Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1975 1
1991 1
2001 1
2002 2
2003 1
2006 3
2007 2
2008 2
2009 2
2010 1
2011 2
2012 5
2013 2
2014 1
2015 1
2016 2
2017 7
2018 13
2019 13
2020 28
2021 24
2022 21
Text availability
Article attribute
Article type
Publication date

Search Results

114 results
Results by year
Filters applied: . Clear all
Page 1
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome.
Drivas TG, Li D, Nair D, Alaimo JT, Alders M, Altmüller J, Barakat TS, Bebin EM, Bertsch NL, Blackburn PR, Blesson A, Bouman AM, Brockmann K, Brunelle P, Burmeister M, Cooper GM, Denecke J, Dieux-Coëslier A, Dubbs H, Ferrer A, Gal D, Bartik LE, Gunderson LB, Hasadsri L, Jain M, Karimov C, Keena B, Klee EW, Kloth K, Lace B, Macchiaiolo M, Marcadier JL, Milunsky JM, Napier MP, Ortiz-Gonzalez XR, Pichurin PN, Pinner J, Powis Z, Prasad C, Radio FC, Rasmussen KJ, Renaud DL, Rush ET, Saunders C, Selcen D, Seman AR, Shinde DN, Smith ED, Smol T, Snijders Blok L, Stoler JM, Tang S, Tartaglia M, Thompson ML, van de Kamp JM, Wang J, Weise D, Weiss K, Woitschach R, Wollnik B, Yan H, Zackai EH, Zampino G, Campeau P, Bhoj E. Drivas TG, et al. Among authors: renaud dl. Eur J Hum Genet. 2020 Oct;28(10):1422-1431. doi: 10.1038/s41431-020-0654-4. Epub 2020 Jun 1. Eur J Hum Genet. 2020. PMID: 32483341 Free PMC article.
Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3.
Schirwani S, Albaba S, Carere DA, Guillen Sacoto MJ, Milan Zamora F, Si Y, Rabin R, Pappas J, Renaud DL, Hauser N, Reid E, Blanchet P, Foulds N, Dixit A, Fisher R, Armstrong R, Isidor B, Cogne B, Schrier Vergano S, Demirdas S, Dykzeul N, Cohen JS, Grand K, Morel D, Slavotinek A, Albassam HF, Naik S, Dean J, Ragge N, Cinzia C, Tedesco MG, Harrison RE, Bouman A, Palen E, Challman TD, Willemsen MH, Vogt J, Cunniff C, Bergstrom K, Walia JS, Bruel AL, Kini U, Alkuraya FS, Slegesky V, Meeks N, Girotto P, Johnson D; DDD Study, Newbury-Ecob R, Ockeloen CW, Prontera P, Lynch SA, Li D, Graham JM Jr, Balasubramanian M. Schirwani S, et al. Among authors: renaud dl. Am J Med Genet A. 2021 Nov;185(11):3446-3458. doi: 10.1002/ajmg.a.62465. Epub 2021 Aug 26. Am J Med Genet A. 2021. PMID: 34436830 Free article.
Inherited leukoencephalopathies.
Renaud DL. Renaud DL. Semin Neurol. 2012 Feb;32(1):3-8. doi: 10.1055/s-0032-1306380. Epub 2012 Mar 15. Semin Neurol. 2012. PMID: 22422201 No abstract available.
Adult-Onset Leukoencephalopathies.
Renaud DL. Renaud DL. Continuum (Minneap Minn). 2016 Apr;22(2 Dementia):559-78. doi: 10.1212/CON.0000000000000303. Continuum (Minneap Minn). 2016. PMID: 27042908 Review.
Leukoencephalopathies in adulthood.
Tillema JM, Renaud DL. Tillema JM, et al. Among authors: renaud dl. Semin Neurol. 2012 Feb;32(1):85-94. doi: 10.1055/s-0032-1306391. Epub 2012 Mar 15. Semin Neurol. 2012. PMID: 22422211 Review.
Pseudopapilledema in Cockayne syndrome.
Brodsky MC, Renaud DL. Brodsky MC, et al. Among authors: renaud dl. Am J Ophthalmol Case Rep. 2021 Feb 18;22:101035. doi: 10.1016/j.ajoc.2021.101035. eCollection 2021 Jun. Am J Ophthalmol Case Rep. 2021. PMID: 33681529 Free PMC article.
Childhood onset of stiff-man syndrome.
Clardy SL, Lennon VA, Dalmau J, Pittock SJ, Jones HR Jr, Renaud DL, Harper CM Jr, Matsumoto JY, McKeon A. Clardy SL, et al. Among authors: renaud dl. JAMA Neurol. 2013 Dec;70(12):1531-6. doi: 10.1001/jamaneurol.2013.4442. JAMA Neurol. 2013. PMID: 24100349 Free PMC article. Review.
114 results