Overview
Ida Schwartz practices in Porto Alegre, Brazil. Ms. Schwartz is rated as a Distinguished expert by MediFind in the treatment of Fructose-1,6-Bisphosphatase Deficiency. Her top areas of expertise are Maple Syrup Urine Disease, Mucolipidosis Type 4, Mucolipidosis 3, Sialidosis, and Liver Transplant.
Her clinical research consists of co-authoring 198 peer reviewed articles and participating in 3 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Fructose-1,6-Bisphosphatase Deficiency.
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
- Maple Syrup Urine DiseaseMs. Schwartz isElite. Learn about Maple Syrup Urine Disease.
- 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.
- Gaucher Disease Type 1Ms. Schwartz isDistinguished. Learn about Gaucher Disease Type 1.
- Advanced
- Chondrodysplasia Punctata with Steroid Sulfatase Deficiency
- 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.
- Inborn Amino Acid Metabolism DisorderMs. Schwartz isAdvanced. Learn about Inborn Amino Acid Metabolism Disorder.
- 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.