Overview
Sema Ucar practices practicing medicine in Ege, Turkey.
Ms. Ucar is highly rated in 8 conditions, according to our data. Her clinical expertise encompasses Mitochondrial Neurogastrointestinal Encephalopathy Disease, Carnitine Palmitoyltransferase 2 Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Von Gierke Disease.
She is actively involved in clinical research, co-authoring 46 peer reviewed articles and participating in 2 clinical trials.
Gender
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.
2 Clinical Trials
Frequently Asked Questions about Sema K. Ucar
Is Sema K. Ucar a top-rated expert for Mitochondrial Neurogastrointestinal Encephalopathy Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Sema K. Ucar is classified as an Distinguished expert for Mitochondrial Neurogastrointestinal Encephalopathy Disease, 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 Sema K. Ucar participate in research or clinical trials?
Yes. Sema K. Ucar has published 46 articles and abstracts on conditions like Mitochondrial Neurogastrointestinal Encephalopathy Disease. You can view a list of Sema K. Ucar'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
- Mitochondrial Neurogastrointestinal Encephalopathy Disease
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Beta-Ketothiolase DeficiencyMs. Ucar isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Biotinidase DeficiencyMs. Ucar isAdvanced. Learn about Biotinidase Deficiency.
- Carnitine Palmitoyltransferase 2 Deficiency
- Multiple Carboxylase Deficiency
- Oculopharyngeal Muscular Dystrophy
- Von Gierke DiseaseMs. Ucar isAdvanced. Learn about Von Gierke Disease.
- Experienced
- Adrenal Insufficiency PediatricMs. Ucar isExperienced. Learn about Adrenal Insufficiency Pediatric.
- AgranulocytosisMs. Ucar isExperienced. Learn about Agranulocytosis.
- AlkaptonuriaMs. Ucar isExperienced. Learn about Alkaptonuria.
- Alpha MannosidosisMs. Ucar isExperienced. Learn about Alpha Mannosidosis.
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Brown SyndromeMs. Ucar isExperienced. Learn about Brown Syndrome.
- Carnitine Palmitoyltransferase 1 Deficiency
- CataractMs. Ucar isExperienced. Learn about Cataract.
- Classic GalactosemiaMs. Ucar isExperienced. Learn about Classic Galactosemia.
- Coarctation of the AortaMs. Ucar isExperienced. Learn about Coarctation of the Aorta.
- Congenital CataractMs. Ucar isExperienced. Learn about Congenital Cataract.
- CystinosisMs. Ucar isExperienced. Learn about Cystinosis.
- Cytochrome C Oxidase DeficiencyMs. Ucar isExperienced. Learn about Cytochrome C Oxidase Deficiency.
- Defective Apolipoprotein B-100Ms. Ucar isExperienced. Learn about Defective Apolipoprotein B-100.
- Fabry DiseaseMs. Ucar isExperienced. Learn about Fabry Disease.
- Familial HypercholesterolemiaMs. Ucar isExperienced. Learn about Familial Hypercholesterolemia.
- Galactokinase DeficiencyMs. Ucar isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Ucar isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Ucar isExperienced. Learn about Galactosemia.
- GangliosidosisMs. Ucar isExperienced. Learn about Gangliosidosis.
- Hearing LossMs. Ucar isExperienced. Learn about Hearing Loss.
- High CholesterolMs. Ucar isExperienced. Learn about High Cholesterol.
- Homozygous Familial Hypercholesterolemia (HoFH)
- Infantile NeutropeniaMs. Ucar isExperienced. Learn about Infantile Neutropenia.
- Intestinal Pseudo-ObstructionMs. Ucar isExperienced. Learn about Intestinal Pseudo-Obstruction.
- Leigh SyndromeMs. Ucar isExperienced. Learn about Leigh Syndrome.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- MacroglossiaMs. Ucar isExperienced. Learn about Macroglossia.
- Maple Syrup Urine DiseaseMs. Ucar isExperienced. Learn about Maple Syrup Urine Disease.
- MELAS SyndromeMs. Ucar isExperienced. Learn about MELAS Syndrome.
- Methylmalonic AcidemiaMs. Ucar isExperienced. Learn about Methylmalonic Acidemia.
- Mitochondrial Trifunctional Protein Deficiency
- Mucopolysaccharidoses (MPS)Ms. Ucar isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- OchronosisMs. Ucar isExperienced. Learn about Ochronosis.
- RhabdomyolysisMs. Ucar isExperienced. Learn about Rhabdomyolysis.
- Sensorimotor PolyneuropathyMs. Ucar isExperienced. Learn about Sensorimotor Polyneuropathy.
- Severe Congenital NeutropeniaMs. Ucar isExperienced. Learn about Severe Congenital Neutropenia.
- Short Bowel SyndromeMs. Ucar isExperienced. Learn about Short Bowel Syndrome.
- Tay-Sachs DiseaseMs. Ucar isExperienced. Learn about Tay-Sachs Disease.