Katalóg evidencie publikačnej činnosti PU

ID záznamu:	PU.Prešov.2011033010280809
Kategória:	ADE
Autor:	Behulová Regína (50%)
Autor:	Varga Ivan (7%)
Autor:	Strháková Ľubica (7%)
Autor:	Bôžiková Alexandra (10%)
Autor:	Dojčáková Dana (10%)
Autor:	Boroňová Iveta (9%)
Autor:	Repiská Vanda (7%)
Názov:	Incidence of microdeletions in the AZF region of the Y chromosome in Slovak patients with azoospermia [print, elektronický dokument]
Zdroj:	Biomedical papers [print, elektronický dokument]
Lokácia:	Roč. 155, č. 1. - Olomouc : Univerzita Palackého v Olomouci, (2011), s. 33-38
ISSN:	1213-8118. - ISSN 1804-7521
URL:	https://www.webofscience.com/wos/woscc/full-record/WOS:000288766200005
Ohlas:	[1] 2012. SUN, K., CHEN, X.-F., ZHU, X.-B. et al. A new molecular diagnostic approach to assess Y chromosome microdeletions in infertile men. In Journal of international medical research, ISSN 0300-0605. 2012, vol. 40, no. 1, s. 237-248.
Ohlas:	[1] 2013. ZHANG, H.-G., ZHANG, Z.-B., WANG, R.-X. et al. Male infertility in Northeast China: Molecular detection of Y chromosome microdeletions in azoospermic patients with Klinefelter`s syndrome. In Genetics and molecular research, ISSN 1676-5680. 2013, vol. 12, no. 4, s. 4972-4980.
Ohlas:	[1] 2013. LU, L.-H., HU, F.-X., GE, S. Investigation on azoospermia factor (AZF) microdeletion and sex-determining region Y (SRY) of the Y chromosome in male infertility. In Journal of reproduction and contraception, ISSN 1001-7844. 2013, vol. 24, no. 2, s. 88-94.
Ohlas:	[1] 2013. ALHALABI, M., KENJ, M., MONEM, F. et al. High prevalence of genetic abnormalities in Middle Eastern patients with idiopathic non-obstructive azoospermia. In Journal of assisted reproduction and genetics, ISSN 1058-0468. 2013, vol. 30, no. 6, s. 799-805.
Ohlas:	[1] 2013. ZHANG, F., LI, L., WANG, L. Clinical characteristics and treatment of azoospermia and severe oligospermia patients with Y-chromosome microdeletions. In Molecular reproduction and development, ISSN 1040-452X. 2013, vol. 80, no. 11, s. 908-915.
Ohlas:	[1] 2014. KHABOUR, O.F., FARARJEH, A.F.S., ALFAOURI, A.A. Genetic screening for AZF Y chromosome microdeletions in Jordanian azoospermic infertile men. In International journal of molecular epidemiology and genetics, ISSN 1948-1756. 2014, vol. 5, no. 1, s. 47-50.
Ohlas:	[1] 2014. HAMMAMI, W., KILANI, O., KHELIFA, M.B. et al. Prevalence of y chromosome microdeletions in infertile Tunisian men. In Annales de biolgie clinique, ISSN 0003-3898. 2014, vol. 72, no. 3, s. 331-336.
Ohlas:	[1] 2013. ZAIMY, M.A., KALANTAR, S.M., SHEIKHHA, M.H. et al. The frequency of Yq microdeletion in azoospermic and oligospermic Iranian infertile men. In Iranian journal of reproductive medicine, ISSN 1680-6433. 2013, vol. 11, no. 6, s. 453-458.
Ohlas:	[1] 2013. SHEIKHHA, M.H., ZAIMY, M.A., SOLEIMANIAN, S. et al. Multiplex PCR Screening of Y-chromosome microdeletions in azoospermic ICSI candidate men. In Iranian journal of reproductive medicine, ISSN 1680-6433. 2013, vol. 11, no. 4, s. 335-338.
Ohlas:	[1] 2015. TORRES, T.P., ROJAS, X.B., NARVÁEZ, M.B. et al. Triplex real-time polymerase chain reaction optimization for azf y-chromosome microdeletion analysis. In Jornal Brasileiro de reproducao assistida, ISSN 1517-5693. 2015, vol. 19, no. 2, s. 37-43.
