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Turkish Archives of Pediatrics

59 138 2024

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A recently explored aspect of the iceberg named COVID-19: multisystem inflammatory syndrome in children (MIS-C)

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Coronavirus infections in childhood and vaccine studies

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Multisystemic inflammatory syndrome in children associated with COVID-19: a single center experience in Turkey

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Associations between parenting styles and excessive screen usage in preschool children

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Comparison of nasal airway obstruction with sonoelastography and nose obstruction symptom evaluation scores in children with allergic rhinitis

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Call for Emergency Action to Limit Global Temperature Increases, Restore Biodiversity, and Protect Health

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Birth Weight Reference Percentiles by Gestational Age for Turkish Twin Neonates

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The Ideal Timing of Bedside Surgical Ligation of Patent Ductus Arteriosus in Premature Babies Less Than 30 Gestational Weeks

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How often do neurological disorders lead to dizziness in childhood?

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The impact of the COVID-19 pandemic on the assessment of autism spectrum disorder

By: Posar, A; Visconti, P and Giuberti, V

Graphical Abstract

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Vaccine hesitancy - vaccine refusal

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The Turkish Neonatal Society proposal for the management of COVID-19 in the neonatal intensive care unit

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Behcet's disease in children: single-center experience

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Evaluation of foreign body aspiration cases in our pediatric intensive care unit: Single-center experience

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A case of Type 1 Dent disease presenting with isolated persistent proteinuria

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Long-term outcome of autism spectrum disorder

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Scientific Letter

Transcobalamin II Deficiency in an Infant with a Novel Mutation

Ersin Toret ¹ , Zeynep Canan Özdemir ¹ , Özcan Bor ¹

Author Affiliation(s)

1.

Department of Pediatric Hematology-Oncology, Eskişehir Osmangazi University, School of Medicine, Eskişehir, Turkey

Turk Arch Pediatr 2022; 57: 670-672

DOI: 10.5152/TurkArchPediatr.2022.22100

Read: 891 Downloads: 385 Published: 01 November 2022

Volume 57, Issue 6, November 2022

Previous Article

Cite this article as: Toret E, Özdemir ZC, Bor Ö. Transcobalamin II deficiency in an infant with a novel mutation. Turk Arch Pediatr. 2022;57(6):670-672.

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