Overview
Melis Kose practices practicing medicine in Ismet Kaptan, Turkey.
Ms. Kose is highly rated in 4 conditions, according to our data. Her clinical expertise encompasses Lysinuric Protein Intolerance, Leigh Syndrome, Cytochrome C Oxidase Deficiency, and Severe Congenital Neutropenia.
She is actively involved in clinical research, co-authoring 41 peer reviewed articles.
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.
Frequently Asked Questions about Melis D. Kose
Is Melis D. Kose a top-rated expert for Lysinuric Protein Intolerance?
MediFind is an objective health platform that identifies experts based on real-world data. Melis D. Kose is classified as an Advanced expert for Lysinuric Protein Intolerance, 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 Melis D. Kose participate in research or clinical trials?
Yes. Melis D. Kose has published 41 articles and abstracts on conditions like Lysinuric Protein Intolerance. You can view a list of Melis D. Kose'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
- Cytochrome C Oxidase Deficiency
- Leigh SyndromeMs. Kose isAdvanced. Learn about Leigh Syndrome.
- Lysinuric Protein IntoleranceMs. Kose isAdvanced. Learn about Lysinuric Protein Intolerance.
- Severe Congenital NeutropeniaMs. Kose isAdvanced. Learn about Severe Congenital Neutropenia.
- Experienced
- Absence SeizureMs. Kose isExperienced. Learn about Absence Seizure.
- AgranulocytosisMs. Kose isExperienced. Learn about Agranulocytosis.
- Alpha ThalassemiaMs. Kose isExperienced. Learn about Alpha Thalassemia.
- Batten DiseaseMs. Kose isExperienced. Learn about Batten Disease.
- Biotinidase DeficiencyMs. Kose isExperienced. Learn about Biotinidase Deficiency.
- CACH SyndromeMs. Kose isExperienced. Learn about CACH Syndrome.
- CitrullinemiaMs. Kose isExperienced. Learn about Citrullinemia.
- Classic GalactosemiaMs. Kose isExperienced. Learn about Classic Galactosemia.
- CLN1 DiseaseMs. Kose isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMs. Kose isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseMs. Kose isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseMs. Kose isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseMs. Kose isExperienced. Learn about CLN5 Disease.
- Cockayne SyndromeMs. Kose isExperienced. Learn about Cockayne Syndrome.
- Congenital Myasthenic SyndromeMs. Kose isExperienced. Learn about Congenital Myasthenic Syndrome.
- Defective Apolipoprotein B-100Ms. Kose isExperienced. Learn about Defective Apolipoprotein B-100.
- EpilepsyMs. Kose isExperienced. Learn about Epilepsy.
- Familial DysautonomiaMs. Kose isExperienced. Learn about Familial Dysautonomia.
- Familial HypercholesterolemiaMs. Kose isExperienced. Learn about Familial Hypercholesterolemia.
- Farber LipogranulomatosisMs. Kose isExperienced. Learn about Farber Lipogranulomatosis.
- Fetal EdemaMs. Kose isExperienced. Learn about Fetal Edema.
- Folate DeficiencyMs. Kose isExperienced. Learn about Folate Deficiency.
- Galactokinase DeficiencyMs. Kose isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Kose isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Kose isExperienced. Learn about Galactosemia.
- Gaucher DiseaseMs. Kose isExperienced. Learn about Gaucher Disease.
- Generalized Tonic-Clonic SeizureMs. Kose isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Hemolytic Disease of the NewbornMs. Kose isExperienced. Learn about Hemolytic Disease of the Newborn.
- Heterozygous Familial Hypercholesterolemia (HeFH)
- High CholesterolMs. Kose isExperienced. Learn about High Cholesterol.
- Homozygous Familial Hypercholesterolemia (HoFH)
- Hydrops FetalisMs. Kose isExperienced. Learn about Hydrops Fetalis.
- HypotoniaMs. Kose isExperienced. Learn about Hypotonia.
- Infantile NeutropeniaMs. Kose isExperienced. Learn about Infantile Neutropenia.
- Krabbe DiseaseMs. Kose isExperienced. Learn about Krabbe Disease.
- Liver FailureMs. Kose isExperienced. Learn about Liver Failure.
- MalnutritionMs. Kose isExperienced. Learn about Malnutrition.
- Maple Syrup Urine DiseaseMs. Kose isExperienced. Learn about Maple Syrup Urine Disease.
- MELAS SyndromeMs. Kose isExperienced. Learn about MELAS Syndrome.
- Metabolic AcidosisMs. Kose isExperienced. Learn about Metabolic Acidosis.
- Movement DisordersMs. Kose isExperienced. Learn about Movement Disorders.
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Multiple Carboxylase DeficiencyMs. Kose isExperienced. Learn about Multiple Carboxylase Deficiency.
- Ornithine Transcarbamylase Deficiency
- RhabdomyolysisMs. Kose isExperienced. Learn about Rhabdomyolysis.
- SeizuresMs. Kose isExperienced. Learn about Seizures.
- Striatonigral Degeneration Infantile
- Urea Cycle Disorders (UCD)Ms. Kose isExperienced. Learn about Urea Cycle Disorders (UCD).
- Vitamin B12 Deficiency AnemiaMs. Kose isExperienced. Learn about Vitamin B12 Deficiency Anemia.