Ida Vanessa Schwartz

40PUBLICATIONS
164CO-AUTHORS
Foetal development and medicineDevelopmental genetics (incl. sex determination)PsychopharmacologyMedical biochemistry - lipidsMetabolic medicine
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Publications (40)

|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.

|Mar 20, 2026
The Diagnostic Odyssey of a Biochemically Confirmed Case of ML II: The First Western Patient With LYSET Deficiency.

Fernanda Sperb-Ludwig, Taciane Alegra, Leonardo Martinello da Rosa

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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