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Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A.
Wang ZQ, Chen XJ, Murong SX, Wang N, Wu ZY. Wang ZQ, et al. J Mol Med (Berl). 2011 Jun;89(6):569-76. doi: 10.1007/s00109-011-0725-7. Epub 2011 Feb 24. J Mol Med (Berl). 2011. PMID: 21347544
Rhabdomyolysis and respiratory insufficiency due to the common ETFDH mutation of c.250G>A in two patients with late-onset multiple acyl-CoA dehydrogenase deficiency.
Chen HZ, Jin M, Cai NQ, Lin XD, Liu XY, Xu LQ, Lin MT, Lin F, Wang N, Wang ZQ, Xu GR. Chen HZ, et al. Chin Med J (Engl). 2019 Jul 5;132(13):1615-1618. doi: 10.1097/CM9.0000000000000288. Chin Med J (Engl). 2019. PMID: 31058673 Free PMC article.
Limb-girdle muscular dystrophy type 2I: two Chinese families and a review in Asian patients.
Wang DN, Wang ZQ, Chen YQ, Xu GR, Lin MT, Wang N. Wang DN, et al. Int J Neurosci. 2018 Mar;128(3):199-207. doi: 10.1080/00207454.2017.1380640. Epub 2017 Oct 2. Int J Neurosci. 2018. PMID: 28931339 Review.
Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.
Fu HX, Liu XY, Wang ZQ, Jin M, Wang DN, He JJ, Lin MT, Wang N. Fu HX, et al. Neurol Sci. 2016 Jul;37(7):1099-105. doi: 10.1007/s10072-016-2549-2. Epub 2016 Mar 21. Neurol Sci. 2016. PMID: 27000805
Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations.
Liu XY, Jin M, Wang ZQ, Wang DN, He JJ, Lin MT, Fu HX, Wang N. Liu XY, et al. Chin Med J (Engl). 2016 Jun 20;129(12):1425-31. doi: 10.4103/0366-6999.183423. Chin Med J (Engl). 2016. PMID: 27270537 Free PMC article.
A Historical Cohort Study on the Efficacy of Glucocorticoids and Riboflavin Among Patients with Late-onset Multiple Acyl-CoA Dehydrogenase Deficiency.
Liu XY, Wang ZQ, Wang DN, Lin MT, Wang N. Liu XY, et al. Chin Med J (Engl). 2016 Jan 20;129(2):142-6. doi: 10.4103/0366-6999.173438. Chin Med J (Engl). 2016. PMID: 26830983 Free PMC article.
Value of muscle enzyme measurement in evaluating different neuromuscular diseases.
Zhang Y, Huang JJ, Wang ZQ, Wang N, Wu ZY. Zhang Y, et al. Clin Chim Acta. 2012 Feb 18;413(3-4):520-4. doi: 10.1016/j.cca.2011.11.016. Epub 2011 Nov 25. Clin Chim Acta. 2012. PMID: 22137979
New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 Patients.
Lin F, Wang ZQ, Lin MT, Murong SX, Wang N. Lin F, et al. Chin Med J (Engl). 2015 Jul 5;128(13):1707-13. doi: 10.4103/0366-6999.159336. Chin Med J (Engl). 2015. PMID: 26112708 Free PMC article.
Nanog inhibits lipopolysaccharide-induced expression of pro-inflammatory cytokines by blocking NF-κB transcriptional activity in rat primary microglial cells.
Zhou H, Chen S, Wang W, Wang Z, Wu X, Zhang Z. Zhou H, et al. Mol Med Rep. 2012 Mar;5(3):842-6. doi: 10.3892/mmr.2011.719. Epub 2011 Dec 19. Mol Med Rep. 2012. PMID: 22200792
[Characteristics of gene structure in facioscapulohumeral muscular dystrophy-related 4q35 subtelomere and genotype-phenotype correlation in Chinese Han population].
Wang ZQ, Wu ZY, Wang N, Lin MT, Murong SX. Wang ZQ, et al. Zhonghua Yi Xue Za Zhi. 2009 Feb 10;89(5):304-9. Zhonghua Yi Xue Za Zhi. 2009. PMID: 19563705 Chinese.
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