Rıza Taner Baran

Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations

Hüseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Özbek et al. · European Journal of Endocrinology · 2015 · 66 citations · Full text

Genotype and Phenotype Characteristics in 22 Patients with Vitamin D-Dependent Rickets Type I

Sophia Tahir, Hüseyin Demirbilek, Mehmet Nuri Özbek et al. · Hormone Research in Paediatrics · 2016 · 32 citations

Clinical characteristics and phenotype–genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations

Hüseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Özbek et al. · European Journal of Endocrinology · 2014 · 26 citations · Full text

Mutations in BTD gene causing biotinidase deficiency: a regional report

Çiğdem Seher Kasapkara, Melek Akar, Mehmet Nuri Özbek et al. · Journal of Pediatric Endocrinology and Metabolism · 2014 · 17 citations

Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism

Mehmet Nuri Özbek, Hüseyin Demirbilek, Rıza Taner Baran et al. · Journal of Clinical Research in Pediatric Endocrinology · 2016 · 16 citations · Full text