Overview
Ida Schwartz practices in Rio Grande, Brazil. Ms. Schwartz is highly rated in 27 conditions, according to our data. Her top areas of expertise are Gaucher Disease Type 1, Mucolipidosis Type 4, Maple Syrup Urine Disease, Sialidosis, and Liver Transplant.
Her clinical research consists of co-authoring 200 peer reviewed articles and participating in 3 clinical trials. MediFind looks at clinical research from the past 15 years.
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. Experts 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.
3 Clinical Trials
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
- Gaucher Disease Type 1Ms. Schwartz isElite. Learn about Gaucher Disease Type 1.
- Maple Syrup Urine DiseaseMs. Schwartz isElite. Learn about Maple Syrup Urine Disease.
- Mucolipidosis Type 4Ms. Schwartz isElite. Learn about Mucolipidosis Type 4.
- Distinguished
- Biotinidase DeficiencyMs. Schwartz isDistinguished. Learn about Biotinidase Deficiency.
- Dihydrolipoamide Dehydrogenase DeficiencyMs. Schwartz isDistinguished. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Farber LipogranulomatosisMs. Schwartz isDistinguished. Learn about Farber Lipogranulomatosis.
- Fructose-1,6-Bisphosphatase DeficiencyMs. Schwartz isDistinguished. Learn about Fructose-1,6-Bisphosphatase Deficiency.
- Gaucher DiseaseMs. Schwartz isDistinguished. Learn about Gaucher Disease.
- HomocystinuriaMs. Schwartz isDistinguished. Learn about Homocystinuria.
- Advanced
- Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
- Classic GalactosemiaMs. Schwartz isAdvanced. Learn about Classic Galactosemia.
- Enlarged LiverMs. Schwartz isAdvanced. Learn about Enlarged Liver.
- Gaucher Disease Type 3Ms. Schwartz isAdvanced. Learn about Gaucher Disease Type 3.
- Hereditary Fructose IntoleranceMs. Schwartz isAdvanced. Learn about Hereditary Fructose Intolerance.
- HypotoniaMs. Schwartz isAdvanced. Learn about Hypotonia.
- Experienced
- Achalasia Microcephaly SyndromeMs. Schwartz isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Acid Sphingomyelinase Deficiency (ASMD)Ms. Schwartz isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Andersen DiseaseMs. Schwartz isExperienced. Learn about Andersen Disease.
- AnhidrosisMs. Schwartz isExperienced. Learn about Anhidrosis.
- Attention Deficit Hyperactivity Disorder (ADHD)
- Brachydactyly Mononen TypeMs. Schwartz isExperienced. Learn about Brachydactyly Mononen Type.