Çiğdem Seher Kasapkara (Cigdem S Kasapkara)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 6

Top Topics

Duchenne Muscular Dystrophy

Autism Spectrum Disorder

Gene Expression

Top Venues

European journal of pediatrics

Cardiology in the young

Journal of clinical research in pediatric endocrinology

Journal of pediatric endocrinology & metabolism : JPEM

This page only lists publications with an associated author ORCID identifier.

Publications

Aynur Küçükçongar Yavaş, Ayşenur Engin Erdal, Berrak Bilginer Gürbüz, Aysel Ünlüsoy Aksu, Çiğdem Seher Kasapkara
Assessment of the diagnosis, treatment, and follow-up of a group of Turkish pediatric glycogen storage disease type 1b patients with varying clinical presentations and a novel mutation. Journal of pediatric endocrinology & metabolism : JPEM (2023)
Begüm Yılmaz, Ahmet Cevdet Ceylan, Mehmet Gündüz, Özlem Ünal Uzun, Aynur Küçükcongar Yavaş, Berrak Bilginer Gürbüz, Ümmühan Öncül, Gülay Güleç Ceylan, Çiğdem Seher Kasapkara
Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency. European journal of pediatrics (2023)
Begüm Yılmaz, Ahmet Cevdet Ceylan, Mehmet Gündüz, Özlem Ünal Uzun, Aynur Küçükcongar Yavaş, Berrak Bilginer Gürbüz, Ümmühan Öncül, Gülay Güleç Ceylan, Çiğdem Seher Kasapkara
Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency. European journal of pediatrics 183 (3) (2023)
Begüm Yılmaz, Ahmet Cevdet Ceylan, Mehmet Gündüz, Özlem Ünal Uzun, Aynur Küçükcongar Yavaş, Berrak Bilginer Gürbüz, Ümmühan Öncül, Gülay Güleç Ceylan, Çiğdem Seher Kasapkara
Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency. European journal of pediatrics 183 (3) (2023)
Çiğdem Seher Kasapkara, Burcu Civelek Ürey, Ahmet C Ceylan, Özlem Ünal Uzun, Ibrahim I Çetin
Malonyl coenzyme A decarboxylase deficiency with a novel mutation. Cardiology in the young 31 (9) (2021)
Husniye Yucel, Çiğdem Genç Sel, Çiğdem Seher Kasapkara, Gülin Karacan Küçükali, Senay Savas Erdeve, Ülkühan Öztoprak, Serdar Ceylaner, Saliha Şenel, Meltem Akcaboy
Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation Journal of clinical research in pediatric endocrinology 13 (1) (2020)