Overview
Rebecca Ganetzky is a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Ganetzky is rated as an Experienced provider by MediFind in the treatment of X-Linked Creatine Deficiency. Her top areas of expertise are Leigh Syndrome, Kearns-Sayre Syndrome, Pyruvate Carboxylase Deficiency, Dihydrolipoamide Dehydrogenase Deficiency, and Splenectomy.
Her clinical research consists of co-authoring 92 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER MEDICARE PART D
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE SNP
- OTHER MEDICARE PART D
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- EPO
- HMO
- PPO
- EPO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- 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
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. 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.
Childrens Health Care Associates Inc
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 X-Linked Creatine Deficiency. His top areas of expertise are Classic Galactosemia, Urea Cycle Disorders (UCD), Galactose Epimerase Deficiency, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
Childrens Health Care Associates Inc
Kim Ng is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Ng is rated as an Advanced provider by MediFind in the treatment of X-Linked Creatine Deficiency. Her top areas of expertise are Citrullinemia, Maple Syrup Urine Disease, Beta-Ketothiolase Deficiency, and Argininosuccinic Aciduria.
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 X-Linked Creatine Deficiency. Her top areas of expertise are Multiple Sulfatase Deficiency, Cardiomyopathic Lentiginosis, Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, and Noonan Syndrome.
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
- Elite
- Leigh SyndromeDr. Ganetzky isElite. Learn about Leigh Syndrome.
- Distinguished
- Dihydrolipoamide Dehydrogenase DeficiencyDr. Ganetzky isDistinguished. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Kearns-Sayre SyndromeDr. Ganetzky isDistinguished. Learn about Kearns-Sayre Syndrome.
- Pyruvate Carboxylase DeficiencyDr. Ganetzky isDistinguished. Learn about Pyruvate Carboxylase Deficiency.
- Advanced
- Autosomal Recessive Congenital Methemoglobinemia
- Maternally Inherited Leigh SyndromeDr. Ganetzky isAdvanced. Learn about Maternally Inherited Leigh Syndrome.
- PEPCK 1 DeficiencyDr. Ganetzky isAdvanced. Learn about PEPCK 1 Deficiency.
- Urea Cycle Disorders (UCD)Dr. Ganetzky isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- AminoaciduriaDr. Ganetzky isExperienced. Learn about Aminoaciduria.
- AnemiaDr. Ganetzky isExperienced. Learn about Anemia.
- Arthrogryposis Multiplex CongenitaDr. Ganetzky isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Carnitine Palmitoyltransferase 1 DeficiencyDr. Ganetzky isExperienced. Learn about Carnitine Palmitoyltransferase 1 Deficiency.
- Carnitine Palmitoyltransferase 2 DeficiencyDr. Ganetzky isExperienced. Learn about Carnitine Palmitoyltransferase 2 Deficiency.
- CHARGE SyndromeDr. Ganetzky isExperienced. Learn about CHARGE Syndrome.