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weihai ling
(28 results)?
A De Novo SEMA6B Variant in a Chinese Patient with Progressive Myoclonic Epilepsy-11 and Review of the Literature.
J Mol Neurosci. 2021 Sep;71(9):1944-1950. doi: 10.1007/s12031-021-01880-0. Epub 2021 Jul 4.
J Mol Neurosci. 2021.
PMID: 34218423
Review.
Treating GNAO1 mutation-related severe movement disorders with oxcarbazepine: a case report.
Ling W, Huang D, Yang F, Yang Z, Liu M, Zhu Q, Huang J, Zhou R, Chen X.
Ling W, et al.
Transl Pediatr. 2022 Sep;11(9):1577-1587. doi: 10.21037/tp-22-297.
Transl Pediatr. 2022.
PMID: 36247896
Free PMC article.
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De novo ATP1A2 variants in two Chinese children with alternating hemiplegia of childhood upgraded the gene-disease relationship and variant classification: a case report.
Huang D, Liu M, Wang H, Zhang B, Zhao D, Ling W, Wang M, Feng J, Shen Y, Chen X.
Huang D, et al. Among authors: ling w.
BMC Med Genomics. 2021 Apr 1;14(1):95. doi: 10.1186/s12920-021-00947-6.
BMC Med Genomics. 2021.
PMID: 33794876
Free PMC article.
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Optic neuritis associated with anti-NMDA receptor antibody in the remission phase of anti-NMDA receptor encephalitis.
Liu X, Giri M, Ling W, Li T.
Liu X, et al. Among authors: ling w.
Neurol India. 2020 Mar-Apr;68(2):474-477. doi: 10.4103/0028-3886.283754.
Neurol India. 2020.
PMID: 32415028
Free article.
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