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Refinado por: Base de dados/Biblioteca: MEDLINE Complete remover
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1
Erratum to "Clinical Characteristics and Molecular Genetics Analysis of Korean Patients with GNE myopathy" by Sim JE, et al. (Yonsei Med J 2013;54:578-82.)
Erratum to "Clinical Characteristics and Molecular Genetics Analysis of Korean Patients with GNE myopathy" by Sim JE, et al. (Yonsei Med J 2013;54:578-82.)
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Erratum to "Clinical Characteristics and Molecular Genetics Analysis of Korean Patients with GNE myopathy" by Sim JE, et al. (Yonsei Med J 2013;54:578-82.)

최영철

Yonsei Medical Journal, 2013, 54(6), , pp.1558-1559 [Periódico revisado por pares]

Yonsei University College of Medicine

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2
The Author Reply: Genotypic and Phenotypic Heterogeneity of LGMD1D due to DNAJB6 Mutations
The Author Reply: Genotypic and Phenotypic Heterogeneity of LGMD1D due to DNAJB6 Mutations
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The Author Reply: Genotypic and Phenotypic Heterogeneity of LGMD1D due to DNAJB6 Mutations

김기태 ; 최영철

Yonsei medical journal, 2018-10, p.1010-1011 [Periódico revisado por pares]

연세대학교의과대학

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3
Erratum to “Clinical Characteristics and Molecular Genetics Analysis of Korean Patients with GNE myopathy”by Sim JE, et al. (Yonsei Med J 2013;54:578-82.)
Erratum to “Clinical Characteristics and Molecular Genetics Analysis of Korean Patients with GNE myopathy”by Sim JE, et al. (Yonsei Med J 2013;54:578-82.)
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Erratum to “Clinical Characteristics and Molecular Genetics Analysis of Korean Patients with GNE myopathy”by Sim JE, et al. (Yonsei Med J 2013;54:578-82.)

최영철

Yonsei medical journal, 2013-11, p.1558-1559 [Periódico revisado por pares]

연세대학교의과대학

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4
Two Cases of Facioscapulohumeral Muscular Dystrophy 2 in Korea
Two Cases of Facioscapulohumeral Muscular Dystrophy 2 in Korea
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Two Cases of Facioscapulohumeral Muscular Dystrophy 2 in Korea

이정환 ; 박형준 ; 성문우 ; 박성섭 ; 최영철

Yonsei medical journal, 2021-01, p.95-98 [Periódico revisado por pares]

연세대학교의과대학

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5
Clinical Characteristics of Spinal Muscular Atrophy in Korea Confirmed by Genetic Analysis
Clinical Characteristics of Spinal Muscular Atrophy in Korea Confirmed by Genetic Analysis
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Clinical Characteristics of Spinal Muscular Atrophy in Korea Confirmed by Genetic Analysis

황희원 ; 최영철 ; 이정환

Yonsei medical journal, 2017-09, p.1051-1054 [Periódico revisado por pares]

연세대학교의과대학

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6
Long Noncoding RNA Expression Profiling Reveals Upregulation of Uroplakin 1A and Uroplakin 1A Antisense RNA 1 under Hypoxic Conditions in Lung Cancer Cells
Long Noncoding RNA Expression Profiling Reveals Upregulation of Uroplakin 1A and Uroplakin 1A Antisense RNA 1 under Hypoxic Conditions in Lung Cancer Cells
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Long Noncoding RNA Expression Profiling Reveals Upregulation of Uroplakin 1A and Uroplakin 1A Antisense RNA 1 under Hypoxic Conditions in Lung Cancer Cells

Byun, Yuree ; Choi, Young-Chul ; Jeong, Yongsu ; Yoon, Jaeseung ; Baek, Kwanghee

Molecules and Cells, 2020, 43(12), , pp.975-988 [Periódico revisado por pares]

United States: Korean Society for Molecular and Cellular Biology

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7
Clinical Features and Brain MRI Findings in Korean Patients with AGel Amyloidosis
Clinical Features and Brain MRI Findings in Korean Patients with AGel Amyloidosis
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Clinical Features and Brain MRI Findings in Korean Patients with AGel Amyloidosis

정이내 ; 백우열 ; 최영철 ; 임영민 ; 김현진 ; 심우현 ; 박형준

Yonsei medical journal, 2021-05, p.431-438 [Periódico revisado por pares]

연세대학교의과대학

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8
The Author Reply: Genotypic and Phenotypic Heterogeneity of LGMD1D due to DNAJB6 Mutations
The Author Reply: Genotypic and Phenotypic Heterogeneity of LGMD1D due to DNAJB6 Mutations
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The Author Reply: Genotypic and Phenotypic Heterogeneity of LGMD1D due to DNAJB6 Mutations

Kim, Kitae ; Choi, Young Chul

Yonsei Medical Journal, 2018, 59(8), , pp.1010-1011 [Periódico revisado por pares]

Korea (South): Yonsei University College of Medicine

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9
Cortical Thickness and White Matter Integrity are Associated with CTG Expansion Size in Myotonic Dystrophy Type I
Cortical Thickness and White Matter Integrity are Associated with CTG Expansion Size in Myotonic Dystrophy Type I
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Cortical Thickness and White Matter Integrity are Associated with CTG Expansion Size in Myotonic Dystrophy Type I

유우경 ; 박윤길 ; 최영철 ; 김선미

Yonsei medical journal, 2017-07, p.807-815 [Periódico revisado por pares]

연세대학교의과대학

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10
Homozygous SMN2 deletion is a major risk factor among twenty-five Korean sporadic amyotrophic lateral sclerosis patients
Homozygous SMN2 deletion is a major risk factor among twenty-five Korean sporadic amyotrophic lateral sclerosis patients
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Homozygous SMN2 deletion is a major risk factor among twenty-five Korean sporadic amyotrophic lateral sclerosis patients

Lee, Jun-Beom ; Lee, Kyung-A ; Hong, Ji-Man ; Suh, Gyoung-Im ; Choi, Young-Chul

Yonsei Medical Journal, 2012, 53(1), , pp.53-57 [Periódico revisado por pares]

Korea (South): Yonsei University College of Medicine

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