Overview
Turgay Coskun practices practicing medicine in Ankara, Turkey.
Coskun is highly rated in 17 conditions, according to our data. Their clinical expertise encompasses Phenylketonuria (PKU), Fucosidosis, Glutaric Acidemia Type 2, Isovaleric Acidemia, and Bone Marrow Aspiration.
They are actively involved in clinical research, co-authoring 75 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 Turgay Coskun
Is Turgay Coskun a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Turgay Coskun is classified as an Distinguished expert for Phenylketonuria (PKU), 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 Turgay Coskun participate in research or clinical trials?
Yes. Turgay Coskun has published 75 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Turgay Coskun'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
- Distinguished
- Phenylketonuria (PKU)Coskun isDistinguished. Learn about Phenylketonuria (PKU).
- Advanced
- Carnitine-Acylcarnitine Translocase Deficiency
- Cerebrotendinous Xanthomatosis
- Enlarged LiverCoskun isAdvanced. Learn about Enlarged Liver.
- FucosidosisCoskun isAdvanced. Learn about Fucosidosis.
- Glutaric Acidemia Type 2Coskun isAdvanced. Learn about Glutaric Acidemia Type 2.
- Guanidinoacetate Methyltransferase Deficiency
- Inborn Amino Acid Metabolism Disorder
- Isovaleric AcidemiaCoskun isAdvanced. Learn about Isovaleric Acidemia.
- Lysinuric Protein Intolerance
- Maple Syrup Urine DiseaseCoskun isAdvanced. Learn about Maple Syrup Urine Disease.
- Maternal Hyperphenylalaninemia
- Metabolic AcidosisCoskun isAdvanced. Learn about Metabolic Acidosis.
- Methylmalonic AcidemiaCoskun isAdvanced. Learn about Methylmalonic Acidemia.
- Propionic AcidemiaCoskun isAdvanced. Learn about Propionic Acidemia.
- VisceromegalyCoskun isAdvanced. Learn about Visceromegaly.
- XanthomaCoskun isAdvanced. Learn about Xanthoma.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Absence SeizureCoskun isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly SyndromeCoskun isExperienced. Learn about Achalasia Microcephaly Syndrome.
- AlbinismCoskun isExperienced. Learn about Albinism.
- AspartylglucosaminuriaCoskun isExperienced. Learn about Aspartylglucosaminuria.
- Bone Marrow AspirationCoskun isExperienced. Learn about Bone Marrow Aspiration.
- CataractCoskun isExperienced. Learn about Cataract.
- Congenital CataractCoskun isExperienced. Learn about Congenital Cataract.
- Corpus Callosum AgenesisCoskun isExperienced. Learn about Corpus Callosum Agenesis.
- Cortical DysplasiaCoskun isExperienced. Learn about Cortical Dysplasia.
- Developmental Reading DisorderCoskun isExperienced. Learn about Developmental Reading Disorder.
- GalactosemiaCoskun isExperienced. Learn about Galactosemia.
- GangliosidosisCoskun isExperienced. Learn about Gangliosidosis.
- Generalized Tonic-Clonic Seizure
- Gestational Trophoblastic Disease
- Glutaric Acidemia Type 1Coskun isExperienced. Learn about Glutaric Acidemia Type 1.
- GM1 GangliosidosisCoskun isExperienced. Learn about GM1 Gangliosidosis.
- HomocystinuriaCoskun isExperienced. Learn about Homocystinuria.
- Hydatidiform MoleCoskun isExperienced. Learn about Hydatidiform Mole.
- Low Blood SugarCoskun isExperienced. Learn about Low Blood Sugar.
- MicrocephalyCoskun isExperienced. Learn about Microcephaly.
- Mucolipidosis 3Coskun isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Coskun isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidoses (MPS)Coskun isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- PMM2-Congenital Disorder of Glycosylation
- Primary Carnitine DeficiencyCoskun isExperienced. Learn about Primary Carnitine Deficiency.
- Primary Lateral SclerosisCoskun isExperienced. Learn about Primary Lateral Sclerosis.
- Riboflavin Transporter Deficiency Neuronopathy
- SeizuresCoskun isExperienced. Learn about Seizures.
- SialidosisCoskun isExperienced. Learn about Sialidosis.
- Vici SyndromeCoskun isExperienced. Learn about Vici Syndrome.
- Vitamin B12 Deficiency AnemiaCoskun isExperienced. Learn about Vitamin B12 Deficiency Anemia.
- X-Linked Creatine DeficiencyCoskun isExperienced. Learn about X-Linked Creatine Deficiency.