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1965
2025

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Year Number of Results
1965 1
1970 1
1974 1
1985 1
1987 1
1988 1
1992 2
1993 2
1994 1
1996 2
1997 3
1998 1
2000 3
2001 5
2003 3
2004 2
2005 2
2006 4
2007 5
2008 2
2009 1
2012 3
2013 4
2014 3
2015 4
2016 2
2017 1
2018 2
2019 2
2020 2
2025 0

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60 results

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Page 1
Ciliopathy: Sjogren-Larsson Syndrome.
Tsang SH, Aycinena ARP, Sharma T. Tsang SH, et al. Adv Exp Med Biol. 2018;1085:181-182. doi: 10.1007/978-3-319-95046-4_36. Adv Exp Med Biol. 2018. PMID: 30578509 Review.
Sjogren-Larsson syndrome.
Dutra LA, Braga-Neto P, Pedroso JL, Povoas Barsottini OG. Dutra LA, et al. Adv Exp Med Biol. 2012;724:344-50. doi: 10.1007/978-1-4614-0653-2_26. Adv Exp Med Biol. 2012. PMID: 22411255 Review.
Sjogren-Larsson syndrome is a rare disease characterized by the occurrence of mental retardation, spastic diplegia and ichthyosis. ...
Sjogren-Larsson syndrome is a rare disease characterized by the occurrence of mental retardation, spastic diplegia and
Sjogren-Larsson syndrome.
Gordon N. Gordon N. Dev Med Child Neurol. 2007 Feb;49(2):152-4. doi: 10.1111/j.1469-8749.2007.00152.x. Dev Med Child Neurol. 2007. PMID: 17254005 Free article. Review.
Sjogren-Larsson syndrome is a recessively inherited syndrome caused by deficiency of fatty aldehyde dehydrogenase. ...
Sjogren-Larsson syndrome is a recessively inherited syndrome caused by deficiency of fatty aldehyde dehydrogenas
Sjogren-Larsson syndrome associated hypermelanosis.
Xu YC, Hou JQ, Zhu WJ, Li P. Xu YC, et al. J Cosmet Dermatol. 2020 Apr;19(4):789-798. doi: 10.1111/jocd.13209. Epub 2019 Nov 7. J Cosmet Dermatol. 2020. PMID: 31697031 Review.
BACKGROUND/OBJECTIVES: Sjogren - Larsson syndrome (SLS) is a rare autosomal recessive disease of the mutation ALDH3A2 that identifies a part of fatty acids for fatty aldehyde dehydrogenase: NAD-oxidoreductase enzyme complex. ...METHODS: In Nov 2018, we perfor …
BACKGROUND/OBJECTIVES: Sjogren - Larsson syndrome (SLS) is a rare autosomal recessive disease of the mutation ALDH3A2 t …
Phytol in a pharma-medico-stance.
Islam MT, de Alencar MV, da Conceição Machado K, da Conceição Machado K, de Carvalho Melo-Cavalcante AA, de Sousa DP, de Freitas RM. Islam MT, et al. Chem Biol Interact. 2015 Oct 5;240:60-73. doi: 10.1016/j.cbi.2015.07.010. Epub 2015 Aug 19. Chem Biol Interact. 2015. PMID: 26296761 Review.
In addition, it may be considered as an important biomarker for some diseases such as Refsum's Disease (RD), Sjogren Larsson syndrome (SLS), rhizomelic chondrodysplasia punctata (RZCP), chronic polyneuropathy (CP), Zellweger's disease hyperpipecolic academia …
In addition, it may be considered as an important biomarker for some diseases such as Refsum's Disease (RD), Sjogren Larsson
Clinical, biochemical, and genetic aspects of Sjogren-Larsson syndrome.
Cho KH, Shim SH, Kim M. Cho KH, et al. Clin Genet. 2018 Apr;93(4):721-730. doi: 10.1111/cge.13058. Epub 2017 Sep 17. Clin Genet. 2018. PMID: 28543186 Review.
Sjogren-Larsson syndrome (SLS) is caused by an autosomal recessive mutation in ALDH3A2, which encodes the fatty aldehyde dehydrogenase responsible for the metabolism of long-chain aliphatic aldehydes and alcohols. ...In addition, the differential diagnoses of
Sjogren-Larsson syndrome (SLS) is caused by an autosomal recessive mutation in ALDH3A2, which encodes the fatty aldehyd
Inherited ichthyosis: Syndromic forms.
Yoneda K. Yoneda K. J Dermatol. 2016 Mar;43(3):252-63. doi: 10.1111/1346-8138.13284. J Dermatol. 2016. PMID: 26945533 Review.
Although these syndromes are very rare, Netherton syndrome, Sjogren-Larsson syndrome, Conradi-Hunermann-Happle syndrome, Dorfman-Chanarin syndrome, ichthyosis follicularis, atrichia and photophobia (IFAP) syndrome, and Refsum sy
Although these syndromes are very rare, Netherton syndrome, Sjogren-Larsson syndrome, Conradi-Hunermann-Happle …
[Sjogren-Larsson syndrome].
Morice F, Léauté-Labrèze C. Morice F, et al. Ann Dermatol Venereol. 2006 Jan;133(1):83-90. doi: 10.1016/s0151-9638(06)70854-7. Ann Dermatol Venereol. 2006. PMID: 16495864 Review. French. No abstract available.
Sjogren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency.
Rizzo WB. Rizzo WB. Mol Genet Metab. 2007 Jan;90(1):1-9. doi: 10.1016/j.ymgme.2006.08.006. Epub 2006 Sep 22. Mol Genet Metab. 2007. PMID: 16996289 Free PMC article. Review.
Sjogren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder caused by mutations in the ALDH3A2 gene that encodes fatty aldehyde dehydrogenase (FALDH), an enzyme that catalyzes the oxidation of fatty aldehyde to fatty acid. ...
Sjogren-Larsson syndrome (SLS) is an inherited neurocutaneous disorder caused by mutations in the ALDH3A2 gene that enc
Sjogren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2).
Rizzo WB, Carney G. Rizzo WB, et al. Hum Mutat. 2005 Jul;26(1):1-10. doi: 10.1002/humu.20181. Hum Mutat. 2005. PMID: 15931689 Review.
Sjogren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, and spastic diplegia or tetraplegia. ...
Sjogren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, and
60 results