Overview
Ida Schwartz practices practicing medicine in Porto Alegre, Brazil.
Ms. Schwartz is highly rated in 29 conditions, according to our data. Her clinical expertise encompasses Maple Syrup Urine Disease, Mucolipidosis 3, Mucolipidosis Type 4, Sialidosis, and Liver Transplant.
She is actively involved in clinical research, co-authoring 199 peer reviewed articles and participating in 4 clinical trials.
Gender
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.
4 Clinical Trials
Frequently Asked Questions about Ida D. Schwartz
Is Ida D. Schwartz a top-rated expert for Maple Syrup Urine Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Ida D. Schwartz is classified as an Elite expert for Maple Syrup Urine Disease, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Ida D. Schwartz participate in research or clinical trials?
Yes. Ida D. Schwartz has published 199 articles and abstracts on conditions like Maple Syrup Urine Disease. You can view a list of Ida D. Schwartz's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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.
- Early Infantile Epileptic EncephalopathyMs. Schwartz isDistinguished. Learn about Early Infantile Epileptic Encephalopathy.
- 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.
- 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.
- Homocystinuria due to MTHFR Deficiency
- 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.