Yoon-Myung Kim
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Explore the profile of Yoon-Myung Kim including associated specialties, affiliations and a list of published articles.
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Articles
28
Citations
201
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Recent Articles
1.
Kim Y, Lee Y, Choi Y, Choi I, Heo S, Choi J, et al.
BMC Med Genomics
. 2022 Sep;
15(1):206.
PMID: 36175890
Background: The genetic features and treatment strategies of lateralized overgrowth have been elusive. We performed this study to analyze the genetic characteristics and treatment results of propranolol- or alpelisib-treated patients...
2.
Choi I, Seo G, Park J, Kim Y, Cheon C, Kim Y, et al.
Medicine (Baltimore)
. 2022 Jul;
101(28):e29424.
PMID: 35838999
The artificial intelligence (AI)-based genetic diagnostic program has been applied to genome sequencing to facilitate the diagnostic process. The objective of the current study was to evaluate the experience and...
3.
Son J, Seo G, Kim Y, Kim G, Jin H, Bae J, et al.
Medicine (Baltimore)
. 2022 Feb;
101(5):e28793.
PMID: 35119049
Pearson syndrome (PS) is a multisystem mitochondrial cytopathy arising from deletions in mitochondrial DNA. Pearson syndrome is a sporadic disease that affects the hematopoietic system, pancreas, eyes, liver, and heart...
4.
Kang E, Kim Y, Choi Y, Lee Y, Kim J, Choi I, et al.
Orphanet J Rare Dis
. 2022 Jan;
17(1):24.
PMID: 35093157
Background: Neurofibromatosis type 1 (NF1) is a common human genetic disease with age-dependent phenotype progression. The overview of clinical and radiological findings evaluated by whole-body magnetic resonance imaging (WBMRI) in...
5.
Woo S, Ju Y, Seo Y, Kim Y, Lim H, Park K
Nutrients
. 2022 Jan;
14(2).
PMID: 35057568
This study compared the effects of a real-world multidisciplinary intervention with additional exercise or nutritional elements and investigated the effectiveness of a booster intervention after weight regain. A total of...
6.
Park J, Woo S, Ju Y, Seo Y, Lim H, Kim Y, et al.
Obes Res Clin Pract
. 2020 Oct;
14(6):566-572.
PMID: 33004301
Background: Significant dropout rates remain a serious concern in pediatric weight control program, but few studies have identified predictors of dropout. Aims: The objective of the study is to identify...
7.
Kang E, Kim Y, Seo G, Oh A, Yoon H, Ra Y, et al.
J Hum Genet
. 2019 Nov;
65(2):79-89.
PMID: 31776437
Neurofibromatosis type 1 (NF1) is caused by heterozygous mutation in the NF1 gene. NF1 is one of the most common human genetic diseases. However, the overall genotype-phenotype correlation has not...
8.
Kim Y, Yum M, Heo S, Kim T, Jin H, Bae J, et al.
J Med Genet
. 2019 Oct;
57(2):124-131.
PMID: 31649052
Background: Ambroxol (ABX) has been suggested as an augmentative pharmacological agent for neuronopathic Gaucher disease (nGD). This study assessed the long-term safety and efficacy of combined therapy with high-dose ABX...
9.
Lee H, Jeong W, Choi Y, Seo Y, Noh H, Song H, et al.
Korean J Fam Med
. 2018 Nov;
40(3):159-164.
PMID: 30466203
Background: This study aimed to investigate the association between physical fitness and cardiometabolic health of Korean children and adolescents. Methods: In total, 168 participants (89 boys and 79 girls) aged...
10.
Kim D, Ko J, Kim Y, Seo G, Kim G, Lee B, et al.
J Hum Genet
. 2018 May;
63(8):911-917.
PMID: 29773863
Argininosuccinic aciduria (ASA), which is considered to be the second most common urea cycle disorder (UCD), is caused by an argininosuccinate lyase deficiency and is biochemically characterized by elevation of...