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Quoted phrase not found in phrase index: "Turner syndrome due to structural X chromosome anomalies"
Page 1
The patient with Turner syndrome: puberty and medical management concerns.
Gonzalez L, Witchel SF. Gonzalez L, et al. Fertil Steril. 2012 Oct;98(4):780-6. doi: 10.1016/j.fertnstert.2012.07.1104. Epub 2012 Aug 9. Fertil Steril. 2012. PMID: 22884020 Free PMC article. Review.
Turner syndrome (TS), which affects approximately 1 in 2,500 live-born females, is characterized by loss or structural anomalies of an X chromosome. ...Involvement of cardiologists is important because approximately 50% of patients with T
Turner syndrome (TS), which affects approximately 1 in 2,500 live-born females, is characterized by loss or structural
The effects of estrogen induction therapy on pubertal presentations in turner syndrome patients.
Lee YC, Huang CY, Lin CH, Cheng BW, Huang SK, Yeh SN, Lee YJ, Ting WH. Lee YC, et al. Taiwan J Obstet Gynecol. 2022 Sep;61(5):788-793. doi: 10.1016/j.tjog.2022.05.014. Taiwan J Obstet Gynecol. 2022. PMID: 36088045 Free article. Review.
Sixty-six patients were enrolled and distributed into 45,X monosomy group, X chromosome structural abnormalities group and X mosaicism group. ...CONCLUSION: The karyotypes were highly correlated with pubertal presentations at Turner syndrome
Sixty-six patients were enrolled and distributed into 45,X monosomy group, X chromosome structural abnormalities
Autoimmune Disease in Turner Syndrome in Sweden: An up to 25 Years' Controlled Follow-up Study.
Naessén S, Eliasson M, Berntorp K, Kitlinski M, Trimpou P, Amundson E, Thunström S, Ekman B, Wahlberg J, Karlsson A, Isaksson M, Bergström I, Levelind C, Bryman I, Landin-Wilhelmsen K. Naessén S, et al. J Clin Endocrinol Metab. 2024 Jan 18;109(2):e602-e612. doi: 10.1210/clinem/dgad566. J Clin Endocrinol Metab. 2024. PMID: 37758506 Free PMC article.
CONTEXT: Turner syndrome (TS) is the most common chromosomal aberration in women; it is the result of structural or numeric abnormalities in the X chromosome. ...A random population sample of women, n = 401, aged 25 to 44 years, fr …
CONTEXT: Turner syndrome (TS) is the most common chromosomal aberration in women; it is the result of structural or num …
Precocious puberty in Turner Syndrome: report of a case and review of the literature.
Improda N, Rezzuto M, Alfano S, Parenti G, Vajro P, Pignata C, Salerno M. Improda N, et al. Ital J Pediatr. 2012 Oct 17;38:54. doi: 10.1186/1824-7288-38-54. Ital J Pediatr. 2012. PMID: 23075274 Free PMC article. Review.
INTRODUCTION: Turner Syndrome (TS) is caused by monosomy or structural abnormalities of the X chromosome, with a prevalence of about 1/2000 females live birth. Most important clinical features of TS are short stature and gonadal fa …
INTRODUCTION: Turner Syndrome (TS) is caused by monosomy or structural abnormalities of the X chromoso
Thyroid autoantibodies, Turner's syndrome and growth hormone therapy.
Ivarsson SA, Ericsson UB, Nilsson KO, Gustafsson J, Hagenäs L, Häger A, Moell C, Tuvemo T, Westphal O, Albertsson-Wikland K, et al. Ivarsson SA, et al. Acta Paediatr. 1995 Jan;84(1):63-5. doi: 10.1111/j.1651-2227.1995.tb13485.x. Acta Paediatr. 1995. PMID: 7734902 Clinical Trial.
The patients were divided into four groups according to karyotype as follows: group 1, 45, X (n = 63); group 2 with structural abnormalities of the X chromosome (n = 10); group 3 with mosaicism but no structural abnormalities of the X
The patients were divided into four groups according to karyotype as follows: group 1, 45, X (n = 63); group 2 with structural abn
Brain anatomy in Turner syndrome: evidence for impaired social and spatial-numerical networks.
