Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Razvan Danau"'
Autor:
Aida Petca, Ioana Rotar, Andreea Borislavschi, Razvan-Cosmin Petca, Razvan Danau, Mihai Dumitrascu, Florica Sandru, Irina Pacu
Publikováno v:
Experimental and therapeutic medicine. 24(5)
Surgical site infections (SSIs) are a complication in any surgical field and they are responsible for 38% of surgery-related patient deaths. Identifying appropriate prophylaxis and solutions to combat SSIs is of global interest. Several studies and r
Autor:
Cristian Toma, Viorel Jinga, Paul D. Iordache, Titus Valentin Grigorean, Dumitru Cristinel Badiu, George Daniel Radavoi, Viorica Radoi, Radu Ursu, Mihaela Mandu, Cristian Sorin Sima, Bogdan Braticevici, Razvan Danau, Stefan Rascu
Publikováno v:
ROMANIAN BIOTECHNOLOGICAL LETTERS. 24:100-107
Autor:
Serban Radian, Catalina Poiana, Radu Iorgulescu, Razvan Danau, Isabela Gaita, Terzea Dana Cristina
Publikováno v:
Endocrine Abstracts.
Autor:
Bjarni Gunnarsson, Viorel Jinga, Angelica Voinoiu, Hrefna Johannsdottir, Stefan Rascu, Stefania Benonisdottir, Violeta Calota, Sorin Cristian Sima, Jon G. Jonasson, Razvan Danau, Dana Mates, Viorica Radoi, Daniel Badescu, Radu Ursu, Camelia Nicolae, Gudny A. Arnadottir, Cătălin Alexandru Staicu, Bjarni V. Halldorsson, Thorunn Rafnar, Paul D. Iordache, Aslaug Jonasdottir, Asgeir Sigurdsson, Kari Stefansson, Mihai Dobra, Irma Eva Csiki, Hannes P. Eggertsson, Sigrun Kristjansdottir, Ioan Nicolae Mates, Mariana Jinga, Louise le Roux, Andrei Manolescu, Brynjar O. Jensson, Nicoleta Suciu, Daniel Radavoi, Gabriel Rosoga, Patrick Sulem
Publikováno v:
Journal of Cellular and Molecular Medicine
Publisher's version (útgefin grein)
Two familial forms of colorectal cancer (CRC), Lynch syndrome (LS) and familial adenomatous polyposis (FAP), are caused by rare mutations in DNA mismatch repair genes (MLH1, MSH2, MSH6, PMS2) and the genes AP
Two familial forms of colorectal cancer (CRC), Lynch syndrome (LS) and familial adenomatous polyposis (FAP), are caused by rare mutations in DNA mismatch repair genes (MLH1, MSH2, MSH6, PMS2) and the genes AP
Autor:
Thorunn Rafnar, Viorel Jinga, Stefan Rascu, Viorica Radoi, Daniel Badescu, Stefania Benonisdottir, Bjarni V. Halldorsson, Angelica Voinoiu, Radu Ursu, Hannes P. Eggertsson, Bjarni Gunnarsson, Paul D. Iordache, Razvan Danau, Cătălin Alexandru Staicu, Irma Eva Csiki, Mariana Jinga, Violeta Calota, Dana Mates, Nicoleta Suciu, Patrick Sulem, Daniel Radavoi, Gabriel Rosoga, Kari Stefansson, Sorin Cristian Sima, Andrei Manolescu, Júlíus Guðmundsson
Publikováno v:
Journal of Cellular and Molecular Medicine
To find sequence variants affecting prostate cancer (PCA) susceptibility in an unscreened Romanian population we use a genome‐wide association study (GWAS). The study population included 990 unrelated pathologically confirmed PCA cases and 1034 mal