Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Porphobilin"'
Autor:
Christian Homann, Christian Heckl, Ronald Sroka, Michael Vogeser, Georg Hennig, Thomas Stauch, Alexander Lang, Herbert Stepp
Publikováno v:
Journal of biomedical optics. 23(5)
Autosomal-dominant acute porphyria, a group of rare metabolic diseases, can lead to life-threatening neurovisceral attacks. Currently, no efficient screening test is available. Elevated urinary porphobilinogen (PBG) in addition to elevated porphyrins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0aa7c1bae43ebf7f7931052d21ea5f32
https://pubmed.ncbi.nlm.nih.gov/29855177
https://pubmed.ncbi.nlm.nih.gov/29855177
Publikováno v:
Experientia. 33(7)
It rats after i.v. prophobilin, blood pressure and pulse rate remained stable, the animals were calm and moved freely with no symptoms or signs of nervous effect. Prophobilin was rapidly excreted in the urine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d7243850c098599b22245739c2a1aa
https://pubmed.ncbi.nlm.nih.gov/891759
https://pubmed.ncbi.nlm.nih.gov/891759
Autor:
Charles H. Gray
Publikováno v:
Archives of Internal Medicine. 85:459
ACUTE porphyria is a familial metabolic disease of unknown etiology characterized by repeated attacks of severe abdominal colic, associated usually with constipation and often with vomiting, and accompanied with abnormalities of the central nervous s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17d52014ce431eeac15f3ff0656d49ee
https://doi.org/10.1001/archinte.1950.00230090096006
https://doi.org/10.1001/archinte.1950.00230090096006