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

Year Number of Results
1953 2
1954 10
1955 14
1956 6
1957 10
1958 6
1959 8
1960 10
1961 6
1962 5
1964 2
1965 21
1966 63
1967 62
1968 74
1969 96
1970 106
1971 99
1972 105
1973 100
1974 100
1975 63
1976 79
1977 70
1978 76
1979 78
1980 87
1981 102
1982 82
1983 82
1984 77
1985 72
1986 74
1987 78
1988 75
1989 73
1990 71
1991 59
1992 104
1993 96
1994 112
1995 104
1996 78
1997 104
1998 95
1999 103
2000 137
2001 106
2002 113
2003 114
2004 142
2005 133
2006 168
2007 156
2008 173
2009 159
2010 219
2011 182
2012 208
2013 191
2014 212
2015 196
2016 178
2017 166
2018 170
2019 84
2020 0
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5,850 results
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Page 1
Fertility in disorders of sex development: A review.
Van Batavia JP and Kolon TF. J Pediatr Urol 2016 - Review. PMID 27856173
INTRODUCTION: Disorders of sex development (DSD) are a heterogeneous group of complex conditions that can affect chromosomal, gonadal, and/or phenotypical sex. ...Original research articles and relevant reviews were examinedand a synopsis of these data was generated for a comprehensive review of fertility potential in disorders of sex development. ...
INTRODUCTION: Disorders of sex development (DSD) are a heterogeneous group of complex conditions that can affect chromo …
Fertility Issues in Disorders of Sex Development.
Guercio G, et al. Endocrinol Metab Clin North Am 2015 - Review. PMID 26568498
Fertility potential should be considered by the multidisciplinary team when addressing gender assignment, surgical management, and patient and family counselling of individuals with disorders of sex development. ...
Fertility potential should be considered by the multidisciplinary team when addressing gender assignment, surgical management, and patient a …
Clinical review of 95 patients with 46,XX disorders of sex development based on the new Chicago classification.
Öcal G, et al. J Pediatr Adolesc Gynecol 2015. PMID 25444050
STUDY OBJECTIVE: The aim of our study was to determine the etiologic distribution of 46,XX disorder of sexual development (DSD) according to the new DSD classification system and to evaluate the clinical features of this DSD subgroup in our patient cohort. ...RESULTS: Types and ratios of each presentation of our 95 patients with 46,XX DSD were as follows: 82 had androgen excess (86.3%): (74 had classical congenital adrenal hyperplasia, 2 had CAH variant possibility of P450-oxidoreductase gene defect), 6 had disorders of ovarian development (6.3%): (1 patient had gonadal dysgenesis with virilization at birth with bilateral streak gonad, 4 patients had complete gonadal dysgenesis, and 1 patient had ovotesticular DSD) and 7 had other 46,XX DSD. ...
STUDY OBJECTIVE: The aim of our study was to determine the etiologic distribution of 46,XX disorder of sexual development (DSD) accor …
Gonadal malignancy in 202 female patients with disorders of sex development containing Y-chromosome material.
Jiang JF, et al. Gynecol Endocrinol 2016. PMID 26608236
The objective of this study was to examine risks for gonadal malignancy in a large sample of adult female patients with disorders of sex development (DSD). ...
The objective of this study was to examine risks for gonadal malignancy in a large sample of adult female patients with disorders of …
Cardiovascular risk in Turner syndrome
Donato B and Ferreira MJ. Rev Port Cardiol 2018 - Review. PMID 29866389 Free article.
Turner syndrome is a relatively common genetic disorder of female development, characterized by partial or complete absence of an X chromosome, with a variable clinical presentation. ...The most feared complication is aortic dissection, which can occur at a very young age and requires careful assessment of its risk factors. ...
Turner syndrome is a relatively common genetic disorder of female development, characterized by partial or complete absence of an X c …
Etiology and management of primary amenorrhoea: A study of 102 cases at tertiary centre
Kriplani A, et al. Taiwan J Obstet Gynecol 2017. PMID 29241916 Free article.
Cases were analysed according to clinical profile, development of secondary sexual characteristics, physical examination, pelvic and rectal examination, X-ray of chest and lumbo-sacral spine, hormone profile, pelvic USG, MRI, and cytogenetic study including karyotype. ...
Cases were analysed according to clinical profile, development of secondary sexual characteristics, physical examination, pelvic and …
Klinefelter syndrome: cardiovascular abnormalities and metabolic disorders.
Calogero AE, et al. J Endocrinol Invest 2017 - Review. PMID 28258556
The aim of this review is to explore more in depth cardiovascular and metabolic disorders associated to KS. KS patients have an increased risk of cerebrovascular disease (standardized mortality ratio, SMR, 2.2; 95% confidence interval, CI, 1.6-3.0), but it is not clear whether the cause of the death is of thrombotic or hemorrhagic nature. Cardiovascular congenital anomalies (SMR, 7.3; 95% CI, 2.4-17.1) and the development of thrombosis or leg ulcers (SMR, 7.9; 95% CI, 2.9-17.2) are also more frequent in these subjects. ...
The aim of this review is to explore more in depth cardiovascular and metabolic disorders associated to KS. KS patients have an incre …
Disorders of sex development presenting as unilateral cryptorchidism.
Østergren P, et al. Scand J Urol 2013. PMID 23373508
Disorders of sex development (DSD) present in different forms but, in most cases, with visible anomalies of the external genitalia. ...
Disorders of sex development (DSD) present in different forms but, in most cases, with visible anomalies of the externa
[Association of 45, X/46, XY mosaicism with disorders of sex development: the clinical analysis of 5 cases].
Chang GY, et al. Zhonghua Er Ke Za Zhi 2011. PMID 21924060 Chinese.
CONCLUSION: Patients with mosaic 45, X/46, XY karyotypes had a wide range of phenotypic manifestations, and disorders of sex development and short stature were the main clinical features. However, the disorders of sex development varied among these patients. And the management for them depends upon many factors and needs to be individualized based on the cooperation with different clinical departments....
CONCLUSION: Patients with mosaic 45, X/46, XY karyotypes had a wide range of phenotypic manifestations, and disorders of sex
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