Overview
Ayca Kahraman practices practicing medicine in Konya, Turkey.
Kahraman is highly rated in 6 conditions, according to our data. Their clinical expertise encompasses Propionic Acidemia, Tyrosinemia Type 3, Rhabdomyolysis, and Phenylketonuria (PKU).
They are actively involved in clinical research, co-authoring 31 peer reviewed articles.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Frequently Asked Questions about Ayca B. Kahraman
Is Ayca B. Kahraman a top-rated expert for Propionic Acidemia?
MediFind is an objective health platform that identifies experts based on real-world data. Ayca B. Kahraman is classified as an Advanced expert for Propionic Acidemia, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Ayca B. Kahraman participate in research or clinical trials?
Yes. Ayca B. Kahraman has published 31 articles and abstracts on conditions like Propionic Acidemia. You can view a list of Ayca B. Kahraman's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Phenylketonuria (PKU)Kahraman isAdvanced. Learn about Phenylketonuria (PKU).
- Propionic AcidemiaKahraman isAdvanced. Learn about Propionic Acidemia.
- RhabdomyolysisKahraman isAdvanced. Learn about Rhabdomyolysis.
- Tyrosinemia Type 3Kahraman isAdvanced. Learn about Tyrosinemia Type 3.
- VisceromegalyKahraman isAdvanced. Learn about Visceromegaly.
- Experienced
- Acromicric DysplasiaKahraman isExperienced. Learn about Acromicric Dysplasia.
- Alpha MannosidosisKahraman isExperienced. Learn about Alpha Mannosidosis.
- Biotinidase DeficiencyKahraman isExperienced. Learn about Biotinidase Deficiency.
- Carpal Tunnel SyndromeKahraman isExperienced. Learn about Carpal Tunnel Syndrome.
- CholestasisKahraman isExperienced. Learn about Cholestasis.
- Compartment SyndromeKahraman isExperienced. Learn about Compartment Syndrome.
- Fanconi Bickel SyndromeKahraman isExperienced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeKahraman isExperienced. Learn about Fanconi Syndrome.
- GangliosidosisKahraman isExperienced. Learn about Gangliosidosis.
- GM1 GangliosidosisKahraman isExperienced. Learn about GM1 Gangliosidosis.
- Hearing LossKahraman isExperienced. Learn about Hearing Loss.
- Hereditary HyperekplexiaKahraman isExperienced. Learn about Hereditary Hyperekplexia.
- HistiocytosisKahraman isExperienced. Learn about Histiocytosis.
- HypotoniaKahraman isExperienced. Learn about Hypotonia.
- Infant Hearing LossKahraman isExperienced. Learn about Infant Hearing Loss.
- Infantile NeutropeniaKahraman isExperienced. Learn about Infantile Neutropenia.
- Lactic AcidosisKahraman isExperienced. Learn about Lactic Acidosis.
- Leukocyte Adhesion Deficiency Type 1
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Low Blood SugarKahraman isExperienced. Learn about Low Blood Sugar.
- Maple Syrup Urine DiseaseKahraman isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaKahraman isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Metabolic AcidosisKahraman isExperienced. Learn about Metabolic Acidosis.
- Mitochondrial Trifunctional Protein Deficiency
- Multiple Carboxylase DeficiencyKahraman isExperienced. Learn about Multiple Carboxylase Deficiency.
- Niemann-Pick DiseaseKahraman isExperienced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell HistiocytosisKahraman isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- Osteogenesis ImperfectaKahraman isExperienced. Learn about Osteogenesis Imperfecta.
- OsteopetrosisKahraman isExperienced. Learn about Osteopetrosis.
- Osteosclerosis Autosomal DominantKahraman isExperienced. Learn about Osteosclerosis Autosomal Dominant.
- ReticulohistiocytomaKahraman isExperienced. Learn about Reticulohistiocytoma.
- SeizuresKahraman isExperienced. Learn about Seizures.
- Severe Acute Respiratory Syndrome (SARS)
- Stiff Person SyndromeKahraman isExperienced. Learn about Stiff Person Syndrome.
- Urinary Tract Infection (UTI)Kahraman isExperienced. Learn about Urinary Tract Infection (UTI).
- Von Gierke DiseaseKahraman isExperienced. Learn about Von Gierke Disease.