Overview
Ebru Canda practices practicing medicine in Bornova, Turkey.
Ms. Canda is highly rated in 11 conditions, according to our data. Her clinical expertise encompasses Biotinidase Deficiency, Multiple Carboxylase Deficiency, Galactokinase Deficiency, and Galactose Epimerase Deficiency.
She is actively involved in clinical research, co-authoring 57 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 Ebru E. Canda
Is Ebru E. Canda a top-rated expert for Biotinidase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Ebru E. Canda 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 Ebru E. Canda participate in research or clinical trials?
Yes. Ebru E. Canda has published 57 articles and abstracts on conditions like Biotinidase Deficiency. You can view a list of Ebru E. Canda'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 DeficiencyMs. Canda isDistinguished. Learn about Biotinidase Deficiency.
- Multiple Carboxylase DeficiencyMs. Canda isDistinguished. Learn about Multiple Carboxylase Deficiency.
- Advanced
- Cerebrotendinous XanthomatosisMs. Canda isAdvanced. Learn about Cerebrotendinous Xanthomatosis.
- Classic GalactosemiaMs. Canda isAdvanced. Learn about Classic Galactosemia.
- DPAGT1-CDGMs. Canda isAdvanced. Learn about DPAGT1-CDG.
- Galactokinase DeficiencyMs. Canda isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Canda isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Canda isAdvanced. Learn about Galactosemia.
- Maple Syrup Urine DiseaseMs. Canda isAdvanced. Learn about Maple Syrup Urine Disease.
- SRD5A3-CDGMs. Canda isAdvanced. Learn about SRD5A3-CDG.
- XanthomaMs. Canda isAdvanced. Learn about Xanthoma.
- Experienced
- AgranulocytosisMs. Canda isExperienced. Learn about Agranulocytosis.
- AlkaptonuriaMs. Canda isExperienced. Learn about Alkaptonuria.
- Aplasia Cutis CongenitaMs. Canda isExperienced. Learn about Aplasia Cutis Congenita.
- Apolipoprotein C2 DeficiencyMs. Canda isExperienced. Learn about Apolipoprotein C2 Deficiency.
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- CACH SyndromeMs. Canda isExperienced. Learn about CACH Syndrome.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- CataractMs. Canda isExperienced. Learn about Cataract.
- Childhood PancreatitisMs. Canda isExperienced. Learn about Childhood Pancreatitis.
- Clouston SyndromeMs. Canda isExperienced. Learn about Clouston Syndrome.
- Coarctation of the AortaMs. Canda isExperienced. Learn about Coarctation of the Aorta.
- Congenital CataractMs. Canda isExperienced. Learn about Congenital Cataract.
- Cytochrome C Oxidase DeficiencyMs. Canda isExperienced. Learn about Cytochrome C Oxidase Deficiency.
- Defective Apolipoprotein B-100Ms. Canda isExperienced. Learn about Defective Apolipoprotein B-100.
- Dilated Cardiomyopathy (DCM)Ms. Canda isExperienced. Learn about Dilated Cardiomyopathy (DCM).
- Drug Induced DyskinesiaMs. Canda isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaMs. Canda isExperienced. Learn about Dysarthria.
- Ectodermal DysplasiasMs. Canda isExperienced. Learn about Ectodermal Dysplasias.
- Familial HypercholesterolemiaMs. Canda isExperienced. Learn about Familial Hypercholesterolemia.
- Familial Lipoprotein Lipase Deficiency
- Farber LipogranulomatosisMs. Canda isExperienced. Learn about Farber Lipogranulomatosis.
- GangliosidosisMs. Canda isExperienced. Learn about Gangliosidosis.
- Gaucher DiseaseMs. Canda isExperienced. Learn about Gaucher Disease.
- Glutaric Acidemia Type 1Ms. Canda isExperienced. Learn about Glutaric Acidemia Type 1.
- Glycogen Storage Disease Type 3Ms. Canda isExperienced. Learn about Glycogen Storage Disease Type 3.
- Glycogen Storage Disease Type 6Ms. Canda isExperienced. Learn about Glycogen Storage Disease Type 6.
