Brazilian registry of patients with porphyria: REBRAPPO study

BACKGROUND: Porphyrias are a rare group of disease due to inherited defects of heme synthesis with important systemic manifestations and great burden of disease for patients and families due to the exceptional course of disease with disabling chronic symptoms interposed by life-threatening acute att...

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Detalles Bibliográficos
Autores principales: Souza, Paulo Victor Sgobbi, Afonso, Gliciane, de Rezende Pinto, Wladimir Bocca Vieira, de Lima Serrano, Paulo, de Mattos Lombardi Badia, Bruno, Farias, Igor Braga, dos Santos Jorge, Ana Carolina, Machado, Roberta Ismael Lacerda, Pinto, Icaro França Navarro, Barros, Glenda Barbosa, de Oliveira, Helvia Bertoldo, Calil, Samia Rogatis, Franz, Cibele, Oliveira, Acary Souza Bulle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996884/
https://www.ncbi.nlm.nih.gov/pubmed/36890577
http://dx.doi.org/10.1186/s13023-023-02653-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996884/
https://www.ncbi.nlm.nih.gov/pubmed/36890577
http://dx.doi.org/10.1186/s13023-023-02653-1

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