Suchergebnisse - "Seong, Moon-Woo"

PubPharm (339)

101

COVID-19 Molecular Testing in Korea : Practical Essentials and Answers From Experts Based on Experiences of Emergency Use Authorization Assays

enthalten in: Annals of laboratory medicine | 2020

von Sung, H. | Roh, K. | Hong, K. | +11

ErratumIn: Ann Lab Med. 2021 Jan;41(1):126-127 Yoo, Sookwon [corrected to Ryu, Sook Won]. - PMID 32829590

102

No association between POU4F1, POU4F2, ISL1 polymorphisms and normal-tension glaucoma

enthalten in: Ophthalmic genetics | 2020

von Lee, J. | Jeoung, J. | Oh, S. | +6

103

Viral RNA Load in Mildly Symptomatic and Asymptomatic Children with COVID-19, Seoul, South Korea

enthalten in: Emerging infectious diseases | 2020

von Han, M. | Seong, M. | Kim, N. | +6

104

Novel compound heterozygous ACO2 mutations in an infant with progressive encephalopathy : A newly identified neurometabolic syndrome

enthalten in: Brain & development | 2020

von Park, J. | Kim, M. | Kim, S. | +5

105

Nationwide External Quality Assessment of SARS-CoV-2 Molecular Testing, South Korea

enthalten in: Emerging infectious diseases | 2020

von Sung, H. | Han, M. | Yoo, C. | +12

106

Lentigo maligna in a patient with xeroderma pigmentosum, variant type : A case report with dermoscopic findings and review of the literature

enthalten in: Photodermatology, photoimmunology & photomedicine | 2020

von Bang, E. | Kim, Y. | Ko, J. | +4

107

Guidelines for Laboratory Diagnosis of Coronavirus Disease 2019 (COVID-19) in Korea

enthalten in: Annals of laboratory medicine | 2020

von Hong, K. | Lee, S. | Kim, T. | +15

108

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 | 2020

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

109

Detailed analysis of phenotypes and genotypes in megalencephaly-capillary malformation-polymicrogyria syndrome caused by somatic mosaicism of PIK3CA mutations

enthalten in: Orphanet journal of rare diseases | 2020

von Park, H. | Shin, C. | Yoo, W. | +7

110

Detailed analysis of phenotypes and genotypes in megalencephaly-capillary malformation-polymicrogyria syndrome caused by somatic mosaicism of PIK3CA mutations

enthalten in: Orphanet journal of rare diseases | 2020

von Park, H. | Shin, C. | Yoo, W. | +7