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    This review discusses how systematic data collection for sickle cell disease through a longitudinal clinical registry and a national surveillance program can improve resource use and patient outcomes and provide an equitable foundation for care.

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    • Revisit this #Year1 special communication that says sickle cell disease needs federal funding equal to other inherited conditions including hemophilia and cystic fibrosis to improve outcomes. #AnniversaryMonth @jkw4444 https://t.co/aG2cKNn7as

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    After 2 years of a seemingly relentless pandemic that has upended work, education, and social interactions, the questions many are asking are when will we get back to normal and what will life be like after the COVID-19 pandemic? In truth, science cannot fully predict what SARS-CoV-2 variants will…

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    • Thank you @LawrenceGostin for contributing #JAMAForum articles during our #Year1 as a peer-reviewed journal, including most recently: "Life After the COVID-19 Pandemic" #AnniversaryMonth https://t.co/9S7Z5mBYzy