühan, Kahveci, Fevzi, Okulu, Emel, Kraja, Elvis, Köse, Engin, Kendirli, Tanıl

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Serum biotin interference: A troublemaker in hormone immunoassays von Öncül, Ümmühan, Eminoğlu, Fatma Tuba, Köse, Engin, Doğan, Özlem, Özsu, Elif, Aycan, Zehra

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ALG1-CDG: A Patient with a Mild Phenotype and Literature Review von Öncül, Ümmühan, Kose, Engin, Eminoğlu, Fatma Tuba

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Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency von Yılmaz, Begüm, Ceylan, Ahmet Cevdet, Gündüz, Mehmet, Ünal Uzun, Özlem, Küçükcongar Yavaş, Aynur, Bilginer Gürbüz, Berrak, Öncül, Ümmühan, Güleç Ceylan, Gülay, Kasapkara, Çiğdem Seher

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Is Ultrasonography a Reliable Approach for the Evaluation of Carpal Tunnel Syndrome in Patients With Mucopolysaccharidosis? von Koç Yekedüz, Merve, Köse, Engin, İnci, Aslı, Yüksel, Merve Feyza, Doğulu, Neslihan, Şen Akova, Birsel, Yeniay Süt, Nurşah, Öncül, Ümmühan, Yildirim, Miraç, Fitoz, Suat, Teber, Serap, Tümer, Leyla, Eminoğlu, Fatma Tuba

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Genetic variants of GBA and GLA in a Turkish cohort of Parkinson's disease: A preliminary report von Yekedüz, Merve Koç, Yilmaz, Rezzak, Kayis, Gorkem, Doğulu, Neslihan, Öncül, Ümmühan, Abali, Talha, Temizyurek, Akar Diyar, Çelik, Gökalp, Çöklü, Hilal, Gemci, Emine, Yalcin, Ahmet, Ceylaner, Serdar, Akbostancı, M Cenk, Eminoğlu, Fatma Tuba

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A Patient with Recurrent Severe Hypoglycemic Attacks and Mitochondrial Complex III Deficiency, Nuclear Type 3: a Novel UQCRB Variant von Koç Yekedüz, Merve, Öncül, Ümmühan, Köse, Engin, Ezgü, Fatih, Eminoğlu, Fatma Tuba

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Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy von Kasapkara, Çiğdem Seher, Civelek Ürey, Burcu, Bilginer Gürbüz, Berrak, Küçükçongar Yavaş, Aynur, Keçeli, Avni Merter, Öncül, Ümmühan, Gündüz, Mehmet, Biberoğlu, Gürsel, Çıtak Kurt, Ayşegül Neşe, Gürkaş, Esra, Kılıç, Esra, Güleç Ceylan, Gülay, Özbek, Namık Yaşar

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A Case of Combined Oxidative Phosphorylation Deficiency 35 Associated with a Novel Missense Variant of the TRIT1 Gene von Yıldırım, Miraç, Bektaş, Ömer, Tunçez, Ebru, Yeniay Süt, Nurşah, Sayar, Yavuz, Öncül, Ümmühan, Teber, Serap

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Inherited metabolic disorders in the neonatal intensive care unit: Red flags to look out for von Eminoğlu, Fatma Tuba, Koç Yekedüz, Merve, Doğulu, Neslihan, Öncül, Ümmühan, Köse, Engin, Okulu, Emel, Erdeve, Ömer, Atasay, Begüm, Arsan, Saadet

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An Atypical Presentation of Mevalonate Kinase Deficiency in Response to Colchicine Treatment von Koç Yekedüz, Merve, Doğulu, Neslihan, Öncül, Ümmühan, Köse, Engin, Ceylaner, Serdar, Eminoğlu, Fatma Tuba

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Unmet Needs of Children with Inherited Metabolic Disorders in the COVID-19 Pandemic von Özalp Akın, Ezgi, Eminoğlu, Fatma Tuba, Doğulu, Neslihan, Koç Yekeduz, Merve, Öncül, Ummuhan, Akpınar, Funda, Hayran, Gamze

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Asthma control test and pediatric asthma quality of life questionnaire association in children with poor asthma control von Karadeniz, Pınar, Özdoğan, Şebnem, Ayyıldız-Emecen, Durdugül, Öncül, Ümmühan

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Use of procalcitonin as a biomarker for sepsis in pediatric burns von Oncul, Ummuhan, Dalgıç, Nazan, Demir, Mesut, Karadeniz, Pınar, Karadağ, Çetin Ali

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A Mild Phenotype of Mitochondrial DNA Depletion Syndrome Type 13 with a Novel FBXL4 Variant von Oncul, Ummuhan, Kose, Engin, Eminoglu, Fatma Tuba

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Early neuroimaging findings of infants diagnosed with inherited metabolic disorders in neonatal period: A case-control study von Koç Yekedüz, Merve, Şen Akova, Birsel, Köse, Engin, Doğulu, Neslihan, Öncül, Ümmühan, Okulu, Emel, Arsan, Saadet, Fitöz, Suat, Eminoğlu, Fatma Tuba

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Coexistence of Megaconial Congenital Muscular Dystrophy and Cystinuria: Mimicking Hypotonia-Cystinuria Syndrome von Surucu Kara, Ilknur, Oncul, Ummuhan, Kose, Engin, Turan, Husnu Mutlu, Ceylan, Ahmet Cevdet, Eminoglu, Fatma Tuba

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BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening von Tangeraas, Trine, Constante, Juliana R, Backe, Paul Hoff, Oyarzábal, Alfonso, Neugebauer, Julia, Weinhold, Natalie, Boemer, Francois, Debray, François G, Ozturk-Hism, Burcu, Evren, Gumus, Tuba, Eminoglu F, Ummuhan, Oncul, Footitt, Emma, Davison, James, Martinez, Caroline, Bueno, Clarissa, Machado, Irene, Rodríguez-Pombo, Pilar, Al-Sannaa, Nouriya, De Los Santos, Mariela, López, Jordi Muchart, Ozturkmen-Akay, Hatice, Karaca, Meryem, Tekin, Mustafa, Pajares, Sonia, Ormazabal, Aida, Stoway, Stephanie D, Artuch, Rafael, Dixon, Marjorie, Mørkrid, Lars, García-Cazorla, Angeles

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Mitochondrial DNA Depletion Syndromes Gene Panel versus Clinical Exome Sequencing in Children with Suspected Mitochondrial Hepatopathies von Doğulu, Neslihan, Köse, Engin, Ceylaner, Serdar, Kasapkara, Çiğdem Seher, Bozaci, Ayşe Ergul, Oncul, Ummuhan, Eminoğlu, Fatma Tuba

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A Fatal Case of Opioid Intoxication After Raw Poppy Plant Ingestion von Bozan, Gurkan, Ulukapi, Hasan Bora, Oncul, Ummuhan, Levent, Serkan, Dinleyici, Ener C

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