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

Year Number of Results
1993 780
1998 29
1999 30
2000 38
2001 32
2002 42
2003 55
2004 47
2005 44
2006 47
2007 44
2008 49
2009 36
2010 24
2011 23
2012 47
2013 46
2014 60
2015 81
2016 119
2017 112
2018 135
2019 159
2020 90
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Article attribute
Article type
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780 results
Results by year
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Page 1
Hereditary Hearing Loss and Deafness Overview.
Shearer AE, Hildebrand MS, Smith RJH. Shearer AE, et al. 1999 Feb 14 [updated 2017 Jul 27]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301607 Free Books & Documents. Review.
Neurodegeneration with Brain Iron Accumulation Disorders Overview.
Gregory A, Hayflick S. Gregory A, et al. 2013 Feb 28 [updated 2019 Oct 21]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 23447832 Free Books & Documents. Review.
Parkinson Disease Overview.
Cook Shukla L, Schulze J, Farlow J, Pankratz ND, Wojcieszek J, Foroud T. Cook Shukla L, et al. 2004 May 25 [updated 2019 Jul 25]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301402 Free Books & Documents. Review.
Charcot-Marie-Tooth (CMT) Hereditary Neuropathy Overview.
Bird TD. Bird TD. 1998 Sep 28 [updated 2020 May 14]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301532 Free Books & Documents. Review.
Hypertrophic Cardiomyopathy Overview.
Cirino AL, Ho C. Cirino AL, et al. 2008 Aug 5 [updated 2019 Jun 6]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301725 Free Books & Documents. Review.
Hereditary Ataxia Overview.
Bird TD. Bird TD. 1998 Oct 28 [updated 2019 Jul 25]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301317 Free Books & Documents. Review.
Hereditary Spastic Paraplegia Overview.
Hedera P. Hedera P. 2000 Aug 15 [updated 2018 Sep 27]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301682 Free Books & Documents. Review.
Amyotrophic Lateral Sclerosis Overview.
Siddique N, Siddique T. Siddique N, et al. 2001 Mar 23 [updated 2019 Oct 3]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301623 Free Books & Documents. Review.
Nonsyndromic Retinitis Pigmentosa Overview.
Fahim AT, Daiger SP, Weleber RG. Fahim AT, et al. 2000 Aug 4 [updated 2017 Jan 19]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301590 Free Books & Documents. Review.
Sotos Syndrome.
Tatton-Brown K, Cole TRP, Rahman N. Tatton-Brown K, et al. 2004 Dec 17 [updated 2019 Aug 1]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301652 Free Books & Documents. Review.
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