Chu X - Search Results

1

First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-Sarcoglycanopathy.

Xie Z, Sun C, Liu C, Chu X, Gang Q, Yu M, Zheng Y, Meng L, Li F, Xia D, Wang L, Li Y, Deng J, Lv H, Wang Z, Zhang W, Yuan Y. Xie Z, et al. Among authors: chu x. Front Pediatr. 2022 Jun 22;10:900280. doi: 10.3389/fped.2022.900280. eCollection 2022. Front Pediatr. 2022. PMID: 35813381 Free PMC article.

2

Peripheral Nervous System Involvement in Late-Onset Cobalamin C Disease?

Chu X, Meng L, Zhang W, Luo J, Wang Z, Yuan Y. Chu X, et al. Front Neurol. 2020 Nov 26;11:594905. doi: 10.3389/fneur.2020.594905. eCollection 2020. Front Neurol. 2020. PMID: 33324334 Free PMC article.

3

Vagus nerve ultrasound in transthyretin familial amyloid polyneuropathy: A pilot study.

Du K, Xu K, Chu X, Tang Y, Lv H, Zhang W, Wang Z, Yuan Y, Meng L. Du K, et al. Among authors: chu x. J Neuroimaging. 2022 Mar;32(2):285-291. doi: 10.1111/jon.12956. Epub 2021 Dec 29. J Neuroimaging. 2022. PMID: 34964197 Free PMC article.

4

TTR Gly83Arg Mutation: Beyond Familial Vitreous Amyloidosis.

Li Z, Du K, Chu X, Lv H, Zhang W, Wang Z, Yuan Y, Meng L. Li Z, et al. Among authors: chu x. Front Neurol. 2022 Feb 3;12:821003. doi: 10.3389/fneur.2021.821003. eCollection 2021. Front Neurol. 2022. PMID: 35185758 Free PMC article.

5

Skeletal Muscle Involvement Pattern of Hereditary Transthyretin Amyloidosis: A Study Based on Muscle MRI.

Chu X, Du K, Tang Y, Zhao X, Yu M, Zheng Y, Deng J, Lv H, Zhang W, Wang Z, Yuan Y, Meng L. Chu X, et al. Front Neurol. 2022 May 2;13:851190. doi: 10.3389/fneur.2022.851190. eCollection 2022. Front Neurol. 2022. PMID: 35592471 Free PMC article.

6

Patterns of myelinated nerve fibers loss in transthyretin amyloid polyneuropathy and mimics.

Du K, Chu X, Tang Y, Zhao X, Yu M, Zheng Y, Deng J, Lv H, Zhang W, Wang Z, Yuan Y, Meng L. Du K, et al. Among authors: chu x. Ann Clin Transl Neurol. 2022 Jul;9(7):1059-1068. doi: 10.1002/acn3.51599. Epub 2022 Jun 4. Ann Clin Transl Neurol. 2022. PMID: 35665499 Free PMC article.

7

Clinical and biochemical characterization of hereditary transthyretin amyloidosis caused by E61K mutation.

Chu X, Wang M, Tang R, Huang Y, Yu J, Cao Y, Zheng Y, Xie Z, Deng J, Wang Z, Ma W, Song W, Wu Y, Lv H, Zhang W, Wang Z, Yuan Y, Liu Y, Meng L. Chu X, et al. Front Mol Neurosci. 2022 Oct 12;15:1003303. doi: 10.3389/fnmol.2022.1003303. eCollection 2022. Front Mol Neurosci. 2022. PMID: 36311011 Free PMC article.

8

Novel mutations in FLVCR1 cause tremors, sensory neuropathy with retinitis pigmentosa.

Li Z, Li Y, Chu X, Du K, Tang Y, Xie Z, Yu M, Deng J, Lv H, Zhang W, Wang Z, Meng L, Yuan Y. Li Z, et al. Among authors: chu x. Neuropathology. 2024 Apr;44(2):87-95. doi: 10.1111/neup.12936. Epub 2023 Jul 19. Neuropathology. 2024. PMID: 37469134

9

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria.

Chu X, Yan H, Yu M. Chu X, et al. JAMA Neurol. 2024 Jan 1;81(1):81-82. doi: 10.1001/jamaneurol.2023.4387. JAMA Neurol. 2024. PMID: 37983040

10

Novel mutation of SMPX-related scapuloperoneal myopathy and myofibrillar myopathy.

Li Z, Chu X, Li Y, Xie Z, Yu M, Deng J, Lv H, Zhang W, Wang Z, Yuan Y, Meng L. Li Z, et al. Among authors: chu x. Acta Neuropathol. 2024 Sep 4;148(1):38. doi: 10.1007/s00401-024-02798-8. Acta Neuropathol. 2024. PMID: 39230604 No abstract available.

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