Maternal 3-methylcrotonyl-coenzyme A carboxylase deficiency with elevated 3-hydroxyisovalerylcarnitine in breast milk
Article Properties
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LanguageEnglish
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DOI (url)
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Publication Date2016/01/01
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Journal
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Indian UGC (journal)
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Refrences9
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Kyung Lae Cho Department of Pediatrics, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea.
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Yeo Jin Kim Department of Pediatrics, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea.
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Song Hyun Yang Green Cross Reference Laboratory, Seoul, Korea.
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Gu-Hwan Kim Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.
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Jun Hwa Lee Department of Pediatrics, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Korea.
Cite
Cho, Kyung Lae, et al. “Maternal 3-Methylcrotonyl-Coenzyme A Carboxylase Deficiency With Elevated 3-Hydroxyisovalerylcarnitine in Breast Milk”. Korean Journal of Pediatrics, vol. 59, no. Suppl 1, 2016, p. S41, https://doi.org/10.3345/kjp.2016.59.11.s41.
Cho, K. L., Kim, Y. J., Yang, S. H., Kim, G.-H., & Lee, J. H. (2016). Maternal 3-methylcrotonyl-coenzyme A carboxylase deficiency with elevated 3-hydroxyisovalerylcarnitine in breast milk. Korean Journal of Pediatrics, 59(Suppl 1), S41. https://doi.org/10.3345/kjp.2016.59.11.s41
Cho KL, Kim YJ, Yang SH, Kim GH, Lee JH. Maternal 3-methylcrotonyl-coenzyme A carboxylase deficiency with elevated 3-hydroxyisovalerylcarnitine in breast milk. Korean Journal of Pediatrics. 2016;59(Suppl 1):S41.
Journal Category
Medicine
Pediatrics
Refrences
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
Nationwide survey of extended newborn screening by tandem mass spectrometry in Taiwan | Journal of Inherited Metabolic Disease |
| 107 | 2010 |
| 10.1016/S0022-3476(98)70032-0 | The Journal of Pediatrics |
| 1998 | |
| Outcome of infants diagnosed with 3-methyl-crotonyl-CoA-carboxylase deficiency by newborn screening | Molecular Genetics and Metabolism |
| 14 | 2012 |
3-methylcrotonyl-CoA carboxylase deficiency: Clinical, biochemical, enzymatic and molecular studies in 88 individuals | Orphanet Journal of Rare Diseases |
| 52 | 2012 |
| Elevated neonatal 3-OH isovalerylcarnitine due to breast milk sources in maternal 3-MCC deficiency | Molecular Genetics and Metabolism |
| 7 | 2010 |
Refrences Analysis
The category
Science: Biology (General): Genetics 10
is the most frequently represented among the references in this article. It primarily includes studies from Molecular Genetics and Metabolism and Journal of Inherited Metabolic Disease. The chart below illustrates the number of referenced publications per year.