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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1979 1
1987 1
1988 3
1990 1
1992 3
1994 1
1995 2
1996 4
1997 2
1998 2
1999 2
2000 5
2001 2
2002 3
2003 11
2004 7
2005 13
2006 13
2007 18
2008 12
2009 11
2010 11
2011 12
2012 8
2013 11
2014 12
2015 10
2016 13
2017 13
2018 10
2019 12
2020 12
2021 16
2022 9
2023 9
2024 1

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250 results

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Page 1
Oral potentially malignant disorders: A consensus report from an international seminar on nomenclature and classification, convened by the WHO Collaborating Centre for Oral Cancer.
Warnakulasuriya S, Kujan O, Aguirre-Urizar JM, Bagan JV, González-Moles MÁ, Kerr AR, Lodi G, Mello FW, Monteiro L, Ogden GR, Sloan P, Johnson NW. Warnakulasuriya S, et al. Oral Dis. 2021 Nov;27(8):1862-1880. doi: 10.1111/odi.13704. Epub 2020 Nov 26. Oral Dis. 2021. PMID: 33128420 Free article. Review.
The first workshop held in London in 2005 considered a wide spectrum of disorders under the term "potentially malignant disorders of the oral mucosa" (PMD) (now referred to as oral potentially malignant disorders: OPMD) including leukoplakia, erythroplakia, proliferative verrucou …
The first workshop held in London in 2005 considered a wide spectrum of disorders under the term "potentially malignant disorders of the ora …
Dyskeratosis congenita: a literature review.
AlSabbagh MM. AlSabbagh MM. J Dtsch Dermatol Ges. 2020 Sep;18(9):943-967. doi: 10.1111/ddg.14268. Epub 2020 Sep 15. J Dtsch Dermatol Ges. 2020. PMID: 32930426 Review.
Dyskeratosis congenita is a rare hereditary disease that occurs predominantly in males and manifests clinically as the classic triad of reticulate hyperpigmentation, nail dystrophy and leukoplakia. It increases the risk of malignancy and other potentially lethal com
Dyskeratosis congenita is a rare hereditary disease that occurs predominantly in males and manifests clinically as the classic
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.
Numerous genetic discoveries and the advent of clinical telomere length testing have led to the recognition of a spectrum of telomere biology disorders (TBDs) beyond the classic dyskeratosis congenita (DC) triad of nail dysplasia, abnormal skin pigmentation, and ora …
Numerous genetic discoveries and the advent of clinical telomere length testing have led to the recognition of a spectrum of telomere biolog …
Telomeres-structure, function, and regulation.
Lu W, Zhang Y, Liu D, Songyang Z, Wan M. Lu W, et al. Exp Cell Res. 2013 Jan 15;319(2):133-41. doi: 10.1016/j.yexcr.2012.09.005. Epub 2012 Sep 21. Exp Cell Res. 2013. PMID: 23006819 Free PMC article. Review.
Aberrant regulation of telomeric proteins and/or telomerase may lead to abnormalities that can result in diseases such as dyskeratosis congenita (DC) and cancers. Understanding the mechanisms that regulate telomere homeostasis and the factors that contribute to telo …
Aberrant regulation of telomeric proteins and/or telomerase may lead to abnormalities that can result in diseases such as dyskeratosis
Telomeres and aging.
Aubert G, Lansdorp PM. Aubert G, et al. Physiol Rev. 2008 Apr;88(2):557-79. doi: 10.1152/physrev.00026.2007. Physiol Rev. 2008. PMID: 18391173 Free article. Review.
Short telomeres in such patients are implicated in a variety of disorders including dyskeratosis congenita, aplastic anemia, pulmonary fibrosis, and cancer. ...
Short telomeres in such patients are implicated in a variety of disorders including dyskeratosis congenita, aplastic anemia, p …
An update on the biology and management of dyskeratosis congenita and related telomere biology disorders.
Niewisch MR, Savage SA. Niewisch MR, et al. Expert Rev Hematol. 2019 Dec;12(12):1037-1052. doi: 10.1080/17474086.2019.1662720. Epub 2019 Sep 10. Expert Rev Hematol. 2019. PMID: 31478401 Free PMC article. Review.
Possible TBD manifestations range from complex multisystem disorders with onset in childhood such as dyskeratosis congenita (DC), Hoyeraal-Hreidarsson syndrome, Revesz syndrome and Coats plus to adults presenting with one or two DC-related features.Areas covered: Th …
Possible TBD manifestations range from complex multisystem disorders with onset in childhood such as dyskeratosis congenita (D …
Regulation of human telomerase in homeostasis and disease.
Roake CM, Artandi SE. Roake CM, et al. Nat Rev Mol Cell Biol. 2020 Jul;21(7):384-397. doi: 10.1038/s41580-020-0234-z. Epub 2020 Apr 2. Nat Rev Mol Cell Biol. 2020. PMID: 32242127 Free PMC article. Review.
Conversely, germline mutations in telomerase-relevant genes that decrease telomerase function cause a range of genetic disorders, including dyskeratosis congenita, idiopathic pulmonary fibrosis and bone marrow failure. ...
Conversely, germline mutations in telomerase-relevant genes that decrease telomerase function cause a range of genetic disorders, including …
Treatment of telomeropathies.
Vieri M, Brümmendorf TH, Beier F. Vieri M, et al. Best Pract Res Clin Haematol. 2021 Jun;34(2):101282. doi: 10.1016/j.beha.2021.101282. Epub 2021 Jul 1. Best Pract Res Clin Haematol. 2021. PMID: 34404536 Review.
Different degrees of severity are also observed among patients with TBDs, ranging from very severe syndromes manifesting themselves in early childhood, such as Revesz syndrome, Hoyeraal-Hreidarsson syndrome, and Coats plus disease, to dyskeratosis congenita (DKC) an …
Different degrees of severity are also observed among patients with TBDs, ranging from very severe syndromes manifesting themselves in early …
Revesz syndrome revisited.
Karremann M, Neumaier-Probst E, Schlichtenbrede F, Beier F, Brümmendorf TH, Cremer FW, Bader P, Dürken M. Karremann M, et al. Orphanet J Rare Dis. 2020 Oct 23;15(1):299. doi: 10.1186/s13023-020-01553-y. Orphanet J Rare Dis. 2020. PMID: 33097095 Free PMC article. Review.
BACKGROUND: Revesz syndrome (RS) is an extremely rare variant of dyskeratosis congenita (DKC) with only anecdotal reports in the literature. ...
BACKGROUND: Revesz syndrome (RS) is an extremely rare variant of dyskeratosis congenita (DKC) with only anecdotal reports in t …
250 results