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1 found in human females with an XO karyotype (Turner syndrome).
2 date for involvement in the short stature of Turner syndrome.
3 in sex differentiation, spermatogenesis, and Turner syndrome.
4 a phenotype significantly more abnormal than Turner syndrome.
5 and subsequent gonadal degeneration found in Turner syndrome.
6 logical manifestations, especially Parsonage-Turner syndrome.
7 ocytes from XO female mice, a mouse model of Turner Syndrome.
8 c requirements of the X chromosome linked to Turner syndrome.
9  1, 2010, was performed of all patients with Turner syndrome.
10 neurysm, and rupture in girls and women with Turner syndrome.
11 ormalities that include trisomies 18 and 21, Turner syndrome.
12 (2.6%) of pilomatricomas among patients with Turner syndrome.
13 disposing finding other than the presence of Turner syndrome.
14  resulting in infertility, sex reversal, and Turner syndrome.
15 om spermatogenic failure to sex reversal and Turner syndrome.
16 100-fold in young and middle-aged women with Turner syndrome.
17 s of hormonal treatments given to women with Turner syndrome.
18  syndromes of gonadal dysgenesis and Ullrich-Turner syndrome.
19  was significantly reduced in the group with Turner syndrome.
20 ir role in the neurological phenotypes of XO Turner syndrome.
21 rful faces in the condition of X-monosomy or Turner syndrome.
22 ated to cause the short stature phenotype in Turner syndrome.
23 sex hormones, and effects of Klinefelter and Turner syndromes.
24 at, Wolf-Hirschhorn, Prader-Willi, Down, and Turner syndromes.
25                      One-third of women with Turner syndrome (45,X) have autism-like social and commu
26                        However, females with Turner syndrome (45,X) have even larger amygdalae than 4
27     DMD may also be observed in females with Turner syndrome (45,X), if the remaining X chromosome ca
28                  Previous work in girls with Turner syndrome (45,XO) has suggested that there are X-l
29 mapping of fear recognition in 93 women with Turner syndrome across the critical region was performed
30 osage variation (X-monosomy) associated with Turner syndrome affects the functional neuroanatomy of t
31                        We derived iPSCs from Turner syndrome and control individuals and examined ger
32 he clinical characteristics among those with Turner syndrome and dissection have received little atte
33 nderstanding brain structure and function in Turner syndrome and identifies several critical research
34 iopathic short stature in humans, as seen in Turner syndrome and Leri-Weill dyschondrosteosis, while
35 some--a near normal phenotype in mice versus Turner syndrome and multiple abnormalities in humans.
36 isuospatial WM functions in individuals with Turner syndrome and normal controls.
37 pulations, where they cause sex reversal and Turner syndrome and predispose individuals to infertilit
38        These abnormalities include Parsonage-Turner syndrome and quadrilateral space syndrome, each o
39 rize aortic valve structure in subjects with Turner syndrome and to determine the prevalence of aorti
40 etic syndromes (for example, Klinefelter and Turner syndromes) and people with disorders of sexual de
41 he growth failure seen in the Leri-Weill and Turner syndromes, and in some familial cases of ISS.
42 2) 12 patients with HEV-associated Parsonage-Turner syndrome; and (3) 16 asymptomatic blood donors (c
43 oluntarily participated in the International Turner Syndrome Aortic Dissection Registry.
44                         Girls and women with Turner syndrome are at risk for aortic dissection and ru
45  anomalies and risk for aortic dissection in Turner syndrome are strongly linked to a history of feta
46 rted neonatal lymphedema, similar to that in Turner syndrome, associated with a t(Y;16)(q12;q24.3) tr
47  significantly increased in individuals with Turner syndrome at all ages, highest during young adult
48  target conditions have mainly been studied: Turner syndrome, coeliac disease, cystic fibrosis, growt
49 gnosis of acute brachial neuritis (Parsonage-Turner syndrome) correlated with MR imaging results in a
50                               A patient with Turner syndrome died of a Stanford type A dissection at
51 lly evaluated for the presence or absence of Turner syndrome features, and their deletions were mappe
52      We obtained an independent sample of 77 Turner syndrome females that we genotyped for 77 SNPs in
53 of genes implicated in gonadal sex reversal, Turner syndrome, graft rejection and spermatogenic failu
54 t find any enriched pathway in the Parsonage-Turner syndrome group or in the controls.
55 rs, and cffDNA from a fetus with monosomy X (Turner syndrome) had decreased hybridization signals on
56 FINDINGS: Recent work on social cognition in Turner syndrome has identified a range of difficulties d
57                             Individuals with Turner syndrome have a spectrum of anatomical, physiolog
58                   Cancer risks in women with Turner syndrome have not been clearly established.
59                     Specifically, girls with Turner syndrome have smaller early visual areas that pro
60 ren with intrauterine growth retardation and Turner syndrome; however, serum insulin levels were elev
61 d by cardiovascular MRI in 208 subjects with Turner syndrome in an institutional review board-approve
62  of the characteristics of aortic disease in Turner syndrome in comparison with Marfan-like syndromes
63 omen who were cytogenetically diagnosed with Turner syndrome in Great Britain between 1959 and 2002.
