Overview
Georgianne Arnold is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Arnold is rated as a Distinguished provider by MediFind in the treatment of Phenylketonuria (PKU). Her top areas of expertise are Phenylketonuria (PKU), Mitochondrial Trifunctional Protein Deficiency, Krabbe Disease, and Inborn Amino Acid Metabolism Disorder.
Her clinical research consists of co-authoring 34 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 7 articles and participated in 1 clinical trial in the study of Phenylketonuria (PKU).
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- OTHER MEDICAID
- STATE MEDICAID
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.
1 Clinical Trials
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 Phenylketonuria (PKU). His top areas of expertise are Classic Galactosemia, Urea Cycle Disorders (UCD), Galactose Epimerase Deficiency, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
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 Phenylketonuria (PKU). Her top areas of expertise are Multiple Sulfatase Deficiency, Cardiomyopathic Lentiginosis, Chondrodysplasia Punctata with Steroid Sulfatase Deficiency, and Noonan Syndrome.
Saint Peters University Hospital
Debra-lynn Day is a Medical Genetics specialist and a Pediatrics provider in New Brunswick, New Jersey. Dr. Day is rated as an Advanced provider by MediFind in the treatment of Phenylketonuria (PKU). Her top areas of expertise are Phenylketonuria (PKU), Gaucher Disease, Gaucher Disease Type 2, and Gaucher Disease Type 1.
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
- Mitochondrial Trifunctional Protein Deficiency
- Phenylketonuria (PKU)Dr. Arnold isDistinguished. Learn about Phenylketonuria (PKU).
- Advanced
- Inborn Amino Acid Metabolism Disorder
- Inborn Renal AminoaciduriaDr. Arnold isAdvanced. Learn about Inborn Renal Aminoaciduria.
- Krabbe DiseaseDr. Arnold isAdvanced. Learn about Krabbe Disease.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maternal HyperphenylalaninemiaDr. Arnold isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Experienced
- Acromicric DysplasiaDr. Arnold isExperienced. Learn about Acromicric Dysplasia.
- AlbinismDr. Arnold isExperienced. Learn about Albinism.
- AlkaptonuriaDr. Arnold isExperienced. Learn about Alkaptonuria.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2