Detalhe da pesquisa
1.
CoERG11 A395T mutation confers azole resistance in Candida orthopsilosis clinical isolates.
J Antimicrob Chemother
; 73(7): 1815-1822, 2018 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29635519
2.
Susceptibility Testing of Common and Uncommon Aspergillus Species against Posaconazole and Other Mold-Active Antifungal Azoles Using the Sensititre Method.
Antimicrob Agents Chemother
; 61(6)2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28416538
3.
Serum Endotoxin Activity Measured with Endotoxin Activity Assay Is Associated with Serum Interleukin-6 Levels in Patients on Chronic Hemodialysis.
Blood Purif
; 42(4): 294-300, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27577953
4.
Advanced tools for BRCA1/2 mutational screening: comparison between two methods for large genomic rearrangements (LGRs) detection.
Clin Chem Lab Med
; 52(8): 1119-27, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24670361
5.
Functional effect of Saffron supplementation and risk genotypes in early age-related macular degeneration: a preliminary report.
J Transl Med
; 11: 228, 2013 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-24067115
6.
Rapid detection of CFH (p.Y402H) and ARMS2 (p.A69S) polymorphisms in age-related macular degeneration using high-resolution melting analysis.
Clin Chem Lab Med
; 50(6): 1031-4, 2012 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22706242
7.
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations.
Clin Chem Lab Med
; 48(8): 1057-62, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20482300
8.
Foreign language effect in decision-making: How foreign is it?
Cognition
; 199: 104245, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32222524
9.
Two novel CYP21A2 missense mutations in Italian patients with 21-hydroxylase deficiency: Identification and functional characterisation.
IUBMB Life
; 61(3): 229-35, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19152428
10.
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form.
BMC Med Genet
; 10: 72, 2009 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-19624807
11.
Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia.
Clin Endocrinol (Oxf)
; 71(4): 470-6, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19170707
12.
A new CYP21A2 nonsense mutation causing severe 21-hydroxylase deficiency.
Clin Chem Lab Med
; 47(7): 824-5, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19499972
13.
Potential Use of MALDI-ToF Mass Spectrometry for Rapid Detection of Antifungal Resistance in the Human Pathogen Candida glabrata.
Sci Rep
; 7(1): 9099, 2017 08 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-28831086
14.
A rapid diagnostic workflow for cefotaxime-resistant Escherichia coli and Klebsiella pneumoniae detection from blood cultures by MALDI-TOF mass spectrometry.
PLoS One
; 12(10): e0185935, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28982134
15.
Multiplex ligation-dependent probe amplification analysis is useful for diagnosing congenital adrenal hyperplasia but requires a deep knowledge of CYP21A2 genetics.
Clin Chem
; 57(7): 1079-80, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21507910
16.
Diagnosis of Nocardia paucivorans central nervous system infection by DNA sequencing from paraffin-embedded tissue.
Infez Med
; 24(2): 147-52, 2016 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27367327
17.
CYP21A2 p.E238 deletion as result of multiple microconversion events: a genetic study on an Italian congenital adrenal hyperplasia (CAH) family.
Diagn Mol Pathol
; 22(1): 48-51, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23370425
18.
Genes, pseudogenes and like genes: the case of 21-hydroxylase in Italian population.
Clin Chim Acta
; 424: 85-9, 2013 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-23721949
19.
The first case of association between postpartum thyroiditis and thyroid hormone resistance in an Italian patient showing a novel p.V283A THRB mutation.
Thyroid
; 23(4): 506-10, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23134553
20.
p.H282N and p.Y191H: 2 novel CYP21A2 mutations in Italian congenital adrenal hyperplasia patients.
Metabolism
; 61(4): 519-24, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22014889