Mehmet Taştan

Prevalence and associated phenotypes of <i>PLXNA1</i> variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism

Leman Damla Kotan, İhsan Turan, Eda Mengen et al. · Clinical Genetics · 2018 · 24 citations

Genetics, Genetic Epidemiology, Pathology +17

Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance

İhsan Turan, Leman Damla Kotan, Mehmet Taştan et al. · Clinical Endocrinology · 2018 · 22 citations

21-Hydroxylase deficiency: Mutational spectrum and Genotype–Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification

İhsan Turan, Mehmet Taştan, Duygu D. Boga et al. · European Journal of Medical Genetics · 2019 · 22 citations

Mendelian Disorder, Genetic Disorder, Medicine +10

Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in &lt;i&gt;GALNT3&lt;/i&gt; Gene: Experience from Southern Turkey

Rabia Miray Kışla Ekinci, Fatih Gürbüz, Sibel Balcı et al. · Journal of Clinical Research in Pediatric Endocrinology · 2019 · 11 citations · Full text

Efficiency of Single Dose of Tolvaptan Treatment During the Triphasic Episode After Surgery for Craniopharyngioma

Fatih Gürbüz, Mehmet Taştan, İhsan Turan et al. · Journal of Clinical Research in Pediatric Endocrinology · 2019 · 11 citations · Full text

Pediatric Neurosurgery, Fluid Restriction, Single Dose +9