Luan X - Search Results

1

Episodic Neurological Dysfunction in X-Linked Charcot-Marie-Tooth Disease: Expansion of the Phenotypic and Genetic Spectrum.

Zhan F, Tian W, Cao Y, Wu J, Ni R, Liu T, Yuan Y, Luan X, Cao L. Zhan F, et al. Among authors: luan x. J Clin Neurol. 2024 Jan;20(1):59-66. doi: 10.3988/jcn.2023.0104. J Clin Neurol. 2024. PMID: 38179633 Free PMC article.

2

Retinal arterial abnormalities correlate with brain white matter lesions in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.

Liu Y, Wu Y, Xie S, Luan XH, Yuan Y. Liu Y, et al. Clin Exp Ophthalmol. 2008 Aug;36(6):532-6. doi: 10.1111/j.1442-9071.2008.01825.x. Clin Exp Ophthalmol. 2008. PMID: 18954315

3

Tubular aggregates in paralysis periodica paramyotonica with T704M mutation of SCN4A.

Luan X, Chen B, Liu Y, Zheng R, Zhang W, Yuan Y. Luan X, et al. Neuropathology. 2009 Oct;29(5):579-84. doi: 10.1111/j.1440-1789.2008.00985.x. Epub 2008 Dec 3. Neuropathology. 2009. PMID: 19077043

4

[Mitochondrial DNA mutation analysis in 97 Chinese patients with mitochondrial cephalomyopathy].

Wang ZX, Luan XH, Zhang Y, Yang YL, Qi Y, Bu DF, Yuan Y. Wang ZX, et al. Zhonghua Yi Xue Za Zhi. 2008 Dec 16;88(46):3254-6. Zhonghua Yi Xue Za Zhi. 2008. PMID: 19159548 Chinese.

5

Clincial and pathological study of distal motor neuropathy with N88S mutation in BSCL2.

Chen B, Zheng R, Luan X, Zhang W, Wang Z, Yuan Y. Chen B, et al. Among authors: luan x. Neuropathology. 2009 Oct;29(5):543-7. doi: 10.1111/j.1440-1789.2009.01011.x. Epub 2009 Mar 23. Neuropathology. 2009. PMID: 19323790

6

Novel human pathological mutations. Gene symbol: SCN4A. Disease: Periodic paralysis.

Hong D, Luan X, Chen B, Zheng R, Wang Z, Yuan Y. Hong D, et al. Among authors: luan x. Hum Genet. 2010 Jan;127(1):113. Hum Genet. 2010. PMID: 20108424 No abstract available.

7

[Two novel mutations of GJB1 gene associated with typical X-linked Charcot-Marie-Tooth disease].

Qiao XH, Li YX, Chang XZ, Luan XH, Chen B, Bu DF, Yuan Y. Qiao XH, et al. Zhonghua Yi Xue Za Zhi. 2009 Dec 22;89(47):3328-31. Zhonghua Yi Xue Za Zhi. 2009. PMID: 20193560 Chinese.

8

Phenotypic patterns of MELAS/LS overlap syndrome associated with m.13513G>A mutation, and neuropathological findings in one autopsy case.

Wang Z, Qi XK, Yao S, Chen B, Luan X, Zhang W, Han M, Yuan Y. Wang Z, et al. Among authors: luan x. Neuropathology. 2010 Dec;30(6):606-14. doi: 10.1111/j.1440-1789.2010.01115.x. Neuropathology. 2010. PMID: 20408961

9

A novel heterozygous deletion-insertion mutation (2695-2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family.

Luan X, Hong D, Zhang W, Wang Z, Yuan Y. Luan X, et al. Neuromuscul Disord. 2010 Jun;20(6):390-6. doi: 10.1016/j.nmd.2010.03.009. Epub 2010 Apr 22. Neuromuscul Disord. 2010. PMID: 20417099

10

Childhood chronic inflammatory demyelinating polyneuropathy with nonuniform pathologic features.

Luan X, Zheng R, Chen B, Yuan Y. Luan X, et al. Pediatr Neurol. 2010 Aug;43(2):103-9. doi: 10.1016/j.pediatrneurol.2010.04.001. Pediatr Neurol. 2010. PMID: 20610120

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,382 results

Search Page

Filters