Overview
Cigdem Kasapkara practices practicing medicine in Yildirim Beyazit, Turkey.
Kasapkara is highly rated in 21 conditions, according to our data. Their clinical expertise encompasses Hypotonia, Glycine Encephalopathy, Malonyl-CoA Decarboxylase Deficiency, and Prolidase Deficiency.
They are actively involved in clinical research, co-authoring 101 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 Cigdem S. Kasapkara
Is Cigdem S. Kasapkara a top-rated expert for Hypotonia?
MediFind is an objective health platform that identifies experts based on real-world data. Cigdem S. Kasapkara is classified as an Advanced expert for Hypotonia, 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 Cigdem S. Kasapkara participate in research or clinical trials?
Yes. Cigdem S. Kasapkara has published 101 articles and abstracts on conditions like Hypotonia. You can view a list of Cigdem S. Kasapkara'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
- AcatalasemiaKasapkara isAdvanced. Learn about Acatalasemia.
- Alpha MannosidosisKasapkara isAdvanced. Learn about Alpha Mannosidosis.
- Arginase DeficiencyKasapkara isAdvanced. Learn about Arginase Deficiency.
- Biotinidase DeficiencyKasapkara isAdvanced. Learn about Biotinidase Deficiency.
- Cerebrotendinous XanthomatosisKasapkara isAdvanced. Learn about Cerebrotendinous Xanthomatosis.
- Decorticate PostureKasapkara isAdvanced. Learn about Decorticate Posture.
- Enlarged LiverKasapkara isAdvanced. Learn about Enlarged Liver.
- Glycine EncephalopathyKasapkara isAdvanced. Learn about Glycine Encephalopathy.
- Glycogen Storage Disease Type 0Kasapkara isAdvanced. Learn about Glycogen Storage Disease Type 0.
- HypotoniaKasapkara isAdvanced. Learn about Hypotonia.
- Lactic AcidosisKasapkara isAdvanced. Learn about Lactic Acidosis.
- Leigh SyndromeKasapkara isAdvanced. Learn about Leigh Syndrome.
- Magnesium DeficiencyKasapkara isAdvanced. Learn about Magnesium Deficiency.
- Malonyl-CoA Decarboxylase Deficiency
- Mitochondrial Complex 2 Deficiency
- Multiple Carboxylase DeficiencyKasapkara isAdvanced. Learn about Multiple Carboxylase Deficiency.
- Prolidase DeficiencyKasapkara isAdvanced. Learn about Prolidase Deficiency.
- SeizuresKasapkara isAdvanced. Learn about Seizures.
- Urea Cycle Disorders (UCD)Kasapkara isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Von Gierke DiseaseKasapkara isAdvanced. Learn about Von Gierke Disease.
- XanthomaKasapkara isAdvanced. Learn about Xanthoma.
- Experienced
- Absence SeizureKasapkara isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly SyndromeKasapkara isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Addison's DiseaseKasapkara isExperienced. Learn about Addison's Disease.
- Adrenoleukodystrophy (ALD)Kasapkara isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Batten DiseaseKasapkara isExperienced. Learn about Batten Disease.
- CACH SyndromeKasapkara isExperienced. Learn about CACH Syndrome.
- CalcinosisKasapkara isExperienced. Learn about Calcinosis.
- CardiomyopathyKasapkara isExperienced. Learn about Cardiomyopathy.
- CholestasisKasapkara isExperienced. Learn about Cholestasis.
- CLN1 DiseaseKasapkara isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseKasapkara isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseKasapkara isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseKasapkara isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseKasapkara isExperienced. Learn about CLN5 Disease.
- Corpus Callosum AgenesisKasapkara isExperienced. Learn about Corpus Callosum Agenesis.
- Cortical DysplasiaKasapkara isExperienced. Learn about Cortical Dysplasia.
- Crouzon SyndromeKasapkara isExperienced. Learn about Crouzon Syndrome.
- Dihydrolipoamide Dehydrogenase Deficiency
- Drug Induced DyskinesiaKasapkara isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaKasapkara isExperienced. Learn about Dysarthria.
- EpilepsyKasapkara isExperienced. Learn about Epilepsy.
- Fabry DiseaseKasapkara isExperienced. Learn about Fabry Disease.
- Fructose-1,6-Bisphosphatase Deficiency
- GalactosemiaKasapkara isExperienced. Learn about Galactosemia.
- GangliosidosisKasapkara isExperienced. Learn about Gangliosidosis.
- Gaucher Disease Type 1Kasapkara isExperienced. Learn about Gaucher Disease Type 1.