- Glycogen Storage Disease Type 9Ms. Canda isExperienced. Learn about Glycogen Storage Disease Type 9.
- GTP Cyclohydrolase 1 DeficiencyMs. Canda isExperienced. Learn about GTP Cyclohydrolase 1 Deficiency.
- Hearing LossMs. Canda isExperienced. Learn about Hearing Loss.
- Heterozygous Familial Hypercholesterolemia (HeFH)
- High CholesterolMs. Canda isExperienced. Learn about High Cholesterol.
- Homozygous Familial Hypercholesterolemia (HoFH)
- Hypophosphatasia (HPP)Ms. Canda isExperienced. Learn about Hypophosphatasia (HPP).
- HypotoniaMs. Canda isExperienced. Learn about Hypotonia.
- Infantile NeutropeniaMs. Canda isExperienced. Learn about Infantile Neutropenia.
- Intestinal Pseudo-ObstructionMs. Canda isExperienced. Learn about Intestinal Pseudo-Obstruction.
- JaundiceMs. Canda isExperienced. Learn about Jaundice.
- Leigh SyndromeMs. Canda isExperienced. Learn about Leigh Syndrome.
- Low Blood SugarMs. Canda isExperienced. Learn about Low Blood Sugar.
- MacroglossiaMs. Canda isExperienced. Learn about Macroglossia.
- Methylmalonic AcidemiaMs. Canda isExperienced. Learn about Methylmalonic Acidemia.
- Mitochondrial Neurogastrointestinal Encephalopathy Disease
- MPI-CDGMs. Canda isExperienced. Learn about MPI-CDG.
- Mucolipidosis 3Ms. Canda isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Ms. Canda isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidoses (MPS)Ms. Canda isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- NephrocalcinosisMs. Canda isExperienced. Learn about Nephrocalcinosis.
- Newborn JaundiceMs. Canda isExperienced. Learn about Newborn Jaundice.
- Newborn Low Blood SugarMs. Canda isExperienced. Learn about Newborn Low Blood Sugar.
- Niemann-Pick DiseaseMs. Canda isExperienced. Learn about Niemann-Pick Disease.
- OchronosisMs. Canda isExperienced. Learn about Ochronosis.
- Oculopharyngeal Muscular DystrophyMs. Canda isExperienced. Learn about Oculopharyngeal Muscular Dystrophy.
- Optic Nerve AtrophyMs. Canda isExperienced. Learn about Optic Nerve Atrophy.
- Ornithine Transcarbamylase DeficiencyMs. Canda isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- Phenylketonuria (PKU)Ms. Canda isExperienced. Learn about Phenylketonuria (PKU).
- PMM2-Congenital Disorder of Glycosylation
- Primary Carnitine DeficiencyMs. Canda isExperienced. Learn about Primary Carnitine Deficiency.
- RhabdomyolysisMs. Canda isExperienced. Learn about Rhabdomyolysis.
- SeizuresMs. Canda isExperienced. Learn about Seizures.
- Sensorimotor PolyneuropathyMs. Canda isExperienced. Learn about Sensorimotor Polyneuropathy.
- Severe Congenital NeutropeniaMs. Canda isExperienced. Learn about Severe Congenital Neutropenia.
- Short Bowel SyndromeMs. Canda isExperienced. Learn about Short Bowel Syndrome.
- SialidosisMs. Canda isExperienced. Learn about Sialidosis.
- SplenomegalyMs. Canda isExperienced. Learn about Splenomegaly.
- Tay-Sachs DiseaseMs. Canda isExperienced. Learn about Tay-Sachs Disease.
- Transient Familial HyperbilirubinemiaMs. Canda isExperienced. Learn about Transient Familial Hyperbilirubinemia.
- Undescended TesticleMs. Canda isExperienced. Learn about Undescended Testicle.
- Urea Cycle Disorders (UCD)Ms. Canda isExperienced. Learn about Urea Cycle Disorders (UCD).
- Von Gierke DiseaseMs. Canda isExperienced. Learn about Von Gierke Disease.