Dr. Georgianne L. Arnold, MD
Pediatrician
4401 PENN AVE STE 1200 PITTSBURGH PA, 15224About
Dr. Georgianne Arnold is a pediatrician practicing in Rochester, NY. Dr. Arnold is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Arnold diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Arnold can oversee and manage the physical, mental and emotional health of their patients.
Education and Training
Suny-Hlth Sci Ctr At Syracuse, Coll of Med, Syracuse Ny 1986
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Protein insufficiency and linear growth restriction in phenylketonuria.
- Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food.
- A Delphi-based consensus clinical practice protocol for the diagnosis and management of 3-methylcrotonyl CoA carboxylase deficiency.
- Universal nephroblastomatosis with bilateral hyperplastic nephromegaly in siblings.
- Parents' experiences of expanded newborn screening evaluations.
- Thoroughly modern medicine.
- Internet use by parents of infants with positive newborn screens.
- Development of clinical guidelines for inborn errors of metabolism: commentary.
- Introduction: Neurodevelopmental issues in inborn errors of metabolism.
- Isolated Sagittal Synostosis in a Boy with Craniofrontonasal Dysplasia and a Novel EFNB1 Mutation.
- Outcomes of cases with 3-methylcrotonyl-CoA carboxylase (3-MCC) deficiency - Report from the Inborn Errors of Metabolism Information System.
- Outcomes and genotype-phenotype correlations in 52 individuals with VLCAD deficiency diagnosed by NBS and enrolled in the IBEM-IS database.
- 221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative.
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