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Results by year

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

Year Number of Results
1965 1
1969 2
1971 1
1991 2
1992 1
1993 2
1997 1
2001 2
2004 3
2005 3
2006 3
2007 1
2011 4
2012 4
2013 6
2014 6
2015 6
2016 11
2017 12
2018 13
2019 6
2020 15
2021 21
2022 11
2023 16
2024 5

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137 results

Results by year

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Page 1
Snyder-Robinson Syndrome.
Schwartz CE, Peron A, Kutler MJ. Schwartz CE, et al. Among authors: peron a. 2013 Jun 27 [updated 2020 Feb 13]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2013 Jun 27 [updated 2020 Feb 13]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 23805436 Free Books & Documents. Review.
Tuberous sclerosis complex.
Peron A, Northrup H. Peron A, et al. Am J Med Genet C Semin Med Genet. 2018 Sep;178(3):274-277. doi: 10.1002/ajmg.c.31657. Epub 2018 Oct 16. Am J Med Genet C Semin Med Genet. 2018. PMID: 30325570 No abstract available.
BCL11A-Related Intellectual Disability.
Peron A, Bradbury K, Viskochil DH, Dias C. Peron A, et al. 2019 Sep 26. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2019 Sep 26. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 31556984 Free Books & Documents. Review.
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays.
Ganapathi M, Matsuoka LS, March M, Li D, Brokamp E, Benito-Sanz S, White SM, Lachlan K, Ahimaz P, Sewda A, Bastarache L, Thomas-Wilson A, Stoler JM, Bramswig NC, Baptista J, Stals K, Demurger F, Cogne B, Isidor B, Bedeschi MF, Peron A, Amiel J, Zackai E, Schacht JP, Iglesias AD, Morton J, Schmetz A; Undiagnosed Diseases Network; Seidel V, Lucia S, Baskin SM, Thiffault I, Cogan JD, Gordon CT, Chung WK, Bowdin S, Bhoj E. Ganapathi M, et al. Among authors: peron a. Eur J Hum Genet. 2023 Oct;31(10):1117-1124. doi: 10.1038/s41431-023-01434-5. Epub 2023 Jul 27. Eur J Hum Genet. 2023. PMID: 37500725
Current concepts on epilepsy management in tuberous sclerosis complex.
Canevini MP, Kotulska-Jozwiak K, Curatolo P, La Briola F, Peron A, Słowińska M, Strzelecka J, Vignoli A, Jóźwiak S. Canevini MP, et al. Among authors: peron a. Am J Med Genet C Semin Med Genet. 2018 Sep;178(3):299-308. doi: 10.1002/ajmg.c.31652. Epub 2018 Sep 26. Am J Med Genet C Semin Med Genet. 2018. PMID: 30255982 Review.
Ungual Keratoacanthoma With Features of Regression.
Fernandez-Flores A, García-Paíno L, Perón ÁS, Cassarino D. Fernandez-Flores A, et al. Among authors: peron as. Am J Dermatopathol. 2023 Feb 1;45(2):113-116. doi: 10.1097/DAD.0000000000002351. Am J Dermatopathol. 2023. PMID: 36669075
137 results