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  2. Hypervitaminosis A - Wikipedia

    en.wikipedia.org/wiki/Hypervitaminosis_A

    Stopping high vitamin A intake is the standard treatment. Most people fully recover. Phosphatidylcholine (in the form of PPC or DLPC), the substrate for lecithin retinol acyltransferase, which converts retinol into retinyl esters (the storage forms of vitamin A). Vitamin E may alleviate hypervitaminosis A. [34]

  3. How Often Should You Use Retinol? Here's What Dermatologists Say

    www.aol.com/lifestyle/often-retinol-heres...

    A quick rundown on ideal retinol application frequency. For premium support please call: 800-290-4726 more ways to reach us

  4. Dog skin disorders - Wikipedia

    en.wikipedia.org/wiki/Dog_skin_disorders

    The condition of a dog's skin and coat is also an important indicator of its general health. Skin disorders of dogs vary from acute, self-limiting problems to chronic or long-lasting problems requiring life-time treatment. Skin disorders may be primary or secondary (due to scratching, itch) in nature, making diagnosis complicated.

  5. Vitamin A - Wikipedia

    en.wikipedia.org/wiki/Vitamin_A

    Vitamin A is a fat-soluble vitamin that is an essential nutrient.The term "vitamin A" encompasses a group of chemically related organic compounds that includes retinol, retinyl esters, and several provitamin (precursor) carotenoids, most notably β-carotene (beta-carotene).

  6. National Dog Day: Holistic treatments increasingly used by ...

    www.aol.com/national-dog-day-holistic-treatments...

    About 15% of the nearly 50,000 participants enrolled in the Dog Aging Project, a nationwide study of healthy aging in companion dogs and pet dogs, have participated in some sort of alternative ...

  7. Retinyl palmitate - Wikipedia

    en.wikipedia.org/wiki/Retinyl_palmitate

    Retinyl palmitate, or vitamin A palmitate, is the ester of retinol and palmitic acid, with formula C 36 H 60 O 2. It is the most abundant form of vitamin A storage in animals. [2] An alternate spelling, retinol palmitate, which violates the -yl organic chemical naming convention for esters, is also frequently seen. [citation needed]