Suchergebnisse - "Seong, Moon-Woo"

PubPharm (339)

61

Association of Tandem Repeat Number Variabilities in Subunit S of the Type I Restriction-Modification System with Macrolide Resistance in Mycoplasma pneumoniae

enthalten in: Journal of clinical medicine | 2022

von Lee, J. | Seong, M. | Yun, K. | +1

62

Characteristics of germline mutations in Korean patients with pheochromocytoma/paraganglioma

enthalten in: Journal of medical genetics | 2022

von Kim, J. | Kim, M. | Kong, S. | +6

63

Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader-Willi Syndrome and Angelman Syndrome

enthalten in: Annals of laboratory medicine | 2022

von Kim, B. | Park, Y. | Cho, S. | +5

64

Rates of Coinfection Between SARS-CoV-2 and Other Respiratory Viruses in Korea

enthalten in: Annals of laboratory medicine | 2022

von Kim, Y. | Park, H. | Kim, S. | +5

65

Clinical and Molecular Characteristics of PRKACA L206R Mutant Cortisol-Producing Adenomas in Korean Patients

enthalten in: Endocrinology and metabolism (Seoul, Korea) | 2021

von Jang, I. | Kim, S. | Song, R. | +7

66

Evidence of Severe Acute Respiratory Syndrome Coronavirus 2 Reinfection After Recovery from Mild Coronavirus Disease 2019

enthalten in: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America | 2021

von Lee, J. | Kim, S. | Kim, T. | +18

CommentIn: Clin Infect Dis. 2021 Nov 2;73(9):e3009-e3012. - PMID 33035308

67

Determination of Clinical Characteristics of Mycobacterium kansasii-Derived Species by Reanalysis of Isolates Formerly Reported as M. kansasii

enthalten in: Annals of laboratory medicine | 2021

von Kim, Y. | Lee, H. | Kwak, N. | +7

68

Early-onset autosomal dominant GTP-cyclohydrolase I deficiency : Diagnostic delay and residual motor signs

enthalten in: Brain & development | 2021

von Kim, W. | Cho, J. | Shim, Y. | +11

69

Accuracy and Performance Evaluation of Triplet Repeat Primed PCR as an Alternative to Conventional Diagnostic Methods for Fragile X Syndrome

enthalten in: Annals of laboratory medicine | 2021

von Gu, H. | Kim, M. | Yang, D. | +4

70

SLC20A2 mutation manifesting as very late-onset orofacial dyskinesia

enthalten in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2021

von Woo, K. | Yoo, D. | Lee, J. | +4