Suchergebnisse - "Seong, Moon Woo"

PubPharm (340)

1

Diagnostic algorithm for neonatal intrahepatic cholestasis integrating single-gene testing and next-generation sequencing in East Asia

enthalten in: Journal of gastroenterology and hepatology | 2024

von Hahn, J. | Lee, H. | Shin, M. | +3

2

In-depth blood proteome profiling analysis revealed distinct functional characteristics of plasma proteins between severe and non-severe COVID-19 patients

enthalten in: bioRxiv.org | 2024

von Park, J. | Kim, H. | Kim, S. | +4

3

Mutations in TMEM43 cause autosomal dominant auditory neuropathy spectrum disorder via interaction with connexin-mediated passive conductance channels

enthalten in: bioRxiv.org | 2024

von Jang, M. | Oh, D. | Yi, E. | +40

4

Poor visual prognosis of Asian patients with 3460 mitochondrial DNA mutation in Leber's hereditary optic neuropathy

enthalten in: Canadian journal of ophthalmology. Journal canadien d'ophtalmologie | 2024

von Yang, H. | Seong, M. | Kim, J. | +2

5

Mitochondrial DNA mutations in Korean patients with Leber's hereditary optic neuropathy

enthalten in: Scientific reports | 2024

von Yang, H. | Seong, M. | Hwang, J.

6

Comparison of Measurable Residual Disease in Pediatric B-Lymphoblastic Leukemia Using Multiparametric Flow Cytometry and Next-Generation Sequencing

enthalten in: Annals of laboratory medicine | 2024

von Hwang, S. | Oh, I. | Kwon, S. | +2

7

Utility of Next-Generation Sequencing-Based Chimerism Analysis for Early Relapse Prediction following Allogenic Hematopoietic Cell Transplantation

enthalten in: International journal of molecular sciences | 2024

von Lee, H. | Chae, S. | Cho, S. | +3

8

Clinical Characteristics of Diabetes in People with Mitochondrial DNA 3243A>G Mutation in Korea

enthalten in: Diabetes & metabolism journal | 2024

von Rho, E. | Baek, S. | Lee, H. | +4

9

Analysis of HTT CAG repeat expansion among healthy individuals and patients with chorea in Korea

enthalten in: Parkinsonism & related disorders | 2024

von Kim, R. | Seong, M. | Oh, B. | +7

10

The First Case of Congenital Nephrogenic Diabetes Insipidus Caused by AVPR2 Disruption Because of 4q25 Insertional Translocation

enthalten in: Annals of laboratory medicine | 2024

von Kim, B. | Ahn, Y. | Park, J. | +6

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