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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1956 1
1963 1
1964 1
1966 1
1968 1
1969 1
1970 2
1973 1
1975 6
1976 4
1977 5
1978 5
1979 5
1980 2
1981 4
1982 4
1983 4
1984 4
1985 2
1986 2
1987 2
1988 7
1989 3
1990 4
1991 2
1992 3
1993 7
1994 3
1995 3
1996 5
1997 2
1998 8
1999 7
2000 6
2001 6
2002 8
2003 7
2004 7
2005 10
2006 11
2007 13
2008 7
2009 12
2010 20
2011 24
2012 28
2013 17
2014 20
2015 19
2016 24
2017 22
2018 27
2019 29
2020 46
2021 32
2022 39
2023 30
2024 5

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514 results

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Page 1
The Klinefelter Syndrome and Testicular Sperm Retrieval Outcomes.
Sá R, Ferraz L, Barros A, Sousa M. Sá R, et al. Genes (Basel). 2023 Mar 4;14(3):647. doi: 10.3390/genes14030647. Genes (Basel). 2023. PMID: 36980920 Free PMC article. Review.
Klinefelter syndrome (KS), caused by the presence of an extra X chromosome, is the most prevalent chromosomal sexual anomaly, with an estimated incidence of 1:500/1000 per male live birth (karyotype 47,XXY). ...Despite testicular atrophy, reproductive treatments all
Klinefelter syndrome (KS), caused by the presence of an extra X chromosome, is the most prevalent chromosomal sexual anomaly,
Tall stature in children and adolescents.
Urakami T. Urakami T. Minerva Pediatr. 2020 Dec;72(6):472-483. doi: 10.23736/S0026-4946.20.05971-X. Epub 2020 Aug 4. Minerva Pediatr. 2020. PMID: 32748612 Review.
Pathological causes for tall statute include endocrine disorders, such as excessive growth hormone secretion, hyperthyroidism, precocious puberty and lipodystrophy, chromosome disorders, such as Trisomy X (47, XXX female), Klinefelter Syndrome (47, XXY), XYY syndrom …
Pathological causes for tall statute include endocrine disorders, such as excessive growth hormone secretion, hyperthyroidism, precocious pu …
Deciphering the Molecular Characteristics of Human Idiopathic Nonobstructive Azoospermia from the Perspective of Germ Cells.
Chen Y, Liu X, Zhang L, Zhu F, Yan L, Tang W, Zhang Z, Liu Q, Jiang H, Qiao J. Chen Y, et al. Adv Sci (Weinh). 2023 Jun;10(17):e2206852. doi: 10.1002/advs.202206852. Epub 2023 Apr 21. Adv Sci (Weinh). 2023. PMID: 37083227 Free PMC article.
Moreover, BOD1L2, C1orf194, and KRTCAP2 are found to indicate testicular spermatogenic capacity in a variety of testicular diseases, such as Y-chromosome microdeletions and Klinefelter syndrome. In general, this study analyzes the pathogenesis of iNOA from the persp …
Moreover, BOD1L2, C1orf194, and KRTCAP2 are found to indicate testicular spermatogenic capacity in a variety of testicular diseases, such as …
Klinefelter Syndrome and Diabetes.
O'Connor MJ, Snyder EA, Hayes FJ. O'Connor MJ, et al. Curr Diab Rep. 2019 Jul 31;19(9):71. doi: 10.1007/s11892-019-1197-3. Curr Diab Rep. 2019. PMID: 31367971 Review.
PURPOSE OF REVIEW: Klinefelter syndrome (KS) is associated with increased insulin resistance and high rates of type 2 diabetes (T2DM). Our aim was to review what is known about the prevalence of diabetes in men with KS, potential mechanisms underlying the observe
PURPOSE OF REVIEW: Klinefelter syndrome (KS) is associated with increased insulin resistance and high rates of type 2 diabetes …
Epigenetics and genomics in Klinefelter syndrome.
