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

Year Number of Results
1967 1
1974 1
1975 3
1976 2
1977 2
1978 1
1980 2
1981 1
1982 2
1984 4
1986 3
1987 1
1988 6
1989 7
1990 7
1991 5
1992 4
1993 4
1994 4
1995 10
1996 5
1997 8
1998 5
1999 9
2000 9
2001 12
2002 7
2003 20
2004 12
2005 15
2006 16
2007 14
2008 14
2009 14
2010 19
2011 21
2012 21
2013 20
2014 24
2015 13
2016 16
2017 17
2018 25
2019 27
2020 35
2021 32
2022 34
2023 30
2024 5

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506 results

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Page 1
Lung cancer is also a hereditary disease.
Benusiglio PR, Fallet V, Sanchis-Borja M, Coulet F, Cadranel J. Benusiglio PR, et al. Eur Respir Rev. 2021 Oct 20;30(162):210045. doi: 10.1183/16000617.0045-2021. Print 2021 Dec 31. Eur Respir Rev. 2021. PMID: 34670806 Free PMC article. Review.
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. ...
Dyskeratosis congenita is a rare hereditary disease that occurs predominantly in males and manifests clinically as the classic …
Retinoblastoma.
Lohmann D. Lohmann D. Adv Exp Med Biol. 2010;685:220-7. doi: 10.1007/978-1-4419-6448-9_21. Adv Exp Med Biol. 2010. PMID: 20687510 Review.
In families, Rb predisposition is transmitted as an autosomal dominant trait (familial Rb). In addition to Rb, patients with hereditary disease also have an increased risk of tumors outside the eye (second cancer). ...
In families, Rb predisposition is transmitted as an autosomal dominant trait (familial Rb). In addition to Rb, patients with hereditary
Recent Status in Brugada Syndrome.
Bayrak F, Brugada P. Bayrak F, et al. Turk Kardiyol Dern Ars. 2022 Mar 1;50(2):137-144. doi: 10.5543/tkda.2022.21020. Turk Kardiyol Dern Ars. 2022. PMID: 35400636 Free article. Review.
Brugada Syndrome is one of the most common reasons for sudden cardiac death (4-12%) and is a hereditary disease with an autosomal dominant pattern of transmission with nearly 300 pathogenic variants in 19 responsible genes published. ...
Brugada Syndrome is one of the most common reasons for sudden cardiac death (4-12%) and is a hereditary disease with an autoso …
Fanconi anemia.
Bagby GC, Alter BP. Bagby GC, et al. Semin Hematol. 2006 Jul;43(3):147-56. doi: 10.1053/j.seminhematol.2006.04.005. Semin Hematol. 2006. PMID: 16822457 Review.
Fanconi anemia (FA) is a rare hereditary disease characterized by bone marrow failure and developmental anomalies; a high incidence of myelodysplasia (MDS), acute nonlymphocytic leukemia (AML), and solid tumors; and cellular hypersensitivity to cross-linking agents. …
Fanconi anemia (FA) is a rare hereditary disease characterized by bone marrow failure and developmental anomalies; a high inci …
Pathology and genetics of phaeochromocytoma and paraganglioma.
Turchini J, Cheung VKY, Tischler AS, De Krijger RR, Gill AJ. Turchini J, et al. Histopathology. 2018 Jan;72(1):97-105. doi: 10.1111/his.13402. Histopathology. 2018. PMID: 29239044 Review.
Advances in molecular understanding have led to the recognition that at least 30-40% arise in the setting of hereditary disease. Germline mutations in the succinate dehydrogenase genes SDHA, SDHB, SDHC, SDHD and SDHAF2 are the most prevalent of the more than 19 here …
Advances in molecular understanding have led to the recognition that at least 30-40% arise in the setting of hereditary disease
Germline genetic factors in the pathogenesis of myeloproliferative neoplasms.
Bellanné-Chantelot C, Rabadan Moraes G, Schmaltz-Panneau B, Marty C, Vainchenker W, Plo I. Bellanné-Chantelot C, et al. Blood Rev. 2020 Jul;42:100710. doi: 10.1016/j.blre.2020.100710. Epub 2020 May 29. Blood Rev. 2020. PMID: 32532454 Review.
Finally, some extremely rare genetic variants can induce MPN-like hereditary disease. We will review these different subtypes of germline genetic variants and discuss how they impact the initiation and/or development of the MPN disease....
Finally, some extremely rare genetic variants can induce MPN-like hereditary disease. We will review these different subtypes …
Cats: a gold mine for ophthalmology.
Narfström K, Deckman KH, Menotti-Raymond M. Narfström K, et al. Annu Rev Anim Biosci. 2013 Jan;1:157-77. doi: 10.1146/annurev-animal-031412-103629. Epub 2013 Jan 1. Annu Rev Anim Biosci. 2013. PMID: 25387015 Review.
Over 200 hereditary diseases have been identified and reported in the cat, several of which affect the eye, with homology to human hereditary disease. Compared with traditional murine models, the cat demonstrates more features in common with humans, including many a …
Over 200 hereditary diseases have been identified and reported in the cat, several of which affect the eye, with homology to human heredi
506 results