Overview
Yilmaz Yildiz practices practicing medicine in Ankara, Turkey.
Yildiz is highly rated in 5 conditions, according to our data. Their clinical expertise encompasses Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), Pyruvate Decarboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, and Glycogen Storage Disease Type 0.
They are actively involved in clinical research, co-authoring 19 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 Yilmaz Yildiz
Is Yilmaz Yildiz a top-rated expert for Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)?
MediFind is an objective health platform that identifies experts based on real-world data. Yilmaz Yildiz is classified as an Advanced expert for Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), 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 Yilmaz Yildiz participate in research or clinical trials?
Yes. Yilmaz Yildiz has published 19 articles and abstracts on conditions like Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). You can view a list of Yilmaz Yildiz'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
- Glycogen Storage Disease Type 0
- Maternal Hyperphenylalaninemia
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Pyruvate Decarboxylase Deficiency
- Pyruvate Dehydrogenase Deficiency
- Experienced
- Achalasia Microcephaly SyndromeYildiz isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Cortical DysplasiaYildiz isExperienced. Learn about Cortical Dysplasia.
- Dihydrolipoamide Dehydrogenase Deficiency
- Drug Induced DyskinesiaYildiz isExperienced. Learn about Drug Induced Dyskinesia.
- Early Infantile Epileptic Encephalopathy
- Gestational Trophoblastic Disease
- Hydatidiform MoleYildiz isExperienced. Learn about Hydatidiform Mole.
- HypotoniaYildiz isExperienced. Learn about Hypotonia.
- MicrocephalyYildiz isExperienced. Learn about Microcephaly.
- Mitochondrial Complex V Deficiency
- Mucopolysaccharidoses (MPS)Yildiz isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Niemann-Pick DiseaseYildiz isExperienced. Learn about Niemann-Pick Disease.
- Ornithine Transcarbamylase Deficiency
- Phenylketonuria (PKU)Yildiz isExperienced. Learn about Phenylketonuria (PKU).
- Spastic Paraplegia Type 2Yildiz isExperienced. Learn about Spastic Paraplegia Type 2.
- Urea Cycle Disorders (UCD)Yildiz isExperienced. Learn about Urea Cycle Disorders (UCD).