Overview
Mahmut Coker practices practicing medicine in Bornova, Turkey.
Coker is highly rated in 12 conditions, according to our data. Their clinical expertise encompasses Biotinidase Deficiency, Multiple Carboxylase Deficiency, Maple Syrup Urine Disease, and Pyruvate Decarboxylase Deficiency.
They are actively involved in clinical research, co-authoring 79 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 Mahmut Coker
Is Mahmut Coker a top-rated expert for Biotinidase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Mahmut Coker is classified as an Advanced 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 Mahmut Coker participate in research or clinical trials?
Yes. Mahmut Coker has published 79 articles and abstracts on conditions like Biotinidase Deficiency. You can view a list of Mahmut Coker'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
- Beta-Ketothiolase Deficiency
- Biotinidase DeficiencyCoker isAdvanced. Learn about Biotinidase Deficiency.
- DPAGT1-CDGCoker isAdvanced. Learn about DPAGT1-CDG.
- Gaucher DiseaseCoker isAdvanced. Learn about Gaucher Disease.
- Glycogen Storage Disease Type 3
- Maple Syrup Urine Disease
- Mucopolysaccharidoses (MPS)
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)
- Multiple Carboxylase Deficiency
- Pyruvate Decarboxylase Deficiency
- Pyruvate Dehydrogenase Deficiency
- SRD5A3-CDGCoker isAdvanced. Learn about SRD5A3-CDG.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Acid Sphingomyelinase Deficiency (ASMD)
- AlkaptonuriaCoker isExperienced. Learn about Alkaptonuria.
- Aplasia Cutis CongenitaCoker isExperienced. Learn about Aplasia Cutis Congenita.
- Apolipoprotein C2 DeficiencyCoker isExperienced. Learn about Apolipoprotein C2 Deficiency.
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- CACH SyndromeCoker isExperienced. Learn about CACH Syndrome.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- CataractCoker isExperienced. Learn about Cataract.
- Childhood PancreatitisCoker isExperienced. Learn about Childhood Pancreatitis.
- Classic GalactosemiaCoker isExperienced. Learn about Classic Galactosemia.
- Clouston SyndromeCoker isExperienced. Learn about Clouston Syndrome.
- Coarctation of the AortaCoker isExperienced. Learn about Coarctation of the Aorta.
- Congenital CataractCoker isExperienced. Learn about Congenital Cataract.
- CystinosisCoker isExperienced. Learn about Cystinosis.
- Cytochrome C Oxidase Deficiency
- Defective Apolipoprotein B-100
- Dihydrolipoamide Dehydrogenase Deficiency
- Drug Induced DyskinesiaCoker isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaCoker isExperienced. Learn about Dysarthria.
- Early Infantile Epileptic Encephalopathy
- Ectodermal DysplasiasCoker isExperienced. Learn about Ectodermal Dysplasias.
- Fabry DiseaseCoker isExperienced. Learn about Fabry Disease.
- Familial HypercholesterolemiaCoker isExperienced. Learn about Familial Hypercholesterolemia.
- Familial Lipoprotein Lipase Deficiency
- Farber LipogranulomatosisCoker isExperienced. Learn about Farber Lipogranulomatosis.
- Galactokinase DeficiencyCoker isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase Deficiency
- GalactosemiaCoker isExperienced. Learn about Galactosemia.
- GangliosidosisCoker isExperienced. Learn about Gangliosidosis.
- Glutaric Acidemia Type 1Coker isExperienced. Learn about Glutaric Acidemia Type 1.
- Glycogen Storage Disease Type 6
- Glycogen Storage Disease Type 9
- GTP Cyclohydrolase 1 Deficiency
- Hearing LossCoker isExperienced. Learn about Hearing Loss.
- Heterozygous Familial Hypercholesterolemia (HeFH)
- High CholesterolCoker isExperienced. Learn about High Cholesterol.
- HistiocytosisCoker isExperienced. Learn about Histiocytosis.
- Homozygous Familial Hypercholesterolemia (HoFH)
- Hypophosphatasia (HPP)Coker isExperienced. Learn about Hypophosphatasia (HPP).
- HypotoniaCoker isExperienced. Learn about Hypotonia.
- Intestinal Pseudo-ObstructionCoker isExperienced. Learn about Intestinal Pseudo-Obstruction.
- Leigh SyndromeCoker isExperienced. Learn about Leigh Syndrome.
- Low Blood SugarCoker isExperienced. Learn about Low Blood Sugar.
- MacroglossiaCoker isExperienced. Learn about Macroglossia.
- Methylmalonic AcidemiaCoker isExperienced. Learn about Methylmalonic Acidemia.
- Mitochondrial Neurogastrointestinal Encephalopathy Disease
- MPI-CDGCoker isExperienced. Learn about MPI-CDG.
- Mucolipidosis 3Coker isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Coker isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- NephrocalcinosisCoker isExperienced. Learn about Nephrocalcinosis.
- Niemann-Pick DiseaseCoker isExperienced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell Histiocytosis
- OchronosisCoker isExperienced. Learn about Ochronosis.
- Oculopharyngeal Muscular Dystrophy
- Phenylketonuria (PKU)Coker isExperienced. Learn about Phenylketonuria (PKU).
- PMM2-Congenital Disorder of Glycosylation
- Pompe DiseaseCoker isExperienced. Learn about Pompe Disease.
- ReticulohistiocytomaCoker isExperienced. Learn about Reticulohistiocytoma.
- RhabdomyolysisCoker isExperienced. Learn about Rhabdomyolysis.
- SeizuresCoker isExperienced. Learn about Seizures.
- Sensorimotor PolyneuropathyCoker isExperienced. Learn about Sensorimotor Polyneuropathy.
- Severe Congenital NeutropeniaCoker isExperienced. Learn about Severe Congenital Neutropenia.
- Short Bowel SyndromeCoker isExperienced. Learn about Short Bowel Syndrome.
- SialidosisCoker isExperienced. Learn about Sialidosis.
- SpasticityCoker isExperienced. Learn about Spasticity.
- SplenomegalyCoker isExperienced. Learn about Splenomegaly.
- Tay-Sachs DiseaseCoker isExperienced. Learn about Tay-Sachs Disease.
- Undescended TesticleCoker isExperienced. Learn about Undescended Testicle.
- Urea Cycle Disorders (UCD)Coker isExperienced. Learn about Urea Cycle Disorders (UCD).
- Von Gierke DiseaseCoker isExperienced. Learn about Von Gierke Disease.