Overview
Havva Yazıcı practices practicing medicine in Ege, Turkey.
Yazıcı is highly rated in 6 conditions, according to our data. Their clinical expertise encompasses Carnitine Palmitoyltransferase 2 Deficiency, Mitochondrial Neurogastrointestinal Encephalopathy Disease, Rhabdomyolysis, and Cerebrotendinous Xanthomatosis.
They are actively involved in clinical research, co-authoring 28 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 Havva Yazıcı
Is Havva Yazıcı a top-rated expert for Carnitine Palmitoyltransferase 2 Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Havva Yazıcı is classified as an Advanced expert for Carnitine Palmitoyltransferase 2 Deficiency, 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 Havva Yazıcı participate in research or clinical trials?
Yes. Havva Yazıcı has published 28 articles and abstracts on conditions like Carnitine Palmitoyltransferase 2 Deficiency. You can view a list of Havva Yazıcı'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
- Carnitine Palmitoyltransferase 2 Deficiency
- Cerebrotendinous Xanthomatosis
- Defective Apolipoprotein B-100
- Mitochondrial Neurogastrointestinal Encephalopathy Disease
- RhabdomyolysisYazıcı isAdvanced. Learn about Rhabdomyolysis.
- XanthomaYazıcı isAdvanced. Learn about Xanthoma.
- Experienced
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Carnitine Palmitoyltransferase 1 Deficiency
- Chanarin-Dorfman SyndromeYazıcı isExperienced. Learn about Chanarin-Dorfman Syndrome.
- Coarctation of the AortaYazıcı isExperienced. Learn about Coarctation of the Aorta.
- Erythrokeratodermia Variabilis et Progressiva
- Familial HypercholesterolemiaYazıcı isExperienced. Learn about Familial Hypercholesterolemia.
- GangliosidosisYazıcı isExperienced. Learn about Gangliosidosis.
- Glycogen Storage Disease Type 3Yazıcı isExperienced. Learn about Glycogen Storage Disease Type 3.
- Glycogen Storage Disease Type 6Yazıcı isExperienced. Learn about Glycogen Storage Disease Type 6.
- Glycogen Storage Disease Type 9Yazıcı isExperienced. Learn about Glycogen Storage Disease Type 9.
- Heterozygous Familial Hypercholesterolemia (HeFH)
- High CholesterolYazıcı isExperienced. Learn about High Cholesterol.
- Homozygous Familial Hypercholesterolemia (HoFH)
- Intestinal Pseudo-ObstructionYazıcı isExperienced. Learn about Intestinal Pseudo-Obstruction.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maple Syrup Urine DiseaseYazıcı isExperienced. Learn about Maple Syrup Urine Disease.
- Methylmalonic AcidemiaYazıcı isExperienced. Learn about Methylmalonic Acidemia.
- Mitochondrial Trifunctional Protein Deficiency
- Mucolipidosis 3Yazıcı isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Yazıcı isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidoses (MPS)Yazıcı isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Nonbullous Congenital Ichthyosiform Erythroderma
- Oculopharyngeal Muscular Dystrophy
- Sensorimotor PolyneuropathyYazıcı isExperienced. Learn about Sensorimotor Polyneuropathy.
- Short Bowel SyndromeYazıcı isExperienced. Learn about Short Bowel Syndrome.
- SialidosisYazıcı isExperienced. Learn about Sialidosis.
- Tay-Sachs DiseaseYazıcı isExperienced. Learn about Tay-Sachs Disease.
- Von Gierke DiseaseYazıcı isExperienced. Learn about Von Gierke Disease.