Doğa Türkkahraman

Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

Anne Raimondo, Ali Chakera, Soren K. Thomsen et al. · Human Molecular Genetics · 2014 · 64 citations · Full text

Successful Granulocyte Colony-stimulating Factor Treatment of Relapsing Candida albicans Meningoencephalitis Caused by CARD9 Deficiency

Fatih Çelmeli, Nefise Öztoprak, Doğa Türkkahraman et al. · The Pediatric Infectious Disease Journal · 2015 · 61 citations

Autoimmune Disease, Medicine, Immunodeficiencies +14

Permanent Neonatal Diabetes Mellitus Caused by a Novel Homozygous (T168A) Glucokinase (GCK) Mutation: Initial Response to Oral Sulphonylurea Therapy

Doğa Türkkahraman, İffet Bircan, Nicholas D. Tribble et al. · The Journal of Pediatrics · 2008 · 54 citations

Diabetes Management, Diabetes, Pediatrics +7

P300 auditory event-related potentials in children with obesity: is childhood obesity related to impairment in cognitive functions?

Mehmet Emre Taşçılar, Doğa Türkkahraman, Oğuzhan Öz et al. · Pediatric Diabetes · 2011 · 46 citations

A family with a novel TSH receptor activating germline mutation (p.Ala485Val)

Sema Akçurin, Doğa Türkkahraman, Carolyn Tysoe et al. · European Journal of Pediatrics · 2008 · 35 citations

Molecular Physiology, Signal Transduction, Novel Tsh Receptor +11