Ke Q - Search Results

1

Progress in treatment and newborn screening for Duchenne muscular dystrophy and spinal muscular atrophy.

Ke Q, Zhao ZY, Mendell JR, Baker M, Wiley V, Kwon JM, Alfano LN, Connolly AM, Jay C, Polari H, Ciafaloni E, Qi M, Griggs RC, Gatheridge MA. Ke Q, et al. World J Pediatr. 2019 Jun;15(3):219-225. doi: 10.1007/s12519-019-00242-6. Epub 2019 Mar 23. World J Pediatr. 2019. PMID: 30904991 Review.

2

Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment.

Ke Q, Zhao ZY, Griggs R, Wiley V, Connolly A, Kwon J, Qi M, Sheehan D, Ciafaloni E, Howell RR, Furu P, Sazani P, Narayana A, Gatheridge M. Ke Q, et al. World J Pediatr. 2017 Jun;13(3):197-201. doi: 10.1007/s12519-017-0036-3. Epub 2017 May 17. World J Pediatr. 2017. PMID: 28466241 Review.

3

Population-Wide Duchenne Muscular Dystrophy Carrier Detection by CK and Molecular Testing.

Han S, Xu H, Zheng J, Sun J, Feng X, Wang Y, Ye W, Ke Q, Ren Y, Yao S, Zhang S, Chen J, Griggs RC, Zhao Z, Qi M, Gatheridge MA. Han S, et al. Among authors: ke q. Biomed Res Int. 2020 Sep 27;2020:8396429. doi: 10.1155/2020/8396429. eCollection 2020. Biomed Res Int. 2020. PMID: 33029525 Free PMC article.

4

China's shift from population control to population quality: Implications for neurology.

Ke Q, Zhang L, He C, Zhao Z, Qi M, Griggs RC, Gatheridge MA. Ke Q, et al. Neurology. 2016 Aug 23;87(8):e85-8. doi: 10.1212/WNL.0000000000003010. Neurology. 2016. PMID: 27550901 Free PMC article. No abstract available.

5

Rare disease centers for periodic paralysis: China versus the United States and United Kingdom.

Ke Q, Qi M, Wu W, Luo B, Hanna M, Herr B, Griggs RC; Consortium for Investigation of Neurological Channelopathies (CINCH). Ke Q, et al. Muscle Nerve. 2014 Feb;49(2):171-4. doi: 10.1002/mus.23970. Muscle Nerve. 2014. PMID: 23893386

6

Development of a comprehensive real-time PCR assay for dystrophin gene analysis and prenatal diagnosis of Chinese families.

Zhang T, Liu S, Wei T, Yong J, Mao Y, Lu X, Xie J, Ke Q, Jin F, Qi M. Zhang T, et al. Among authors: ke q. Clin Chim Acta. 2013 Sep 23;424:33-8. doi: 10.1016/j.cca.2013.05.006. Epub 2013 May 13. Clin Chim Acta. 2013. PMID: 23680072

7

Gender differences in penetrance and phenotype in hypokalemic periodic paralysis.

Ke Q, Luo B, Qi M, Du Y, Wu W. Ke Q, et al. Muscle Nerve. 2013 Jan;47(1):41-5. doi: 10.1002/mus.23460. Epub 2012 Sep 27. Muscle Nerve. 2013. PMID: 23019082

8

Clinical comparison and functional study of the L703P: a recurrent mutation in human SCN4A that causes sodium channel myotonia.

Ke Q, Zhao Y, Li Y, Ye J, Tang S, He F, Ji F, Dai X, Ni J, Li Y, Griggs RC, Cheng X. Ke Q, et al. Neuromuscul Disord. 2022 Oct;32(10):811-819. doi: 10.1016/j.nmd.2022.08.004. Epub 2022 Aug 17. Neuromuscul Disord. 2022. PMID: 36050252

9

The R900S mutation in CACNA1S associated with hypokalemic periodic paralysis.

Ke Q, He F, Lu L, Yu P, Jiang Y, Weng C, Huang H, Yi X, Qi M. Ke Q, et al. Neuromuscul Disord. 2015 Dec;25(12):955-8. doi: 10.1016/j.nmd.2015.09.006. Epub 2015 Sep 9. Neuromuscul Disord. 2015. PMID: 26433613

10

ATP1A3 mutation in rapid-onset dystonia parkinsonism: New data and genotype-phenotype correlation analysis.

Yu L, Peng G, Yuan Y, Tang M, Liu P, Liu X, Ni J, Li Y, Ji C, Fan Z, Zhu W, Luo B, Ke Q. Yu L, et al. Among authors: ke q. Front Aging Neurosci. 2022 Aug 1;14:933893. doi: 10.3389/fnagi.2022.933893. eCollection 2022. Front Aging Neurosci. 2022. PMID: 35978945 Free PMC article.

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

794 results

Search Page

Filters