about
The presence of germ cells in the semen of azoospermic, cryptozoospermic and severe oligozoospermic patients: stringent flow cytometric analysis and correlations with hormonal status.EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013.Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.Novel genetic aspects of Klinefelter's syndrome.Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males.Azoospermia and ring chromosome 9--a case report.The FSHB -211G>T variant attenuates serum FSH levels in the supraphysiological gonadotropin setting of Klinefelter syndromeThe haplotype M2 of the ANXA5 gene is not associated with antitrophoblast antibodiesFSHB -211G>T stratification for follicle-stimulating hormone treatment of male infertility patients: making the case for a pharmacogenetic approach in genetic functional secondary hypogonadism.The future of testis research is turning 6! Six years of international network for young researchers in male fertility.Mosaicism for an unbalanced Y;21 translocation in an infertile man: a case reportMinutes of the 5th meeting of the International Network for Young Researchers in Male Fertility.Aquaporins in the human testis and spermatozoa - identification, involvement in sperm volume regulation and clinical relevance.Role of syndecan-3 polymorphisms in obesity and female hyperandrogenism.Further insights into the role of the annexin A5 M2 haplotype as recurrent pregnancy loss factor, assessing timing of miscarriage and partner risk.A common haplotype of protamine 1 and 2 genes is associated with higher sperm counts.Anti-Müllerian hormone in men with normal and reduced sperm concentration and men with maldescended testes.Polymorphisms of the luteinizing hormone/chorionic gonadotropin receptor gene: association with maldescended testes and male infertility.ESHRE Task Force on Ethics and Law 21: genetic screening of gamete donors: ethical issues.Is the FSHR 2039A>G variant associated with susceptibility to testicular germ cell cancer?Effects of the FSH-β-subunit promoter polymorphism -211G->T on the hypothalamic-pituitary-ovarian axis in normally cycling women indicate a gender-specific regulation of gonadotropin secretion.DMRT1 mutations are rarely associated with male infertility.Y-chromosome microdeletions are not associated with SHOX haploinsufficiency.Paternal and maternal carriage of the annexin A5 M2 haplotype are equal risk factors for recurrent pregnancy loss: a pilot study.Gene expression patterns in relation to the clinical phenotype in Klinefelter syndrome.Independent association of the M2/ANXA5 haplotype with recurrent pregnancy loss (RPL) in PCOS patients.Intratesticular testosterone is increased in men with Klinefelter syndrome and may not be released into the bloodstream owing to altered testicular vascularization– a preliminary report.Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiencyRestoration of fertility by gonadotropin replacement in a man with hypogonadotropic azoospermia and testicular adrenal rest tumors due to untreated simple virilizing congenital adrenal hyperplasiaGenetik der männlichen InfertilitätCombined Effects of the VariantsFSHB−211G>T andFSHR2039A>G on Male Reproductive ParametersClinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsyMinutes of the 14th European workshop on molecular and cellular endocrinology of the testisCoiled sperm from infertile patients: characteristics, associated factors and biological implicationIdiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1The X chromosome and male infertility
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description
hulumtues
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հետազոտող
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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Frank Tüttelmann
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P21
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frank-tttelmann
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