논문상세정보
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- 저자 양승
- 제어번호 104297305
- 학술지명 Annals of Pediatirc Endocrinology & Metabolism
- 권호사항 Vol. 22 No. 4 [ 2017 ]
- 발행처 대한소아내분비학회
- 발행처 URL http://www.kspendo.or.kr
- 자료유형 학술저널
- 수록면 226-230
- 언어 English
- 출판년도 2017
- 등재정보 KCI등재
- 판매처
유사주제 논문( 0)
Diagnostic and therapeutic considerations in Turner syndrome
양승
2017년
' Diagnostic and therapeutic considerations in Turner syndrome' 의 참고문헌
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X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome
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Venous thromboembolism risk in relation to use of different types of postmenopausal hormone therapy in a large prospective study
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Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study
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Turner syndrome: update on biology and management across the life span
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Turner syndrome: new insights into an old disorder
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Turner syndrome revisited: review of new data supports the hypothesis that all viable 45,X cases are cryptic mosaics with a rescue cell line, implying an origin by mitotic loss
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Therapeutic effects of growth hormone combined with low-dose stanozolol on growth velocity and final height of girls with Turner syndrome
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The sitting height/height ratio for age in healthy and short individuals and its potential role in selecting short children for SHOX analysis
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The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
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The XO syndrome. A study of the differentiated phenotype in 25 patients
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Single-nucleotide polymorphism array genotyping is equivalent to metaphase cytogenetics for diagnosis of Turner syndrome
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Self-esteem and social adjustment in young women with Turner syndrome--influence of pubertal management and sexuality: population-based cohort study
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Screening of turner syndrome with novel auxological criteria facilitates early diagnosis
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Safety and efficacy of oxandrolone in growth hormone-treated girls with Turner syndrome: evidence from recent studies and recommendations for use
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Quality of life after growth hormone therapy and induced puberty in women with Turner syndrome
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Physiological estrogen replacement therapy for puberty induction in girls: a clinical observational study
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Occurrence of cancer in women with Turner syndrome
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Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma
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Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing
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New approach to phenotypic variability and karyotype-phenotype correlation in Turner syndrome
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Neonatal detection of Turner syndrome by real-time PCR gene quantification of the ARSE and MAGEH1 genes
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Multiethnic WHO growth charts may not be optimal in the screening of disorders affecting height: Turner syndrome as a model
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Morbidity in Turner syndrome
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Mode of initial presentation and chromosomal abnormalities in Irish patients with Turner syndrome: a single-centre experience
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Metabolic effects of oral versus transdermal 17β-estradiol (E₂): a randomized clinical trial in girls with Turner syndrome
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Long-term effects of previous oxandrolone treatment in adult women with Turner syndrome
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Lichen planus-like drug reaction associated with recombinant human growth hormone therapy in a child patient with Turner syndrome
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Individualised vs fixed dose of oral 17β-oestradiol for induction of puberty in girls with Turner syndrome: an open-randomised parallel trial
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Height gain in Ullrich-Turner syndrome after early and late growth hormone treatment start: results from a large retrospective German study and potential basis for an individualized treatment approach
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Growth hormone positive effects on craniofacial complex in Turner syndrome
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Growth curves for girls with Turner syndrome
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Growth curve for girls with Turner syndrome
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Genetic predictors of long-term response to growth hormone (GH) therapy in children with GH deficiency and Turner syndrome: the influence of a SOCS2 polymorphism
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Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome
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GH treatment to final height produces similar height gains in patients with SHOX deficiency and Turner syndrome: results of a multicenter trial
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Features of Turner syndrome among a group of Cameroonian patients
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Efficacy and safety of oxandrolone in growth hormone-treated girls with turner syndrome
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Effects of low-dose estrogen replacement during childhood on pubertal development and gonadotropin concentrations in patients with Turner syndrome: results of a randomized, double-blind, placebo-controlled clinical trial
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Dosage of estradiol, bone and body composition in Turner syndrome: a 5-year randomized controlled clinical trial
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Detailed clinical and molecular study of 20 females with Xq deletions with special reference to menstruation and fertility
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Comparison of body surface area versus weight-based growth hormone dosing for girls with Turner syndrome
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Commentary: launch of a quality improvement network for evidence-based management of uncommon pediatric endocrine disorders: Turner syndrome as a prototype
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Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting
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Anti-Müllerian hormone levels in girls and adolescents with Turner syndrome are related to karyotype, pubertal development and growth hormone treatment
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Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome
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An observational study of the effectiveness and safety of growth hormone (Humatrope(®)) treatment in Japanese children with growth hormone deficiency or Turner syndrome
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Adult height in girls with Turner syndrome treated from before 6 years of age with a fixed per kilogram GH dose
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A syndrome of infantilism, congenital webbed neck, and cubitus valus
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A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome)
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A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome
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50 Years ago in The Journal of Pediatrics: the XO syndrome: a study of the differential phenotype in 25 patients