C
Csilla Krausz
Researcher at University of Florence
Publications - 216
Citations - 12738
Csilla Krausz is an academic researcher from University of Florence. The author has contributed to research in topics: Male infertility & Infertility. The author has an hindex of 60, co-authored 186 publications receiving 10945 citations. Previous affiliations of Csilla Krausz include Pasteur Institute & University of Edinburgh.
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Journal ArticleDOI
European Association of Urology Guidelines on Male Infertility: The 2012 Update
A. Jungwirth,Aleksander Giwercman,Herman Tournaye,Thorsten Diemer,Zsolt Kopa,Gert R. Dohle,Csilla Krausz +6 more
TL;DR: These EAU guidelines are a short comprehensive overview of the updated guidelines of male infertility as recently published by the EAU and are also available in the National Guideline Clearinghouse ( www.guideline.gov/).
Journal ArticleDOI
Oxidative stress, DNA damage and the Y chromosome.
Robert John Aitken,Csilla Krausz +1 more
TL;DR: The factors responsible for Y chromosome deletions in spermatozoa remain unresolved but may be one facet of a central reproductive problem: controlling the amount of oxidative stress experienced by germ cells during their differentiation and maturation in the male reproductive tract.
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Genetics of male infertility.
TL;DR: Large, international, and consortium-based whole-exome and whole-genome studies are the most promising approach for the discovery of the missing genetic aetiology of idiopathic male infertility.
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EAA/EMQN best practice guidelines for molecular diagnosis of y‐chromosomal microdeletions. State of the art 2004
TL;DR: The most recent revision of the 1999 laboratory guidelines summarizes the results of a 'Best Practice Meeting' held in Florence (Italy) in October 2003 as discussed by the authors, and it was agreed that the basic 1999 protocol, based on two multiplex polymerase chain reactions each covering the three AZF regions, is still fully valid and appropriate for accurate diagnosis.
Journal ArticleDOI
EAA/EMQN best practice guidelines for molecular diagnosis of Y‐chromosomal microdeletions: state‐of‐the‐art 2013
TL;DR: The present revision of the 2004 laboratory guidelines summarizes all the clinical novelties related to the Y chromosome (classic, partial and gene‐specific deletions, genotype–phenotype correlations, methodological issues) and provides an update on the results of the quality control programme.