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Puberty: a Model for the Study of Hypothalamic Differentiation

Lee BJ

  • KMID: 2321968
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):1-5.
No abstract available.
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Pathophysiology of Precocious Puberty

Shin HJ

  • KMID: 2321970
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):7-14.
No abstract available.
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Efficacy and Side Effects of GnRH Agonist

Yang S

  • KMID: 2321973
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):30-34.
No abstract available.
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Indication of Combined Treatment of GnRH Agonist and GH

Yi KH

  • KMID: 2321972
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):24-29.
No abstract available.
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Indication of Gonadotropin-Releasing Hormone Agonist: Precocious Puberty or Advanced Puberty?

Kim JD

  • KMID: 2321971
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):15-23.
No abstract available.
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Serum IGF-I and IGFBP-3 in 919 Healthy Korean Children and Adolescents: Normal Values and Correlations with Age, Sex, Height, Body Mass Index and Bone Age

Song AK, Kim HJ, Suk HJ, Hwang JS, Hong CH

  • KMID: 2321974
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):35-41.
PURPOSE: IGF-I and IGFBP-3 are usually used for the diagnosis of growth hormone deficiency. Until now we don't have normal values of IGF-I and IGFBP-3 in Korea. Therefore, we evaluated...
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Short Stature Associated with Polymorphisms in Chromosome 1qh+, and 16qh+

Kim KH, Lee SW, Kim MG, Kim DH, Kim HS

  • KMID: 2321983
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):95-99.
Chromosomal polymorphism of constitutive heterochromatin regions of chromosome 1, 9, 16, and Y is a stable evolutionary feature that is thought to cause no phenotypic alterations. The presence of definite...
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A Case of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome with Amenorrhea and Sexual Precosity

Ahn JG, Baek HS, Shin JH

  • KMID: 2321986
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):110-114.
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is comprised of vaginal atresia with other variable Mullerian duct abnormalities. Its features include an absent or very short vagina and a uterus that can be...
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A Case of Down-Turner Syndrome

Jeong HJ, Lee ES, Choi KH, Park YH

  • KMID: 2321988
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):120-124.
Down-Turner syndrome is a rare disease with the incidence of 1 in 2 million. Although Down syndrome with various Turner's karyotype were reported occasionally since a report in 1962, it...
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Effect on Final Height of Gonadotropin-Releasing Hormone Agonist (GnRHa) in Children with Congenital Adrenal Hyperplasia

Yi KH

  • KMID: 2321976
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):50-56.
PURPOSE: Object of present study is to identify the effect of gonadotropin-releasing hormone agonis (GnRHa) treatment on final adult height in congenital adrenal hyperplasia (CAH) children with central precocious puberty....
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Two Cases of Kallmann Syndrome Presented with Delayed Puberty

Choi HK, Choi JH, Yoo HW

  • KMID: 2321985
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):105-109.
Kallmann syndrome is caused by the defects of migration of the olfactory and GnRH neurons from the olfactory placodes to the brain, and characterized by hypogonadotropic hypogonadism, and anosmia or...
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A Case of Metabolic Syndrome in a Child with Normal Weight

Park HG, Chung SC, Kim MH, Kim KS, Park JH, Jeon HJ, Seo BK

  • KMID: 2321987
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):115-119.
The worldwide obesity epidemic is realized during the past few decades. The risk of developing metabolic syndrome increases steeply with increasing obesity. Increasing childhood obesity heralds a greater health burden...
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A Case of Thyroid Hormone Resistance (RTH)

Seo JY, Yoon IS, Yoo JH, Ahn SY, Jeong HL, Shin CH, Yang SW

  • KMID: 2321984
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):100-104.
Thyroid hormone resistance (RTH) is a rare autosomal dominant disease characterized by reduced tissue sensitivity to thyroid hormone. Approximately 90% of subjects with RTH have mutation in the thyroid hormone...
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Relationship between Chronologic Age and Bone Age at Diagnosis of Central Precocious Puberty

Han MY, Sohn WY, Paik KH, Jin DK

  • KMID: 2321982
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):90-94.
PURPOSE: Precocious puberty is defined as the development of secondary sexual characteristics in girls younger than 8 years, and boys younger than 9 years. Central precocious puberty (CPP) is gonadotropin...
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Otologic Evaluation in Children with Turner Syndrome

Kim JS, Kim SR, Chung WY

  • KMID: 2321979
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):71-75.
PURPOSE: Patients with Turner syndrome have been frequently suspected to have associated various otologic disorders and hearing loss. The purpose of this study was to evaluate the otologic problems in...
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Insulin Sensitivity in Prepubertal Children born with Low Birth Weight

Chung HR, Hong SY, Yi KH, Shin CH, Yang SW

  • KMID: 2321980
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):76-83.
PURPOSE: We aimed to determine whether prepubertal children born with low birth weight (LBW) have decreased insulin sensitivity, compared with children born with normal birth weight and to know a...
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Gender Difference of Insulin Resistance in Obese Children and Adolescents

Kim DH, Yoon JH, Kim HS, Kim DK, Cheong MY

  • KMID: 2321981
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):84-89.
PURPOSE: It is known that insulin resistance is important because it may precede the development of Diabetes Mellitus. We evaluated the gender difference of insulin resistance in obese children &...
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The Behavioral and Psychic Masculinizing Scores and Its Related Factors in Female Patients with Congenital Adrenal Hyperplasia Caused by 21-Hydroxylase Deficiency

Hwang IT, Ryu SG, Yi KH

  • KMID: 2321978
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):64-70.
OBJECTIVE: We analyzed the degree of behavioral and psychic masculinization as well as factors influencing the masculinization in female patients with CAH caused by 21-hydroxylase deficiency. METHODS: We studied 26 patients...
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Final Adult Height and Its Influencing Factors in Patients with Congenital Adrenal Hyperplasia Caused by 21-Hydroxylase Deficiency

Hong SY, Chung HR, Kim SY, Yi KH, Shin CH, Yang SW

  • KMID: 2321975
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):42-49.
PURPOSE: We evaluated adult final height and factors influencing adult height outcome in patients with congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency. METHOD: We retrospectively reviewed medical records of 20...
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A Sustained Release Human Growth Hormone (LB03002):Efficacy and Safety Following Six-month Treatment in Children with Growth Hormone Deficiency (GHD)

Kim DH, Lee BC, Shin JH, Yang SW, Yoo HW, Jin DK, Ko CW, Chung WY, Suh BK, Lee KH, Kim HJ, Ji HJ, Kim J

  • KMID: 2321969
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):6-6.
BACKGROUND: LB03002[somatropin(rDNA origin) for injectable suspension] is a sustained release formulation of human growth hormone to be administered by once-a-week subcutaneous injections. Less frequent administration could provide a considerable improvement...
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