ライフサイエンスコーパス: Turner syndrome

1 found in human females with an XO karyotype (Turner syndrome).

2 neurysm, and rupture in girls and women with Turner syndrome.

3 ormalities that include trisomies 18 and 21, Turner syndrome.

4 (2.6%) of pilomatricomas among patients with Turner syndrome.

5 disposing finding other than the presence of Turner syndrome.

6 resulting in infertility, sex reversal, and Turner syndrome.

7 om spermatogenic failure to sex reversal and Turner syndrome.

8 100-fold in young and middle-aged women with Turner syndrome.

9 s of hormonal treatments given to women with Turner syndrome.

10 c requirements of the X chromosome linked to Turner syndrome.

11 syndromes of gonadal dysgenesis and Ullrich-Turner syndrome.

12 was significantly reduced in the group with Turner syndrome.

13 ir role in the neurological phenotypes of XO Turner syndrome.

14 rful faces in the condition of X-monosomy or Turner syndrome.

15 1, 2010, was performed of all patients with Turner syndrome.

16 ated to cause the short stature phenotype in Turner syndrome.

17 date for involvement in the short stature of Turner syndrome.

18 in sex differentiation, spermatogenesis, and Turner syndrome.

19 a phenotype significantly more abnormal than Turner syndrome.

20 and subsequent gonadal degeneration found in Turner syndrome.

21 One-third of women with Turner syndrome (45,X) have autism-like social and commu

22 However, females with Turner syndrome (45,X) have even larger amygdalae than 4

23 DMD may also be observed in females with Turner syndrome (45,X), if the remaining X chromosome ca

24 Previous work in girls with Turner syndrome (45,XO) has suggested that there are X-l

25 mapping of fear recognition in 93 women with Turner syndrome across the critical region was performed

26 We derived iPSCs from Turner syndrome and control individuals and examined ger

27 he clinical characteristics among those with Turner syndrome and dissection have received little atte

28 nderstanding brain structure and function in Turner syndrome and identifies several critical research

29 iopathic short stature in humans, as seen in Turner syndrome and Leri-Weill dyschondrosteosis, while

30 some--a near normal phenotype in mice versus Turner syndrome and multiple abnormalities in humans.

31 isuospatial WM functions in individuals with Turner syndrome and normal controls.

32 pulations, where they cause sex reversal and Turner syndrome and predispose individuals to infertilit

33 These abnormalities include Parsonage-Turner syndrome and quadrilateral space syndrome, each o

34 rize aortic valve structure in subjects with Turner syndrome and to determine the prevalence of aorti

35 he growth failure seen in the Leri-Weill and Turner syndromes, and in some familial cases of ISS.

36 oluntarily participated in the International Turner Syndrome Aortic Dissection Registry.

37 Girls and women with Turner syndrome are at risk for aortic dissection and ru

38 anomalies and risk for aortic dissection in Turner syndrome are strongly linked to a history of feta

39 rted neonatal lymphedema, similar to that in Turner syndrome, associated with a t(Y;16)(q12;q24.3) tr

40 significantly increased in individuals with Turner syndrome at all ages, highest during young adult

41 target conditions have mainly been studied: Turner syndrome, coeliac disease, cystic fibrosis, growt

42 gnosis of acute brachial neuritis (Parsonage-Turner syndrome) correlated with MR imaging results in a

43 A patient with Turner syndrome died of a Stanford type A dissection at

44 lly evaluated for the presence or absence of Turner syndrome features, and their deletions were mappe

45 We obtained an independent sample of 77 Turner syndrome females that we genotyped for 77 SNPs in

46 of genes implicated in gonadal sex reversal, Turner syndrome, graft rejection and spermatogenic failu

47 rs, and cffDNA from a fetus with monosomy X (Turner syndrome) had decreased hybridization signals on

48 FINDINGS: Recent work on social cognition in Turner syndrome has identified a range of difficulties d

49 Individuals with Turner syndrome have a spectrum of anatomical, physiolog

50 Cancer risks in women with Turner syndrome have not been clearly established.

51 ren with intrauterine growth retardation and Turner syndrome; however, serum insulin levels were elev

52 d by cardiovascular MRI in 208 subjects with Turner syndrome in an institutional review board-approve

53 of the characteristics of aortic disease in Turner syndrome in comparison with Marfan-like syndromes

54 omen who were cytogenetically diagnosed with Turner syndrome in Great Britain between 1959 and 2002.

