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Quoted phrase not found in phrase index: "Turner syndrome due to structural X chromosome anomalies"
Page 1
Turner syndrome: contemporary thoughts and reproductive issues.
Reindollar RH. Reindollar RH. Semin Reprod Med. 2011 Jul;29(4):342-52. doi: 10.1055/s-0031-1280919. Epub 2011 Oct 3. Semin Reprod Med. 2011. PMID: 21969268 Review.
Turner syndrome is a common genetic disorder that has been classically associated with a 45,X karyotype. ...Amenorrheic women with Turner syndrome truly have ovarian failure. Although I have adopted the term POI in this article for women with Turner
Turner syndrome is a common genetic disorder that has been classically associated with a 45,X karyotype. ...Amenorrheic women
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. ...METHODS: A cross-sectional, longitudinal, 25-year follow-up study was conduc …
CONTEXT: Turner syndrome (TS) is the most common chromosomal aberration in women; it is the result of structural or num …
Endocrine autoimmunity in Turner syndrome.
Grossi A, Crinò A, Luciano R, Lombardo A, Cappa M, Fierabracci A. Grossi A, et al. Ital J Pediatr. 2013 Dec 20;39:79. doi: 10.1186/1824-7288-39-79. Ital J Pediatr. 2013. PMID: 24355069 Free PMC article.
BACKGROUND: Turner syndrome is caused by numeric and structural abnormalities of the X chromosome. An increased frequency of autoimmunity as well as an elevated incidence of autoantibodies was observed in Turner patients. The aim o …
BACKGROUND: Turner syndrome is caused by numeric and structural abnormalities of the X chromosome. …
Gonadoblastoma in patients with Ullrich-Turner syndrome.
Zelaya G, López Marti JM, Marino R, Garcia de Dávila MT, Gallego MS. Zelaya G, et al. Pediatr Dev Pathol. 2015 Mar-Apr;18(2):117-21. doi: 10.2350/14-08-1539-OA.1. Epub 2014 Dec 23. Pediatr Dev Pathol. 2015. PMID: 25535833
Ullrich-Turner syndrome (UTS) is a common chromosomal abnormality caused by partial or complete X chromosome monosomy. One half of the patients have a 45,X karyotype, whereas the remaining patients display other X chromosome anomalies
Ullrich-Turner syndrome (UTS) is a common chromosomal abnormality caused by partial or complete X chromosome mon …
Ovarian function and in vitro fertilization (IVF) in Turner syndrome.
Hovatta O. Hovatta O. Pediatr Endocrinol Rev. 2012 May;9 Suppl 2:713-7. Pediatr Endocrinol Rev. 2012. PMID: 22946282
Ovarian follicles have been found in some 40% of teenagers with Turner syndrome. Serum concentrations of antimullerian hormone (AMH) and follicle stimulation hormone (FSH), karyotype with mosaicism or structural chromosomal abnormalities, and spontaneo …
Ovarian follicles have been found in some 40% of teenagers with Turner syndrome. Serum concentrations of antimullerian hormone …
Pheochromocytoma as a rare cause of hypertension in a 46 X, i(X)(q10) turner syndrome: a case report and literature review.
Shin JY, Kim BH, Kim YK, Kim TH, Kim EH, Lee MJ, Kim JH, Jeon YK, Kim SS, Kim IJ. Shin JY, et al. BMC Endocr Disord. 2018 May 10;18(1):27. doi: 10.1186/s12902-018-0253-3. BMC Endocr Disord. 2018. PMID: 29747617 Free PMC article. Review.
The aetiology of hypertension in Turner syndrome varies, even in the absence of cardiac anomalies and obvious structural renal abnormalities. Pheochromocytoma is an extremely rare cause among various etiologies for hypertension in patients with …
The aetiology of hypertension in Turner syndrome varies, even in the absence of cardiac anomalies and obvious struct
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 …
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
The influence of sex chromosome aneuploidy on brain asymmetry.
Rezaie R, Daly EM, Cutter WJ, Murphy DG, Robertson DM, DeLisi LE, Mackay CE, Barrick TR, Crow TJ, Roberts N. Rezaie R, et al. Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):74-85. doi: 10.1002/ajmg.b.30772. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18454450
The cognitive deficits present in individuals with sex chromosome aneuploidies suggest that hemispheric differentiation of function is determined by an X-Y homologous gene [Crow (1993); Lancet 342:594-598]. In particular, females with Turner's syndrome (TS) who have …
The cognitive deficits present in individuals with sex chromosome aneuploidies suggest that hemispheric differentiation of function is deter …
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