Overview
Carlos Milla is a Pediatric Pulmonologist and a Pediatrics provider in Palo Alto, California. Dr. Milla is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. His top areas of expertise are Cystic Fibrosis, Ciliary Dyskinesia-Bronchiectasis, Pseudomonas Stutzeri Infections, Situs Inversus, and Lung Transplant.
His clinical research consists of co-authoring 117 peer reviewed articles and participating in 6 clinical trials. 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
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- EPO
- HMO
- PPO
Accepted plan types not found. Please verify directly with the provider.
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- POS
- PPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER MEDICARE
- POS
- PPO
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- PPO
- HMO
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
725 Welch Rd, Palo Alto, CA 94304
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.
6 Clinical Trials
Lpch Medical Group Div Of Lucile
Brenda Porter is a Pediatric Neurologist and a Neurologist in Palo Alto, California. Dr. Porter is rated as an Elite provider by MediFind in the treatment of PEPCK 1 Deficiency. Her top areas of expertise are Tuberous Sclerosis, Tuberous Sclerosis Complex, Seizures, Epilepsy, and Deep Brain Stimulation.
Lpch Medical Group Div Of Lucile
Jean Chia is a Pediatrics provider in Palo Alto, California. Dr. Chia is rated as an Advanced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her top areas of expertise are Microcephaly Deafness Syndrome, Early Infantile Epileptic Encephalopathy, CHARGE Syndrome, and Koolen De Vries Syndrome.
Monica Penon-Portmann is a Pediatrics specialist and a Medical Genetics provider in San Francisco, California. Dr. Penon-Portmann is rated as an Experienced provider by MediFind in the treatment of PEPCK 1 Deficiency. Her top areas of expertise are Glycogen Storage Disease Type 0, Glycogen Storage Disease Type 13, Andersen Disease, and Phosphoglycerate Mutase Deficiency. Dr. Penon-Portmann is currently accepting new patients.
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
- Ciliary Dyskinesia-Bronchiectasis
- Cystic FibrosisDr. Milla isElite. Learn about Cystic Fibrosis.
- Distinguished
- Pseudomonas Stutzeri InfectionsDr. Milla isDistinguished. Learn about Pseudomonas Stutzeri Infections.
- Situs InversusDr. Milla isDistinguished. Learn about Situs Inversus.
- Advanced
- Primary Ciliary Dyskinesia (PCD)
- Experienced
- Autosomal Recessive Congenital Methemoglobinemia
- Bronchopulmonary DysplasiaDr. Milla isExperienced. Learn about Bronchopulmonary Dysplasia.
- CHARGE SyndromeDr. Milla isExperienced. Learn about CHARGE Syndrome.
- Congenital Unilateral Pulmonary Hypoplasia
- DiGeorge SyndromeDr. Milla isExperienced. Learn about DiGeorge Syndrome.
- Dihydrolipoamide Dehydrogenase Deficiency