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Commentary on "Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience"
- Hye Young Jin
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Ann Pediatr Endocrinol Metab. 2024;29(1):1-2.
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Editorial
February 29, 2024
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An overview of growth hormone therapy in pediatric cases documented in the Kabi International Growth Study (Pfizer International Growth Database)
- Mitchell E. Geffner, Michael B. Ranke, Michael P. Wajnrajch,
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Ann Pediatr Endocrinol Metab. 2024;29(1):3-11.
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Review Article
February 29, 2024
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Pediatric and adult osteoporosis: a contrasting mirror
- Hanene Lassoued Ferjani, Ines Cherif, Dorra Ben Nessib, Dhia Kaffel, Kaouther Maatallah, Wafa Hamdi
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Ann Pediatr Endocrinol Metab. 2024;29(1):12-18.
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Review Article
February 29, 2024
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Association of maternal insulin resistance with neonatal insulin resistance and body composition/size: a prospective cohort study in a sub-Saharan African population
- Ibironke J. Akinola, Peter O. Ubuane, Adeyemi O. Dada, Joy O. Chionuma, Taiwo O. Kuku-Kuye, Folasade D. Olalere
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Ann Pediatr Endocrinol Metab. 2024;29(1):19-28.
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Original Article
February 29, 2024
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Comparison of anthropometric, metabolic, and body compositional abnormalities in Korean children and adolescents born small, appropriate, and large for gestational age: a population-based study from KNHANES V (2010–2011)
- Tae Kwan Lee, Yoo Mi Kim, Han Hyuk Lim
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Ann Pediatr Endocrinol Metab. 2024;29(1):29-37.
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Original Article
February 29, 2024
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Genetic evaluation using next-generation sequencing of children with short stature: a single tertiary-center experience
- Su Jin Kim, Eunyoung Joo, Jisun Park, Chang Ahn Seol, Ji-Eun Lee
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Ann Pediatr Endocrinol Metab. 2024;29(1):38-45.
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Original Article
February 29, 2024
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Effectiveness and safety of pamidronate treatment in nonambulatory children with low bone mineral density
- Myeongseob Lee, Ahreum Kwon, Kyungchul Song, Hae In Lee, Han Saem Choi, Junghwan Suh, Hyun Wook Chae, Ho-Seong Kim
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Ann Pediatr Endocrinol Metab. 2024;29(1):46-53.
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Original Article
February 29, 2024
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Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene
- Ji-Hee Yoon, Soojin Hwang, Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
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Ann Pediatr Endocrinol Metab. 2024;29(1):54-59.
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Original Article
February 29, 2024
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Familial male-limited precocious puberty due to an activating mutation of the LHCGR: a case report and literature review
- Jihyun Ha, Yunha Choi,, Mo Kyung Jung, Eun-Gyong Yoo, Han-Wook Yoo
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Ann Pediatr Endocrinol Metab. 2024;29(1):60-66.
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Case Report
February 29, 2024
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Resistance to thyroid hormone and nonfunctioning pituitary microadenoma in a 13-year-old boy with THRB mutation
- Jiyeon Kim, Eu Seon Noh, Min-Sun Kim, Jong-Moon Choi, Sae-Mi Lee, Sung Yoon Cho
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Ann Pediatr Endocrinol Metab. 2024;29(1):67-69.
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Letter to the Editor
February 29, 2024
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The first case of hyperosmolar diabetic ketoacidosis in a patient diagnosed with MODY 5 (maturity-onset diabetes of the young type 5) and 17q12 microdeletion syndrome
- Jun Lee, Minji Kim, Sukdong Yoo, Ju Young Yoon, Chong Kun Cheon
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Ann Pediatr Endocrinol Metab. 2024;29(1):70-72.
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Letter to the Editor
February 29, 2024
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