55 to the X chromosome is the genetic basis of Turner syndrome in human females.

56 of interventions to assist individuals with Turner syndrome in visual-spatial, mathematical, and soc

57 Principle features of Turner syndrome include short stature, ovarian failure,

58 sts recommended GH therapy for children with Turner syndrome, insurer policies covered GH therapy for

59 Turner syndrome is a genetic disorder that results from

60 Turner syndrome is a relatively common disorder of femal

61 Turner syndrome is caused by complete or partial loss of

62 Turner syndrome is characterized by short stature and is

63 Turner syndrome is the complex human phenotype associate

64 Turner syndrome is the most common established cause of

65 l subjects should refine the localization of Turner syndrome loci and provide a rational basis for ex

66 -of-origin influences on social cognition in Turner syndrome might be due to the presence of imprinte

67 The abnormalities seen in Turner syndrome (monosomy X) presumably result from hapl

68 Thoracic aortic dilation in Turner syndrome must be evaluated in relation to body su

69 studies have examined spatial WM function in Turner syndrome, none have directly compared the neural

70 Aortic valve abnormalities in Turner syndrome occur with a spectrum of severity and ar

71 Aortic dissection in Turner syndrome occurs in young individuals at smaller a

72 Turner syndrome, one of the most common cytogenetic abno

73 erapy in 78% of children with GH deficiency, Turner syndrome, or renal failure; of those recommended

74 female volunteers and eight individuals with Turner syndrome performed a delayed-response WM task dur

75 ci responsible for various components of the Turner syndrome phenotype.

76 and dicentric Xq isochromosomes (i(Xq)) from Turner syndrome probands, using FISH with cosmids and YA

77 For some, like Turner syndrome, recombinant human growth hormone has be

78 In the combined Turner syndrome samples, the most strongly associated SN

79 increased risk of gonadoblastoma, women with Turner syndrome seem to be at increased risk for meningi

80 valence of pilomatricoma among patients with Turner syndrome served as the catalyst for this multicen

81 Additionally, Turner Syndrome subjects, who are predisposed to chronic

82 Variability in fear recognition accuracy in Turner syndrome suggested the existence of a quantitativ

83 during visuospatial executive processing in Turner syndrome, suggesting a significant role for the X

84 henotype correlations, we mapped one or more Turner syndrome traits to a critical region in Xp11.2-p2

85 Turner syndrome (TS) is a neurogenetic disorder characte

86 Turner syndrome (TS) is associated with a characteristic

87 Turner syndrome (TS) is associated with aortic coarctati

88 Turner syndrome (TS) results from whole or partial monos

89 lthy controls and 40 prepubescent girls with Turner syndrome (TS), a condition caused by the absence

90 examine this framework in humans, including Turner syndrome (TS), where females are missing one X-ch

91 women with monosomy for the X chromosome, or Turner syndrome (TS).

92 increased among relatively young women with Turner syndrome (TS).

93 Using a mouse model for Turner syndrome, we searched for locus-specific imprinti

94 In total, 311 patients with Turner syndrome were identified from these 3 institution

95 PURPOSE OF REVIEW: Turner syndrome, which results from the complete or part

96 Individuals with Turner syndrome who are >18 years of age with an ascendi

97 rstanding of brain structure and function in Turner syndrome will generate new therapeutic approaches

98 ce across both verbal and spatial domains in Turner syndrome, with greater impairment on tasks with W

99 tion However, aortic dissection can occur in Turner syndrome without cardiac malformations or hyperte

100 Previous research found Turner syndrome women of normal verbal intelligence are