Maria Helena Vaisbich

11PUBLICATIONS
41CO-AUTHORS
Neurology and neuromuscular diseasesCardiovascular medicine and haematology not elsewhere classifiedEpidemiological modellingComputational physiologyInfant and child health
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Publications (11)

|Jan 30, 2026
Nephrocalcinosis: unveiling renal tubulopathies in the genomic era.

Elenice Andrade Milhomem Ayoub, Maria Helena Vaisbich, Daniel Ribeiro Rocha

|Feb 07, 2025
Recommendations for diagnosis and treatment of Atypical Hemolytic Uremic Syndrome (aHUS): an expert consensus statement from the Rare Diseases Committee of the Brazilian Society of Nephrology (COMDORA-SBN).

Maria Helena Vaisbich, Luis Gustavo Modelli de Andrade, Maria Izabel Neves de Holanda Barbosa

|Feb 10, 2024
Real-world data of Brazilian adults with X-linked hypophosphatemia (XLH) treated with burosumab and comparison with other worldwide cohorts.

Maria Helena Vaisbich, Antônio César Paulillo de Cillo, Bárbara Campolina C Silva

|Nov 23, 2023
A comprehensive model for assessing and classifying patients with thrombotic microangiopathy: the TMA-INSIGHT score.

Vanessa Vilani Addad, Lilian Monteiro Pereira Palma, Maria Helena Vaisbich

|Mar 03, 2022
Recommendations for the diagnosis and management of Fabry disease in pediatric patients: a document from the Rare Diseases Committee of the Brazilian Society of Nephrology (Comdora-SBN).

Maria Helena Vaisbich, Luís Gustavo Modelli de Andrade, Cassiano Augusto Braga Silva

|Feb 25, 2022
Brazilian consensus recommendations for the diagnosis, screening, and treatment of individuals with fabry disease: Committee for Rare Diseases - Brazilian Society of Nephrology/2021.

Cassiano Augusto Braga Silva, Luis Gustavo Modelli de Andrade, Maria Helena Vaisbich

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Frequent Collaborators

5 joint publications

Luis Gustavo Modelli de Andrade

4 joint publications

Fellype de Carvalho Barreto

4 joint publications

Cassiano Augusto Braga Silva

3 joint publications

Lilian Monteiro Pereira Palma