Similar articles for PMID: 15793835

Year	Number of Results
2003	3
2004	7
2005	9
2006	7
2007	9
2008	5
2009	7
2011	8
2012	6
2013	6
2014	8
2015	6
2016	6
2017	5
2018	7
2019	3
2020	5
2021	5
2022	4
2023	1
2024	0

1

Somatic and gonadal mosaicism in Hutchinson-Gilford progeria.

Wuyts W, Biervliet M, Reyniers E, D'Apice MR, Novelli G, Storm K. Wuyts W, et al. Am J Med Genet A. 2005 May 15;135(1):66-8. doi: 10.1002/ajmg.a.30663. Am J Med Genet A. 2005. PMID: 15793835

2

A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome.

Bar DZ, Arlt MF, Brazier JF, Norris WE, Campbell SE, Chines P, Larrieu D, Jackson SP, Collins FS, Glover TW, Gordon LB. Bar DZ, et al. J Med Genet. 2017 Mar;54(3):212-216. doi: 10.1136/jmedgenet-2016-104295. Epub 2016 Dec 5. J Med Genet. 2017. PMID: 27920058 Free PMC article.

3

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.

Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. Eriksson M, et al. Nature. 2003 May 15;423(6937):293-8. doi: 10.1038/nature01629. Epub 2003 Apr 25. Nature. 2003. PMID: 12714972 Free PMC article.

4

Paternal origin of LMNA mutations in Hutchinson-Gilford progeria.

D'Apice MR, Tenconi R, Mammi I, van den Ende J, Novelli G. D'Apice MR, et al. Clin Genet. 2004 Jan;65(1):52-4. doi: 10.1111/j..2004.00181.x. Clin Genet. 2004. PMID: 15032975 No abstract available.

5

Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress.

Paradisi M, McClintock D, Boguslavsky RL, Pedicelli C, Worman HJ, Djabali K. Paradisi M, et al. BMC Cell Biol. 2005 Jun 27;6:27. doi: 10.1186/1471-2121-6-27. BMC Cell Biol. 2005. PMID: 15982412 Free PMC article.

6

Hutchinson-Gilford progeria syndrome with G608G LMNA mutation.

Kim HK, Lee JY, Bae EJ, Oh PS, Park WI, Lee DS, Kim JI, Lee HJ. Kim HK, et al. J Korean Med Sci. 2011 Dec;26(12):1642-5. doi: 10.3346/jkms.2011.26.12.1642. Epub 2011 Nov 29. J Korean Med Sci. 2011. PMID: 22148005 Free PMC article.

7

[Hutchinson-Gilford progeria in the light of contemporary genetics].

Madej-Pilarczyk A. Madej-Pilarczyk A. Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):355-62. Med Wieku Rozwoj. 2006. PMID: 17028399 Review. Polish.

8

[Hutchinson-Gilford progeria syndrome: clinical and molecular analysis in an African patient].

Mutesa L, Pierquin G, Cwiny-Ay N, Buzizi P, Bours V. Mutesa L, et al. Rev Med Liege. 2007 Mar;62(3):155-8. Rev Med Liege. 2007. PMID: 17511383 Free article. French.

9

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome.

Plasilova M, Chattopadhyay C, Pal P, Schaub NA, Buechner SA, Mueller H, Miny P, Ghosh A, Heinimann K. Plasilova M, et al. J Med Genet. 2004 Aug;41(8):609-14. doi: 10.1136/jmg.2004.019661. J Med Genet. 2004. PMID: 15286156 Free PMC article. No abstract available.

10

Emerging candidate treatment strategies for Hutchinson-Gilford progeria syndrome.

Strandgren C, Revêchon G, Sola-Carvajal A, Eriksson M. Strandgren C, et al. Biochem Soc Trans. 2017 Dec 15;45(6):1279-1293. doi: 10.1042/BST20170141. Epub 2017 Nov 10. Biochem Soc Trans. 2017. PMID: 29127216 Review.

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