Publications by authors named "Bahattin Ciftci"

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Correction to: Clinical, laboratory and molecular features of glycogen storage disease type 1a and 1b patients from Turkey: novel mutations and phenotypes.
Ayşe Akyüz, İlyas Okur, Leyla Tümer, Fatma Tuba Eminoğlu, Engin Köse

Eur J Pediatr· September 2025

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Clinical, laboratory and molecular features of glycogen storage disease type 1a and 1b patients from Turkey: novel mutations and phenotypes.
Ayşe Akyüz, İlyas Okur, Leyla Tümer, Fatma Tuba Eminoğlu, Engin Köse

Eur J Pediatr· August 2025

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Hypophosphatasia: is it an underdiagnosed disease even by expert physicians?
Aslı İnci, Filiz Başak Cengiz Ergin, Burcu Topcu Yüce, Bahattin Çiftçi, Ercan Demir

J Bone Miner Metab· July 2021

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High incidence of co-existing factors significantly modifying the phenotype in patients with Fabry disease.
Serhat Koca, Leyla Tümer, İlyas Okur, Yasemin Erten, Sevcan Bakkaloğlu

Gene· March 2019

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Investigating the Impacts of Preoperative Steroid Treatment on Tumor Necrosis Factor-Alpha and Duration of Extubation Time underwent Ventricular Septal Defect Surgery.
H Hakan Poyrazoğlu, Zeynel Duman, Şerafettin Demir, M Kemal Avşar, Atakan Atalay

Balkan Med J· March 2016

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Diagnosis of glycine encephalopathy in a pediatric patient by detection of a GLDC mutation during initial next generation DNA sequencing.
Fatih Ezgu, Bahattin Çiftci, Burcu Topçu, Gülcan Adıyaman, Hatice Gökmenoğlu

Metab Brain Dis· March 2014

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