Overview
Louise Pyle is a Pediatrics specialist and a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Pyle is rated as an Experienced provider by MediFind in the treatment of Medium-Chain Acyl-CoA Dehydrogenase Deficiency. Her top areas of expertise are Intersex, CHARGE Syndrome, Penis Agenesis, and Klinefelter Syndrome.
Her clinical research consists of co-authoring 34 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- EPO
- HMO
- PPO
- EPO
- HMO
- POS
- 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 Medium-Chain Acyl-CoA Dehydrogenase Deficiency. His top areas of expertise are Classic Galactosemia, Urea Cycle Disorders (UCD), Galactose Epimerase Deficiency, and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).
Georgianne Arnold is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Arnold is rated as an Advanced provider by MediFind in the treatment of Medium-Chain Acyl-CoA Dehydrogenase Deficiency. Her top areas of expertise are Phenylketonuria (PKU), Mitochondrial Trifunctional Protein Deficiency, Krabbe Disease, and Inborn Amino Acid Metabolism Disorder.
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 Medium-Chain Acyl-CoA Dehydrogenase 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
- Advanced
- CHARGE SyndromeDr. Pyle isAdvanced. Learn about CHARGE Syndrome.
- IntersexDr. Pyle isAdvanced. Learn about Intersex.
- Experienced
- 46XX Testicular Disorder of Sex Development
- AcheiropodyDr. Pyle isExperienced. Learn about Acheiropody.
- Acromicric DysplasiaDr. Pyle isExperienced. Learn about Acromicric Dysplasia.
- Crouzon SyndromeDr. Pyle isExperienced. Learn about Crouzon Syndrome.
- HoloprosencephalyDr. Pyle isExperienced. Learn about Holoprosencephaly.
- HypospadiasDr. Pyle isExperienced. Learn about Hypospadias.