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

Year Number of Results
1975 1
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1987 1
1988 3
1990 1
1992 3
1994 1
1995 2
1996 4
1997 2
1998 2
1999 2
2000 6
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
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2020 13
2021 16
2022 9
2023 10
2024 3

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254 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 …
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 …
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 …
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 …
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 …
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 …
Hereditary myeloid malignancies.
Rafei H, DiNardo CD. Rafei H, et al. Best Pract Res Clin Haematol. 2019 Jun;32(2):163-176. doi: 10.1016/j.beha.2019.05.001. Epub 2019 May 3. Best Pract Res Clin Haematol. 2019. PMID: 31203998 Free PMC article. Review.
Genetic predispositions to myeloid malignancies can be classified into three categories: familial cancer syndromes associated with increased risk of various malignancies including myelodysplasia and acute myeloid leukemia such as Li-Fraumeni syndrome and constitutional mis …
Genetic predispositions to myeloid malignancies can be classified into three categories: familial cancer syndromes associated with increased …
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 …
Different degrees of severity are also observed among patients with TBDs, ranging from very severe syndromes manifesting themselves in early …
Unraveling the pathogenesis of Hoyeraal-Hreidarsson syndrome, a complex telomere biology disorder.
Glousker G, Touzot F, Revy P, Tzfati Y, Savage SA. Glousker G, et al. Br J Haematol. 2015 Aug;170(4):457-71. doi: 10.1111/bjh.13442. Epub 2015 May 4. Br J Haematol. 2015. PMID: 25940403 Free PMC article. Review.
Hoyeraal-Hreidarsson (HH) syndrome is a multisystem genetic disorder characterized by very short telomeres and considered a clinically severe variant of dyskeratosis congenita. ...
Hoyeraal-Hreidarsson (HH) syndrome is a multisystem genetic disorder characterized by very short telomeres and consider …
254 results