Ida Vanessa Schwartz

41PUBLICATIONS
187CO-AUTHORS
Respiratory diseasesFoetal development and medicineDevelopmental genetics (incl. sex determination)PsychopharmacologyMedical biochemistry - lipids
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Publications (41)

|Sep 15, 2026
Rare diseases in Brazil: a nationwide analysis of the diagnostic odyssey.

|Aug 26, 2026
Cobalamin-Related Remethylation Disorders: Pregnancy Outcomes and Prenatal Treatment-New Cases and a Literature Study.

|Aug 25, 2026
Glucose Transporter Deficiency Syndrome Type 1 (Glut1-DS): New Insights From a Brazilian Cohort of Patients.

|Jul 10, 2026
Genetic landscape of phenylketonuria in Brazil.

|Jul 09, 2026
Long-Chain Fatty Acid Oxidation Disorder Genes: A Comprehensive Genetic Database of LC-FAOD Variants, Genotypes, and Phenotypes.

|Jun 03, 2026
First Revision of the Guidelines for the Diagnosis and Management of Remethylation Disorders.

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Frequent Collaborators

11 joint publications

Fernanda Sperb-Ludwig

4 joint publications

Katia Irie Teruya

4 joint publications

Eduardo Remor

3 joint publications

Fernanda Staniscuaski