Similar articles for PMID: 28620780

Year	Number of Results
1996	1
2004	2
2006	2
2007	3
2008	6
2009	2
2010	4
2011	5
2012	5
2013	7
2014	6
2015	9
2016	6
2017	12
2018	9
2019	7
2020	8
2021	4
2022	10
2023	4
2024	0

1

A novel large fragment deletion in PLS3 causes rare X-linked early-onset osteoporosis and response to zoledronic acid.

Lv F, Ma M, Liu W, Xu X, Song Y, Li L, Jiang Y, Wang O, Xia W, Xing X, Qiu Z, Li M. Lv F, et al. Osteoporos Int. 2017 Sep;28(9):2691-2700. doi: 10.1007/s00198-017-4094-0. Epub 2017 Jun 16. Osteoporos Int. 2017. PMID: 28620780

2

A novel splice mutation in PLS3 causes X-linked early onset low-turnover osteoporosis.

Laine CM, Wessman M, Toiviainen-Salo S, Kaunisto MA, Mäyränpää MK, Laine T, Pekkinen M, Kröger H, Välimäki VV, Välimäki MJ, Lehesjoki AE, Mäkitie O. Laine CM, et al. J Bone Miner Res. 2015 Mar;30(3):510-8. doi: 10.1002/jbmr.2355. J Bone Miner Res. 2015. PMID: 25209159 Free article.

3

PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants.

Kämpe AJ, Costantini A, Mäkitie RE, Jäntti N, Valta H, Mäyränpää M, Kröger H, Pekkinen M, Taylan F, Jiao H, Mäkitie O. Kämpe AJ, et al. Osteoporos Int. 2017 Oct;28(10):3023-3032. doi: 10.1007/s00198-017-4150-9. Epub 2017 Jul 26. Osteoporos Int. 2017. PMID: 28748388 Free PMC article.

4

Identification of a novel splicing mutation and genotype-phenotype correlations in rare PLS3-related childhood-onset osteoporosis.

Wu Z, Feng Z, Zhu X, Dai Z, Min K, Qiu Y, Yi L, Xu L, Zhu Z. Wu Z, et al. Orphanet J Rare Dis. 2022 Jun 25;17(1):247. doi: 10.1186/s13023-022-02380-z. Orphanet J Rare Dis. 2022. PMID: 35752817 Free PMC article.

5

A novel mutation in PLS3 causes extremely rare X-linked osteogenesis imperfecta.

Hu J, Li LJ, Zheng WB, Zhao DC, Wang O, Jiang Y, Xing XP, Li M, Xia W. Hu J, et al. Mol Genet Genomic Med. 2020 Dec;8(12):e1525. doi: 10.1002/mgg3.1525. Epub 2020 Nov 9. Mol Genet Genomic Med. 2020. PMID: 33166085 Free PMC article.

6

Novel PLS3 variants in X-linked osteoporosis: Exploring bone material properties.

Balasubramanian M, Fratzl-Zelman N, O'Sullivan R, Bull M, Fa Peel N, Pollitt RC, Jones R, Milne E, Smith K, Roschger P, Klaushofer K, Bishop NJ. Balasubramanian M, et al. Am J Med Genet A. 2018 Jul;176(7):1578-1586. doi: 10.1002/ajmg.a.38830. Epub 2018 May 7. Am J Med Genet A. 2018. PMID: 29736964 Free article.

7

Teriparatide Treatment in Patients With WNT1 or PLS3 Mutation-Related Early-Onset Osteoporosis: A Pilot Study.

Välimäki VV, Mäkitie O, Pereira R, Laine C, Wesseling-Perry K, Määttä J, Kirjavainen M, Viljakainen H, Välimäki MJ. Välimäki VV, et al. J Clin Endocrinol Metab. 2017 Feb 1;102(2):535-544. doi: 10.1210/jc.2016-2423. J Clin Endocrinol Metab. 2017. PMID: 27732335

8

PLS3 Mutations in X-Linked Osteoporosis: Clinical and Bone Characteristics of Two Novel Mutations.

Kannu P, Mahjoub A, Babul-Hirji R, Carter MT, Harrington J. Kannu P, et al. Horm Res Paediatr. 2017;88(3-4):298-304. doi: 10.1159/000477242. Epub 2017 Jun 12. Horm Res Paediatr. 2017. PMID: 28605746

9

A novel frameshift deletion in PLS3 causing severe primary osteoporosis.

Costantini A, Krallis PΝ, Kämpe A, Karavitakis EM, Taylan F, Mäkitie O, Doulgeraki A. Costantini A, et al. J Hum Genet. 2018 Aug;63(8):923-926. doi: 10.1038/s10038-018-0472-5. Epub 2018 Jun 8. J Hum Genet. 2018. PMID: 29884797

10

PLS3 mutations in X-linked osteoporosis with fractures.

van Dijk FS, Zillikens MC, Micha D, Riessland M, Marcelis CL, de Die-Smulders CE, Milbradt J, Franken AA, Harsevoort AJ, Lichtenbelt KD, Pruijs HE, Rubio-Gozalbo ME, Zwertbroek R, Moutaouakil Y, Egthuijsen J, Hammerschmidt M, Bijman R, Semeins CM, Bakker AD, Everts V, Klein-Nulend J, Campos-Obando N, Hofman A, te Meerman GJ, Verkerk AJ, Uitterlinden AG, Maugeri A, Sistermans EA, Waisfisz Q, Meijers-Heijboer H, Wirth B, Simon ME, Pals G. van Dijk FS, et al. N Engl J Med. 2013 Oct 17;369(16):1529-36. doi: 10.1056/NEJMoa1308223. Epub 2013 Oct 2. N Engl J Med. 2013. PMID: 24088043 Free article.

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