Overview
Can Ficicioglu is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Ficicioglu has been practicing medicine for over 40 years and is rated as an Experienced provider by MediFind in the treatment of Pyruvate Dehydrogenase Deficiency. His top areas of expertise are Classic Galactosemia, Multiple Sulfatase Deficiency, Cholesteryl Ester Storage Disease, and Homocystinuria.
His clinical research consists of co-authoring 86 peer reviewed articles and participating in 12 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Pyruvate Dehydrogenase Deficiency.
Insurance
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Locations
3401 Civic Ctr Blvd, Philadelphia, PA 19104
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers 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.
12 Clinical Trials
Parith Wongkittichote is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Wongkittichote and is rated as an Advanced provider by MediFind in the treatment of Pyruvate Dehydrogenase Deficiency. His top areas of expertise are Dihydrolipoamide Dehydrogenase Deficiency, Glutaric Acidemia Type 1, Multiple Sulfatase Deficiency, and Mucolipidosis Type 4.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Cholesteryl Ester Storage Disease
- Classic Galactosemia
- Homocystinuria
- Lysosomal Acid Lipase Deficiency
- Multiple Sulfatase Deficiency
- Urea Cycle Disorders (UCD)
- Advanced
- Cardiomyopathy Hypogonadism Metabolic Anomalies
- Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
- Citrullinemia
- Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism
- Galactokinase Deficiency
- Galactose Epimerase Deficiency
- Experienced
- Adrenoleukodystrophy (ALD)
- ALG1-CDG
- Alpha Mannosidosis
- Argininosuccinic Aciduria
- Brachydactyly Mononen Type
- Carbamoyl Phosphate Synthetase 1 Deficiency