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

Year Number of Results
1938 1
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1946 3
1947 1
1948 4
1949 6
1950 7
1951 5
1952 12
1953 8
1954 12
1955 15
1956 16
1957 16
1958 17
1959 12
1960 28
1961 24
1962 29
1963 24
1964 18
1965 33
1966 33
1967 31
1968 34
1969 49
1970 37
1971 63
1972 43
1973 57
1974 84
1975 109
1976 110
1977 126
1978 152
1979 139
1980 136
1981 159
1982 156
1983 177
1984 172
1985 186
1986 194
1987 224
1988 226
1989 229
1990 224
1991 241
1992 252
1993 250
1994 240
1995 288
1996 294
1997 287
1998 292
1999 328
2000 326
2001 343
2002 364
2003 325
2004 367
2005 435
2006 473
2007 474
2008 477
2009 494
2010 479
2011 564
2012 567
2013 638
2014 656
2015 639
2016 659
2017 671
2018 695
2019 675
2020 743
2021 754
2022 768
2023 675
2024 264

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17,836 results

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Page 1
Sjogren-Larsson syndrome: a complex metabolic disease with a distinctive ocular phenotype.
Fouzdar-Jain S, Suh DW, Rizzo WB. Fouzdar-Jain S, et al. Ophthalmic Genet. 2019 Aug;40(4):298-308. doi: 10.1080/13816810.2019.1660379. Epub 2019 Sep 12. Ophthalmic Genet. 2019. PMID: 31512987 Review.
Purpose: Sjogren-Larsson Syndrome (SLS) is a rare genetic disorder characterized by a distinctive crystalline maculopathy, congenital ichthyosis, spasticity and intellectual disability. ...
Purpose: Sjogren-Larsson Syndrome (SLS) is a rare genetic disorder characterized by a distinctive crystalline maculopathy, congenital …
A Neurodegenerative Phenotype Associated With Sjogren-Larsson Syndrome.
Warrack S, Love T, Rizzo WB. Warrack S, et al. J Child Neurol. 2021 Oct;36(11):1011-1016. doi: 10.1177/08830738211029390. Epub 2021 Jul 28. J Child Neurol. 2021. PMID: 34315315 Free PMC article.
Sjogren-Larsson syndrome (SLS) is a rare neurologic disorder caused by pathogenic sequence variants in ALDH3A2 and characterized by ichthyosis, spasticity, intellectual disability, and a crystalline retinopathy. ...Together with 7 additional published cases of these atypic …
Sjogren-Larsson syndrome (SLS) is a rare neurologic disorder caused by pathogenic sequence variants in ALDH3A2 and characterized by i …
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 ichthyosis. .. …
Sjogren-Larsson Syndrome: A Rare Presentation With Developmental Delay.
J SK, Waheed MD, Batool S, Holder SS, Rodriguez Reyes Y, Guntha M. J SK, et al. Cureus. 2023 Feb 18;15(2):e35159. doi: 10.7759/cureus.35159. eCollection 2023 Feb. Cureus. 2023. PMID: 36950004 Free PMC article.
Sjogren-Larsson syndrome (SLS) is a rare, inherited disorder passed down through families in an autosomal recessive pattern. ...
Sjogren-Larsson syndrome (SLS) is a rare, inherited disorder passed down through families in an autosomal recessive pattern. ...
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 dehydrogenase. ...
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 performed a literatu …
BACKGROUND/OBJECTIVES: Sjogren - Larsson syndrome (SLS) is a rare autosomal recessive disease of the mutation ALDH3A2 that identifies …
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.
A rare case of Sjogren-Larsson syndrome with recurrent pneumonia and asthma.
Tavasoli A, Sayyahfar S, Behnam B. Tavasoli A, et al. Korean J Pediatr. 2016 Jun;59(6):276-9. doi: 10.3345/kjp.2016.59.6.276. Epub 2016 Jun 30. Korean J Pediatr. 2016. PMID: 27462357 Free PMC article.
Sjogren-Larsson syndrome (SLS) is a rare autosomal recessive neurocutaneous disorder with worldwide incidence of 0.4 per 100,000 people. ...
Sjogren-Larsson syndrome (SLS) is a rare autosomal recessive neurocutaneous disorder with worldwide incidence of 0.4 per 100,000 peop …
[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: Anesthetic considerations and practical recommendations.
Franzen MH, LeRiger MM, Pellegrino KP, Kugler JA, Rizzo WB. Franzen MH, et al. Paediatr Anaesth. 2020 Dec;30(12):1390-1395. doi: 10.1111/pan.14034. Epub 2020 Oct 26. Paediatr Anaesth. 2020. PMID: 33037729 Free PMC article.
Most individuals with Sjogren-Larsson syndrome live well into adulthood and often require surgical intervention to manage their symptomatology. ...CONCLUSIONS: We found that anesthesia can be safely administered in patients with Sjogren-Larsson syndrome. Providers s …
Most individuals with Sjogren-Larsson syndrome live well into adulthood and often require surgical intervention to manage their sympt …
17,836 results
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