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

Year Number of Results
1870 1
1878 1
1880 1
1911 1
1912 1
1913 1
1915 1
1917 1
1922 3
1923 1
1927 1
1929 1
1932 2
1936 1
1945 1
1946 3
1947 7
1948 2
1949 1
1950 5
1951 7
1952 11
1953 11
1954 16
1955 11
1956 11
1957 15
1958 26
1959 17
1960 16
1961 19
1962 29
1963 53
1964 53
1965 30
1966 14
1967 11
1968 17
1969 21
1970 31
1971 53
1972 41
1973 44
1974 52
1975 60
1976 49
1977 86
1978 65
1979 53
1980 54
1981 62
1982 61
1983 73
1984 76
1985 68
1986 56
1987 67
1988 59
1989 65
1990 97
1991 90
1992 106
1993 92
1994 98
1995 106
1996 99
1997 96
1998 97
1999 97
2000 97
2001 137
2002 142
2003 164
2004 186
2005 207
2006 208
2007 238
2008 221
2009 240
2010 306
2011 311
2012 310
2013 379
2014 448
2015 488
2016 496
2017 542
2018 593
2019 648
2020 813
2021 920
2022 891
2023 836
2024 320

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11,363 results

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The following term was not found in PubMed: Yong-Haur
Page 1
Did you mean yong hua tang (11 results)?
Tay-Sachs disease.
Fernandes Filho JA, Shapiro BE. Fernandes Filho JA, et al. Arch Neurol. 2004 Sep;61(9):1466-8. doi: 10.1001/archneur.61.9.1466. Arch Neurol. 2004. PMID: 15364698 Review. No abstract available.
New Approaches to Tay-Sachs Disease Therapy.
Solovyeva VV, Shaimardanova AA, Chulpanova DS, Kitaeva KV, Chakrabarti L, Rizvanov AA. Solovyeva VV, et al. Front Physiol. 2018 Nov 20;9:1663. doi: 10.3389/fphys.2018.01663. eCollection 2018. Front Physiol. 2018. PMID: 30524313 Free PMC article. Review.
Tay-Sachs disease belongs to the group of autosomal-recessive lysosomal storage metabolic disorders. ...This review discusses the possibilities of new therapeutic strategies in Tay-Sachs disease therapy aimed at preventing neurodegeneration and neuroinflammation....
Tay-Sachs disease belongs to the group of autosomal-recessive lysosomal storage metabolic disorders. ...This review discusses the pos
Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene.
Myerowitz R. Myerowitz R. Hum Mutat. 1997;9(3):195-208. doi: 10.1002/(SICI)1098-1004(1997)9:3<195::AID-HUMU1>3.0.CO;2-7. Hum Mutat. 1997. PMID: 9090523 Review.
Tay-Sachs disease is an autosomal recessive disorder affecting the central nervous system. ...Six nonsense mutations and 14 splice site lesions result from single base substitutions, and all but one of the splice site lesions cause a severe form of Tay-Sachs disease
Tay-Sachs disease is an autosomal recessive disorder affecting the central nervous system. ...Six nonsense mutations and 14 splice si
Tay-Sachs disease.
Gelbart M. Gelbart M. Nurs Times. 1998 Mar 18-24;94(11):39. Nurs Times. 1998. PMID: 9697531 Review. No abstract available.
[Tay-Sachs disease].
Tanaka A. Tanaka A. Nihon Rinsho. 1993 Sep;51(9):2281-5. Nihon Rinsho. 1993. PMID: 8411703 Review. Japanese.
In the severest phenotype of Tay-Sachs disease (infantile form), mRNA of beta-hexosaminidase alpha subunit is not produced or is unstable such as in French Canadian patients or in Jewish patients with infantile Tay-Sachs disease, or the polypeptide does not have any …
In the severest phenotype of Tay-Sachs disease (infantile form), mRNA of beta-hexosaminidase alpha subunit is not produced or is unst …
Attention-Deficit/Hyperactivity Disorder and Transitional Aged Youth.
Wilens TE, Isenberg BM, Kaminski TA, Lyons RM, Quintero J. Wilens TE, et al. Curr Psychiatry Rep. 2018 Sep 17;20(11):100. doi: 10.1007/s11920-018-0968-x. Curr Psychiatry Rep. 2018. PMID: 30221318 Review.
The purpose of this review is to provide an update on the evaluation, diagnosis, and treatment of TAY-ADHD. RECENT FINDINGS: Recent studies discovering ADHD symptoms emerging in TAY call the classification of ADHD as a disorder necessarily developing in childhood in …
The purpose of this review is to provide an update on the evaluation, diagnosis, and treatment of TAY-ADHD. RECENT FINDINGS: Recent s …
[Tay-Sachs disease].
Itoh T, Miura AB. Itoh T, et al. Ryoikibetsu Shokogun Shirizu. 1998;(22 Pt 3):389-92. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9851170 Review. Japanese. No abstract available.
Genetics and Therapies for GM2 Gangliosidosis.
Cachon-Gonzalez MB, Zaccariotto E, Cox TM. Cachon-Gonzalez MB, et al. Curr Gene Ther. 2018;18(2):68-89. doi: 10.2174/1566523218666180404162622. Curr Gene Ther. 2018. PMID: 29618308 Free PMC article. Review.
Tay-Sachs disease, caused by impaired beta-N-acetylhexosaminidase activity, was the first GM2 gangliosidosis to be studied and one of the most severe and earliest lysosomal diseases to be described. ...
Tay-Sachs disease, caused by impaired beta-N-acetylhexosaminidase activity, was the first GM2 gangliosidosis to be studied and one of
Late-onset Tay-Sachs disease.
Barritt AW, Anderson SJ, Leigh PN, Ridha BH. Barritt AW, et al. Pract Neurol. 2017 Oct;17(5):396-399. doi: 10.1136/practneurol-2017-001665. Epub 2017 Jul 24. Pract Neurol. 2017. PMID: 28739864
(Gly269Ser)), confirming the very rare diagnosis of adult-onset Tay-Sachs disease....
(Gly269Ser)), confirming the very rare diagnosis of adult-onset Tay-Sachs disease....
Cherry-red spot.
Suvarna JC, Hajela SA. Suvarna JC, et al. J Postgrad Med. 2008 Jan-Mar;54(1):54-7. doi: 10.4103/0022-3859.39196. J Postgrad Med. 2008. PMID: 18296811 No abstract available.
11,363 results
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