Risultati della ricerca - Seong, Moon-Woo

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  1. 1
    Molecular basis and diagnosis of thalassemia

    Molecular basis and diagnosis of thalassemia di Lee, Jee-Soo, Cho, Sung Im, Park, Sung Sup, Seong, Moon-Woo

    Pubblicazione 2021
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  2. 2
    Skewed X-Chromosome Inactivation in a Korean Girl with Severe Mucopolysaccharidosis Type II

    Skewed X-Chromosome Inactivation in a Korean Girl with Severe Mucopolysaccharidosis Type II di Kim, Hwa Young, Kim, Man Jin, Seong, Moon-Woo, Ko, Jung Min

    Pubblicazione 2022
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  3. 3
    Association of Tandem Repeat Number Variabilities in Subunit S of the Type I Restriction-Modification System with Macrolide Resistance in Mycoplasma pneumoniae

    Association of Tandem Repeat Number Variabilities in Subunit S of the Type I Restriction-Modification System with Macrolide Resistance in Mycoplasma pneumoniae di Lee, Joon-Kee, Seong, Moon-Woo, Yun, Ki-Wook, Choi, Eun-Hwa

    Pubblicazione 2022
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  4. 4
    Frequency and clinical implications of the isolation of rare nontuberculous mycobacteria

    Frequency and clinical implications of the isolation of rare nontuberculous mycobacteria di Kim, Junghyun, Seong, Moon-Woo, Kim, Eui-Chong, Han, Sung Koo, Yim, Jae-Joon

    Pubblicazione 2015
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  5. 5
    Genotypic profile and phenotype correlations of ABCA4-associated retinopathy in Koreans

    Genotypic profile and phenotype correlations of ABCA4-associated retinopathy in Koreans di Joo, Kwangsic, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon

    Pubblicazione 2019
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  6. 6
    Neonatal invasive Streptococcus gallolyticus subsp. pasteurianus infection with delayed central nervous system complications

    Neonatal invasive Streptococcus gallolyticus subsp. pasteurianus infection with delayed central nervous system complications di Park, Jung-Weon, Eun, So-Hee, Kim, Eui-Chong, Seong, Moon-Woo, Kim, Yun-Kyung

    Pubblicazione 2015
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  7. 7
    Retinitis Pigmentosa Associated with Bardet-Biedl Syndrome with BBS9 Gene Mutation in a Korean Patient

    Retinitis Pigmentosa Associated with Bardet-Biedl Syndrome with BBS9 Gene Mutation in a Korean Patient di Kim, Yong Hoon, Joo, Kwang Sic, Seong, Moon-Woo, Park, Sung Sup, Woo, Se Joon

    Pubblicazione 2020
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  8. 8
    Two Cases of Facioscapulohumeral Muscular Dystrophy 2 in Korea

    Two Cases of Facioscapulohumeral Muscular Dystrophy 2 in Korea di Lee, Jung Hwan, Park, Hyung Jun, Seong, Moon-Woo, Park, Sung Sup, Choi, Young-Chul

    Pubblicazione 2021
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  9. 9
    Genetic mutation spectrum of pantothenate kinase-associated neurodegeneration expanded by breakpoint sequencing in pantothenate kinase 2 gene

    Genetic mutation spectrum of pantothenate kinase-associated neurodegeneration expanded by breakpoint sequencing in pantothenate kinase 2 gene di Yang, Dahae, Cho, Sanghyun, Cho, Sung Im, Kim, Manjin, Seong, Moon-Woo, Park, Sung Sup

    Pubblicazione 2022
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  10. 10
    The First Study on Nucleotide-level Identification of Hb Koriyama in a Patient with Severe Hemolytic Anemia

    The First Study on Nucleotide-level Identification of Hb Koriyama in a Patient with Severe Hemolytic Anemia di Park, Seungman, Park, Jun Eun, Cho, Sung Im, Jeon, Yongbum, Park, Sung Sup, Seong, Moon-Woo

    Pubblicazione 2012
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  11. 11
    The First Korean Case of Lysinuric Protein Intolerance: Presented with Short Stature and Increased Somnolence

