Overview
Yuval Landau is a Medical Genetics provider in Brookline, Massachusetts. Dr. Landau is rated as an Experienced provider by MediFind in the treatment of Galactosemia. His top areas of expertise are Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Urea Cycle Disorders (UCD), and Orotic Aciduria Type 1.
His clinical research consists of co-authoring 30 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 2 articles in the study of Galactosemia.
Insurance
Accepted insurance can change. Please verify directly with the provider.
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.
Children's Hospital Pediatric Associates, Inc
Olaf Bodamer is a Medical Genetics provider in Boston, Massachusetts. Dr. Bodamer is rated as a Distinguished provider by MediFind in the treatment of Galactosemia. His top areas of expertise are Kabuki Syndrome, Classic Galactosemia, Niemann-Pick Disease, and Mucopolysaccharidoses (MPS). Dr. Bodamer is currently accepting new patients.
Gerard Berry is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Berry is rated as an Advanced provider by MediFind in the treatment of Galactosemia. His top areas of expertise are Classic Galactosemia, Galactose Epimerase Deficiency, Galactosemia, and Maple Syrup Urine Disease. Dr. Berry is currently accepting new patients.
Children's Hospital Pediatric Associates, Inc
Stephanie Sacharow is a Medical Genetics specialist and a Pediatrics provider in Boston, Massachusetts. Dr. Sacharow is rated as a Distinguished provider by MediFind in the treatment of Galactosemia. Her top areas of expertise are Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, Cat Eye Syndrome, and Dihydropteridine Reductase Deficiency. Dr. Sacharow 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
- Distinguished
- Classic GalactosemiaDr. Landau isDistinguished. Learn about Classic Galactosemia.
- Advanced
- Maple Syrup Urine DiseaseDr. Landau isAdvanced. Learn about Maple Syrup Urine Disease.
- Orotic Aciduria Type 1Dr. Landau isAdvanced. Learn about Orotic Aciduria Type 1.
- Urea Cycle Disorders (UCD)Dr. Landau isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Carbamoyl Phosphate Synthetase 1 Deficiency
- CitrullinemiaDr. Landau isExperienced. Learn about Citrullinemia.
- Cortical DysplasiaDr. Landau isExperienced. Learn about Cortical Dysplasia.
- Dihydrolipoamide Dehydrogenase Deficiency
- Galactokinase DeficiencyDr. Landau isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Landau isExperienced. Learn about Galactose Epimerase Deficiency.