Overview
Sema Ucar-Kalkan practices practicing medicine in Ege, Turkey.
Ms. Ucar-Kalkan is highly rated in 6 conditions, according to our data. Her clinical expertise encompasses Mohr-Tranebjaerg Syndrome, Pyruvate Decarboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, and DPAGT1-CDG.
She is actively involved in clinical research, co-authoring 37 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 Sema Ucar-Kalkan
Is Sema Ucar-Kalkan a top-rated expert for Mohr-Tranebjaerg Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Sema Ucar-Kalkan is classified as an Advanced expert for Mohr-Tranebjaerg Syndrome, 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 Ucar-Kalkan participate in research or clinical trials?
Yes. Sema Ucar-Kalkan has published 37 articles and abstracts on conditions like Mohr-Tranebjaerg Syndrome. You can view a list of Sema Ucar-Kalkan'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
- DPAGT1-CDGMs. Ucar-Kalkan isAdvanced. Learn about DPAGT1-CDG.
- Glycogen Storage Disease Type 6Ms. Ucar-Kalkan isAdvanced. Learn about Glycogen Storage Disease Type 6.
- Mohr-Tranebjaerg SyndromeMs. Ucar-Kalkan isAdvanced. Learn about Mohr-Tranebjaerg Syndrome.
- Pyruvate Decarboxylase DeficiencyMs. Ucar-Kalkan isAdvanced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMs. Ucar-Kalkan isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- SRD5A3-CDGMs. Ucar-Kalkan isAdvanced. Learn about SRD5A3-CDG.
- Experienced
- Acute Cerebellar AtaxiaMs. Ucar-Kalkan isExperienced. Learn about Acute Cerebellar Ataxia.
- Aplasia Cutis CongenitaMs. Ucar-Kalkan isExperienced. Learn about Aplasia Cutis Congenita.
- Apolipoprotein C2 DeficiencyMs. Ucar-Kalkan isExperienced. Learn about Apolipoprotein C2 Deficiency.
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Biotinidase DeficiencyMs. Ucar-Kalkan isExperienced. Learn about Biotinidase Deficiency.
- CACH SyndromeMs. Ucar-Kalkan isExperienced. Learn about CACH Syndrome.
- Chanarin-Dorfman SyndromeMs. Ucar-Kalkan isExperienced. Learn about Chanarin-Dorfman Syndrome.
- Childhood PancreatitisMs. Ucar-Kalkan isExperienced. Learn about Childhood Pancreatitis.
- Classic GalactosemiaMs. Ucar-Kalkan isExperienced. Learn about Classic Galactosemia.
- Clouston SyndromeMs. Ucar-Kalkan isExperienced. Learn about Clouston Syndrome.
- Defective Apolipoprotein B-100Ms. Ucar-Kalkan isExperienced. Learn about Defective Apolipoprotein B-100.
- Dihydrolipoamide Dehydrogenase DeficiencyMs. Ucar-Kalkan isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Dilated Cardiomyopathy (DCM)Ms. Ucar-Kalkan isExperienced. Learn about Dilated Cardiomyopathy (DCM).
- Drug Induced DyskinesiaMs. Ucar-Kalkan isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaMs. Ucar-Kalkan isExperienced. Learn about Dysarthria.
- Early Infantile Epileptic EncephalopathyMs. Ucar-Kalkan isExperienced. Learn about Early Infantile Epileptic Encephalopathy.
- Ectodermal DysplasiasMs. Ucar-Kalkan isExperienced. Learn about Ectodermal Dysplasias.
- Erythrokeratodermia Variabilis et ProgressivaMs. Ucar-Kalkan isExperienced. Learn about Erythrokeratodermia Variabilis et Progressiva.
- Fabry DiseaseMs. Ucar-Kalkan isExperienced. Learn about Fabry Disease.
- Familial HypercholesterolemiaMs. Ucar-Kalkan isExperienced. Learn about Familial Hypercholesterolemia.
- Familial Lipoprotein Lipase DeficiencyMs. Ucar-Kalkan isExperienced. Learn about Familial Lipoprotein Lipase Deficiency.
- Galactokinase DeficiencyMs. Ucar-Kalkan isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Ucar-Kalkan isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Ucar-Kalkan isExperienced. Learn about Galactosemia.
- Glutaric Acidemia Type 1Ms. Ucar-Kalkan isExperienced. Learn about Glutaric Acidemia Type 1.
- Glycogen Storage Disease Type 3Ms. Ucar-Kalkan isExperienced. Learn about Glycogen Storage Disease Type 3.
- Glycogen Storage Disease Type 9Ms. Ucar-Kalkan isExperienced. Learn about Glycogen Storage Disease Type 9.
- GTP Cyclohydrolase 1 DeficiencyMs. Ucar-Kalkan isExperienced. Learn about GTP Cyclohydrolase 1 Deficiency.
- Hearing LossMs. Ucar-Kalkan isExperienced. Learn about Hearing Loss.
- High CholesterolMs. Ucar-Kalkan isExperienced. Learn about High Cholesterol.
- HistiocytosisMs. Ucar-Kalkan isExperienced. Learn about Histiocytosis.
- Hypophosphatasia (HPP)Ms. Ucar-Kalkan isExperienced. Learn about Hypophosphatasia (HPP).
- HypotoniaMs. Ucar-Kalkan isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderMs. Ucar-Kalkan isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Low Blood SugarMs. Ucar-Kalkan isExperienced. Learn about Low Blood Sugar.
- Lysinuric Protein IntoleranceMs. Ucar-Kalkan isExperienced. Learn about Lysinuric Protein Intolerance.
- MPI-CDGMs. Ucar-Kalkan isExperienced. Learn about MPI-CDG.
- Mucolipidosis 3Ms. Ucar-Kalkan isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Ms. Ucar-Kalkan isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Multiple Carboxylase DeficiencyMs. Ucar-Kalkan isExperienced. Learn about Multiple Carboxylase Deficiency.
- NephrocalcinosisMs. Ucar-Kalkan isExperienced. Learn about Nephrocalcinosis.
- Niemann-Pick DiseaseMs. Ucar-Kalkan isExperienced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell HistiocytosisMs. Ucar-Kalkan isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- Nonbullous Congenital Ichthyosiform ErythrodermaMs. Ucar-Kalkan isExperienced. Learn about Nonbullous Congenital Ichthyosiform Erythroderma.
- Optic Nerve AtrophyMs. Ucar-Kalkan isExperienced. Learn about Optic Nerve Atrophy.
- PMM2-Congenital Disorder of GlycosylationMs. Ucar-Kalkan isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.
- Primary Carnitine DeficiencyMs. Ucar-Kalkan isExperienced. Learn about Primary Carnitine Deficiency.
- ReticulohistiocytomaMs. Ucar-Kalkan isExperienced. Learn about Reticulohistiocytoma.
- RhabdomyolysisMs. Ucar-Kalkan isExperienced. Learn about Rhabdomyolysis.
- SeizuresMs. Ucar-Kalkan isExperienced. Learn about Seizures.
- SialidosisMs. Ucar-Kalkan isExperienced. Learn about Sialidosis.
- SpasticityMs. Ucar-Kalkan isExperienced. Learn about Spasticity.
- SplenomegalyMs. Ucar-Kalkan isExperienced. Learn about Splenomegaly.
- Undescended TesticleMs. Ucar-Kalkan isExperienced. Learn about Undescended Testicle.
- Von Gierke DiseaseMs. Ucar-Kalkan isExperienced. Learn about Von Gierke Disease.