Found: 27
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Delayed Bone Age Might Accelerate the Response to Human Growth Hormone Treatment in Small for Gestational Age Children with Short Stature.
- Published in:
- International Journal of Endocrinology, 2019, p. 1, doi. 10.1155/2019/8454303
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- Publication type:
- Article
Recombinant growth hormone therapy in children with Turner Syndrome in Korea: a phase III Randomized Trial.
- Published in:
- BMC Endocrine Disorders, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12902-021-00904-5
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- Publication type:
- Article
Precocious puberty in Korean girls with and without exposure to endocrine-disrupting chemicals in toy slime: a comparative analysis.
- Published in:
- BMC Endocrine Disorders, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12902-021-00855-x
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- Publication type:
- Article
A de novo <italic>KMT2D</italic> mutation in a girl with Kabuki syndrome associated with endocrine symptoms: a case report.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Recurrent pancreatitis after renal transplantation in a child.
- Published in:
- Pediatric Transplantation, 2008, v. 12, n. 5, p. 593, doi. 10.1111/j.1399-3046.2008.00922.x
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- Publication type:
- Article
Post hoc subgroup analysis of Asian children with paediatric GHD from the global phase 3 efficacy and safety study of once-weekly somatrogon vs. once-daily somatropin.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2024, v. 37, n. 6, p. 525, doi. 10.1515/jpem-2023-0512
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- Publication type:
- Article
Fulminant type 1 diabetes mellitus in Korean adolescents.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2011, v. 24, n. 9/10, p. 679, doi. 10.1515/JPEM.2011.233
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- Publication type:
- Article
Efficacy and safety of LB03002, a once-weekly sustained-release human GH for 12-month treatment in Korean children with GH deficiency.
- Published in:
- European Journal of Endocrinology, 2013, v. 169, n. 2, p. 179, doi. 10.1530/EJE-13-0148
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- Publication type:
- Article
Metabolic Impacts of Discontinuation and Resumption of Recombinant Human Growth Hormone Treatment during the Transition Period in Patients with Childhood-Onset Growth Hormone Deficiency.
- Published in:
- Endocrinology & Metabolism, 2022, v. 37, n. 2, p. 359, doi. 10.3803/EnM.2021.1384
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- Publication type:
- Article
Effect of Growth Hormone Therapy on Height Velocity in Korean Children with Idiopathic Short Stature: A Phase III Randomised Controlled Trial.
- Published in:
- Hormone Research in Paediatrics, 2018, v. 90, n. 1, p. 44, doi. 10.1159/000491016
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- Publication type:
- Article
Once-Weekly Administration of Sustained-Release Growth Hormone in Korean Prepubertal Children with Idiopathic Short Stature: A Randomized, Controlled Phase II Study.
- Published in:
- Hormone Research in Paediatrics, 2018, v. 90, n. 1, p. 54, doi. 10.1159/000489262
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- Publication type:
- Article
Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing.
- Published in:
- Hormone Research in Paediatrics, 2015, v. 83, n. 4, p. 242, doi. 10.1159/000368657
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- Publication type:
- Article
Efficacy of Short-Term Growth Hormone Treatment in Prepubertal Children with Idiopathic Short Stature.
- Published in:
- Yonsei Medical Journal, 2014, v. 55, n. 1, p. 53, doi. 10.3349/ymj.2014.55.1.53
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- Publication type:
- Article
Combined surgical and medical treatment in an adolescent with severe gynecomastia due to excessive estradiol secretion: a case report.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Long-term Therapeutic Efficacy of Lamivudine Compared With Interferon-α in Children with Chronic Hepatitis B: The Younger the Better.
- Published in:
- Journal of Pediatric Gastroenterology & Nutrition, 2007, v. 44, n. 1, p. 92, doi. 10.1097/01.mpg.0000243439.47334.4e
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- Publication type:
- Article
A cell function study on calcium regulation of a novel calcium-sensing receptor mutation (p.Tyr825Phe).
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2021, v. 26, n. 1, p. 24, doi. 10.6065/apem.2040022.011
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- Publication type:
- Article
An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2020, v. 25, n. 2, p. 132, doi. 10.6065/apem.1938074.037
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- Publication type:
- Article
Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2020, v. 25, n. 2, p. 97, doi. 10.6065/apem.1938152.076
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- Publication type:
- Article
Severe recurrent nocturnal hypoglycemia during chemotherapy with 6-mercaptopurine in a child with acute lymphoblastic leukemia.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2018, v. 23, n. 4, p. 227, doi. 10.6065/apem.2018.23.4.226
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- Publication type:
- Article
De novo a novel variant of CaSR gene in a neonate with congenital hypoparathyroidism.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2018, v. 23, n. 2, p. 107, doi. 10.6065/apem.2018.23.2.107
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- Publication type:
- Article
Delayed diagnosis of pituitary stalk interruption syndrome with severe recurrent hyponatremia caused by adrenal insufficiency.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Delayed diagnosis of pituitary stalk interruption syndrome with severe recurrent hyponatremia caused by adrenal insufficiency.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Changes of antithroglobulin antibody in children with congenital hypothyroidism.
- Published in:
- Annals of Pediatric Endocrinology & Metabolism, 2013, v. 18, n. 4, p. 179, doi. 10.6065/apem.2013.18.4.179
- By:
- Publication type:
- Article
Interleukin-8 and tumor necrosis factor-alpha are increased in minimal change disease but do not alter albumin permeability.
- Published in:
- 2003
- By:
- Publication type:
- journal article
Pathophysiology of minimal change nephrotic syndrome and focal segmental glomerulosclerosis.
- Published in:
- Nephrology, 2007, v. 12, p. S11, doi. 10.1111/j.1440-1797.2007.00875.x
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- Publication type:
- Article
Clinical characterization and identification of two novel mutations of the GNAS gene in patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism.
- Published in:
- Clinical Endocrinology, 2011, v. 75, n. 2, p. 207, doi. 10.1111/j.1365-2265.2011.04026.x
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- Publication type:
- Article
A pilot study on children with bone-age advancement without early sexual maturation; auxological and laboratory (GNRH stimulation) characteristics.
- Published in:
- 2013
- By:
- Publication type:
- Abstract