A new proof of evidence of cysteamine quantification for therapeutic drug monitoring in patients with cystinosis

Overview of attention for article published in Orphanet Journal of Rare Diseases, November 2022

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Top story: A new proof of evidence of cysteamine quantification for therapeutic drug monitoring in patients with cystinosis | Orphanet Journal of Rare Diseases | Full Text https://t.co/DMCkLLr4OU, see more https://t.co/6X0FQJCIbA

05 Nov 2022

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A new proof of evidence of cysteamine quantification for therapeutic drug monitoring in patients with cystinosis #OJRD #MassSpec https://t.co/0BCsP9F5hH

04 Nov 2022

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A new proof of evidence of cysteamine quantification for therapeutic drug monitoring in patients with cystinosis https://t.co/eAYe0dSwKb

04 Nov 2022

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