Ge P - Search Results

1

Association of circulating branched-chain amino acids with risk of moyamoya disease.

Zeng C, Ge P, Liu C, Yu X, Zhai Y, Liu W, He Q, Li J, Liu X, Wang J, Ye X, Zhang Q, Wang R, Zhang Y, Zhao J, Zhang D. Zeng C, et al. Among authors: ge p. Front Nutr. 2022 Sep 2;9:994286. doi: 10.3389/fnut.2022.994286. eCollection 2022. Front Nutr. 2022. PMID: 36118742 Free PMC article.

2

Prediction of High-Grade Pediatric Meningiomas: Magnetic Resonance Imaging Features Based on T1-Weighted, T2-Weighted, and Contrast-Enhanced T1-Weighted Images.

Li H, Zhao M, Jiao Y, Ge P, Li Z, Ma J, Wang S, Cao Y, Zhao J. Li H, et al. Among authors: ge p. World Neurosurg. 2016 Jul;91:89-95. doi: 10.1016/j.wneu.2016.03.079. Epub 2016 Mar 30. World Neurosurg. 2016. PMID: 27046015

3

Clinical Features and Long-Term Outcomes of Unilateral Moyamoya Disease.

Zhang Q, Wang R, Liu Y, Zhang Y, Wang S, Cao Y, Zhao Y, Liu X, Wang J, Deng X, Gao F, Yang Z, Zhao M, Ge P, Ma Y, Zhao J, Zhang D. Zhang Q, et al. Among authors: ge p. World Neurosurg. 2016 Dec;96:474-482. doi: 10.1016/j.wneu.2016.09.018. Epub 2016 Sep 16. World Neurosurg. 2016. PMID: 27647029

4

The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature.

Zhang Q, Liu Y, Yu L, Duan R, Ma Y, Ge P, Zhang D, Zhang Y, Wang R, Wang S, Zhao Y, Cao Y, Liu X, Deng X, Zhao J, Zhang X. Zhang Q, et al. Among authors: ge p. World Neurosurg. 2017 Mar;99:701-708.e1. doi: 10.1016/j.wneu.2016.12.119. Epub 2017 Jan 5. World Neurosurg. 2017. PMID: 28063898 Review.

5

Clinical Features, Surgical Treatment, and Long-Term Outcome in Elderly Patients with Moyamoya Disease.

Ge P, Zhang Q, Ye X, Liu X, Deng X, Wang R, Zhang Y, Zhang D, Zhao J. Ge P, et al. World Neurosurg. 2017 Apr;100:459-466. doi: 10.1016/j.wneu.2017.01.055. Epub 2017 Jan 26. World Neurosurg. 2017. PMID: 28132922

6

Long-Term Outcome After Conservative Treatment and Direct Bypass Surgery of Moyamoya Disease at Late Suzuki Stage.

Ge P, Zhang Q, Ye X, Liu X, Deng X, Li H, Wang R, Zhang Y, Zhang D, Zhao J. Ge P, et al. World Neurosurg. 2017 Jul;103:283-290. doi: 10.1016/j.wneu.2017.03.101. Epub 2017 Mar 30. World Neurosurg. 2017. PMID: 28366750

7

Clinical Features of Hemorrhagic Moyamoya Disease in China.

Ge P, Zhang Q, Ye X, Liu X, Deng X, Li H, Wang R, Zhang Y, Zhang D, Cao Y, Wang S, Zhao J. Ge P, et al. World Neurosurg. 2017 Oct;106:224-230. doi: 10.1016/j.wneu.2017.06.145. Epub 2017 Jul 1. World Neurosurg. 2017. PMID: 28673885

8

Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome.

Zhang Q, Si N, Liu Y, Zhang D, Wang R, Zhang Y, Wang S, Liu X, Deng X, Ma Y, Ge P, Zhao J, Zhang X. Zhang Q, et al. Among authors: ge p. Gene. 2017 Sep 10;628:103-108. doi: 10.1016/j.gene.2017.07.030. Epub 2017 Jul 12. Gene. 2017. PMID: 28710038

9

In Reply To "Moyamoya Disease: From Hypoperfusion to Network Disruption".

Ge P, Zhang Q, Zhao J. Ge P, et al. World Neurosurg. 2017 Aug;104:1038-1039. doi: 10.1016/j.wneu.2017.05.116. World Neurosurg. 2017. PMID: 28732427 No abstract available.

10

Encephaloduroateriosynangiosis versus conservative treatment for patients with moyamoya disease at late Suzuki stage.

Ge P, Ye X, Zhang Q, Zhang D, Wang S, Zhao J. Ge P, et al. J Clin Neurosci. 2018 Apr;50:277-280. doi: 10.1016/j.jocn.2017.12.004. Epub 2018 Feb 1. J Clin Neurosci. 2018. PMID: 29366619

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