Aromatic L-Amino acid decarboxylase deficiency: A new case from Turkey with a novel mutation

by Kivilcim Gucuyener, Cigdem Seher Kasapkara, Leyla Tumer, Marcel M. Verbeek
Published 2014-01-01

Siblings with Ethylmalonic Encephalopathy: Case Report

by Çiğdem Seher Kasapkara, Ayşe Aksoy, Emine Polat, Mustafa Kılıç, Serdar Ceylaner
Published 2018-03-01

The Evaluation of Skeletal Manifestations in Patients with Gaucher Disease

by Çiğdem Seher Kasapkara, Asburçe Olgaç, İlyas Okur, Fatih Süheyl Ezgu, Leyla Tümer
Published 2021-09-01

Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation

by Hüsniye Yücel, Çiğdem Genç Sel, Çiğdem Seher Kasapkara, Gülin Karacan Küçükali, Senay Savas-Erdeve, Ülkühan Öztoprak, Serdar Ceylaner, Saliha Şenel, Meltem Akçaboy
Published 2021-03-01