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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.   Published online February 29, 2024
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Genetic aspects of type 1 diabetes
Hae Sang Lee, Jin Soon Hwang
Ann Pediatr Endocrinol Metab. 2019;24(3):143-148.   Published online September 30, 2019
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Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family
Myo-Jing Kim, Young-Eun Kim, Chang-Seok Ki, Jae-Ho Yoo
Ann Pediatr Endocrinol Metab. 2014;19(4):220-224.   Published online December 31, 2014
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Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center
Yangho Yoo, Mi Sun Chang, Jieun Lee, Sung Yoon Cho, Sung Won Park, Dong-Kyu Jin, Hyung-Doo Park
Ann Pediatr Endocrinol Metab. 2013;18(3):128-134.   Published online September 30, 2013
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A Single-Arm, Phase III Study to Assess Efficacy and Safety after 6-Month-Treatment of Eutropin(TM) Inj. (Recombinant Human Growth Hormone) in Prepubertal Children with Short Stature due to Small for Gestational Age.
Kee Hyoung Lee, Byung Churl Lee, Cheol Woo Ko, Dong Kyu Jin, Sei Won Yang, Han Wook Yoo, Woo Yeong Chung, Duk Hee Kim, Byung Kyu Suh
Ann Pediatr Endocrinol Metab. 2011;16(3):157-164.
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