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

Year Number of Results
1987 1
1991 1
1992 3
1993 1
1994 2
1995 3
1996 4
1997 3
1998 8
1999 9
2000 11
2001 8
2002 12
2003 10
2004 6
2005 7
2006 3
2007 6
2008 7
2009 3
2010 4
2011 6
2012 7
2013 2
2014 7
2015 6
2016 3
2017 3
2018 9
2019 2
2020 5
2021 3
2022 4
2023 5
2024 0

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161 results

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Page 1
Birt-Hogg-Dubé Syndrome.
Sattler EC, Steinlein OK. Sattler EC, et al. Among authors: steinlein ok. 2006 Feb 27 [updated 2020 Jan 30]. 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. 2006 Feb 27 [updated 2020 Jan 30]. 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: 20301695 Free Books & Documents. Review.
Response.
Sattler EC, Syunyaeva Z, Mansmann U, Steinlein OK. Sattler EC, et al. Among authors: steinlein ok. Chest. 2020 Oct;158(4):1793-1794. doi: 10.1016/j.chest.2020.05.522. Chest. 2020. PMID: 33036104 No abstract available.
[Cancer-associated genodermatoses].
Frommherz LH, Steinlein OK, French LE, Sattler EC. Frommherz LH, et al. Among authors: steinlein ok. Hautarzt. 2021 Apr;72(4):288-294. doi: 10.1007/s00105-021-04779-4. Epub 2021 Mar 4. Hautarzt. 2021. PMID: 33661338 Review. German.
Update of penetrance estimates in Birt-Hogg-Dubé syndrome.
Bruinsma FJ, Dowty JG, Win AK, Goddard LC, Agrawal P, Attina' D, Bissada N, De Luise M, Eisen DB, Furuya M, Gasparre G, Genuardi M, Gerdes AM, Hansen TVO, Houweling AC, Johannesma PC, Lencastre A, Lim D, Lindor NM, Luzzi V, Lynch M, Maffé A, Menko FH, Michels G, Pulido JS, Ryu JH, Sattler EC, Steinlein OK, Tomassetti S, Tucker K, Turchetti D, van de Beek I, van Riel L, van Steensel M, Zenone T, Zompatori M, Walsh J, Bondavalli D, Maher ER, Winship IM; Genetic Susceptibility Working Group I-CONFIRM. Bruinsma FJ, et al. Among authors: steinlein ok. J Med Genet. 2023 Apr;60(4):317-326. doi: 10.1136/jmg-2022-109104. Epub 2023 Feb 27. J Med Genet. 2023. PMID: 36849229 Review.
Epilepsy-aphasia syndromes.
Steinlein OK. Steinlein OK. Expert Rev Neurother. 2009 Jun;9(6):825-33. doi: 10.1586/ern.09.49. Expert Rev Neurother. 2009. PMID: 19496686 Review.
Congenital myasthenic syndromes.
Sieb JP, Kraner S, Steinlein OK. Sieb JP, et al. Among authors: steinlein ok. Semin Pediatr Neurol. 2002 Jun;9(2):108-19. doi: 10.1053/spen.2002.33803. Semin Pediatr Neurol. 2002. PMID: 12138995 Review.
Preface. Genetics of epilepsy.
Steinlein OK. Steinlein OK. Prog Brain Res. 2014;213:vii. doi: 10.1016/B978-0-444-63326-2.10000-6. Prog Brain Res. 2014. PMID: 25194495 No abstract available.
Calcium signaling and epilepsy.
Steinlein OK. Steinlein OK. Cell Tissue Res. 2014 Aug;357(2):385-93. doi: 10.1007/s00441-014-1849-1. Epub 2014 Apr 11. Cell Tissue Res. 2014. PMID: 24723228 Review.
161 results