    The First Korean Case of Lysinuric Protein Intolerance: Presented with Short Stature and Increased Somnolence di Ko, Jung Min, Shin, Choong Ho, Yang, Sei Won, Seong, Moon Woo, Park, Sung Sup, Song, Junghan

    Pubblicazione 2012
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  12. 12
    Comparison of 3 Automated Immunoassays for Detection of Anti-Hepatitis A Virus Immunoglobulin M in a Tertiary Care Hospital

    Comparison of 3 Automated Immunoassays for Detection of Anti-Hepatitis A Virus Immunoglobulin M in a Tertiary Care Hospital di Park, Hyewon, Lee, Yu-joo, Seong, Moon-Woo, Lee, Do-Hoon, Park, Myoung Hee, Song, Eun Young

    Pubblicazione 2013
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  13. 13
    Analytical and Clinical Validation of Six Commercial Middle East Respiratory Syndrome Coronavirus RNA Detection Kits Based on Real-Time Reverse-Transcription PCR

    Analytical and Clinical Validation of Six Commercial Middle East Respiratory Syndrome Coronavirus RNA Detection Kits Based on Real-Time Reverse-Transcription PCR di Kim, Mi-Na, Ko, Young Jin, Seong, Moon-Woo, Kim, Jae-Seok, Shin, Bo-Moon, Sung, Heungsup

    Pubblicazione 2016
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  14. 14
    Cardiomyopathies with Mixed and Inapparent Morphological Features in Cardiac Troponin I3 Mutation

    Cardiomyopathies with Mixed and Inapparent Morphological Features in Cardiac Troponin I3 Mutation di Sohn, Dae-Won, Kim, Hyung-Kwan, Kim, Yong-Jin, Oh, Seil, Seong, Moon-Woo, Park, Sung-Sup

    Pubblicazione 2017
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  15. 15
    Erratum: Cardiomyopathies with Mixed and Inapparent Morphological Features in Cardiac Troponin I3 Mutation

    Erratum: Cardiomyopathies with Mixed and Inapparent Morphological Features in Cardiac Troponin I3 Mutation di Sohn, Dae-Won, Kim, Hyung-Kwan, Kim, Yong-Jin, Oh, Seil, Seong, Moon-Woo, Park, Sung-Sup

    Pubblicazione 2017
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  16. 16
    Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient

    Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient di Lee, Yun Jeong, Joo, Kwangsic, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon

    Pubblicazione 2020
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  17. 17
    Molecular characterization of Leber congenital amaurosis in Koreans

    Molecular characterization of Leber congenital amaurosis in Koreans di Seong, Moon-Woo, Kim, Seong Yeon, Yu, Young Suk, Hwang, Jeong-Min, Kim, Ji Yeon, Park, Sung Sup

    Pubblicazione 2008
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  18. 18
    A Novel Mutation of the TAZ Gene in Barth Syndrome: Acute Exacerbation after Contrast-Dye Injection

    A Novel Mutation of the TAZ Gene in Barth Syndrome: Acute Exacerbation after Contrast-Dye Injection di Kim, Gi Beom, Kwon, Bo Sang, Bae, Eun Jung, Noh, Chung Il, Seong, Moon-Woo, Park, Sung Sup

    Pubblicazione 2013
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  19. 19
    Hereditary Spastic Paraplegia with a Novel SPAST Mutation Misdiagnosed with Subacute Combined Degeneration

    Hereditary Spastic Paraplegia with a Novel SPAST Mutation Misdiagnosed with Subacute Combined Degeneration di Yang, Ji Won, Han, Ji-Young, Seong, Moon-Woo, Sung, Jung-Joon, Park, Sung Sup, Lee, Kwang-Woo

    Pubblicazione 2013
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  20. 20
    Characteristics of hereditary nonpolyposis colorectal cancer patients with double primary cancers in endometrium and colorectum

    Characteristics of hereditary nonpolyposis colorectal cancer patients with double primary cancers in endometrium and colorectum di Shin, So Hyun, Yu, Eun Jeong, Lee, Yoo-Kyung, Song, Yong-Sang, Seong, Moon-Woo, Park, Sung Sup

    Pubblicazione 2015
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