|1.||Flåøyen, A: 2 articles (06/2003 - 06/2003)|
|2.||Scheie, E: 2 articles (06/2003 - 06/2003)|
|3.||Karlsen, Jan: 1 article (09/2013)|
|4.||Laane, Carl M M: 1 article (09/2013)|
|5.||Skulberg, Olav M: 1 article (09/2013)|
|6.||Hegge, Anne Bee: 1 article (09/2013)|
|7.||Schumacher, Trond: 1 article (09/2013)|
|8.||Mysterud, Ivar: 1 article (09/2013)|
|9.||Tønnesen, Hanne Hjorth: 1 article (09/2013)|
|10.||Sharma, I: 1 article (06/2010)|
06/01/2010 - "The sera of facial eczema-affected cattle and sheep had concentrations of phytoporphyrin ranging from 0.4 to 1.8 and 0.9 to 2.8 microM, respectively. "
06/01/2003 - "To establish a method for measuring phylloerythrin in plasma or serum and skin from lambs photosensitised after ingestion of the plant, Narthecium ossifragum, which induces an hepatogenous photosensitisation similar to the disease known as facial eczema in sheep. "
06/01/2003 - "To study the increase in phylloerythrin concentration in plasma and the disposition of phylloerythrin in skin and other tissues of sheep in which the hepatogenous photosensitisation,facial eczema, had been experimentally induced by dosing with the mycotoxin, sporidesmin. "
03/01/1983 - "While an obliterative cholangitis is responsible for the retention of phylloerythrin in facial eczema, the occlusion of bile ducts with crystalloid material (microliths) appear to perform a similar function in geeldikkop. "
06/01/2003 - "Spectrofluorometric analysis of phylloerythrin (phytoporphyrin) in plasma and tissues from sheep suffering from facial eczema."
|2.||Photosensitivity Disorders (Photodermatitis)
11/01/1976 - "Presence of phylloerythrin in the blood is a prerequisite for the photosensitization. "
12/01/2006 - "Hepatogenous photosensitization occurs in livestock following damage to the liver or biliary apparatus that results in impaired excretion of phytoporphyrin (phylloerythrin), a photosensitizer. "
|5.||Dehydration (Water Stress)
09/14/2007 - "Single dehydration of 2,3-dihydroxychlorin 3 gave a mixture of 2- and 3-(1-hydroxyethyl)porphyrins 7, while that of 12,13-dihydroxychlorin 5 resulted in the sole formation of 131-hydroxyporphyrin 9. The latter was modified smoothly to the phytoporphyrin analogue 2, whose molecular skeleton was similar to that of naturally occurring chlorophylls possessing a 131-oxo group fixed on an exo-five-membered ring."