Similar articles for PMID: 12768443

Year	Number of Results
1997	1
2003	3
2004	4
2005	10
2006	7
2007	11
2008	7
2009	11
2010	3
2011	15
2012	10
2013	12
2014	10
2015	6
2016	8
2017	13
2018	20
2019	23
2020	26
2021	17
2022	23
2023	5
2024	0

1

LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).

Cao H, Hegele RA. Cao H, et al. J Hum Genet. 2003;48(5):271-274. doi: 10.1007/s10038-003-0025-3. Epub 2003 Apr 3. J Hum Genet. 2003. PMID: 12768443

2

Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations.

Lessel D, Ozel AB, Campbell SE, Saadi A, Arlt MF, McSweeney KM, Plaiasu V, Szakszon K, Szőllős A, Rusu C, Rojas AJ, Lopez-Valdez J, Thiele H, Nürnberg P, Nickerson DA, Bamshad MJ, Li JZ, Kubisch C, Glover TW, Gordon LB. Lessel D, et al. Hum Genet. 2018 Dec;137(11-12):921-939. doi: 10.1007/s00439-018-1957-1. Epub 2018 Nov 19. Hum Genet. 2018. PMID: 30450527 Free PMC article.

3

The neonatal progeroid syndrome (Wiedemann-Rautenstrauch): a model for the study of human aging?

Arboleda G, Ramírez N, Arboleda H. Arboleda G, et al. Exp Gerontol. 2007 Oct;42(10):939-43. doi: 10.1016/j.exger.2007.07.004. Epub 2007 Jul 19. Exp Gerontol. 2007. PMID: 17728088 Review.

4

Hutchinson-Gilford progeria syndrome: clinical findings in three patients carrying the G608G mutation in LMNA and review of the literature.

Mazereeuw-Hautier J, Wilson LC, Mohammed S, Smallwood D, Shackleton S, Atherton DJ, Harper JI. Mazereeuw-Hautier J, et al. Br J Dermatol. 2007 Jun;156(6):1308-14. doi: 10.1111/j.1365-2133.2007.07897.x. Epub 2007 Apr 25. Br J Dermatol. 2007. PMID: 17459035 Review.

5

An inherited LMNA gene mutation in atypical Progeria syndrome.

Doubaj Y, De Sandre-Giovannoli A, Vera EV, Navarro CL, Elalaoui SC, Tajir M, Lévy N, Sefiani A. Doubaj Y, et al. Am J Med Genet A. 2012 Nov;158A(11):2881-7. doi: 10.1002/ajmg.a.35557. Epub 2012 Sep 18. Am J Med Genet A. 2012. PMID: 22991222

6

Absence of Lamin A/C gene mutations in four Wiedemann-Rautenstrauch syndrome patients.

Morales LC, Arboleda G, Rodríguez Y, Forero DA, Ramírez N, Yunis JJ, Arboleda H. Morales LC, et al. Am J Med Genet A. 2009 Dec;149A(12):2695-9. doi: 10.1002/ajmg.a.33090. Am J Med Genet A. 2009. PMID: 19938095

7

Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes.

Moulson CL, Fong LG, Gardner JM, Farber EA, Go G, Passariello A, Grange DK, Young SG, Miner JH. Moulson CL, et al. Hum Mutat. 2007 Sep;28(9):882-9. doi: 10.1002/humu.20536. Hum Mutat. 2007. PMID: 17469202

8

p.Pro4Arg mutation in LMNA gene: a new atypical progeria phenotype without metabolism abnormalities.

Guo H, Luo N, Hao F, Bai Y. Guo H, et al. Gene. 2014 Aug 1;546(1):35-9. doi: 10.1016/j.gene.2014.05.042. Epub 2014 May 23. Gene. 2014. PMID: 24861648

9

Telomere length in Hutchinson-Gilford progeria syndrome.

Decker ML, Chavez E, Vulto I, Lansdorp PM. Decker ML, et al. Mech Ageing Dev. 2009 Jun;130(6):377-83. doi: 10.1016/j.mad.2009.03.001. Epub 2009 Mar 20. Mech Ageing Dev. 2009. PMID: 19428457

10

A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation.

Hussain I, Patni N, Ueda M, Sorkina E, Valerio CM, Cochran E, Brown RJ, Peeden J, Tikhonovich Y, Tiulpakov A, Stender SRS, Klouda E, Tayeh MK, Innis JW, Meyer A, Lal P, Godoy-Matos AF, Teles MG, Adams-Huet B, Rader DJ, Hegele RA, Oral EA, Garg A. Hussain I, et al. J Clin Endocrinol Metab. 2018 Mar 1;103(3):1005-1014. doi: 10.1210/jc.2017-02078. J Clin Endocrinol Metab. 2018. PMID: 29267953 Free PMC article.

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