Song YW - Search Results

1

A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfecta.

Xu XJ, Lv F, Liu Y, Wang JY, Song YW, Asan, Wang JW, Song LJ, Jiang Y, Wang O, Xia WB, Xing XP, Li M. Xu XJ, et al. Among authors: song yw, song lj. Clin Chim Acta. 2016 Sep 1;460:33-9. doi: 10.1016/j.cca.2016.06.011. Epub 2016 Jun 14. Clin Chim Acta. 2016. PMID: 27312322

2

Genotype-phenotype analysis of a rare type of osteogenesis imperfecta in four Chinese families with WNT1 mutations.

Liu Y, Song L, Ma D, Lv F, Xu X, Wang J, Xia W, Jiang Y, Wang O, Song Y, Xing X, Asan, Li M. Liu Y, et al. Clin Chim Acta. 2016 Oct 1;461:172-80. doi: 10.1016/j.cca.2016.07.012. Epub 2016 Jul 20. Clin Chim Acta. 2016. PMID: 27450065

3

Novel Mutations in PLOD2 Cause Rare Bruck Syndrome.

Lv F, Xu X, Song Y, Li L, Asan, Wang J, Yang H, Wang O, Jiang Y, Xia W, Xing X, Li M. Lv F, et al. Calcif Tissue Int. 2018 Mar;102(3):296-309. doi: 10.1007/s00223-017-0360-6. Epub 2017 Nov 24. Calcif Tissue Int. 2018. PMID: 29177700

4

Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta.

Lv F, Xu XJ, Wang JY, Liu Y, Asan, Wang JW, Song LJ, Song YW, Jiang Y, Wang O, Xia WB, Xing XP, Li M. Lv F, et al. Among authors: song lj, song yw. J Hum Genet. 2016 Jun;61(6):539-45. doi: 10.1038/jhg.2016.11. Epub 2016 Feb 25. J Hum Genet. 2016. PMID: 26911354

5

Recurrent and novel mutations in the NTRK1 gene lead to rare congenital insensitivity to pain with anhidrosis in two Chinese patients.

Lv F, Xu XJ, Song YW, Li LJ, Wang O, Jiang Y, Xia WB, Xing XP, Gao P, Li M. Lv F, et al. Among authors: song yw. Clin Chim Acta. 2017 May;468:39-45. doi: 10.1016/j.cca.2017.02.007. Epub 2017 Feb 10. Clin Chim Acta. 2017. PMID: 28192073

6

Extremely low level of serum pigment epithelium-derived factor is a special biomarker of Chinese osteogenesis imperfecta patients with SERPINF1 mutations.

Wang JY, Li LJ, Zhang Q, Liu Y, Lv F, Xu XJ, Song YW, Wang O, Jiang Y, Xia WB, Xing XP, Li M. Wang JY, et al. Among authors: song yw. Clin Chim Acta. 2018 Mar;478:216-221. doi: 10.1016/j.cca.2017.10.032. Epub 2017 Nov 6. Clin Chim Acta. 2018. PMID: 29104038

7

Novel mutations in BMP1 induce a rare type of osteogenesis imperfecta.

Xu XJ, Lv F, Song YW, Li LJ, Asan, Wei XX, Zhao XL, Jiang Y, Wang O, Xing XP, Xia WB, Li M. Xu XJ, et al. Among authors: song yw. Clin Chim Acta. 2019 Feb;489:21-28. doi: 10.1016/j.cca.2018.11.004. Epub 2018 Nov 5. Clin Chim Acta. 2019. PMID: 30408480

8

Genotype-phenotype relationship in a large cohort of osteogenesis imperfecta patients with COL1A1 mutations revealed by a new scoring system.

Li LJ, Lyu F, Song YW, Wang O, Jiang Y, Xia WB, Xing XP, Li M. Li LJ, et al. Among authors: song yw. Chin Med J (Engl). 2019 Jan 20;132(2):145-153. doi: 10.1097/CM9.0000000000000013. Chin Med J (Engl). 2019. PMID: 30614853 Free PMC article.

9

Effects of alendronate and alfacalcidol on bone in patients with myasthenia gravis initiating glucocorticoids treatment.

Lv F, Guan Y, Ma D, Xu X, Song Y, Li L, Jiang Y, Wang O, Xia W, Xing X, Li M. Lv F, et al. Clin Endocrinol (Oxf). 2018 Mar;88(3):380-387. doi: 10.1111/cen.13537. Epub 2018 Jan 12. Clin Endocrinol (Oxf). 2018. PMID: 29266368

10

Clinical characteristics and bisphosphonates treatment of rare pregnancy- and lactation-associated osteoporosis.

Li LJ, Zhang J, Gao P, Lv F, Song YW, Chang XY, Zhao DC, Wang O, Jiang Y, Xing XP, Xia WB, Li M. Li LJ, et al. Among authors: song yw. Clin Rheumatol. 2018 Nov;37(11):3141-3150. doi: 10.1007/s10067-018-4185-0. Epub 2018 Jun 26. Clin Rheumatol. 2018. PMID: 29946989

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