Ohlas:	[1] 2015. ATIA, T., ABBAS, M., AHMED, A.-F. zoospermia factor microdeletion in infertile men with idiopathic severe oligozoospermia or non-obstructive azoospermia. In African journal of urology, ISSN 1110-5704. 2015, vol. 21, no. 4, s. 246-253.
Ohlas:	[1] 2015. CETINKAYA, M., KABA, M., CETIN, E.S. et al. Case report: Y chromosome microdeletion in an infertile patient with mosaic klinefelter syndrome. In International journal of human genetics, ISSN 0972-3757. 2015, vol. 15, no. 3, s. 145-148.
Ohlas:	[1] 2016. VASAN, Satya Srini. Azoospermia: diagnosis and management. In Male Infertility : a clinical approach. India : Springer India, 2016, s. 85-106. ISBN 978-813223604-7.
Ohlas:	[1] 2017. NAILWAL, M., CHAUHAN, J.B. Gene scanning for microdeletions in the azoospermia factor region of y-chromosome in infertile men of Gujarat, India. In Journal of clinical and diagnostic research, ISSN 2249-782X. 2017, vol. 11, no. 8.
Ohlas:	[1] 2019. SCIARRA, F., PELLONI, M., FAJA, F. Incidence of Y chromosome microdeletions in patients with Klinefelter syndrome. In Journal of endocrinological investigation, ISSN 0391-4097. 2019, vol. 42, no. 7, s. 833-842.
Ohlas:	[1] 2018. KIM, S.Y., LEE, B.Y., OH, A.R. et al. Clinical, hormonal and genetic evaluation of idiopathic nonobstructive azoospermia and Klinefelter syndrome patients. In Cytogenetic and genome research, ISSN 1424-8581. 2018, vol. 153, no. 4, s. 190-197.
Ohlas:	[1] 2017. LIU, X.-Y., ZHANG, H.-Y., PANG, D.-X. et al. AZFa microdeletions: occurrence in chinese infertile men and novel deletions revealed by semiconductor sequencing. In Urology, ISSN 0090-4295. 2017, vol. 107, s. 81.
Ohlas:	[1] 2018. MOJTABANEZHAD SHARIATPANAHI, A., AHMADNIA, H., TORKAMANZEHI, A. et al. Multiplex-polymerase chain reaction for detecting microdeletions in the azoospermia factor region of y chromosome in iranian couples with non-obstructive infertility and recurrent pregnancy loss. In International journal of fertility and sterility, ISSN 2008-076X. 2018, vol. 11, no. 4, s. 257.
Ohlas:	[1] 2013. RANDOLPH, Linda Marie. The cytogenetics of infertility. In The principles of clinical cytogenetics, third edition. New York : Springer , 2013, s. 213-227. ISBN 978-144191688-4.
Ohlas:	[1] 2020. JIA, Y., NIU, Z.-G., LI, W.-Y. et al. A fertile male with a single sY86 deletion on the Y chromosome. In Asian journal of andrology, ISSN 1008-682X. 2020, vol. 22, no. 3, s. 334.
Ohlas:	[1] 2023. WU, F.-T., CHEN, CH.-P., CHEN, S.-W. et al. Concomitance of 47,XXY, a balanced reciprocal translocation of t(4;17)(q12;q11.2) encompassing SPINK2 at 4q12 and NOS at 17q11.2 and an AZFa sY86 deletion in an infertile male. In Taiwanese journal of obstetrics & gynecology [online], ISSN 1028-4559. 2023 [cit. 2024-03-12], roč. 62, č. 2, s. 336-342. WOS:000965301700001; SCOPUS. Dostupný na internete <https://www.sciencedirect.com/science/article/pii/S1028455923000347?via%3Dihub>
Ohlas:	[1] 2023. KALANTARI, H., SABBAGHIAN, M., VOGIATZI, P. et al. Bridging the gap between AZF microdeletions and karyotype: twelve years' experience of an infertility center. In World journal of mens health, ISSN 2287-4208. 2023, roč. 41, č. 3, s. 659-670. WOS:000907683200001;.
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