Molko N, Cachia A, Riviere D, Mangin JF, Bruandet M, LeBihan D, Cohen L, Dehaene S. Molko N, et al. Cereb Cortex. 2004 Aug;14(8):840-50. doi: 10.1093/cercor/bhh042. Epub 2004 Mar 28. Cereb Cortex. 2004. PMID: 15054057 Clinical Trial.
Analysis of brain structure in Turner syndrome (TS) provides the opportunity to identify the consequences of the loss of one X chromosome on brain anatomy and to characterize the neural bases underlying the specific cognitive profile of TS subje …
Analysis of brain structure in Turner syndrome (TS) provides the opportunity to identify the consequences of the loss o …
Spontaneous pubertal development in Turner's syndrome. Italian Study Group for Turner's Syndrome.
Pasquino AM, Passeri F, Pucarelli I, Segni M, Municchi G. Pasquino AM, et al. J Clin Endocrinol Metab. 1997 Jun;82(6):1810-3. doi: 10.1210/jcem.82.6.3970. J Clin Endocrinol Metab. 1997. PMID: 9177387 Clinical Trial.
Karyotype distribution in the whole group was as follows: 52.1% (272 patients) X-monosomy (45,X), 13.2% (69 patients) mosaicism characterized by X-monosomy and cellular line with no structural abnormalities of the second X, 19.9% (104 patients) mosaicism characteriz …
Karyotype distribution in the whole group was as follows: 52.1% (272 patients) X-monosomy (45,X), 13.2% (69 patients) mosaicism characterize …
Karyotype-specific ear and hearing problems in young adults with Turner syndrome and the effect of oxandrolone treatment.
Verver EJ, Freriks K, Sas TC, Huygen PL, Pennings RJ, Smeets DF, Hermus AR, Menke LA, Wit JM, Otten BJ, van Alfen-van der Velden JA, de Muinck Keizer-Schrama SM, Topsakal V, Admiraal RJ, Timmers HJ, Kunst HP. Verver EJ, et al. Otol Neurotol. 2014 Oct;35(9):1577-84. doi: 10.1097/MAO.0000000000000406. Otol Neurotol. 2014. PMID: 25133471 Clinical Trial.
OBJECTIVE: To evaluate karyotype-specific ear and hearing problems in young-adult patients with Turner syndrome (TS) and assess the effects of previous treatment with oxandrolone (Ox). ...MAIN OUTCOME MEASURES: We compared patients with total monosomy of the short a …
OBJECTIVE: To evaluate karyotype-specific ear and hearing problems in young-adult patients with Turner syndrome (TS) and asses …
Lichen sclerosus associated with Turner syndrome treated with photodynamic therapy: A case report.
Wang Y, Liu J. Wang Y, et al. Photodiagnosis Photodyn Ther. 2024 Feb;45:103932. doi: 10.1016/j.pdpdt.2023.103932. Epub 2023 Dec 12. Photodiagnosis Photodyn Ther. 2024. PMID: 38097123 Free article.
Turner syndrome (TS) is a rare clinical condition associated with a completely or partially absence, or structural abnormality of an X chromosome, mainly representing as short stature and skeletal anomalies, female hypergonadotropi
Turner syndrome (TS) is a rare clinical condition associated with a completely or partially absence, or structural
Assessment of X bends in patients with atypical X chromosome phenotypes.
Munn CA, Wenger SL, Steele MW. Munn CA, et al. Ann Genet. 1991;34(2):120-4. Ann Genet. 1991. PMID: 1746882
Several patients with X chromosome structural abnormalities have been more severely affected clinically than expected. ...Five of the 6 patients with a short or long arm deletion or paracentric inversion of Xq were mentally retarded or had other congen …
Several patients with X chromosome structural abnormalities have been more severely affected clinically than exp …
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