Fernanda Sperb-Ludwig

18PUBLICATIONS
60CO-AUTHORS
Developmental genetics (incl. sex determination)PsychopharmacologyMedical molecular engineering of nucleic acids and proteinsRespiratory diseasesMedical biochemistry - proteins and peptides (incl. medical proteomics)
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Publications (18)

|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.

|Mar 20, 2026
Toward the establishment of best practice guidelines for human research in Genomic Medicine in Brazil.

Fernanda Sperb Ludwig, Osvaldo Artigalás, Nureyev Ferreira Rodrigues

|Feb 06, 2026
Chronic Granulomatous Disease: Clinical and Molecular Characterization of Brazilian Patients.

Leonardo Martinello da Rosa, Martha Braun da Rosa, Mariana de Sampaio Leite Jobim Wilson

|Apr 09, 2024
Homocysteine and methylmalonic acid in Phenylketonuria patients.

Giovana Regina Weber Hoss, Fernanda Sperb-Ludwig, Tássia Tonon

|Dec 23, 2023
Glycogen Storage Disease: Expert Opinion on Clinical Diagnosis Revisited after Molecular Testing.

Rafael de Marchi, Tatiele Nalin, Fernanda Sperb-Ludwig

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Frequent Collaborators

11 joint publications

Ida Vanessa Döederlein Schwartz

3 joint publications

Franciele Cabral Pinheiro

2 joint publications

Greice Andreotti de Molfetta

2 joint publications

Adriana Aparecida Marques