- Compound heterozygous mutations of ACADS gene in newborn with short chain acyl-CoA dehydrogenase deficiency: case report and literatures review
- Se Jin An, Sook Za Kim, Gu Hwan Kim et al.
- Clin Exp Pediatr. 2016;59(Suppl 1):S45-S48.
-
- A Case Report Kostmann Syndrome.
- Han Wook Yoo, Son Moon Shin, Hyo Seop Ahn et al.
- Clin Exp Pediatr. 1983;26(3):284-288.
-
- Idiopathic IgA Nepropathy in Children.
- Hae Il Cheong, Han Wook Yoo, Kwang Wook Ko
- Clin Exp Pediatr. 1986;29(6):633-643.
-
- Plasma Basal Cortisol Level and Its Significance in Minimal Change Neprotic syndrom.
- Han Wook Yoo
- Clin Exp Pediatr. 1986;29(6):644-652.
-
- A Clinical Observation on Systemic Lupus Erythematosus in Children.
- Han Wook Yoo, Hae Il Cheong, Hoan Jong Lee et al.
- Clin Exp Pediatr. 1987;30(5):527-535.
-
- Plasma Amino Acid Patterns in Reye's Syndrome.
- Han Wook Yoo, Hee Shang Youn
- Clin Exp Pediatr. 1989;32(10):1377-1383.
-
- Diaphragmatic Movements in Neonates.
- Hee Shang Youn, Han Wook Yoo, Moon Hong Do et al.
- Clin Exp Pediatr. 1990;33(7):901-906.
-
- A Korean boy with atypical X-linked adrenoleukodystrophy confirmed by an unpublished mutation of ABCD1
- Hye Jeong Jwa, Keon Su Lee, Gu Hwan Kim et al.
- Clin Exp Pediatr. 2014;57(9):416-419.
-
- Testicular adrenal rest tumors in a patient with untreated congenital adrenal hyperplasia
- Hye Young Jin, Jin Ho Choi, Gu Hwan Kim et al.
- Clin Exp Pediatr. 2011;54(3):137-140.
-
- A case of thanatophoric dysplasia type I with an R248C mutation in the FGFR3 gene
- Eun Jung Noe, Han Wook Yoo, Kwang Nam Kim et al.
- Clin Exp Pediatr. 2010;53(12):1022-1025.
-
- A family with Townes-Brocks syndrome with congenital hypothyroidism and a novel mutation of the SALL1 gene
- Won Ik Choi, Ji Hye Kim, Han Wook Yoo et al.
- Clin Exp Pediatr. 2010;53(12):1018-1021.
-
- The natural history and prognostic factors of Graves' disease in Korean children and adolescents
- Seung Min Song, Ji-Seok Youn, Jung Min Ko et al.
- Clin Exp Pediatr. 2010;53(4):585-591.
-
- Genetic testing in clinical pediatric practice
- Han Wook Yoo
- Clin Exp Pediatr. 2010;53(3):273-285.
-
- Two cases of Fabry disease identified in brothers
- Ji Eun Cho, Yong Hee Hong, Yang Gyun Lee et al.
- Clin Exp Pediatr. 2010;53(2):235-238.
-
- A Case of CATCH22 Syndrome with First Attack of Hypocalcemic Seizure at 13 Years of Age
- Young Won An, Mi Jin Jung, Jee Suk Yu et al.
- Clin Exp Pediatr. 2004;47(7):794-798.
-
- A Case of Glutaric Aciduria Type 1
- Joon Young Song, Cheol Min Kim, Young Lim Shin et al.
- Clin Exp Pediatr. 2002;45(10):1278-1282.
-
- A Case of Chronic Active Epstein-Barr Virus
Infection with Coronary Aneurysm
- Hee Jeong, Bong Seong Kim, Ok Ja Choi et al.
- Clin Exp Pediatr. 2001;44(6):687-693.
-
- A Case of de novo Interstitial Deletion of 17 Chromosome
- Kyung Hee Yoon, Hee Cheol Lee, Ai Rhan Kim et al.
- Clin Exp Pediatr. 2001;44(4):475-479.
-
- MELAS Syndrome Confirmed by Mitochondrial DNA Analysis in Siblings
- Young Ghil Rah, Soo Ahn Chae, In Suk Lim et al.
- Clin Exp Pediatr. 1999;42(3):412-418.
-
- The Clinical Study on Marfan Syndrome
- Jung Sim Kim, Dong Kyu Jin, See Hwan Ko et al.
- Clin Exp Pediatr. 1998;41(10):1411-1416.
-
- A Case of Dietary Treatment of Vitamin B12 Non-responsive Methylmalonic Acidemia
- Won Young Song, Ki Soo Kim, Han Wook Yoo
- Clin Exp Pediatr. 1997;40(4):549-554.
-
About
Browse articles
For contributors