Çiğdem Seher Kasapkara

Key features and clinical variability of COG6-CDG

Daisy Rymen, Julia Winter, Peter M. van Hasselt et al. · Molecular Genetics and Metabolism · 2015 · 59 citations

Life Sciences, Hematology, Human Genetics +1

N-carbamylglutamate treatment for acute neonatal hyperammonemia in isovaleric acidemia

Çiğdem Seher Kasapkara, Fatih Süheyl Ezgü, İlyas Okur et al. · European Journal of Pediatrics · 2011 · 44 citations

Pharmacy, Pediatrics, Pharmacology +9

Continuous glucose monitoring in children with glycogen storage disease type I

Çiğdem Seher Kasapkara, G Cinasal Demir, Alev Hasanoğlu et al. · European Journal of Clinical Nutrition · 2013 · 40 citations

Medicine, Endocrinology, Pediatrics +14

The variable clinical phenotype of three patients with hepatic glycogen synthase deficiency

Çiğdem Seher Kasapkara, Zehra Aycan, Esma Altınel Açoğlu et al. · Journal of Pediatric Endocrinology and Metabolism · 2017 · 33 citations

Medicine, Endocrinology, Pediatrics +17

Lack of prolidase causes a bone phenotype both in human and in mouse

Roberta Besio, Silvia Maruelli, Roberta Gioia et al. · Bone · 2014 · 26 citations

Medicine, Craniofacial Biology, Orthopaedic Surgery +8