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  1. No Access

    Article

    A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency

    Heterozygous mutations of the gene encoding transcription factor OTX2 were recently shown to be responsible for ocular as well as pituitary abnormalities. Here, we describe a patient with unilateral anophthalmia ...

    Liat Ashkenazi-Hoffnung, Yael Lebenthal, Alexander W. Wyatt… in Human Genetics (2010)

  2. No Access

    Article

    Insulin dose optimization using an automated artificial intelligence-based decision support system in youths with type 1 diabetes

    Despite the increasing adoption of insulin pumps and continuous glucose monitoring devices, most people with type 1 diabetes do not achieve their glycemic goals1. This could be related to a lack of expertise or i...

    Revital Nimri, Tadej Battelino, Lori M. Laffel, Robert H. Slover… in Nature Medicine (2020)