Overview
Engin Kose practices practicing medicine in Ankara, Turkey.
Kose is highly rated in 28 conditions, according to our data. Their clinical expertise encompasses Biotinidase Deficiency, Multiple Carboxylase Deficiency, Metabolic Acidosis, and Transcobalamin Deficiency.
They are actively involved in clinical research, co-authoring 102 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 Engin A. Kose
Is Engin A. Kose a top-rated expert for Biotinidase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Engin A. Kose is classified as an Distinguished expert for Biotinidase 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 Engin A. Kose participate in research or clinical trials?
Yes. Engin A. Kose has published 102 articles and abstracts on conditions like Biotinidase Deficiency. You can view a list of Engin A. 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
- Distinguished
- Biotinidase DeficiencyKose isDistinguished. Learn about Biotinidase Deficiency.
- Metabolic AcidosisKose isDistinguished. Learn about Metabolic Acidosis.
- Multiple Carboxylase DeficiencyKose isDistinguished. Learn about Multiple Carboxylase Deficiency.
- Transcobalamin DeficiencyKose isDistinguished. Learn about Transcobalamin Deficiency.
- Vitamin B12 DeficiencyKose isDistinguished. Learn about Vitamin B12 Deficiency.
- Advanced
- Alpha MannosidosisKose isAdvanced. Learn about Alpha Mannosidosis.
- Batten DiseaseKose isAdvanced. Learn about Batten Disease.
- Cerebrotendinous Xanthomatosis
- CitrullinemiaKose isAdvanced. Learn about Citrullinemia.
- Classic GalactosemiaKose isAdvanced. Learn about Classic Galactosemia.
- CLN1 DiseaseKose isAdvanced. Learn about CLN1 Disease.
- CLN2 DiseaseKose isAdvanced. Learn about CLN2 Disease.
- CLN3 DiseaseKose isAdvanced. Learn about CLN3 Disease.
- CLN4 DiseaseKose isAdvanced. Learn about CLN4 Disease.
- CLN5 DiseaseKose isAdvanced. Learn about CLN5 Disease.
- Cytochrome C Oxidase Deficiency
- GalactosemiaKose isAdvanced. Learn about Galactosemia.
- HyperglycerolemiaKose isAdvanced. Learn about Hyperglycerolemia.
- HypotoniaKose isAdvanced. Learn about Hypotonia.
- Lactic AcidosisKose isAdvanced. Learn about Lactic Acidosis.
- Leigh SyndromeKose isAdvanced. Learn about Leigh Syndrome.
- Maple Syrup Urine Disease
- Mitochondrial Complex 3 Deficiency
- Pyruvate Carboxylase Deficiency
- RhabdomyolysisKose isAdvanced. Learn about Rhabdomyolysis.
- Vitamin B12 Deficiency Anemia
- Von Gierke DiseaseKose isAdvanced. Learn about Von Gierke Disease.
- XanthomaKose isAdvanced. Learn about Xanthoma.
- Experienced
- Absence SeizureKose isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly Syndrome
- ALG1-CDGKose isExperienced. Learn about ALG1-CDG.
- Amyotonia CongenitaKose isExperienced. Learn about Amyotonia Congenita.
- Apolipoprotein C2 Deficiency
- Argininosuccinic AciduriaKose isExperienced. Learn about Argininosuccinic Aciduria.
- Autosomal Recessive Distal Renal Tubular Acidosis
- Bronchiolitis ObliteransKose isExperienced. Learn about Bronchiolitis Obliterans.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- CardiomyopathyKose isExperienced. Learn about Cardiomyopathy.
- Centronuclear MyopathyKose isExperienced. Learn about Centronuclear Myopathy.
- Cholesteryl Ester Storage Disease
- Coenzyme Q Cytochrome C Reductase Deficiency
- Congenital Fiber-Type Disproportion
- Cortical DysplasiaKose isExperienced. Learn about Cortical Dysplasia.
- CystinuriaKose isExperienced. Learn about Cystinuria.
- Defective Apolipoprotein B-100
- Diabetic KetoacidosisKose isExperienced. Learn about Diabetic Ketoacidosis.
- DiarrheaKose isExperienced. Learn about Diarrhea.
- Drug Induced DyskinesiaKose isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaKose isExperienced. Learn about Dysarthria.
- Early Infantile Epileptic Encephalopathy
- Enlarged LiverKose isExperienced. Learn about Enlarged Liver.
- EpilepsyKose isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenKose isExperienced. Learn about Epilepsy in Children.
- Familial Hypercholesterolemia
- Familial Hypertriglyceridemia
- Familial Lipoprotein Lipase Deficiency
- Galactokinase DeficiencyKose isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase Deficiency
- Generalized Tonic-Clonic Seizure
- Hearing LossKose isExperienced. Learn about Hearing Loss.
- HemochromatosisKose isExperienced. Learn about Hemochromatosis.
- Hepatocerebral DegenerationKose isExperienced. Learn about Hepatocerebral Degeneration.
- Heterozygous Familial Hypercholesterolemia (HeFH)
- High CholesterolKose isExperienced. Learn about High Cholesterol.
- HistiocytosisKose isExperienced. Learn about Histiocytosis.
- Hypertrophic Cardiomyopathy (HCM)
- HypothyroidismKose isExperienced. Learn about Hypothyroidism.
- Infantile NeutropeniaKose isExperienced. Learn about Infantile Neutropenia.
- Low Blood SugarKose isExperienced. Learn about Low Blood Sugar.
- Lysosomal Acid Lipase Deficiency
- Magnesium DeficiencyKose isExperienced. Learn about Magnesium Deficiency.
- MalnutritionKose isExperienced. Learn about Malnutrition.
- Maternal Hyperphenylalaninemia
- MELAS SyndromeKose isExperienced. Learn about MELAS Syndrome.
- Methylmalonic AcidemiaKose isExperienced. Learn about Methylmalonic Acidemia.
- Mevalonate Kinase Deficiency
- MicrocephalyKose isExperienced. Learn about Microcephaly.
- Movement DisordersKose isExperienced. Learn about Movement Disorders.
- Mucopolysaccharidoses (MPS)Kose isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Myotonia CongenitaKose isExperienced. Learn about Myotonia Congenita.
- Neonatal HemochromatosisKose isExperienced. Learn about Neonatal Hemochromatosis.
- Neonatal HypothyroidismKose isExperienced. Learn about Neonatal Hypothyroidism.
- Newborn Low Blood SugarKose isExperienced. Learn about Newborn Low Blood Sugar.
- Niemann-Pick DiseaseKose isExperienced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell Histiocytosis
- Optic GliomaKose isExperienced. Learn about Optic Glioma.
- Phenylketonuria (PKU)Kose isExperienced. Learn about Phenylketonuria (PKU).
- Respiratory AlkalosisKose isExperienced. Learn about Respiratory Alkalosis.
- ReticulohistiocytomaKose isExperienced. Learn about Reticulohistiocytoma.
- SeizuresKose isExperienced. Learn about Seizures.
- SplenomegalyKose isExperienced. Learn about Splenomegaly.
- Tubular Aggregate MyopathyKose isExperienced. Learn about Tubular Aggregate Myopathy.
- Urea Cycle Disorders (UCD)Kose isExperienced. Learn about Urea Cycle Disorders (UCD).
- Wolman DiseaseKose isExperienced. Learn about Wolman Disease.
- X-Linked Myotubular Myopathy