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  1. 1
    Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry

    Orthopaedic phenotyping of NGLY1 deficiency using an international, family-led disease registry by Eli M. Cahan, Steven L. Frick

    Published 2019-06-01
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  2. 2
    Mothers of children with major congenital anomalies have increased health care utilization over a 20-year post-birth time horizon

    Mothers of children with major congenital anomalies have increased health care utilization over a 20-year post-birth time horizon by Nirav R. Shah, Kyung Mi Kim, Venus Wong, Eyal Cohen, Sarah Rosenbaum, Eli M. Cahan, Arnold Milstein, Henrik Toft Sørensen, Erzsébet Horváth-Puhó

    Published 2021-01-01
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    Article

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