Skakkebaek A, Viuff M, Nielsen MM, Gravholt CH. Skakkebaek A, et al. Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):216-225. doi: 10.1002/ajmg.c.31802. Epub 2020 Jun 2. Am J Med Genet C Semin Med Genet. 2020. PMID: 32484281 Review.
Since the first description of Klinefelter syndrome (KS) was published in 1942 in The Journal of Clinical Endocrinology, large inter-individual variability in the phenotypic presentation has been demonstrated. ...Unraveling the genetics of KS will be of clinical rel …
Since the first description of Klinefelter syndrome (KS) was published in 1942 in The Journal of Clinical Endocrinology, large …
Klinefelter's syndrome and taurodontism.
Giambersio E, Barile V, Giambersio AM. Giambersio E, et al. Arch Ital Urol Androl. 2019 Jul 2;91(2). doi: 10.4081/aiua.2019.2.130. Arch Ital Urol Androl. 2019. PMID: 31266283 Free article.
The prevalence of taurodontism in normal population is controversial. It has been reported that taurodontism is frequently observed in Klinefelter's patients. The purpose of this study was to assess the prevalence of taurodontism in a group of Italian Klinefelter's patient …
The prevalence of taurodontism in normal population is controversial. It has been reported that taurodontism is frequently observed i …
Fertility management of Klinefelter syndrome.
Fainberg J, Hayden RP, Schlegel PN. Fainberg J, et al. Expert Rev Endocrinol Metab. 2019 Nov;14(6):369-380. doi: 10.1080/17446651.2019.1671821. Epub 2019 Oct 7. Expert Rev Endocrinol Metab. 2019. PMID: 31587581 Review.
Introduction: Klinefelter syndrome (KS) represents the most common chromosomal abnormality in the general population, and one of the most common genetic etiologies of nonobstructive azoospermia (NOA) and in severe oligospermia. ...Presented is a critical review of t …
Introduction: Klinefelter syndrome (KS) represents the most common chromosomal abnormality in the general population, and one …
Klinefelter Syndrome and medical treatment: hypogonadism and beyond.
Chang S, Skakkebæk A, Gravholt CH. Chang S, et al. Hormones (Athens). 2015 Oct-Dec;14(4):531-48. doi: 10.14310/horm.2002.1622. Hormones (Athens). 2015. PMID: 26732150 Free article. Review.
Klinefelter syndrome (KS), though described more than 70 years ago, still imposes significant diagnostic challenges. Based on data from epidemiological studies, KS is associated with increased morbidity and mortality. Although the pathophysiology and etiology behind
Klinefelter syndrome (KS), though described more than 70 years ago, still imposes significant diagnostic challenges. Based on
Sex-linked genetic mechanisms and atrial fibrillation risk.
Wren G, Davies W. Wren G, et al. Eur J Med Genet. 2022 Apr;65(4):104459. doi: 10.1016/j.ejmg.2022.104459. Epub 2022 Feb 19. Eur J Med Genet. 2022. PMID: 35189376 Free article. Review.
Understanding the biological basis of sex differences in AF should allow better prediction of disease risk, identification of novel risk/protective factors, and the development of more effective sex-tailored interventions....
Understanding the biological basis of sex differences in AF should allow better prediction of disease risk, identification of novel r …
Klinefelter syndrome: clinical and molecular aspects.
Giltay JC, Maiburg MC. Giltay JC, et al. Expert Rev Mol Diagn. 2010 Sep;10(6):765-76. doi: 10.1586/erm.10.63. Expert Rev Mol Diagn. 2010. PMID: 20843200 Review.
Klinefelter syndrome is the most common chromosome abnormality in humans. ...Surgical procedures of obtaining sperm in combination with repeated intracytoplasmic sperm injection/in vitro fertilization treatment may allow up to one in four men with Klinefelter
Klinefelter syndrome is the most common chromosome abnormality in humans. ...Surgical procedures of obtaining sperm in combina
514 results