- Generalized Tonic-Clonic SeizureKasapkara isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Glycogen Storage Disease Type 3Kasapkara isExperienced. Learn about Glycogen Storage Disease Type 3.
- GM1 GangliosidosisKasapkara isExperienced. Learn about GM1 Gangliosidosis.
- Gracile SyndromeKasapkara isExperienced. Learn about Gracile Syndrome.
- Hallervorden-Spatz DiseaseKasapkara isExperienced. Learn about Hallervorden-Spatz Disease.
- Hearing LossKasapkara isExperienced. Learn about Hearing Loss.
- Hepatocerebral DegenerationKasapkara isExperienced. Learn about Hepatocerebral Degeneration.
- Hereditary CoproporphyriaKasapkara isExperienced. Learn about Hereditary Coproporphyria.
- Hereditary Fructose IntoleranceKasapkara isExperienced. Learn about Hereditary Fructose Intolerance.
- Hereditary Spastic ParaparesisKasapkara isExperienced. Learn about Hereditary Spastic Paraparesis.
- High CholesterolKasapkara isExperienced. Learn about High Cholesterol.
- HydrocephalusKasapkara isExperienced. Learn about Hydrocephalus.
- Inborn Renal AminoaciduriaKasapkara isExperienced. Learn about Inborn Renal Aminoaciduria.
- Increased Head CircumferenceKasapkara isExperienced. Learn about Increased Head Circumference.
- Infantile NeutropeniaKasapkara isExperienced. Learn about Infantile Neutropenia.
- L-2-Hydroxyglutaric AciduriaKasapkara isExperienced. Learn about L-2-Hydroxyglutaric Aciduria.
- LeukodystrophyKasapkara isExperienced. Learn about Leukodystrophy.
- Liver FailureKasapkara isExperienced. Learn about Liver Failure.
- Low Blood SugarKasapkara isExperienced. Learn about Low Blood Sugar.
- Low Sodium LevelKasapkara isExperienced. Learn about Low Sodium Level.
- MalnutritionKasapkara isExperienced. Learn about Malnutrition.
- Metabolic AcidosisKasapkara isExperienced. Learn about Metabolic Acidosis.
- Metachromatic LeukodystrophyKasapkara isExperienced. Learn about Metachromatic Leukodystrophy.
- MicrocephalyKasapkara isExperienced. Learn about Microcephaly.
- Mitochondrial Complex 1 DeficiencyKasapkara isExperienced. Learn about Mitochondrial Complex 1 Deficiency.
- Mucolipidosis 3Kasapkara isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Kasapkara isExperienced. Learn about Mucolipidosis Type 4.
- N-Acetylglutamate Synthase DeficiencyKasapkara isExperienced. Learn about N-Acetylglutamate Synthase Deficiency.
- Ornithine Transcarbamylase DeficiencyKasapkara isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- ParaplegiaKasapkara isExperienced. Learn about Paraplegia.
- PMM2-Congenital Disorder of Glycosylation
- Pol 3-Related LeukodystrophyKasapkara isExperienced. Learn about Pol 3-Related Leukodystrophy.
- Pompe DiseaseKasapkara isExperienced. Learn about Pompe Disease.
- PorphyriaKasapkara isExperienced. Learn about Porphyria.
- Propionic AcidemiaKasapkara isExperienced. Learn about Propionic Acidemia.
- Protein DeficiencyKasapkara isExperienced. Learn about Protein Deficiency.
- Pyruvate Decarboxylase DeficiencyKasapkara isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyKasapkara isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- RhabdomyolysisKasapkara isExperienced. Learn about Rhabdomyolysis.
- Sandhoff DiseaseKasapkara isExperienced. Learn about Sandhoff Disease.
- SialidosisKasapkara isExperienced. Learn about Sialidosis.
- Sideroblastic AnemiaKasapkara isExperienced. Learn about Sideroblastic Anemia.
- Spastic Paraplegia Type 2Kasapkara isExperienced. Learn about Spastic Paraplegia Type 2.
- SplenomegalyKasapkara isExperienced. Learn about Splenomegaly.
- Status EpilepticusKasapkara isExperienced. Learn about Status Epilepticus.
- Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
- Tay-Sachs DiseaseKasapkara isExperienced. Learn about Tay-Sachs Disease.
- Tyrosinemia Type 1Kasapkara isExperienced. Learn about Tyrosinemia Type 1.
- X-Linked Lymphoproliferative DiseaseKasapkara isExperienced. Learn about X-Linked Lymphoproliferative Disease.
- Zellweger SyndromeKasapkara isExperienced. Learn about Zellweger Syndrome.