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Pituitary apoplexy is not uncommon in pediatric patients and can be a manifestation of neuro-COVID

Finsterer J

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Commentary on "The prevalence of diabetic peripheral neuropathy in youth with diabetes mellitus"

Cho WK

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Reply to Commentary on "Pituitary apoplexy in an adolescent male with macroprolactinoma presenting as middle cerebral artery territory infarction"

Agrawal P, Arya VB

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Commentary on "Effect of gonadotropin-releasing hormone agonist treatment on near final height in girls with central precocious puberty and early puberty"

Kwon A

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Ciliopathies in pediatric enodcrinology

Cicolini I, Blasetti A, Chiarelli F

Ciliopathies are a group of disorders that involve many organs and systems. In this review, we consider the role of the cilium in multiorgan pathology with a focus on endocrinological...
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The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in Korea

Yoo S, Yoon JY, Keum C, Cheon CK

Follicle-stimulating hormone receptor (FSHR) mutation is a rare cause of amenorrhea. We report the first case of FSHR mutations in Korea. Two female siblings, aged 16 (patient 1) and 19...
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Pediatric management challenges of hyperglycemic hyperosmolar state: case series of Korean adolescents with type 2 diabetes

Lee S, Yoo S, Yoon JY, Cheon CK, Kim YA

The hyperglycemic hyperosmolar state (HHS) is considered the most fatal complication of type 2 diabetes mellitus (DM). The number of case reports describing pediatric HHS has increased recently in parallel...
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The prevalence of diabetic peripheral neuropathy in youth with diabetes mellitus

Sophausvaporn P, Boonhong J, Sahakitrungruang T

Purpose: Diabetic neuropathy (DN) is a serious complication in diabetes mellitus. We aimed to determine the prevalence of DN in pediatric-onset diabetes in a tertiary care center and to assess...
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Risk factors of postoperative hypoparathyroidism after total thyroidectomy in pediatric patients with thyroid cancer

Choe Y, Lee YJ, Shin CH, Chung EJ, Lee YA

Purpose: Hypoparathyroidism (hypoPTH) is the most common complication following thyroidectomy. We investigated the frequency and risk factors of hypoPTH after total thyroidectomy (TT) in pediatric patients with thyroid cancer. Methods: This...
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Development of delayed thyroid stimulating hormone elevation in small-for-gestational-age infants: is a second screening needed?

Lee G, Park SY, Park JH, Kang S

Purpose: Recent reports indicate that small for gestational age (SGA) could be a risk factor for delayed thyroid stimulating hormone (dTSH) elevation in preterm infants. The development of dTSH elevation...
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Vitamin D deficiency is a public health emergency among Indonesian children and adolescents: a systematic review and meta-analysis of prevalence

Octavius GS, Shakila A, Meliani M, Halim A

Purpose: This study aimed to describe the prevalence of vitamin D deficiency in Indonesian children and adolescents. Methods: This was a meta-analysis of prevalence using the Hartung-Knapp-Sidik-Jonkman method with a random...
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Factors affecting bone mineral density in children and adolescents with secondary osteoporosis

Jang MJ, Shin C, Kim S, Lee JW, Chung NG, Cho B, Jung MH, Suh BK, Ahn MB

Purpose: This study aimed to investigate the clinical factors associated with bone mineral density (BMD) among children and adolescents with osteoporosis secondary to treatment for underlying clinical conditions. Methods: We retrospectively...
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Effect of gonadotropin-releasing hormone agonist treatment on near final height in girls with central precocious puberty and early puberty

Yang EH, Jo HY, Park SJ, Yoo HW, Choi SH, Kim HY, Park KH, Kim YM, Kwak MJ

Purpose: The aim of this study was to examine whether gonadotropin-releasing hormone (GnRH) agonist treatment is effective in preserving final height in patients with central precocious puberty (CPP) or early...
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First female Korean child with Coffin-Lowry syndrome: a novel variant in RPS6KA3 diagnosed by exome sequencing and a literature review

Song A, Im M, Kim MS, Noh ES, Kim C, Jang J, Lee SM, Ki CS, Cho SY, Jin DK

Coffin-Lowry syndrome (CLS, OMIM # 303600) is a rare X-linked disorder caused by mutations in RPS6KA3. CLS is characterized by facial dysmorphism, digit abnormalities, developmental delays, growth retardation, and progressive...
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