Overview
Berrak Gurbuz-Bilginer practices practicing medicine in Yildirim Beyazit, Turkey.
Their clinical expertise encompasses L-2-Hydroxyglutaric Aciduria, Dubin-Johnson Syndrome, Biotinidase Deficiency, and Multiple Carboxylase Deficiency.
They are actively involved in clinical research, co-authoring 17 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 Berrak Gurbuz-Bilginer
Is Berrak Gurbuz-Bilginer a top-rated expert for L-2-Hydroxyglutaric Aciduria?
MediFind is an objective health platform that identifies experts based on real-world data. Berrak Gurbuz-Bilginer is classified as an Experienced expert for L-2-Hydroxyglutaric Aciduria, 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 Berrak Gurbuz-Bilginer participate in research or clinical trials?
Yes. Berrak Gurbuz-Bilginer has published 17 articles and abstracts on conditions like L-2-Hydroxyglutaric Aciduria. You can view a list of Berrak Gurbuz-Bilginer'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
- Experienced
- Biotinidase DeficiencyGurbuz-Bilginer isExperienced. Learn about Biotinidase Deficiency.
- Dubin-Johnson SyndromeGurbuz-Bilginer isExperienced. Learn about Dubin-Johnson Syndrome.
- Enlarged LiverGurbuz-Bilginer isExperienced. Learn about Enlarged Liver.
- Fanconi Bickel SyndromeGurbuz-Bilginer isExperienced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeGurbuz-Bilginer isExperienced. Learn about Fanconi Syndrome.
- Hearing LossGurbuz-Bilginer isExperienced. Learn about Hearing Loss.
- HypotoniaGurbuz-Bilginer isExperienced. Learn about Hypotonia.
- L-2-Hydroxyglutaric AciduriaGurbuz-Bilginer isExperienced. Learn about L-2-Hydroxyglutaric Aciduria.
- Lactic AcidosisGurbuz-Bilginer isExperienced. Learn about Lactic Acidosis.
- LeukodystrophyGurbuz-Bilginer isExperienced. Learn about Leukodystrophy.
- Low Sodium LevelGurbuz-Bilginer isExperienced. Learn about Low Sodium Level.
- Metachromatic LeukodystrophyGurbuz-Bilginer isExperienced. Learn about Metachromatic Leukodystrophy.
- Mucopolysaccharidoses (MPS)Gurbuz-Bilginer isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Multiple Carboxylase DeficiencyGurbuz-Bilginer isExperienced. Learn about Multiple Carboxylase Deficiency.
- Pompe DiseaseGurbuz-Bilginer isExperienced. Learn about Pompe Disease.
- PorphyriaGurbuz-Bilginer isExperienced. Learn about Porphyria.
- Rotor SyndromeGurbuz-Bilginer isExperienced. Learn about Rotor Syndrome.
- Situs InversusGurbuz-Bilginer isExperienced. Learn about Situs Inversus.
- Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
- Tyrosinemia Type 1Gurbuz-Bilginer isExperienced. Learn about Tyrosinemia Type 1.
- Von Gierke DiseaseGurbuz-Bilginer isExperienced. Learn about Von Gierke Disease.
- X-Linked HypophosphatemiaGurbuz-Bilginer isExperienced. Learn about X-Linked Hypophosphatemia.