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Year | Number of Results |
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2019 | 3 |
2020 | 2 |
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Page 1
Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegia.
Clin Genet. 2019 May;95(5):637-639. doi: 10.1111/cge.13517. Epub 2019 Feb 19.
Clin Genet. 2019.
PMID: 30780198
Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy.
Luo WJ, Wei Q, Dong HL, Yan YT, Chen MJ, Li HF.
Luo WJ, et al. Among authors: chen mj.
Mol Genet Genomic Med. 2020 Jan;8(1):e1065. doi: 10.1002/mgg3.1065. Epub 2019 Nov 27.
Mol Genet Genomic Med. 2020.
PMID: 31777199
Free PMC article.
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Identified novel heterozygous HTRA1 pathogenic variants in Chinese patients with HTRA1-associated dominant cerebral small vessel disease.
Chen MJ, Zhang Y, Luo WJ, Dong HL, Wei Q, Zhang J, Ruan QQ, Ni W, Li HF.
Chen MJ, et al.
Front Genet. 2022 Aug 10;13:909131. doi: 10.3389/fgene.2022.909131. eCollection 2022.
Front Genet. 2022.
PMID: 36035189
Free PMC article.
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Trigeminal Autonomic Cephalalgias Manifested As The Only Initial Symptom Of Ehlers-Danlos Syndrome Type IV.
Chen MJ, Li HF, Mao S.
Chen MJ, et al.
J Pain Res. 2019 Nov 27;12:3215-3220. doi: 10.2147/JPR.S218580. eCollection 2019.
J Pain Res. 2019.
PMID: 31819605
Free PMC article.
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Common genetic variants in PRRC2A are associated with both neuromyelitis optica spectrum disorder and multiple sclerosis in Han Chinese population.
Zhang J, Chen MJ, Zhao GX, Li HF, Wu L, Xu YF, Liao Y, Yuan Z, Wu ZY.
Zhang J, et al. Among authors: chen mj.
J Neurol. 2021 Feb;268(2):506-515. doi: 10.1007/s00415-020-10184-z. Epub 2020 Aug 29.
J Neurol. 2021.
PMID: 32862241
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