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

Year Number of Results
1947 1
1948 1
1949 1
1951 1
1955 1
1956 2
1957 4
1958 2
1961 1
1963 4
1964 1
1965 3
1966 1
1968 1
1970 2
1971 2
1972 2
1973 2
1974 7
1975 4
1977 2
1978 4
1979 5
1980 4
1981 6
1982 9
1983 2
1984 8
1985 7
1986 7
1987 5
1988 9
1989 9
1990 6
1991 3
1992 17
1993 10
1994 15
1995 4
1996 11
1997 14
1998 16
1999 22
2000 16
2001 16
2002 15
2003 33
2004 24
2005 36
2006 39
2007 50
2008 49
2009 59
2010 52
2011 65
2012 49
2013 67
2014 66
2015 66
2016 55
2017 57
2018 51
2019 54
2020 59
2021 70
2022 67
2023 63
2024 47

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1,326 results

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Page 1
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.
Stoopler ET, Shanti RM. Stoopler ET, et al. Mayo Clin Proc. 2019 Sep;94(9):1668-1669. doi: 10.1016/j.mayocp.2019.04.032. Mayo Clin Proc. 2019. PMID: 31486376 Review. No abstract available.
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 …
Dyskeratosis congenita.
Dokal I. Dokal I. Hematology Am Soc Hematol Educ Program. 2011;2011:480-6. doi: 10.1182/asheducation-2011.1.480. Hematology Am Soc Hematol Educ Program. 2011. PMID: 22160078 Review.
Dyskeratosis congenita (DC) is a multisystem inherited syndrome exhibiting marked clinical and genetic heterogeneity. ...
Dyskeratosis congenita (DC) is a multisystem inherited syndrome exhibiting marked clinical and genetic heterogeneity. ...
Dyskeratosis congenita.
Gupta V, Kumar A. Gupta V, et al. Adv Exp Med Biol. 2010;685:215-9. doi: 10.1007/978-1-4419-6448-9_20. Adv Exp Med Biol. 2010. PMID: 20687509 Free article. Review.
Dyskeratosis congenita (DC) is an inheritable bone marrow failure syndrome characterized by reticulated hyperpigmentation, dystrophic nails and oral leukoplakia. ...
Dyskeratosis congenita (DC) is an inheritable bone marrow failure syndrome characterized by reticulated hyperpigmentation, dys …
Dyskeratosis congenita.
Vulliamy T, Dokal I. Vulliamy T, et al. Semin Hematol. 2006 Jul;43(3):157-66. doi: 10.1053/j.seminhematol.2006.04.001. Semin Hematol. 2006. PMID: 16822458 Review.
Dyskeratosis congenita (DC) is a rare inherited multi-system disorder. ...
Dyskeratosis congenita (DC) is a rare inherited multi-system disorder. ...
Dyskeratosis congenita.
Handley TP, McCaul JA, Ogden GR. Handley TP, et al. Oral Oncol. 2006 Apr;42(4):331-6. doi: 10.1016/j.oraloncology.2005.06.007. Epub 2005 Sep 2. Oral Oncol. 2006. PMID: 16140563 Review.
Dyskeratosis congenita is an inherited disorder that usually presents in males, consisting of the triad of leukoplakia of the mucous membranes, nail dystrophy and skin pigmentation. ...
Dyskeratosis congenita is an inherited disorder that usually presents in males, consisting of the triad of leukoplakia of the …
Dyskeratosis Congenita.
Kelmenson DA, Hanley M. Kelmenson DA, et al. N Engl J Med. 2017 Apr 13;376(15):1460. doi: 10.1056/NEJMicm1613081. N Engl J Med. 2017. PMID: 28402761 Free article. No abstract available.
[Research progress of dyskeratosis congenita].
Wang F, Du YQ, Gong W, Sun CK, Zeng X. Wang F, et al. Zhonghua Kou Qiang Yi Xue Za Zhi. 2019 Feb 9;54(2):130-134. doi: 10.3760/cma.j.issn.1002-0098.2019.02.010. Zhonghua Kou Qiang Yi Xue Za Zhi. 2019. PMID: 30695916 Review. Chinese.
Dyskeratosis congenita (DC) is a rare disease and a genetic heterogeneity of bone marrow failure, characterized by muco-cutaneous triad of mucosal leukoplakia, abnormal skin pigmentation, nails dystrophy and often involving multiple organs or systems. ...However, th …
Dyskeratosis congenita (DC) is a rare disease and a genetic heterogeneity of bone marrow failure, characterized by muco-cutane …
Dyskeratosis congenita and telomerase.
Bessler M, Wilson DB, Mason PJ. Bessler M, et al. Curr Opin Pediatr. 2004 Feb;16(1):23-8. doi: 10.1097/00008480-200402000-00006. Curr Opin Pediatr. 2004. PMID: 14758110 Review.
Autosomal dominant dyskeratosis congenita is associated with mutations in the RNA component of telomerase, hTERC, while X-linked dyskeratosis congenita is due to mutations in the gene encoding dyskerin, a protein implicated in both telomerase function …
Autosomal dominant dyskeratosis congenita is associated with mutations in the RNA component of telomerase, hTERC, while X-link …
1,326 results