The proportion of prostate-specific antigen (PSA) complexed to alpha(1)-antichymotrypsin improves the discrimination between prostate cancer and benign prostatic hyperplasia in men with a total PSA of 10 to 30 microg/L.
Autores de IIS La Fe
Participantes ajenos a IIS La Fe
- Royo M
Abstract
The aim of this study was to assess the diagnostic accuracy of the proportion of prostate-specific antigen (PSA) complexed to alpha(1)-antichymotrypsin (PSA-alpha(1)ACT:PSA ratio) in the differential diagnosis of prostate cancer (CaP) and benign prostatic hyperplasia (BPH) in men with total PSA of 10-30 microg/L.
Datos de la publicación
- ISSN/ISSNe:
- 0009-9147, 1530-8561
- Tipo:
- Article
- Páginas:
- 1251-1256
- PubMed:
- 12142381
- Factor de Impacto:
- 1,355 SCImago ℠
- Cuartil:
- Q1 SCImago ℠
CLINICAL CHEMISTRY OXFORD UNIV PRESS INC
Citas Recibidas en Web of Science: 11
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Keywords
- DIGITAL RECTAL EXAMINATION; TRANSITION ZONE VOLUME; REFERENCE RANGES; LONGITUDINAL EVALUATION; MOLECULAR-FORMS; IN-VITRO; SERUM; RATIO; ALPHA-1-ANTICHYMOTRYPSIN; DENSITY
Cita
MARTÍNEZ M,ESPAÑA F,Royo M,ALAPONT JM,NAVARRO S,ESTELLES A,AZNAR J,VERA CD,JIMENEZ J. The proportion of prostate-specific antigen (PSA) complexed to alpha(1)-antichymotrypsin improves the discrimination between prostate cancer and benign prostatic hyperplasia in men with a total PSA of 10 to 30 microg/L. Clin. Chem. 2002. 48. (8):p. 1251-1256. IF:4,788. (1).
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