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Results 1481 - 1490 of 9104 for Abnormalities
  • News - 23 Jul 2004
    Cancers of the gut are one of the major causes of death from cancer, but a review published this week shows that they are also amongst the most preventable through changes in diet.
  • News - 27 Apr 2004
    BioTime, Inc. has announced that it has been awarded a research grant by the National Heart, Lung, and Blood Institute division of the National Institutes of Health (NIH) for use in the development of...
  • News - 13 Apr 2004
    Before the 1960's knowledge of the intrauterine environment was like a black box, limiting clinical understanding, and monitoring of the fetus during pregnancy. Little was known about the fetus until...
  • Health - 21 Jun 2023
    Pancreatic cancer is not usually diagnosed early on in the disease course due to a lack of symptoms in the initial stages.
  • Health - 15 Jun 2023
    There are several disorders that may lead to balance problems. Diagnosis aims at detecting the cause of balance problems. Balance problems thus are symptoms of an underlying condition rather than a...
  • Health - 10 Jun 2023
    Cancer arises when the genes and DNA within the cell are damaged. In a normal cell this DNA guides the actions, functions, growth, maturity, division and ultimately death of the cell.
  • Health - 30 Dec 2022
    First described in the early 20th century, Alport syndrome (AS), also known as hereditary nephritis, is a rare genetic disorder. Mutations in genes encoding type IV collagen give rise to primary...
  • News - 18 Jul 2025
    Parental metabolic health influences childhood asthma severity, with paternal cholesterol showing modest protective effects against exacerbating symptoms.
  • Health - 29 May 2025
    MODY 5 is a rare genetic diabetes subtype caused by HNF1B mutations or deletions, often presenting with early-onset diabetes and kidney, liver, or pancreatic abnormalities. Accurate genetic diagnosis...
  • Health - 12 Sep 2023
    Otopalatodigital spectrum disorders (OPDSD) constitute a group of rare, congenital, X-linked conditions caused by mutations in the filamin A (FLNA) gene.

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