Wiland E - Search Results

1

Chromosomal anomalies as a predisposing factor for male infertility.

Wiland E, Kurpisz M. Wiland E, et al. Folia Histochem Cytobiol. 1997;35(2):55-62. Folia Histochem Cytobiol. 1997. PMID: 9151078 Review.

2

Infertility status of male individuals with abnormal spermiogram evaluated by cytogenetic analysis and in vitro sperm penetration assay.

Wiland E, Wojda A, Kamieniczna M, Szczygieł M, Kurpisz M. Wiland E, et al. Med Sci Monit. 2002 May;8(5):CR394-400. Med Sci Monit. 2002. PMID: 12016421

3

Segregation of the marker chromosome der(20) in the sperm of a male with karyotype 46,XY[961/ 47,XY+mar[4].

Wiland E, Jarmumz M, Kurpisz M. Wiland E, et al. Med Sci Monit. 2005 Mar;11(3):CS9-15. Med Sci Monit. 2005. PMID: 15735571

4

Positioning of chromosome 15, 18, X and Y centromeres in sperm cells of fertile individuals and infertile patients with increased level of aneuploidy.

Olszewska M, Wiland E, Kurpisz M. Olszewska M, et al. Among authors: wiland e. Chromosome Res. 2008;16(6):875-90. doi: 10.1007/s10577-008-1246-2. Epub 2008 Aug 15. Chromosome Res. 2008. PMID: 18696233

5

Comparison of chromosome centromere topology in differentiating cells with myogenic potential.

Mikołajczak B, Wiland E, Rozwadowska N, Rucinski M, Mietkiewski T, Kurpisz M. Mikołajczak B, et al. Among authors: wiland e. Folia Histochem Cytobiol. 2009 Jan;47(3):377-83. doi: 10.2478/v10042-009-0037-8. Folia Histochem Cytobiol. 2009. PMID: 20164021 Free article.

6

Idiopathic infertility in married couples in the light of cytogenetic analysis and sperm penetration assay.

Wiland E, Wojda A, Kamieniczna M, Latos-Bieleńska A, Jedrzejczak P, Kurpisz M. Wiland E, et al. Folia Histochem Cytobiol. 2001;39(1):35-41. Folia Histochem Cytobiol. 2001. PMID: 11261547

7

Risk evaluation of carriers with chromosome reciprocal translocation t(7;13)(q34;q13) and concomitant meiotic segregation analyzed by FISH on ejaculated spermatozoa.

Midro AT, Wiland E, Panasiuk B, Leśniewicz R, Kurpisz M. Midro AT, et al. Among authors: wiland e. Am J Med Genet A. 2006 Feb 1;140(3):245-56. doi: 10.1002/ajmg.a.31083. Am J Med Genet A. 2006. PMID: 16411217

8

The analysis of meiotic segregation patterns and aneuploidy in the spermatozoa of father and son with translocation t(4;5)(p15.1;p12) and the prediction of the individual probability rate for unbalanced progeny at birth.

Wiland E, Midro AT, Panasiuk B, Kurpisz M. Wiland E, et al. J Androl. 2007 Mar-Apr;28(2):262-72. doi: 10.2164/jandrol.106.000919. Epub 2006 Oct 4. J Androl. 2007. PMID: 17021336 Free article.

9

Successful pregnancy after preimplantation genetic diagnosis for carrier of t(2;7)(p11.2;q22) with high rates of unbalanced sperm and embryos: a case report.

Wiland E, Hobel CJ, Hill D, Kurpisz M. Wiland E, et al. Prenat Diagn. 2008 Jan;28(1):36-41. doi: 10.1002/pd.1899. Prenat Diagn. 2008. PMID: 18186141

10

Interindividual differences and alterations in the topology of chromosomes in human sperm nuclei of fertile donors and carriers of reciprocal translocations.

Wiland E, Zegało M, Kurpisz M. Wiland E, et al. Chromosome Res. 2008;16(2):291-305. doi: 10.1007/s10577-007-1194-2. Epub 2008 Feb 11. Chromosome Res. 2008. PMID: 18256895

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