455 results on '"Krausz, C."'
Search Results
2. Safety issues in semen banks during the COVID-19 pandemic: data from a European survey
3. A de novo paradigm for male infertility
4. Testosterone Treatment in Male Patients with Klinefelter’s Syndrome
5. Tall stature and gigantism in transition age: clinical and genetic aspects—a literature review and recommendations.
6. Testosterone Treatment in Male Patients with Klinefelter’s Syndrome
7. Spermatogenic failure and the Y chromosome
8. Evaluation of sperm DNA quality in men presenting with testicular cancer and lymphoma using alkaline and neutral Comet assays
9. P-068 Oxidative stress and DNA fragmentation of spermatozoa in patients with cancer
10. Pubertal induction and transition to adult sex hormone replacement in patients with congenital pituitary or gonadal reproductive hormone deficiency: an Endo-ERN clinical practice guideline
11. A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships
12. Sellar and parasellar lesions in the transition age: a retrospective Italian multi-centre study.
13. European Association of Urology guidelines on vasectomy
14. Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia
15. A global approach to addressing the policy, research and social challenges of male reproductive health
16. The X chromosome and male infertility
17. Genetics of Male Infertility
18. The Y chromosome-linked copy number variations and male fertility
19. The need of continuous focus on improved mentoring of trainees and young investigators in the field of andrology: highlights of current programs and opportunities for the future
20. Epidemiology; diagnosis, and treatment of male hypogonadotropic hypogonadism
21. Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility
22. Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency
23. Persistence of expression of the TMPRSS2:ERG fusion gene after pre-surgery androgen ablation may be associated with early prostate specific antigen relapse of prostate cancer: Preliminary results
24. EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013
25. The European Academy of Andrology (EAA) ultrasound study on healthy, fertile men: Scrotal ultrasound reference ranges and associations with clinical, seminal, and biochemical characteristics
26. Y-chromosome microdeletions are not associated with SHOX haploinsufficiency
27. Short anogenital distance is associated with testicular germ cell tumour development
28. gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study (vol 27, pg 1578, 2019)
29. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest (vol 34, pg 978, 2020)
30. Difficulties in achieving vs maintaining erection: organic, psychogenic and relational determinants
31. Varicocele and infertility
32. The relationship between Y chromosome DNA haplotypes and Y chromosome deletions leading to male infertility
33. Further insights into the role of T222P variant of RXFP2 in non-syndromic cryptorchidism in two Mediterranean populations
34. Corrigendum. Sequencing of a ‘mouse azoospermia’ gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest
35. European Academy of Andrology (EAA) guidelines on investigation, treatment and monitoring of functional hypogonadism in males
36. Genetic testing in infertile males
37. The association between varicocele, premature ejaculation and prostatitis symptoms: Possible mechanisms: PS-05–004
38. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independent of Y-chromosomal background
39. Florence–Utah Symposium corner: from genetics to epigenetics of male infertility
40. Florence–Utah Symposium on the Genetics of Male Infertility
41. The Y chromosome and its fragility
42. Phenotypic variation within European carriers of the Y-chromosomal gr/gr deletion is independentof Y-chromosomal background
43. Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest
44. Whole exome sequencing in non-obstructive azoospermia allows the identification of a high-risk subgroup of infertile men for undiagnosed Fanconi Anemia, a cancer-prone disease
45. Genetics of ncHH: from a peculiar inheritance of a novel GNRHR mutation to a comprehensive review of the literature
46. From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia
47. Partial AZFc deletions in infertile men with cryptorchidism
48. Molecular analysis of estrogen receptor alpha gene AGATA haplotype and SNP12 in European populations: potential protective effect for cryptorchidism and lack of association with male infertility
49. Y chromosome and male infertility
50. The gr/gr deletion(s): a new genetic test in male infertility?
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