Search research articles
Contact Us
Filters
Showing results (21-30 of 47) with videos related to
Page
of 5
Sort By:
Journal of Korean Medical Science
|
August 29, 2022
Serial Long-Term Growth and Neurodevelopment of Very-Low-Birth-Weight Infants: 2022 Update on the Korean Neonatal Network
Ga Won Jeon, Jang Hoon Lee, Minkyung Oh, et al.
Korean Journal of Pediatrics
|
December 31, 2010
A case of Pfeiffer syndrome with c833_834GC>TG (Cys278Leu) mutation in the FGFR2 gene
Min Young Lee, Ga Won Jeon, Ji Mi Jung, et al.
Children (Basel, Switzerland)
|
November 27, 2024
A Predictive Model for Perinatal Brain Injury Using Machine Learning Based on Early Birth Data
Ga Won Jeon, Yeong Seok Lee, Won-Ho Hahn, et al.
Korean Journal of Pediatrics
|
July 28, 2015
Thyroid dysfunction in very low birth weight preterm infants
Ji Hoon Lee, Sung Woo Kim, Ga Won Jeon, et al.
Japanese Journal of Infectious Diseases
|
June 2, 2020
Prevalence of Eleven Infectious Viruses Causing Diarrhea in Korea
Gyu Ri Kim, Si Hyun Kim, Ga Won Jeon, et al.
Journal of Korean Medical Science
|
January 31, 2023
Proper Depth of Percutaneous Central Venous Catheter via the Great Saphenous Vein for Very Low Birth Weight Infants: A Single-Center, Prospective Cohort Study
Jin Ho Kim, Ga Won Jeon, Hyun Ho Kim, et al.
Scientific Reports
|
October 27, 2022
Comparison of definitions of bronchopulmonary dysplasia to reflect the long-term outcomes of extremely preterm infants
Ga Won Jeon, Minkyung Oh, Juyoung Lee, et al.
Journal of Korean Medical Science
|
September 3, 2010
The first Korean case of cutaneous lung tissue heterotopia
Ga Won Jeon, Seong Woo Han, Ji Mi Jung, et al.
Annals of Clinical and Laboratory Science
|
March 2, 2016
Identification of the KCNJ2 Mutation in a Korean Family with Andersen-Tawil Syndrome and Developmental Delay
Na Ri Kim, Ja-Hyun Jang, Ga Won Jeon, et al.
Annals of Clinical and Laboratory Science
|
March 7, 2013
Clinical and genetic analysis of a Korean patient with X-linked chondrodysplasia punctata: identification of a novel splicing mutation in the ARSE gene
Ga Won Jeon, Min-Jung Kwon, Sun Joo Lee, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 47) with videos related to
Sort By:
Page
of 5
Journal of Korean Medical Science
|
August 29, 2022
Serial Long-Term Growth and Neurodevelopment of Very-Low-Birth-Weight Infants: 2022 Update on the Korean Neonatal Network
Ga Won Jeon, Jang Hoon Lee, Minkyung Oh, et al.
Korean Journal of Pediatrics
|
December 31, 2010
A case of Pfeiffer syndrome with c833_834GC>TG (Cys278Leu) mutation in the FGFR2 gene
Min Young Lee, Ga Won Jeon, Ji Mi Jung, et al.
Children (Basel, Switzerland)
|
November 27, 2024
A Predictive Model for Perinatal Brain Injury Using Machine Learning Based on Early Birth Data
Ga Won Jeon, Yeong Seok Lee, Won-Ho Hahn, et al.
Korean Journal of Pediatrics
|
July 28, 2015
Thyroid dysfunction in very low birth weight preterm infants
Ji Hoon Lee, Sung Woo Kim, Ga Won Jeon, et al.
Japanese Journal of Infectious Diseases
|
June 2, 2020
Prevalence of Eleven Infectious Viruses Causing Diarrhea in Korea
Gyu Ri Kim, Si Hyun Kim, Ga Won Jeon, et al.
Journal of Korean Medical Science
|
January 31, 2023
Proper Depth of Percutaneous Central Venous Catheter via the Great Saphenous Vein for Very Low Birth Weight Infants: A Single-Center, Prospective Cohort Study
Jin Ho Kim, Ga Won Jeon, Hyun Ho Kim, et al.
Scientific Reports
|
October 27, 2022
Comparison of definitions of bronchopulmonary dysplasia to reflect the long-term outcomes of extremely preterm infants
Ga Won Jeon, Minkyung Oh, Juyoung Lee, et al.
Journal of Korean Medical Science
|
September 3, 2010
The first Korean case of cutaneous lung tissue heterotopia
Ga Won Jeon, Seong Woo Han, Ji Mi Jung, et al.
Annals of Clinical and Laboratory Science
|
March 2, 2016
Identification of the KCNJ2 Mutation in a Korean Family with Andersen-Tawil Syndrome and Developmental Delay
Na Ri Kim, Ja-Hyun Jang, Ga Won Jeon, et al.
Annals of Clinical and Laboratory Science
|
March 7, 2013
Clinical and genetic analysis of a Korean patient with X-linked chondrodysplasia punctata: identification of a novel splicing mutation in the ARSE gene
Ga Won Jeon, Min-Jung Kwon, Sun Joo Lee, et al.
Page
of 5