Overview
Fehime Erdem practices practicing medicine in Ege, Turkey.
Erdem is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses DPAGT1-CDG, SRD5A3-CDG, Glycogen Storage Disease Type 6, and Rhabdomyolysis.
They are actively involved in clinical research, co-authoring 21 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 Fehime H. Erdem
Is Fehime H. Erdem a top-rated expert for DPAGT1-CDG?
MediFind is an objective health platform that identifies experts based on real-world data. Fehime H. Erdem is classified as an Advanced expert for DPAGT1-CDG, 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 Fehime H. Erdem participate in research or clinical trials?
Yes. Fehime H. Erdem has published 21 articles and abstracts on conditions like DPAGT1-CDG. You can view a list of Fehime H. Erdem'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-CDGErdem isAdvanced. Learn about DPAGT1-CDG.
- SRD5A3-CDGErdem isAdvanced. Learn about SRD5A3-CDG.
- Experienced
- Apolipoprotein C2 DeficiencyErdem isExperienced. Learn about Apolipoprotein C2 Deficiency.
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Childhood PancreatitisErdem isExperienced. Learn about Childhood Pancreatitis.
- Defective Apolipoprotein B-100
- DysarthriaErdem isExperienced. Learn about Dysarthria.
- Familial HypercholesterolemiaErdem isExperienced. Learn about Familial Hypercholesterolemia.
- Familial Lipoprotein Lipase Deficiency
- Glutaric Acidemia Type 1Erdem isExperienced. Learn about Glutaric Acidemia Type 1.
- Glycogen Storage Disease Type 3
- Glycogen Storage Disease Type 6
- Glycogen Storage Disease Type 9
- High CholesterolErdem isExperienced. Learn about High Cholesterol.
- Homozygous Familial Hypercholesterolemia (HoFH)
- Intestinal Pseudo-ObstructionErdem isExperienced. Learn about Intestinal Pseudo-Obstruction.
- Low Blood SugarErdem isExperienced. Learn about Low Blood Sugar.
- Mitochondrial Neurogastrointestinal Encephalopathy Disease
- MPI-CDGErdem isExperienced. Learn about MPI-CDG.
- Mucolipidosis 3Erdem isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Erdem isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Niemann-Pick DiseaseErdem isExperienced. Learn about Niemann-Pick Disease.
- Oculopharyngeal Muscular Dystrophy
- PMM2-Congenital Disorder of Glycosylation
- RhabdomyolysisErdem isExperienced. Learn about Rhabdomyolysis.
- Sensorimotor PolyneuropathyErdem isExperienced. Learn about Sensorimotor Polyneuropathy.
- Short Bowel SyndromeErdem isExperienced. Learn about Short Bowel Syndrome.
- SialidosisErdem isExperienced. Learn about Sialidosis.
- SplenomegalyErdem isExperienced. Learn about Splenomegaly.
- Von Gierke DiseaseErdem isExperienced. Learn about Von Gierke Disease.