Desensitization of olipudase alfa-induced anaphylaxis in a child with chronic neurovisceral acid sphingomyelinase deficiency

Author:

Fiori Laura,Tagi Veronica Maria,Montanari Chiara,Gambino Mirko,Carlevatti Veronica,Zizzo Carmela,D'Auria Enza,Dilillo Dario,Verduci Elvira,Zuccotti Gianvincenzo

Funder

Romeo and Enrica Invernizzi Foundation

Publisher

Elsevier BV

Reference42 articles.

1. Enzyme replacement therapy for children with acid sphingomyelinase deficiency in the real world: a single center experience in Taiwan;Pan;Mol. Genet. Metab. Rep.,2023

2. Consensus clinical management guidelines for acid sphingomyelinase deficiency (Niemann-pick disease types A, B and A/B);Geberhiwot;Orphanet J. Rare Dis.,2023

3. Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): literature review and report of new cases;Cassiman;Mol. Genet. Metab.,2016

4. Types a and B Niemann-pick disease;Schuchman;Best Pract. Res. Clin. Endocrinol. Metab.,2015

5. The natural history of type B Niemann-pick disease: results from a 10-year longitudinal study;Wasserstein;Pediatrics,2004

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1. Multiple drugs;Reactions Weekly;2024-08-10

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