Intra- and interreader reproducibility of PI-RADSv2: A multireader study

Autor: Smith, CP, Harmon, SA, Barrett, T, Bittencourt, LK, Law, YM, Shebel, H, An, JY, Czarniecki, M, Mehralivand, S, Coskun, M, Wood, BJ, Pinto, PA, Shih, JH, Choyke, PL, Turkbey, B

Background: The Prostate Imaging Reporting and Data System version 2 (PI-RADSv2) has been in use since 2015; while interreader reproducibility has been studied, there has been a paucity of studies investigating the intrareader reproducibility of PI-R

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4bc838b1bca2c4b7b0e340544687f89
https://www.repository.cam.ac.uk/handle/1810/296797

Diffusion-weighted MRI for detecting and monitoring cancer: a review of

Autor: Turkbey, B, Aras, O, Karabulut, N, Turgut, AT, Akpinar, E, Alibek, S, Pang, YX, Erturk, SM, El Khouli, RH, Bluemke, DA, Choyke, PL

Diffusion-weighted magnetic resonance imaging (MRI), Which involves the acquisition of a magnetic resonance signal related to the Brownian motion of water protons in tissue, has become a useful technique for assessing tumors. In this article, we revi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::457b85193be23ea993d3c697eb89c6b5
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/21133

Ruolo della risonanza magnetica nello studio dei feocromocitomi benigni e maligni: analisi quantitativa dell'intensità del segnale di risonanza

Autor: MAUREA, SIMONE, Cuocolo A, Reynolds JC, Choyke PL, Keiser HR, Neuman RD, Salvatore M.

In order to assess the clinical role of Magnetic Resonance (MR) imaging in patients with benign or malignant pheochromocytomas, the MR signal intensity ratios of benign and malignant tumors were evaluated. Eighteen patients (9 men and 9 women, mean a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3730::1ede7d3533d8d579a34207aa8949c5a9
http://hdl.handle.net/11588/344422

GENETIC FLANKING MARKERS REFINE DIAGNOSTIC-CRITERIA AND PROVIDE INSIGHTS INTO THE GENETICS OF VONHIPPEL LINDAU DISEASE

Autor: SEIZINGER, BR, SMITH, DI, FILLINGKATZ, MR, NEUMANN, H, GREEN, JS, CHOYKE, PL, ANDERSON, KM, FREIMAN, RN, KLAUCK, SM, WHALEY, J, DECKER, HJH, HSIA, YE, COLLINS, D, HALPERIN, J, LAMIELL, JM, OOSTRA, B, WAZIRI, MH, GORIN, MB, SCHERER, G, DRABKIN, HA, ARONIN, N, SCHINZEL, A, MARTUZA, RL, GUSELLA, JF, HAINES, JL

Publikováno v: SEIZINGER, BR; SMITH, DI; FILLINGKATZ, MR; NEUMANN, H; GREEN, JS; CHOYKE, PL; et al.(1991). GENETIC FLANKING MARKERS REFINE DIAGNOSTIC-CRITERIA AND PROVIDE INSIGHTS INTO THE GENETICS OF VONHIPPEL LINDAU DISEASE. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 88(7), 2864-2868. doi: 10.1073/pnas.88.7.2864. UCLA: Retrieved from: http://www.escholarship.org/uc/item/5831j1dv

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::ffe35534cc027a4c85356778286c42d1
http://www.escholarship.org/uc/item/5831j1dv

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