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Items: 1 to 20 of 42


Drug price, dosage and safety: Real-world evidence of oral hypoglycemic agents.

Lin YS, Lin MT, Cheng SH.

Health Policy. 2019 Aug 20. pii: S0168-8510(19)30189-7. doi: 10.1016/j.healthpol.2019.08.005. [Epub ahead of print]


The influence of initial symptoms on phenotypes in spinocerebellar ataxia type 3.

Xu HL, Su QN, Shang XJ, Sikandar A, Lin MT, Wang N, Lin H, Gan SR.

Mol Genet Genomic Med. 2019 Jul;7(7):e00719. doi: 10.1002/mgg3.719. Epub 2019 May 23.


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.

Chin Med J (Engl). 2019 Jul 5;132(13):1615-1618. doi: 10.1097/CM9.0000000000000288. No abstract available.


A "Triple Trouble" Case of Facioscapulohumeral Muscular Dystrophy Accompanied by Peripheral Neuropathy and Myoclonic Epilepsy.

Lin XD, He JJ, Lin F, Chen HZ, Xu LQ, Hu W, Cai NQ, Lin MT, Wang N, Wang ZQ, Xu GR.

Chin Med J (Engl). 2018 Sep 20;131(18):2164-2171. doi: 10.4103/0366-6999.240797.


Homozygote of spinocerebellar Ataxia type 3 correlating with severe phenotype based on analyses of clinical features.

Shang XJ, Xu HL, Yang JS, Chen PP, Lin MT, Qian MZ, Lin HX, Chen XP, Chen YC, Jiang B, Chen YJ, Chen WJ, Wang N, Zhou ZM, Gan SR.

J Neurol Sci. 2018 Jul 15;390:111-114. doi: 10.1016/j.jns.2018.04.026. Epub 2018 Apr 18.


Bidirectional Connections between Depression and Ataxia Severity in Spinocerebellar Ataxia Type 3 Patients.

Lin MT, Yang JS, Chen PP, Qian MZ, Lin HX, Chen XP, Shang XJ, Wang DN, Chen YC, Jiang B, Chen YJ, Chen WJ, Wang N, Gan SR.

Eur Neurol. 2018;79(5-6):266-271. doi: 10.1159/000489398. Epub 2018 May 15.


High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis.

Xu GR, Hu W, Zhan LL, Wang C, Xu LQ, Lin MT, Chen WJ, Wang N, Zhang QJ.

BMC Neurol. 2018 Apr 5;18(1):35. doi: 10.1186/s12883-018-1028-1.


Association Between Body Mass Index and Disease Severity in Chinese Spinocerebellar Ataxia Type 3 Patients.

Yang JS, Chen PP, Lin MT, Qian MZ, Lin HX, Chen XP, Shang XJ, Wang DN, Chen YC, Jiang B, Chen YJ, Wang N, Chen WJ, Gan SR.

Cerebellum. 2018 Aug;17(4):494-498. doi: 10.1007/s12311-018-0929-2.


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.

Int J Neurosci. 2018 Mar;128(3):199-207. doi: 10.1080/00207454.2017.1380640. Epub 2017 Oct 2. Review.


Clinical and mutational characteristics of Duchenne muscular dystrophy patients based on a comprehensive database in South China.

Wang DN, Wang ZQ, Yan L, He J, Lin MT, Chen WJ, Wang N.

Neuromuscul Disord. 2017 Aug;27(8):715-722. doi: 10.1016/j.nmd.2017.02.010. Epub 2017 Feb 21.


[Metabolites Identification for Alkaloids from Nelumbinis Plumula in Caco-2 Cells by LC/MS/MS].

Lin MT, Zhang C, Tang SL, Zhao ZZ, Chen HB, Zhang JY.

Zhong Yao Cai. 2015 Dec;38(12):2531-4. Chinese.


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.

Chin Med J (Engl). 2016 Jun 20;129(12):1425-31. doi: 10.4103/0366-6999.183423.


Bruceine D induces apoptosis in human chronic myeloid leukemia K562 cells via mitochondrial pathway.

Zhang JY, Lin MT, Tung HY, Tang SL, Yi T, Zhang YZ, Tang YN, Zhao ZZ, Chen HB.

Am J Cancer Res. 2016 Mar 15;6(4):819-26. eCollection 2016.


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.

Neurol Sci. 2016 Jul;37(7):1099-105. doi: 10.1007/s10072-016-2549-2. Epub 2016 Mar 21.


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.

Chin Med J (Engl). 2016 Jan 20;129(2):142-6. doi: 10.4103/0366-6999.173438.


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.

Chin Med J (Engl). 2015 Jul 5;128(13):1707-13. doi: 10.4103/0366-6999.159336.


Combinational Treatment of Curcumin and Quercetin against Gastric Cancer MGC-803 Cells in Vitro.

Zhang JY, Lin MT, Zhou MJ, Yi T, Tang YN, Tang SL, Yang ZJ, Zhao ZZ, Chen HB.

Molecules. 2015 Jun 22;20(6):11524-34. doi: 10.3390/molecules200611524.


Anticancer activity and mechanism investigation of beauvericin isolated from secondary metabolites of the mangrove endophytic fungi.

Tao YW, Lin YC, She ZG, Lin MT, Chen PX, Zhang JY.

Anticancer Agents Med Chem. 2015;15(2):258-66.


Growth hormone deficiency in a dopa-responsive dystonia patient with a novel mutation of guanosine triphosphate cyclohydrolase 1 gene.

Lin Y, Wang DN, Chen WJ, Lin X, Lin MT, Wang N.

J Child Neurol. 2015 May;30(6):796-9. doi: 10.1177/0883073814538498. Epub 2014 Jun 17.


Apoptosis sensitization by Euphorbia factor L1 in ABCB1-mediated multidrug resistant K562/ADR cells.

Zhang JY, Lin MT, Yi T, Tang YN, Fan LL, He XC, Zhao ZZ, Chen HB.

Molecules. 2013 Oct 16;18(10):12793-808. doi: 10.3390/molecules181012793.

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