Similar articles for PMID: 22458992

Year	Number of Results
1993	1
2001	1
2004	2
2005	5
2006	1
2007	3
2008	3
2009	8
2010	5
2011	10
2012	14
2013	9
2014	8
2015	6
2016	7
2017	11
2018	8
2019	4
2021	1
2022	7
2023	3
2024	1

1

Neuropsychiatric conditions among patients with dyskeratosis congenita: a link with telomere biology?

Rackley S, Pao M, Seratti GF, Giri N, Rasimas JJ, Alter BP, Savage SA. Rackley S, et al. Psychosomatics. 2012 May-Jun;53(3):230-5. doi: 10.1016/j.psym.2011.09.003. Epub 2012 Mar 27. Psychosomatics. 2012. PMID: 22458992 Free PMC article.

2

Telomere length in inherited bone marrow failure syndromes.

Alter BP, Giri N, Savage SA, Rosenberg PS. Alter BP, et al. Haematologica. 2015 Jan;100(1):49-54. doi: 10.3324/haematol.2014.114389. Epub 2014 Oct 10. Haematologica. 2015. PMID: 25304614 Free PMC article.

3

Telomere length in blood, buccal cells, and fibroblasts from patients with inherited bone marrow failure syndromes.

Gadalla SM, Cawthon R, Giri N, Alter BP, Savage SA. Gadalla SM, et al. Aging (Albany NY). 2010 Nov;2(11):867-74. doi: 10.18632/aging.100235. Aging (Albany NY). 2010. PMID: 21113082 Free PMC article.

4

Evaluation and Management of Hematopoietic Failure in Dyskeratosis Congenita.

Agarwal S. Agarwal S. Hematol Oncol Clin North Am. 2018 Aug;32(4):669-685. doi: 10.1016/j.hoc.2018.04.003. Epub 2018 May 28. Hematol Oncol Clin North Am. 2018. PMID: 30047419 Free PMC article. Review.

5

The role of telomere biology in bone marrow failure and other disorders.

Savage SA, Alter BP. Savage SA, et al. Mech Ageing Dev. 2008 Jan-Feb;129(1-2):35-47. doi: 10.1016/j.mad.2007.11.002. Epub 2007 Nov 19. Mech Ageing Dev. 2008. PMID: 18160098 Free PMC article. Review.

6

Dyskeratosis congenita and telomere biology disorders.

Savage SA. Savage SA. Hematology Am Soc Hematol Educ Program. 2022 Dec 9;2022(1):637-648. doi: 10.1182/hematology.2022000394. Hematology Am Soc Hematol Educ Program. 2022. PMID: 36485133 Free PMC article. Review.

7

p53 Mediates Failure of Human Definitive Hematopoiesis in Dyskeratosis Congenita.

Fok WC, Niero ELO, Dege C, Brenner KA, Sturgeon CM, Batista LFZ. Fok WC, et al. Stem Cell Reports. 2017 Aug 8;9(2):409-418. doi: 10.1016/j.stemcr.2017.06.015. Epub 2017 Jul 27. Stem Cell Reports. 2017. PMID: 28757166 Free PMC article.

8

Refining the phenotype associated with biallelic DNAJC21 mutations.

D'Amours G, Lopes F, Gauthier J, Saillour V, Nassif C, Wynn R, Alos N, Leblanc T, Capri Y, Nizard S, Lemyre E, Michaud JL, Pelletier VA, Pastore YD, Soucy JF. D'Amours G, et al. Clin Genet. 2018 Aug;94(2):252-258. doi: 10.1111/cge.13370. Epub 2018 Jun 7. Clin Genet. 2018. PMID: 29700810

9

Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenita.

Ballew BJ, Yeager M, Jacobs K, Giri N, Boland J, Burdett L, Alter BP, Savage SA. Ballew BJ, et al. Hum Genet. 2013 Apr;132(4):473-80. doi: 10.1007/s00439-013-1265-8. Epub 2013 Jan 18. Hum Genet. 2013. PMID: 23329068 Free PMC article. Clinical Trial.

10

The genomics of inherited bone marrow failure: from mechanism to the clinic.

Wegman-Ostrosky T, Savage SA. Wegman-Ostrosky T, et al. Br J Haematol. 2017 May;177(4):526-542. doi: 10.1111/bjh.14535. Epub 2017 Feb 17. Br J Haematol. 2017. PMID: 28211564 Free article. Review.

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