Zheng RL - Search Results

1

[Tumor-like inflammatory demyelinating diseases of the central nervous system with relapse onset: a case report and review].

Qi XL, Chen J, Zheng RL, Li Y, Huang YN, Yuan Y. Qi XL, et al. Among authors: zheng rl. Beijing Da Xue Xue Bao Yi Xue Ban. 2009 Oct 18;41(5):588-9. Beijing Da Xue Xue Bao Yi Xue Ban. 2009. PMID: 19829680 Free article. Chinese.

2

[Rheumatoid leptomeningitis: a case report and literature review].

Zheng RL, Lv H, Zhang W, Yu MX, Yuan Y. Zheng RL, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Jun 18;38(3):324-5. Beijing Da Xue Xue Bao Yi Xue Ban. 2006. PMID: 16778982 Free article. Review. Chinese.

3

The overlap of corticobasal degeneration and Alzheimer changes: an autopsy case.

Zhang W, Zheng R, Wang Z, Yuan Y. Zhang W, et al. Neuropathology. 2009 Dec;29(6):720-6. doi: 10.1111/j.1440-1789.2009.01012.x. Epub 2009 Mar 23. Neuropathology. 2009. PMID: 19323789

4

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

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. 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

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

7

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

8

[The clinical and pathological characteristics of a patient with glycogen storage disease IV].

Yao S, Qi XK, Xiong B, Zhang W, Zheng RL, Yuan Y. Yao S, et al. Among authors: zheng rl. Zhonghua Nei Ke Za Zhi. 2009 May;48(5):380-2. Zhonghua Nei Ke Za Zhi. 2009. PMID: 19615154 Chinese.

9

Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.

Zhao D, Hong D, Zhang W, Yao S, Qi X, Lv H, Zheng R, Feng L, Huang Y, Yuan Y, Wang Z. Zhao D, et al. J Hum Genet. 2011 Nov;56(11):759-64. doi: 10.1038/jhg.2011.96. Epub 2011 Aug 18. J Hum Genet. 2011. PMID: 21850008

10

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. 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.

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