Overview
Can Ficicioglu is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Ficicioglu is rated as a Distinguished provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Classic Galactosemia, Urea Cycle Disorders (UCD), Galactose Epimerase Deficiency, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
His clinical research consists of co-authoring 92 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 3 articles and participated in 3 clinical trials in the study of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER MEDICARE PART D
- PPO
- EPO
- HMO
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE SNP
- OTHER MEDICARE PART D
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- EPO
- HMO
- PPO
- EPO
- POS
- EPO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
- EPO
- PPO
- MEDICARE DISCOUNT CARD
- MEDICARE PDP
- OTHER MEDICARE
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
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
Michael Bober is a Medical Genetics specialist and a Pediatrics provider in Wilmington, Delaware. Dr. Bober is rated as an Elite provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). His top areas of expertise are Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Adenoidectomy. Dr. Bober is currently accepting new patients.
Childrens Health Care Associates Inc
Rebecca Ahrens-Nicklas is a Pediatrics specialist and a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Ahrens-Nicklas is rated as an Elite provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Multiple Sulfatase Deficiency, Cardiomyopathic Lentiginosis, Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, and Noonan Syndrome.
Mary Pipan is a Developmental and Behavioral Pediatrics specialist and a Physiatrist in Philadelphia, Pennsylvania. Dr. Pipan is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). Her top areas of expertise are Autism Spectrum Disorder, Delayed Growth, Apraxia, Cardiofaciocutaneous Syndrome, and Myringotomy.
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
- Cholesteryl Ester Storage DiseaseDr. Ficicioglu isDistinguished. Learn about Cholesteryl Ester Storage Disease.
- Classic GalactosemiaDr. Ficicioglu isDistinguished. Learn about Classic Galactosemia.
- Galactokinase DeficiencyDr. Ficicioglu isDistinguished. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Ficicioglu isDistinguished. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Ficicioglu isDistinguished. Learn about Galactosemia.
- Gaucher DiseaseDr. Ficicioglu isDistinguished. Learn about Gaucher Disease.
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Argininosuccinic AciduriaDr. Ficicioglu isAdvanced. Learn about Argininosuccinic Aciduria.
- Beta-Ketothiolase DeficiencyDr. Ficicioglu isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Biotinidase DeficiencyDr. Ficicioglu isAdvanced. Learn about Biotinidase Deficiency.
- Cardiomyopathy Hypogonadism Metabolic Anomalies
- Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
- Experienced
- Activated PI3K Delta Syndrome (APDS)Dr. Ficicioglu isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- Adrenoleukodystrophy (ALD)Dr. Ficicioglu isExperienced. Learn about Adrenoleukodystrophy (ALD).
- ALG1-CDGDr. Ficicioglu isExperienced. Learn about ALG1-CDG.
- Alpha MannosidosisDr. Ficicioglu isExperienced. Learn about Alpha Mannosidosis.
- AminoaciduriaDr. Ficicioglu isExperienced. Learn about Aminoaciduria.
- Arginase DeficiencyDr. Ficicioglu isExperienced. Learn about Arginase Deficiency.