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Volume 29(1); Feb 2024
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):1-2.
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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,
Ann Pediatr Endocrinol Metab.
2024;29(1):3-11.
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):12-18.
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):19-28.
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):29-37.
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):38-45.
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):46-53.
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):54-59.
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):60-66.
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):67-69.
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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
Ann Pediatr Endocrinol Metab.
2024;29(1):70-72.
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