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Results 2921 - 2930 of 3032 for Absent
  • Health - 1 Jun 2022
    Carnosinemia, also known as carnosinase deficiency, is an extremely rare inherited metabolic disorder.
  • Health - 19 May 2022
    This article explains jejunal atresia, a congenital birth defect that is a leading cause of bowel obstruction in newborns.
  • Health - 19 May 2022
    Bannayan-Riley-Ruvalcaba Syndrome (BRRS) is a congenital genetic condition defined by a group of characteristic features. This article discusses the condition in depth.
  • White Paper - 23 Mar 2022
    Bispecific antibodies are emerging as rising stars in antibody therapeutics. This article delves into why they are desirable therapeutic targets and what this could mean for healthcare.
  • Health - 7 Feb 2022
    PMDD is similar to PMS in that it occurs before the menstrual period, however, PMDD is more extreme.
  • Health - 10 Jan 2022
    Rare diseases affect 6-8% of the world’s population and most people wait several years before they are diagnosed and potentially treated.
  • Health - 10 Jan 2022
    Bartter syndrome refers to a set of rare genetic disorders characterized by distinct kidney function abnormalities.
  • Health - 22 Dec 2021
    As modern-day humans began to emerge from Africa, the divergent characteristics of archaic groups began to overlap spatially and temporally.
  • Health - 8 Oct 2021
    The ongoing pandemic has highlighted the difficulty of achieving satisfaction within and outside of work hours. In this article the importance of a work-life balance.
  • Health - 30 Sep 2021
    The term metatarsalgia refers to pain at one or more of the metatarsal heads in the foot, which is commonly described as forefoot pain.

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