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Malnutrition-Related Fulminant Type 1 Diabetes in a Patient with Sturge-Weber Syndrome

Oh JS, Yu J

Fulminant type 1 diabetes is a subtype of idiopathic type 1 diabetes and is characterized by a short duration of symptom onset and an absence of anti-islet autoantibodies. It has...
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Successful Pamidronate Treatment of Osteogenesis Imperfecta Type III Infant with Multiple Fractures

Yoon JH, Baek JU, Shim EJ, Hwang IT

Osteogenesis imperfect (OI) is a generalized connective tissue disorder. We report the female neonate case with OI type III who showed severe bone deformities and fractures in utero. At birth,...
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Issues in Infants with Prader-Will Syndrome: Special Review on Early Dietary Intervention and Early Use of Growth Hormone

Cho SY, Jin DK

Prader-Willi syndrome (PWS) is a complex multisystem genetic disorder characterized by hypothalamic-pituitary dysfunction. The main clinical features consist of neonatal hypotonia, distinctive facial features, delayed overall development with mental deficiency,...
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Sterile Abscess Formation Associated with Two Different Forms of Gonadotropin-Releasing Hormone Agonist in Central Precocious Puberty

Kim JM, Shin YL

Long-acting formulations of gonadotropin-releasing hormone (GnRH) agonists are indicated for treating central precocious puberty. Leuprolide acetate and triptorelin acetate are widely used in Korea. Local reactions related to GnRH agonists,...
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Differential Diagnosis of Disorders of Sex Development (DSD) by Molecular Genetic Analyses

Choi JH, Yoo HW

Sex determination and differentiation require the balanced and sequential activation of transcription factors, signaling molecules, hormones and their receptors. Disorders of sex development (DSD) have heterogeneous groups of etiologies caused...
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Changes in the Predicted Adult Height after Gonadotropin-Releasing Hormone Agonist Treatment in Girls with Idiopathic True Precocious Puberty

Kwon EB, Lee SJ, Cha M, Kim SY

PURPOSE: We evaluated the effects of the timing of treatment initiation with gonadotropin-releasing hormone agonist (GnRHa) on the change in predicted adult height (PAH) in girls with idiopathic true precocious...
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Growth Hormone Treatment and Its Effect on Height in Pediatric Patients with Different Genotypes of Prader-Willi Syndrome

Kwun C, Cho SY, Maeng SH, Jung YJ, Jin DK

PURPOSE: Differences in phenotypes between the two most common subtypes of Prader-Willi syndrome (PWS) indicate that a distinct response to growth hormone (GH) treatment may exist. To test this hypothesis,...
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A Case of Systemic Lupus Erythematosus with Graves Disease in a Child

Kim SH, Yoon KL, Lee SH, Won KY, Shim KS

Autoimmune diseases are occasionally associated with other autoimmune diseases in the same patients. Graves disease has been associated with systemic rheumatic diseases including systemic lupus erythematosus (SLE). The diagnosis of...
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Growth Status and Body Composition in Children with Central Precocious Puberty and Early Puberty

Kim HJ, Kim YH, Chung S

PURPOSE: The aim of this study was to analyze the growth status and body composition in children with central precocious puberty (CPP ) and early puberty (EP). METHODS: One hundred and...
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Efficacy of a Single Luteinizing Hormone Measurement after GnRH Agonist Administration for Therapeutic Monitoring of Girls with Central Precocious Puberty

Kim YM, Choi JH, Lee BH, Yoo HW

PURPOSE: The effectiveness of gonadotropin releasing hormone (GnRH) agonist therapy in central precocious puberty (CPP) depends on the suppression of luteinizing hormone (LH) secretion. The purpose of this study was...
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