- Original Article
- Clinical characteristics of severe meconium aspiration syndrome
-
Chang Won Choi, Beyong Il Kim, Hyun Ju Lee, Kyoung Eun Joung, Gyu Hong Shim, In Suk Lim, Jin-A Lee, Ee-Kyung Kim, Han-Suk Kim, Jung-Hwan Choi
-
Clin Exp Pediatr. 2008;51(7):713-721. Published online July 15, 2008
-
|
|
Purpose : This study aims to describe the clinical characteristics of severe meconium aspiration syndrome (MAS) which required mechanical ventilation over 48 h and to delineate the progress of respiratory failure and radiographic findings in severe MAS.
Methods : Twelve infants admitted to the Neonatal Intensive Care Unit (NICU) of the Seoul National University Bundang Hospital diagnosed with severe MAS from... |
-
-
- A Comparison of Clinical Manifestations in Neonates and Infants Infected by Respiratory Syncytial Virus
-
In Suk Lim, Min Joo Shim, Byung Eui Kim, Ju Young Chung, Chang Keun Kim, Myoung Jae Chey, Sang Woo Kim, Soung Hee Kim, Tae Hee Han
-
Clin Exp Pediatr. 2004;47(9):949-952. Published online September 15, 2004
-
|
|
Purpose : This study was performed to evaluate of clinical manifestations of neonatal respiratory syncytial virus(RSV) infection, and to evaluate of differences of clinical manifestations between the neonates and infants who were infected by RSV.
Methods : We reviewed the medical record of 75 children who were younger than 12 months of age and infected by RSV. We classified then into... |
-
-
- Case Report
- A Case of 4q Deletion with Partial Agenesis of Corpus Callosum
-
Mi Na Kang, In Suk Lim, Byeong Eui Kim, Myoung Jae Chey, Sang Woo Kim
-
Clin Exp Pediatr. 2002;45(2):273-277. Published online February 15, 2002
-
|
|
Syndrome of 4q deletion is characterized by an abnormal shape of the skull, craniofacial dysmorphism, cardiovascular malformations, genitourinary defects, limb and digital anomalies, and developmental delay. We experienced a case of 4q interstitial deletion in a 2 day-old female neonate who showed short extremities, partial agenesis of corpus callosum and congenital heart defects. We report the case with a brief... |
-
-
- Original Article
- MELAS Syndrome Confirmed by Mitochondrial DNA Analysis in Siblings
-
Young Ghil Rah, Soo Ahn Chae, In Suk Lim, Dong Keun Lee, Byoung Hun Yoo, Tae Sung Ko, Han Wook Yoo
-
Clin Exp Pediatr. 1999;42(3):412-418. Published online March 15, 1999
-
|
|
MELAS(mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) syndrome is a major subgroup of mitochondrial myopathy. Recent advances in molecular genetics revealed specific mutations in mitochondrial DNA which cause MELAS. We described here clinical and molecular genetic findings of sister and brother with MELAS syndrome. For molecular genetic studies, DNAs from peripheral blood nucleated cells were used. And the substitution... |
-
-
- A Study of Vascular Reactivity Change in Nephrotic Syndrome Children Using Plethysmography
-
Jae Won Shim, Byoung Hoon Yoo, In Suk Lim
-
Clin Exp Pediatr. 1997;40(5):650-659. Published online May 15, 1997
-
|
|
Purpose : The nephrotic syndrome is characterized by proteinuria, hypoproteinemia, edema and hyperlipidemia. These can change body homeostasis and cause hypertension. This study was designed to determine the relationship between the forearm vasodilating capacity and serum cholesterol level of nephrotic syndrome patients.
Methods : 15 Nephrotic syndrome patients and 17 normal control children who visited Chung-ang University Youngsan Hospital from Sep.... |
-
-
|