64  to the X chromosome is the genetic basis of Turner syndrome in human females.
65  of interventions to assist individuals with Turner syndrome in visual-spatial, mathematical, and soc
66                        Principle features of Turner syndrome include short stature, ovarian failure,
67 sts recommended GH therapy for children with Turner syndrome, insurer policies covered GH therapy for
68                                              Turner syndrome is a genetic disorder that results from
69                                              Turner syndrome is a relatively common disorder of femal
70                                              Turner syndrome is caused by complete or partial loss of
71 suospatial processing.SIGNIFICANCE STATEMENT Turner syndrome is caused by the absence of one of the t
72                                              Turner syndrome is characterized by short stature and is
73                                              Turner syndrome is the complex human phenotype associate
74                                              Turner syndrome is the most common established cause of
75 gic amyotrophy (NA), also known as Parsonage-Turner syndrome, is characterised by sudden pain attacks
76  variation in the number of sex chromosomes: Turner syndrome, Klinefelter syndrome, XYY syndrome, and
77 l subjects should refine the localization of Turner syndrome loci and provide a rational basis for ex
78 -of-origin influences on social cognition in Turner syndrome might be due to the presence of imprinte
79                    The abnormalities seen in Turner syndrome (monosomy X) presumably result from hapl
80                  Thoracic aortic dilation in Turner syndrome must be evaluated in relation to body su
81 studies have examined spatial WM function in Turner syndrome, none have directly compared the neural
82                Aortic valve abnormalities in Turner syndrome occur with a spectrum of severity and ar
83                         Aortic dissection in Turner syndrome occurs in young individuals at smaller a
84                                              Turner syndrome, one of the most common cytogenetic abno
85 erapy in 78% of children with GH deficiency, Turner syndrome, or renal failure; of those recommended
86 female volunteers and eight individuals with Turner syndrome performed a delayed-response WM task dur
87 ci responsible for various components of the Turner syndrome phenotype.
88 and dicentric Xq isochromosomes (i(Xq)) from Turner syndrome probands, using FISH with cosmids and YA
89                                    Parsonage-Turner syndrome (PTS), also known as neuralgic amyotroph
90 e of the several known triggers of Parsonage-Turner syndrome (PTS).
91                               For some, like Turner syndrome, recombinant human growth hormone has be
92                              In the combined Turner syndrome samples, the most strongly associated SN
93 increased risk of gonadoblastoma, women with Turner syndrome seem to be at increased risk for meningi
94 valence of pilomatricoma among patients with Turner syndrome served as the catalyst for this multicen
95                                Additionally, Turner Syndrome subjects, who are predisposed to chronic
96  Variability in fear recognition accuracy in Turner syndrome suggested the existence of a quantitativ
97  during visuospatial executive processing in Turner syndrome, suggesting a significant role for the X
98 henotype correlations, we mapped one or more Turner syndrome traits to a critical region in Xp11.2-p2
99 ) mapping in 20 human females with monosomic Turner syndrome (TS) (mean age, 10.3 +/- 2.0 years) vers
100  thoracic aortic disease (nsHTAD) (n = 378), Turner syndrome (TS) (n = 298), vascular Ehlers-Danlos s
101                                      In both Turner syndrome (TS) and Klinefelter syndrome (KS) copy
102                                              Turner syndrome (TS) is a neurogenetic disorder characte
103                                              Turner syndrome (TS) is associated with a characteristic
104                                              Turner syndrome (TS) is associated with aortic coarctati
105                                 The study of Turner syndrome (TS) offers a unique window of opportuni
106                                              Turner syndrome (TS) results from whole or partial monos
107 lthy controls and 40 prepubescent girls with Turner syndrome (TS), a condition caused by the absence
108               Human monosomy-X (45,X) causes Turner syndrome (TS), altering craniofacial, skeletal, e
109  examine this framework in humans, including Turner syndrome (TS), where females are missing one X-ch
110 women with monosomy for the X chromosome, or Turner syndrome (TS).
111  increased among relatively young women with Turner syndrome (TS).
112                      Using a mouse model for Turner syndrome, we searched for locus-specific imprinti
113                  In total, 311 patients with Turner syndrome were identified from these 3 institution
114                           PURPOSE OF REVIEW: Turner syndrome, which results from the complete or part
115                             Individuals with Turner syndrome who are >18 years of age with an ascendi
116 rstanding of brain structure and function in Turner syndrome will generate new therapeutic approaches
117 arche or premature menopause, Down syndrome, Turner syndrome, Williams syndrome, chronic fatigue synd
118 ce across both verbal and spatial domains in Turner syndrome, with greater impairment on tasks with W
119 tion However, aortic dissection can occur in Turner syndrome without cardiac malformations or hyperte
120                      Previous research found Turner syndrome women of normal verbal intelligence are
121         Sex chromosome aneuploidies, such as Turner syndrome (X0) and Klinefelter syndrome (XXY), are
122                                        Using Turner syndrome (XO) and Klinefelter (XXY) models, we fi

 
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