Chu X - Search Results

1

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

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

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.

4

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.

5

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.

6

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

7

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.

8

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.

9

A novel variant of biallelic MME gene associated with autosomal recessive late-onset distal hereditary motor neuropathy in Chinese families.

Zhang B, Gang Q, Meng L, Li Z, Chu X, Wu H, Yang J, Huang B, Du K. Zhang B, et al. Among authors: chu x. BMC Med Genomics. 2024 Sep 4;17(1):223. doi: 10.1186/s12920-024-01996-3. BMC Med Genomics. 2024. PMID: 39232784 Free PMC article.

10

Spinal and bulbar muscular atrophy combined with hypertrophic cardiomyopathy and Brugada-pattern electrocardiographic changes: A case report.

Liu T, Weng H, Ding W, Chu X, Li J. Liu T, et al. Among authors: chu x. Echocardiography. 2023 Nov;40(11):1276-1279. doi: 10.1111/echo.15690. Epub 2023 Sep 16. Echocardiography. 2023. PMID: 37715620

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