Chen B - Search Results

1

Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene.

Hong D, Luan X, Chen B, Zheng R, Zhang W, Wang Z, Yuan Y. Hong D, et al. Among authors: chen b. J Neurol Neurosurg Psychiatry. 2010 Jun;81(6):703-4. doi: 10.1136/jnnp.2009.177451. J Neurol Neurosurg Psychiatry. 2010. PMID: 20522878 No abstract available.

2

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. Among authors: chen b. Neuropathology. 2009 Oct;29(5):579-84. doi: 10.1111/j.1440-1789.2008.00985.x. Epub 2008 Dec 3. Neuropathology. 2009. PMID: 19077043

3

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. Neuropathology. 2009 Oct;29(5):543-7. doi: 10.1111/j.1440-1789.2009.01011.x. Epub 2009 Mar 23. Neuropathology. 2009. PMID: 19323790

4

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: chen b. Hum Genet. 2010 Jan;127(1):113. Hum Genet. 2010. PMID: 20108424 No abstract available.

5

[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. Among authors: chen b. Zhonghua Yi Xue Za Zhi. 2009 Dec 22;89(47):3328-31. Zhonghua Yi Xue Za Zhi. 2009. PMID: 20193560 Chinese.

6

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: chen b. Neuropathology. 2010 Dec;30(6):606-14. doi: 10.1111/j.1440-1789.2010.01115.x. Neuropathology. 2010. PMID: 20408961

7

Childhood chronic inflammatory demyelinating polyneuropathy with nonuniform pathologic features.

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

8

NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL.

Wang Z, Yuan Y, Zhang W, Lv H, Hong D, Chen B, Liu Y, Luan X, Xie S, Wu S. Wang Z, et al. Among authors: chen b. J Neurol Neurosurg Psychiatry. 2011 May;82(5):534-9. doi: 10.1136/jnnp.2010.209247. Epub 2010 Oct 9. J Neurol Neurosurg Psychiatry. 2011. PMID: 20935329

9

A new pseudoexon activation due to ultrarare branch point formation in Duchenne muscular dystrophy.

Xie Z, Sun C, Liu C, Lu Y, Chen B, Wu R, Liu Y, Liu R, Peng Q, Deng J, Meng L, Wang Z, Zhang W, Yuan Y. Xie Z, et al. Among authors: chen b. Neuromuscul Disord. 2024 Feb;35:8-12. doi: 10.1016/j.nmd.2023.12.009. Epub 2023 Dec 20. Neuromuscul Disord. 2024. PMID: 38194733

10

Novel PNPLA8 variants associated with primary ovarian insufficiency, tremors, cerebellar ataxia and limb weakness: a case report and literature review.

Chen B, Zhang C, Yuan Y, Wang Z, Cui T, Dong G, Pan H, Zhang Z, Li W. Chen B, et al. J Neurol. 2024 Dec 16;272(1):78. doi: 10.1007/s00415-024-12838-8. J Neurol. 2024. PMID: 39680195 Review.

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