Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Daniela Griso"'
Publikováno v:
Archives of Dermatological Research. 284:212-214
The determination of the enzymatic activity of URO-D in erythrocytes is the screening method used for differentiation between hereditary and non-hereditary forms of porphyria cutanea tarda (PCT). The aim of the present work was to establish the relat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d60e362d1c05ad59aa206f4cc20d4174
https://doi.org/10.1007/bf00375795
https://doi.org/10.1007/bf00375795
Publikováno v:
Journal of Investigative Dermatology. 111:1241-1242
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fca6fc70c2988e6866f839e5857ca7ad
https://doi.org/10.1046/j.1523-1747.1998.00400.x
https://doi.org/10.1046/j.1523-1747.1998.00400.x
Autor:
Mauro D'Amato, Annelisa Macri, Simona Barile, Daniela Griso, Margherita Bonuglia, G. Biolcati
Publikováno v:
Human Mutation. 21:448-448
Variegate Porphyria (VP) is one of the acute hepatic porphyrias, and is clinically characterised by skin lesions and acute neuropsychiatric/visceral attacks that occur separately or together. The disorder is caused by a partial deficiency of protopor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::558838e94ca04cca3499308ee6e8cd97
https://doi.org/10.1002/humu.9125
https://doi.org/10.1002/humu.9125
Autor:
Antonella Argiroffo, G. C. Topi, Oreste Zardi, Bernardino Giacalone, Luciana D'Alessandro Gandolfo, Daniela Griso
Publikováno v:
Dermatology. 167:24-32
We examined more than 1,400 dermatologic patients with clinically defined (but having unknown or presumably multiple etiology) affections. The investigation revealed the presence of antitoxoplasm antibodies in more than 50% of the patients, but in on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52977c3ce3437d131a7e8701e07bda52
https://doi.org/10.1159/000249740
https://doi.org/10.1159/000249740
Publikováno v:
Archives of dermatological research. 281(4)
In the present report we describe our findings in 158 cases of PCT, tested for the presence of circulating autoantibodies, and examine the incidence of SLE in a large survey of PCT patients. The results showed no evidence of a PCT + SLE association.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0723ef8680865b6325dd260c8797c543
https://pubmed.ncbi.nlm.nih.gov/2774662
https://pubmed.ncbi.nlm.nih.gov/2774662
Autor:
Daniela Griso, Annelisa Macri, Silvia Fargion, E. Di Pierro, F Martinez di Montemuros, Maria Domenica Cappellini, G. Biolcati, Gemino Fiorelli
Publikováno v:
Scopus-Elsevier
Acute intermittent porphyria (AIP) is an autosomal disorder caused by molecular abnormalities in the hydroxymethylbilane synthase (HMBS) gene coding for the third enzyme in the heme biosynthetic pathway. So far, more than 160 different mutations resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f952c5cc3dc0c1ac08793c321afa52da
http://www.scopus.com/inward/record.url?eid=2-s2.0-17144454533&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-17144454533&partnerID=MN8TOARS
