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You searched for: Author/Creator Scarpa, Maurizio

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1. A column‐switching HPLC‐MS/MS method for mucopolysaccharidosis type I analysis in a multiplex assay for the simultaneous newborn screening of six lysosomal storage disorders. (22nd January 2014)

2. A generic emergency protocol for patients with inborn errors of metabolism causing fasting intolerance: A retrospective, single‐center study and the generation of www.emergencyprotocol.net. Issue 5 (4th May 2021)

4. Easy‐to‐use algorithm would provide faster diagnoses for mucopolysaccharidosis type I and enable patients to receive earlier treatment. (13th July 2018)

5. Efficacy and safety of enzyme replacement therapy with BMN 110 (elosulfase alfa) for Morquio A syndrome (mucopolysaccharidosis IVA): a phase 3 randomised placebo‐controlled study. Issue 6 (9th May 2014)

6. Erratum to: Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders. Issue 1 (December 2016)

8. Fabry cardiomyopathy: Gb3‐induced auto‐reactive panmyocarditis requiring heart transplantation. (29th April 2020)

9. Fabry cardiomyopathy: Gb3‐induced auto‐reactive panmyocarditis requiring heart transplantation. (29th April 2020)

10. Human amniotic fluid stem cells protect rat lungs exposed to moderate hyperoxia. Issue 11 (26th March 2013)