Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Naye Choi

Showing results (1-10 of 23) with videos related to

Pageof 3
Sort By:
Electrolyte & Blood Pressure : E & BP|January 23, 2023
Bartter Syndrome: Perspectives of a Pediatric NephrologistNaye Choi, Hee Gyung Kang
Journal of Clinical Laboratory Analysis|January 2, 2026
Clinical and Genetic Significance of Chromosomal Microarray Screening of Asymptomatic NewbornsNaye Choi, Hwa Young Kim, Jung Min Ko
Pediatrics International : Official Journal of the Japan Pediatric Society|September 4, 2025
Efficacy of avalglucosidase alfa in infantile-onset Pompe disease with high anti-alglucosidase alfa antibody titersA Young Park, Naye Choi, Jung Min Ko
Clinical Genetics|January 24, 2024
Development of disease-specific growth charts for Korean children with Beckwith-Wiedemann syndromeNaye Choi, Hwa Young Kim, Jung Min Ko
Molecular Genetics & Genomic Medicine|November 4, 2024
Deciphering Growth Patterns in Korean Children With Sotos Syndrome Through the Development of a Disease-Specific Growth ChartNaye Choi, Hwa Young Kim, Jung Min Ko
European Journal of Medical Genetics|June 26, 2026
Clinical and Genetic Spectrum of Trichorhinophalangeal Syndrome Type I/III in 20 Children of Korean OriginAyoung Park, Naye Choi, Tae-Joon Cho, et al.
Pediatric Nephrology (Berlin, Germany)|September 8, 2023
Efficacy and safety of long-term repeated use of rituximab in pediatric patients with nephrotic syndromeNaye Choi, Jeesu Min, Ji Hyun Kim, et al.
Frontiers in Pediatrics|January 30, 2023
Case report: Genetic defects in laminin α5 cause infantile steroid-resistant nephrotic syndromeYoon Sunwoo, Naye Choi, Jeesu Min, et al.
Molecular Genetics & Genomic Medicine|August 28, 2024
Dramatic Clinical Improvement With Biotin Mega-Dose Therapy in a Neonate With Holocarboxylase Synthetase DeficiencySeon Woo Kim, Hyeon Joo Lee, Naye Choi, et al.
Molecular Genetics & Genomic Medicine|August 24, 2021
Genetic and clinical heterogeneity in Korean patients with Rubinstein-Taybi syndromeNaye Choi, Hwa Young Kim, Byung Chan Lim, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Electrolyte & Blood Pressure : E & BP|January 23, 2023
Bartter Syndrome: Perspectives of a Pediatric NephrologistNaye Choi, Hee Gyung Kang
Journal of Clinical Laboratory Analysis|January 2, 2026
Clinical and Genetic Significance of Chromosomal Microarray Screening of Asymptomatic NewbornsNaye Choi, Hwa Young Kim, Jung Min Ko
Pediatrics International : Official Journal of the Japan Pediatric Society|September 4, 2025
Efficacy of avalglucosidase alfa in infantile-onset Pompe disease with high anti-alglucosidase alfa antibody titersA Young Park, Naye Choi, Jung Min Ko
Clinical Genetics|January 24, 2024
Development of disease-specific growth charts for Korean children with Beckwith-Wiedemann syndromeNaye Choi, Hwa Young Kim, Jung Min Ko
Molecular Genetics & Genomic Medicine|November 4, 2024
Deciphering Growth Patterns in Korean Children With Sotos Syndrome Through the Development of a Disease-Specific Growth ChartNaye Choi, Hwa Young Kim, Jung Min Ko
European Journal of Medical Genetics|June 26, 2026
Clinical and Genetic Spectrum of Trichorhinophalangeal Syndrome Type I/III in 20 Children of Korean OriginAyoung Park, Naye Choi, Tae-Joon Cho, et al.
Pediatric Nephrology (Berlin, Germany)|September 8, 2023
Efficacy and safety of long-term repeated use of rituximab in pediatric patients with nephrotic syndromeNaye Choi, Jeesu Min, Ji Hyun Kim, et al.
Frontiers in Pediatrics|January 30, 2023
Case report: Genetic defects in laminin α5 cause infantile steroid-resistant nephrotic syndromeYoon Sunwoo, Naye Choi, Jeesu Min, et al.
Molecular Genetics & Genomic Medicine|August 28, 2024
Dramatic Clinical Improvement With Biotin Mega-Dose Therapy in a Neonate With Holocarboxylase Synthetase DeficiencySeon Woo Kim, Hyeon Joo Lee, Naye Choi, et al.
Molecular Genetics & Genomic Medicine|August 24, 2021
Genetic and clinical heterogeneity in Korean patients with Rubinstein-Taybi syndromeNaye Choi, Hwa Young Kim, Byung Chan Lim, et al.
Pageof 3