Lv F - Search Results

1

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. 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

2

[Studies on the chemical constituents of Rabdosia rubescens].

Lv F, Xu XJ. Lv F, et al. Zhong Yao Cai. 2008 Sep;31(9):1340-3. Zhong Yao Cai. 2008. PMID: 19180953 Chinese.

3

Gorham-Stout disease: radiological, histological, and clinical features of 12 cases and review of literature.

Liu Y, Zhong DR, Zhou PR, Lv F, Ma DD, Xia WB, Jiang Y, Wang O, Xing XP, Li M. Liu Y, et al. Among authors: lv f. Clin Rheumatol. 2016 Mar;35(3):813-23. doi: 10.1007/s10067-014-2780-2. Epub 2014 Sep 18. Clin Rheumatol. 2016. PMID: 25227772

4

Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients.

Zhou P, Liu Y, Lv F, Nie M, Jiang Y, Wang O, Xia W, Xing X, Li M. Zhou P, et al. Among authors: lv f. PLoS One. 2014 Sep 19;9(9):e107594. doi: 10.1371/journal.pone.0107594. eCollection 2014. PLoS One. 2014. PMID: 25238597 Free PMC article.

5

A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.

Lv F, Xu XJ, Wang JY, Liu Y, Jiang Y, Wang O, Xia WB, Xing XP, Li M. Lv F, et al. Clin Chim Acta. 2016 Jun 1;457:69-74. doi: 10.1016/j.cca.2016.04.004. Epub 2016 Apr 9. Clin Chim Acta. 2016. PMID: 27067446

6

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: lv f. 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

7

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. Among authors: lv f. 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

8

EFFECTS OF LONG-TERM ALENDRONATE TREATMENT ON A LARGE SAMPLE OF PEDIATRIC PATIENTS WITH OSTEOGENESIS IMPERFECTA.

Lv F, Liu Y, Xu X, Wang J, Ma D, Jiang Y, Wang O, Xia W, Xing X, Yu W, Li M. Lv F, et al. Endocr Pract. 2016 Dec;22(12):1369-1376. doi: 10.4158/EP161322.OR. Epub 2016 Aug 2. Endocr Pract. 2016. PMID: 27482608

9

THE CLINICAL CHARACTERISTICS AND EFFICACY OF BISPHOSPHONATES IN AUDLT PATIENTS WITH OSTEOGENESIS IMPERGECTA.

Xu XJ, Ma DD, Lv F, Wang JY, Liu Y, Xia WB, Jiang Y, Wang O, Xing XP, Yu W, Li M. Xu XJ, et al. Among authors: lv f. Endocr Pract. 2016 Nov;22(11):1267-1276. doi: 10.4158/EP151184.OR. Epub 2016 Aug 2. Endocr Pract. 2016. PMID: 27482615 Clinical Trial.

10

Osteogenesis imperfecta type V: Genetic and clinical findings in eleven Chinese patients.

Liu Y, Wang J, Ma D, Lv F, Xu X, Xia W, Jiang Y, Wang O, Xing X, Zhou P, Wang J, Yu W; ASAN; Li M. Liu Y, et al. Among authors: lv f. Clin Chim Acta. 2016 Nov 1;462:201-209. doi: 10.1016/j.cca.2016.09.019. Epub 2016 Sep 25. Clin Chim Acta. 2016. PMID: 27678411

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

1,910 results

Search Page

Filters