Overview
Renata Gallagher is a Medical Genetics specialist and a Pediatrics provider in San Francisco, California. Dr. Gallagher is rated as an Experienced provider by MediFind in the treatment of Reticulohistiocytoma. Her top areas of expertise are Gaucher Disease Type 2, Gaucher Disease Type 1, Gaucher Disease Type 3, and Gaucher Disease.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
Locations
Jorge Rodriguez-Gil is a Medical Genetics specialist and a Pediatrics provider in Pleasanton, California. Dr. Rodriguez-Gil is rated as an Advanced provider by MediFind in the treatment of Reticulohistiocytoma. His top areas of expertise are Niemann-Pick Disease, Reticulohistiocytoma, Chromosome 7p Deletion, and Acid Sphingomyelinase Deficiency (ASMD).
Office
Ann Marqueling is a Pediatrics provider in Palo Alto, California. Dr. Marqueling is rated as an Advanced provider by MediFind in the treatment of Reticulohistiocytoma. Her top areas of expertise are Linear Hamartoma Syndrome, Stork Bite, Vascular Birthmark, and Familial Multiple Nevi Flammei.
Robert Goldsby is a Pediatrics specialist and a Pediatric Hematologist Oncology provider in San Francisco, California. Dr. Goldsby is rated as an Advanced provider by MediFind in the treatment of Reticulohistiocytoma. His top areas of expertise are Osteosarcoma, Ewing Sarcoma, Adult Soft Tissue Sarcoma, Langerhans Cell Histiocytosis, and Bone Marrow Aspiration.
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
- Acid Sphingomyelinase Deficiency (ASMD)Dr. Gallagher isAdvanced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- AlkaptonuriaDr. Gallagher isAdvanced. Learn about Alkaptonuria.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Coenzyme Q Cytochrome C Reductase Deficiency
- Fabry DiseaseDr. Gallagher isAdvanced. Learn about Fabry Disease.
- Experienced
- Danon DiseaseDr. Gallagher isExperienced. Learn about Danon Disease.
- Dihydropteridine Reductase DeficiencyDr. Gallagher isExperienced. Learn about Dihydropteridine Reductase Deficiency.
- Glutaric Acidemia Type 2Dr. Gallagher isExperienced. Learn about Glutaric Acidemia Type 2.
- Inborn Amino Acid Metabolism DisorderDr. Gallagher isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Maple Syrup Urine DiseaseDr. Gallagher isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaDr. Gallagher isExperienced. Learn about Maternal Hyperphenylalaninemia.