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

Year Number of Results
1912 1
1914 1
1915 1
1922 1
1931 1
1932 1
1946 1
1947 1
1960 1
1964 2
1965 4
1967 2
1968 3
1969 2
1972 1
1973 2
1974 2
1975 5
1976 2
1977 2
1978 4
1979 3
1980 5
1981 6
1982 6
1983 15
1984 7
1985 5
1986 8
1987 5
1988 12
1989 14
1990 13
1991 21
1992 12
1993 22
1994 22
1995 19
1996 52
1997 29
1998 19
1999 24
2000 21
2001 14
2002 19
2003 31
2004 33
2005 36
2006 34
2007 34
2008 30
2009 29
2010 36
2011 32
2012 47
2013 59
2014 59
2015 46
2016 62
2017 56
2018 42
2019 47
2020 73
2021 9
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1,098 results
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Page 1
Canavan Disease.
Bokhari MR, Samanta D, Bokhari SRA. Bokhari MR, et al. 2020 Jul 6. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan–. StatPearls. 2020 Jan–. PMID: 28613566 Free Books & Documents. Review.
Canavan disease, also called Canavan-Van Bogaert-Bertrand disease, is a rare, progressive, and fatal neurological hereditary disorder that begins in infancy. ...
Canavan disease, also called Canavan-Van Bogaert-Bertrand disease, is a rare, progressive, and fatal neurological hereditary d
Canavan Disease.
Matalon R, Delgado L, Michals-Matalon K. Matalon R, et al. 1999 Sep 16 [updated 2018 Sep 13]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. GeneReviews®. 1993–2021. PMID: 20301412 Free Books & Documents. Review.
Surveillance: Neonatal/infantile Canavan disease. Follow up every six months to evaluate developmental status and evidence of any new problems. Mild/juvenile Canavan disease. Annual routine follow up by a pediatric neurologist or a developmental pediatrician is indi …
Surveillance: Neonatal/infantile Canavan disease. Follow up every six months to evaluate developmental status and evidence of any new …
Myrtelle May Canavan.
Akkermans R. Akkermans R. Lancet Neurol. 2020 Jul;19(7):569. doi: 10.1016/S1474-4422(19)30167-X. Epub 2019 May 7. Lancet Neurol. 2020. PMID: 31076243 No abstract available.
[Mild Canavan disease in a child].
Zhou J, Ding CH, Zhuo XW, Ren XT, Zhang WH, Gong S. Zhou J, et al. Zhonghua Er Ke Za Zhi. 2019 Dec 2;57(12):961-963. doi: 10.3760/cma.j.issn.0578-1310.2019.12.014. Zhonghua Er Ke Za Zhi. 2019. PMID: 31795566 Chinese.
Canavan disease: an Arab scenario.
Zayed H. Zayed H. Gene. 2015 Apr 10;560(1):9-14. doi: 10.1016/j.gene.2015.02.009. Epub 2015 Feb 7. Gene. 2015. PMID: 25668701 Review.
The autosomal recessive Canavan disease (CD) is a neurological disorder that begins in infancy. ...
The autosomal recessive Canavan disease (CD) is a neurological disorder that begins in infancy. ...
Pathophysiology and Treatment of Canavan Disease.
Pleasure D, Guo F, Chechneva O, Bannerman P, McDonough J, Burns T, Wang Y, Hull V. Pleasure D, et al. Neurochem Res. 2020 Mar;45(3):561-565. doi: 10.1007/s11064-018-2693-6. Epub 2018 Dec 8. Neurochem Res. 2020. PMID: 30535831 No abstract available.
Severe retinal degeneration in a patient with Canavan disease.
Benson MD, Plemel DJA, Freund PR, Lewis JR, Sass JO, Bähr L, Gemperle-Britschgi C, Ferreira P, MacDonald IM. Benson MD, et al. Ophthalmic Genet. 2020 Sep 25:1-4. doi: 10.1080/13816810.2020.1827441. Online ahead of print. Ophthalmic Genet. 2020. PMID: 32975148
Investigations for an alternative cause for our patient's retinal degeneration were non-revealing. Conclusion: We wonder if retinal degeneration may not have been previously recognized as a feature of Canavan disease. We highlight findings from animal models of C
Investigations for an alternative cause for our patient's retinal degeneration were non-revealing. Conclusion: We wonder if retinal d …
Canavan disease: clinical features and recent advances in research.
Hoshino H, Kubota M. Hoshino H, et al. Pediatr Int. 2014 Aug;56(4):477-83. doi: 10.1111/ped.12422. Pediatr Int. 2014. PMID: 24977939 Review.
Canavan disease (CD) is a genetic neurodegenerative leukodystrophy that results in the spongy degeneration of white matter in the brain. ...
Canavan disease (CD) is a genetic neurodegenerative leukodystrophy that results in the spongy degeneration of white matter in the bra
A thematic review of scientific and family interests in Canavan Disease: where are the developmentalists?
Glicksman S, Borgen C, Blackstein M, Gordon A, Hanon I, Kusin D, Leibowitz B, Halle J. Glicksman S, et al. J Intellect Disabil Res. 2013 Sep;57(9):815-25. doi: 10.1111/j.1365-2788.2012.01576.x. Epub 2012 Jun 8. J Intellect Disabil Res. 2013. PMID: 22676184 Review.
BACKGROUND: Canavan Disease is a degenerative neurological condition resulting in a spongy deterioration of the brain. ...RESULTS: When comparing the topics discussed and information sought among parents with the themes noted in the extant scientific literature, researcher …
BACKGROUND: Canavan Disease is a degenerative neurological condition resulting in a spongy deterioration of the brain. ...RESULTS: Wh …
Canavan's disease.
Pearce JM. Pearce JM. J Neurol Neurosurg Psychiatry. 2004 Oct;75(10):1410. doi: 10.1136/jnnp.2003.022699. J Neurol Neurosurg Psychiatry. 2004. PMID: 15377686 Free PMC article. No abstract available.
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