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Impact of COVID-19 infection in patients with inherited metabolic diseases: a National Multicenter Study from the French IMDs Healthcare Network for Rare Diseases.
The impact of limited healthcare access among patients with light chain and transthyretin amyloidosis: real-world survey during COVID-19 lockdown period in France.
Genetic variants of SLC6A4 and risk of coronary artery disease: insights from North Indian population.
Immunization coverage and timeliness of vaccination in young patients with inborn errors of metabolism: a French multicentric study.
The healthcare burden of pulmonary alveolar proteinosis (PAP).