Similar articles for PMID: 31033143

Year	Number of Results
1993	1
1998	1
2003	1
2004	3
2005	5
2006	5
2007	3
2008	9
2009	9
2010	11
2011	6
2012	15
2013	8
2014	11
2015	13
2016	12
2017	7
2018	4
2019	18
2020	9
2021	19
2022	11
2023	6
2024	1

1

Medium-chain acyl-coenzyme A dehydrogenase deficiency: Six cases in the Chinese population.

Li Y, Zhu R, Liu Y, Song J, Xu J, Yang Y. Li Y, et al. Pediatr Int. 2019 Jun;61(6):551-557. doi: 10.1111/ped.13872. Epub 2019 Jun 14. Pediatr Int. 2019. PMID: 31033143

2

Analysis of gene mutations of medium-chain acyl-coenzyme a dehydrogenase deficiency (MCADD) by next-generation sequencing in Henan, China.

Tian Y, Zhu X, Lv S, Jia C, Zhang L, Ni M, Xu Y, Peng R, Liu S, Zhao D. Tian Y, et al. Clin Chim Acta. 2022 Nov 1;536:155-161. doi: 10.1016/j.cca.2022.09.008. Epub 2022 Sep 9. Clin Chim Acta. 2022. PMID: 36096209

3

Medium-chain acyl-CoA dehydrogenase deficiency in Saudi Arabia: incidence, genotype, and preventive implications.

Al-Hassnan ZN, Imtiaz F, Al-Amoudi M, Rahbeeni Z, Al-Sayed M, Al-Owain M, Al-Zaidan H, Al-Odaib A, Rashed MS. Al-Hassnan ZN, et al. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S263-7. doi: 10.1007/s10545-010-9143-1. Epub 2010 Jun 22. J Inherit Metab Dis. 2010. PMID: 20567907

4

Newborn screening and genetic variation of medium chain acyl-CoA dehydrogenase deficiency in the Chinese population.

Li YY, Xu J, Sun XC, Li HY, Mu K. Li YY, et al. J Pediatr Endocrinol Metab. 2022 Sep 8;35(10):1264-1271. doi: 10.1515/jpem-2022-0394. Print 2022 Oct 26. J Pediatr Endocrinol Metab. 2022. PMID: 36068006

5

First case report of medium-chain acyl-coenzyme A dehydrogenase deficiency in China.

Liang C, Jiang M, Sheng H, Cai Y, Wu D, Yin X, Peng M, Liu L. Liang C, et al. J Pediatr Endocrinol Metab. 2015 May;28(5-6):681-4. doi: 10.1515/jpem-2014-0058. J Pediatr Endocrinol Metab. 2015. PMID: 25503862

6

Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening.

Yusupov R, Finegold DN, Naylor EW, Sahai I, Waisbren S, Levy HL. Yusupov R, et al. Mol Genet Metab. 2010 Sep;101(1):33-9. doi: 10.1016/j.ymgme.2010.05.007. Epub 2010 Jun 9. Mol Genet Metab. 2010. PMID: 20580581

7

Clinical, biochemical and genetic analyses in two Korean patients with medium-chain acyl-CoA dehydrogenase deficiency.

Woo HI, Park HD, Lee YW, Lee DH, Ki CS, Lee SY, Kim JW. Woo HI, et al. Korean J Lab Med. 2011 Jan;31(1):54-60. doi: 10.3343/kjlm.2011.31.1.54. Korean J Lab Med. 2011. PMID: 21239873 Free PMC article.

8

Screening and follow-up results of neonate medium-chain acyl-CoA dehydrogenase deficiency in Zibo, Shandong province.

Dong L, Ji C, Xu J, Cui Y. Dong L, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2022 Jun 25;51(3):284-289. doi: 10.3724/zdxbyxb-2022-0114. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2022. PMID: 36207830 Free PMC article. English.

9

221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative.

Bentler K, Zhai S, Elsbecker SA, Arnold GL, Burton BK, Vockley J, Cameron CA, Hiner SJ, Edick MJ, Berry SA; Inborn Errors of Metabolism Collaborative. Bentler K, et al. Mol Genet Metab. 2016 Sep;119(1-2):75-82. doi: 10.1016/j.ymgme.2016.07.002. Epub 2016 Jul 15. Mol Genet Metab. 2016. PMID: 27477829 Free PMC article.

10

Medium-chain acyl-CoA dehydrogenase deficiency: Two novel ACADM mutations identified in a retrospective screening.

Smon A, Groselj U, Debeljak M, Zerjav Tansek M, Bertok S, Avbelj Stefanija M, Trebusak Podkrajsek K, Battelino T, Repic Lampret B. Smon A, et al. J Int Med Res. 2018 Apr;46(4):1339-1348. doi: 10.1177/0300060517734123. Epub 2018 Jan 19. J Int Med Res. 2018. PMID: 29350094 Free PMC article.

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