Yu XF - Search Results

1

Case report: A patient with brachio-cervical inflammatory myopathy was misdiagnosed as flail arm syndrome.

Sun H, Wei XJ, Han Y, Wang YC, Wang ZY, Yu XF. Sun H, et al. Among authors: yu xf. Front Immunol. 2024 Jul 3;15:1378130. doi: 10.3389/fimmu.2024.1378130. eCollection 2024. Front Immunol. 2024. PMID: 39021570 Free PMC article.

2

A case report: Becker muscular dystrophy presenting with epilepsy and dysgnosia induced by duplication mutation of Dystrophin gene.

Miao J, Feng JC, Zhu D, Yu XF. Miao J, et al. Among authors: yu xf. BMC Neurol. 2016 Dec 12;16(1):255. doi: 10.1186/s12883-016-0777-y. BMC Neurol. 2016. PMID: 27955624 Free PMC article.

3

A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family.

Miao J, Su FF, Liu XM, Wei XJ, Yuan Y, Yu XF. Miao J, et al. Among authors: yu xf. BMC Neurol. 2018 Jun 4;18(1):79. doi: 10.1186/s12883-018-1078-4. BMC Neurol. 2018. PMID: 29866061 Free PMC article.

4

Distal myopathy with rimmed vacuoles: Spectrum of GNE gene mutations in seven Chinese patients.

Su F, Miao J, Liu X, Wei X, Yu X. Su F, et al. Exp Ther Med. 2018 Aug;16(2):1505-1512. doi: 10.3892/etm.2018.6344. Epub 2018 Jun 22. Exp Ther Med. 2018. PMID: 30112071 Free PMC article.

5

A case report: autosomal recessive Myotonia congenita caused by a novel splice mutation (c.1401 + 1G > A) in CLCN1 gene of a Chinese Han patient.

Miao J, Wei XJ, Liu XM, Kang ZX, Gao YL, Yu XF. Miao J, et al. Among authors: yu xf. BMC Neurol. 2018 Sep 22;18(1):154. doi: 10.1186/s12883-018-1153-x. BMC Neurol. 2018. PMID: 30243293 Free PMC article.

6

A family with nemaline myopathy type 6 caused by hseterozygous mutation (c.1222C>T) in the KBTBD13 gene in China: A case report.

Kang ZX, Wei XJ, Miao J, Gao YL, Wang ZY, Yu XF. Kang ZX, et al. Among authors: yu xf. Neuropathology. 2020 Feb;40(1):104-108. doi: 10.1111/neup.12610. Epub 2019 Dec 11. Neuropathology. 2020. PMID: 31828823

7

Complete spinal cord involvement from neuromyelitis optica spectrum disorder in an adult female with anti-synthetase syndrome.

Wang ZY, Guo JJ, Wang M, Wei XJ, Jiang ZZ, Yu XF. Wang ZY, et al. Among authors: yu xf. Mult Scler Relat Disord. 2020 Nov;46:102491. doi: 10.1016/j.msard.2020.102491. Epub 2020 Sep 19. Mult Scler Relat Disord. 2020. PMID: 32979734

8

Acute bilateral cerebral infarction in the presence of neuromyelitis optica spectrum disorder: A case report.

Wang ZY, Wang M, Guo JJ, Gao YL, Yu XF. Wang ZY, et al. Among authors: yu xf. Medicine (Baltimore). 2020 Oct 2;99(40):e22616. doi: 10.1097/MD.0000000000022616. Medicine (Baltimore). 2020. PMID: 33019482 Free PMC article.

9

A case report: identification of a novel exon 1 deletion mutation in the GNE gene in a Chinese patient with GNE myopathy.

Miao J, Wei XJ, Wang X, Yin X, Yu XF. Miao J, et al. Among authors: yu xf. Medicine (Baltimore). 2020 Oct 9;99(41):e22663. doi: 10.1097/MD.0000000000022663. Medicine (Baltimore). 2020. PMID: 33031330 Free PMC article.

10

Adult-onset neuronal intranuclear inclusion disease mimicking Parkinson's disease in a Chinese patient: a case report and literature reviews.

Wang ZY, Guo JJ, Wang M, Wang ZX, Hong DJ, Yu XF. Wang ZY, et al. Among authors: yu xf. Neuro Endocrinol Lett. 2020 Oct;41(4):155-161. Neuro Endocrinol Lett. 2020. PMID: 33307649 Review.

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