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EISSN 2757-6256

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Turkish Archives of Pediatrics

59 138 2024

HIGHLY CITED ARTICLES

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

By: Haslak, F; Yildiz, M; Adrovic, A; et al.

Coronavirus infections in childhood and vaccine studies

By: Aygun, D; Onal, P; Apaydin, G, et al.

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

By: Basar, EZ; Sonmez, HE; Oncel, S; et al.

Associations between parenting styles and excessive screen usage in preschool children

By: Caylan, N; Yalcin, SS; Nergiz, ME; et al.

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

By: Filiz, S; Ozkan, MB; Selcuk, OT; et al.

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

By: Atwoli, L; Baqui, AH; Benfield, T; et al.

Birth Weight Reference Percentiles by Gestational Age for Turkish Twin Neonates

By: Imamoglu, EY; Hayran, M; Kayiran, SM, et al.

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

By: Zubarioglu, AU; Yildirim, O; Zeybek, C, et al.

How often do neurological disorders lead to dizziness in childhood?

By: Karatoprak, E; Sozen, G and Yilmaz, K

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

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

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Vaccine hesitancy - vaccine refusal

By: Gur, Emel

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

By: Erdeve, Omer; Cetinkaya, Merih; Bas, Ahmet Yagmur; et al.

Behcet's disease in children: single-center experience

By: Cirkinoglu, Murat Soner; Demir, Selcan; Bilginer, Yelda; et al.

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

By: Aslan, Nagehan; Yildizdas, Dincer; Ozden, Onder; et al.

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

By: Gungor, Tulin; Eroglu, Fehime Kara; Yazilitas, Fatma; et al.

Long-term outcome of autism spectrum disorder

By: Posar, Annio; Visconti, Paola

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A family with novel homozygous deletion mutation (c.1255delT; p.Phe419Serfs*12) in the glucokinase gene, which is a rare cause of permanent neonatal diabetes mellitus

Semih Bolu, Recep Eröz, Mustafa Doğan, Ilknur Arslanoğlu, Hakan Uzun, Furkan Timur

(Turk Arch Pediatr 2020; 55: 434-437) DOI: 10.14744/TurkPediatriArs.2019.05882

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