Wu S - Search Results

1

Central core disease is due to RYR1 mutations in more than 90% of patients.

Wu S, Ibarra MC, Malicdan MC, Murayama K, Ichihara Y, Kikuchi H, Nonaka I, Noguchi S, Hayashi YK, Nishino I. Wu S, et al. Brain. 2006 Jun;129(Pt 6):1470-80. doi: 10.1093/brain/awl077. Epub 2006 Apr 18. Brain. 2006. PMID: 16621918

2

Malignant hyperthermia in Japan: mutation screening of the entire ryanodine receptor type 1 gene coding region by direct sequencing.

Ibarra M CA, Wu S, Murayama K, Minami N, Ichihara Y, Kikuchi H, Noguchi S, Hayashi YK, Ochiai R, Nishino I. Ibarra M CA, et al. Among authors: wu s. Anesthesiology. 2006 Jun;104(6):1146-54. doi: 10.1097/00000542-200606000-00008. Anesthesiology. 2006. PMID: 16732084 Free article.

3

Distal myopathy in multi-minicore disease.

Mitsuhashi S, Nonaka I, Wu S, Moreno CA, Shalaby S, Hayashi YK, Noguchi S, Nishino I. Mitsuhashi S, et al. Among authors: wu s. Intern Med. 2009;48(19):1759-62. doi: 10.2169/internalmedicine.48.2425. Epub 2009 Oct 1. Intern Med. 2009. PMID: 19797833 Free article.

4

Novel RYR1 missense mutations in six Chinese patients with central core disease.

Gu M, Zhang S, Hu J, Yuan Y, Wang Z, Da Y, Wu S. Gu M, et al. Among authors: wu s. Neurosci Lett. 2014 Apr 30;566:32-5. doi: 10.1016/j.neulet.2014.02.015. Epub 2014 Feb 20. Neurosci Lett. 2014. PMID: 24561095

5

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: wu s. 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

6

Mitochondrial tRNA genes are hotspots for mutations in a cohort of patients with exercise intolerance and mitochondrial myopathy.

Lu Y, Zhao D, Yao S, Wu S, Hong D, Wang Q, Liu J, Smeitink JAM, Yuan Y, Wang Z. Lu Y, et al. Among authors: wu s. J Neurol Sci. 2017 Aug 15;379:137-143. doi: 10.1016/j.jns.2017.05.056. Epub 2017 May 30. J Neurol Sci. 2017. PMID: 28716227

7

Comprehensive genetic characteristics of dystrophinopathies in China.

Ma P, Zhang S, Zhang H, Fang S, Dong Y, Zhang Y, Hao W, Wu S, Zhao Y. Ma P, et al. Among authors: wu s. Orphanet J Rare Dis. 2018 Jul 4;13(1):109. doi: 10.1186/s13023-018-0853-z. Orphanet J Rare Dis. 2018. PMID: 29973226 Free PMC article.

8

FHL1-related clinical, muscle MRI and genetic features in six Chinese patients with reducing body myopathy.

Hu Z, Zhu Y, Liu X, Zhang W, Liu J, Wu S, Xiao J, Yuan Y, Wang Z. Hu Z, et al. Among authors: wu s. J Hum Genet. 2019 Sep;64(9):919-926. doi: 10.1038/s10038-019-0627-z. Epub 2019 Jul 4. J Hum Genet. 2019. PMID: 31273321 Clinical Trial.

9

High-resolution MRI of radiation-induced intracranial vasculopathy.

Li M, Wu SW, Xu WH. Li M, et al. Neurology. 2015 Feb 10;84(6):631. doi: 10.1212/WNL.0000000000001223. Neurology. 2015. PMID: 25666631 No abstract available.

10

Etiology of isolated pontine infarctions: a study based on high-resolution MRI and brain small vessel disease scores.

Xia C, Chen HS, Wu SW, Xu WH. Xia C, et al. BMC Neurol. 2017 Dec 12;17(1):216. doi: 10.1186/s12883-017-0999-7. BMC Neurol. 2017. PMID: 29233158 Free PMC article.

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