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21-hydroxylase deficiency transiently mimicking combined 21- and 11 beta-hydroxylase deficiency
(Walter De Gruyter Gmbh, 2008-05-01)
21-Hydroxylase deficiency (21OHD) is the commonest form of congenital adrenal hyperplasia, while 11 beta OHD represents 5% of cases. Although both result from mutations in distinct genes, cases of 'apparent' combined 210HD ...
Molecular analysis of CYP21 and C4 genes in Brazilian families with the classical form of steroid 21-hydroxylase deficiency
(Assoc Bras Divulg CientificaSao PauloBrasil, 1996)
21-hydroxylase deficiency transiently mimicking combined 21- and 11 beta-hydroxylase deficiency
(Walter De Gruyter GmbhBerlinAlemanha, 2008)
17-hydroxyprogesterone deficiency as a cause of sexual infantilism and arterial hypertension: Laboratory and molecular diagnosis - a case report
(Parthenon Publishing GroupLancasterInglaterra, 2007)
Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency
(Scandinavian University PressOsloNoruega, 1999)
Microbiosensor for salicylate based on modified carbon fibre
(Marcel Dekker IncNew YorkEUA, 2000)
Substrate specificity of a glucosyltransferase and an N-hydroxylase involved in the biosynthesis of cyclic hydroxamic acids in gramineae
(1994)
Microsomal preparations from maize seedlings exhibited N-hydroxylase activity with 2-hydroxy-1,4-benzoxazin-3-one (HBOA) as substrate, but not with its 7-methoxy analogue (HMBOA), or their corresponding 2-O-β-d-glucosides. ...