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Year Number of Results
1943 1
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1946 1
1947 1
1948 4
1949 7
1950 17
1951 14
1952 7
1953 4
1954 4
1955 3
1956 5
1957 7
1958 1
1959 7
1960 10
1961 8
1962 6
1963 9
1964 5
1965 9
1966 8
1967 6
1968 5
1969 11
1970 12
1971 10
1972 11
1973 4
1974 10
1975 24
1976 28
1977 25
1978 26
1979 26
1980 25
1981 13
1982 21
1983 16
1984 21
1985 14
1986 20
1987 19
1988 15
1989 15
1990 25
1991 14
1992 34
1993 33
1994 20
1995 20
1996 22
1997 23
1998 28
1999 29
2000 43
2001 19
2002 31
2003 30
2004 34
2005 32
2006 38
2007 54
2008 49
2009 40
2010 47
2011 55
2012 48
2013 74
2014 72
2015 70
2016 62
2017 68
2018 72
2019 71
2020 75
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2023 72
2024 25

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363 results

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Page 1
Sturge-Weber Syndrome: A Review.
Higueros E, Roe E, Granell E, Baselga E. Higueros E, et al. Actas Dermosifiliogr. 2017 Jun;108(5):407-417. doi: 10.1016/j.ad.2016.09.022. Epub 2017 Jan 23. Actas Dermosifiliogr. 2017. PMID: 28126187 Free article. Review. English, Spanish.
Sturge-Weber syndrome is a sporadic congenital neurocutaneous disorder caused by a somatic activating mutation in GNAQ; it affects 1 in every 20,000 to 50,000 newborns. ...Neuroimaging studies show leptomeningeal angiomatosis, supporting diagnosis. Standard t …
Sturge-Weber syndrome is a sporadic congenital neurocutaneous disorder caused by a somatic activating mutation in GNAQ; …
Consensus Statement for the Management and Treatment of Port-Wine Birthmarks in Sturge-Weber Syndrome.
Sabeti S, Ball KL, Burkhart C, Eichenfield L, Fernandez Faith E, Frieden IJ, Geronemus R, Gupta D, Krakowski AC, Levy ML, Metry D, Nelson JS, Tollefson MM, Kelly KM. Sabeti S, et al. JAMA Dermatol. 2021 Jan 1;157(1):98-104. doi: 10.1001/jamadermatol.2020.4226. JAMA Dermatol. 2021. PMID: 33175124 Free PMC article. Review.
IMPORTANCE: Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome involving the skin, brain, and eyes. ...
IMPORTANCE: Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome involving the skin, brain, and eyes. ...
Sturge-Weber syndrome.
Ho TH, Yang FC, Lin JC, Hsu CH, Lee JT. Ho TH, et al. QJM. 2019 Apr 1;112(4):299. doi: 10.1093/qjmed/hcy246. QJM. 2019. PMID: 30357409 No abstract available.
Ocular Manifestations of the Sturge-Weber Syndrome.
Hassanpour K, Nourinia R, Gerami E, Mahmoudi G, Esfandiari H. Hassanpour K, et al. J Ophthalmic Vis Res. 2021 Jul 29;16(3):415-431. doi: 10.18502/jovr.v16i3.9438. eCollection 2021 Jul-Sep. J Ophthalmic Vis Res. 2021. PMID: 34394871 Free PMC article. Review.
Sturge-Weber syndrome (SWS) or encephalotrigeminal angiomatosis is a non-inherited congenital disorder characterized by neurologic, skin, and ocular abnormalities. ...
Sturge-Weber syndrome (SWS) or encephalotrigeminal angiomatosis is a non-inherited congenital disorder characterized by …
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons.
Bianchi F, Auricchio AM, Battaglia DI, Chieffo DRP, Massimi L. Bianchi F, et al. Childs Nerv Syst. 2020 Oct;36(10):2553-2570. doi: 10.1007/s00381-020-04695-3. Epub 2020 Jun 21. Childs Nerv Syst. 2020. PMID: 32564157 Review.
PURPOSE: Sturge-Weber syndrome (SWS) is a neurocutaneous facomatosis characterized by facial and leptomeningeal angioma, glaucoma, seizures, and neurological disability. ...
PURPOSE: Sturge-Weber syndrome (SWS) is a neurocutaneous facomatosis characterized by facial and leptomeningeal angioma …
Neurological Complications of Sturge-Weber Syndrome: Current Status and Unmet Needs.
Luat AF, Juhász C, Loeb JA, Chugani HT, Falchek SJ, Jain B, Greene-Roethke C, Amlie-Lefond C, Ball KL, Davis A, Pinto A. Luat AF, et al. Pediatr Neurol. 2019 Sep;98:31-38. doi: 10.1016/j.pediatrneurol.2019.05.013. Epub 2019 Jun 6. Pediatr Neurol. 2019. PMID: 31272784 Review.
Each patient with Sturge-Weber syndrome should have an individualized seizure action plan. ...CONCLUSION: We identified the unmet needs in the management of neurological complications in Sturge-Weber syndrome. We define a minimum standard …
Each patient with Sturge-Weber syndrome should have an individualized seizure action plan. ...CONCLUSION: We identified …
Ocular manifestations of Sturge-Weber syndrome.
Silverstein M, Salvin J. Silverstein M, et al. Curr Opin Ophthalmol. 2019 Sep;30(5):301-305. doi: 10.1097/ICU.0000000000000597. Curr Opin Ophthalmol. 2019. PMID: 31313748 Review.
PURPOSE OF REVIEW: Sturge-Weber syndrome (SWS) is a rare, congenital disease which frequently involves the eye. It is important that ophthalmologists recognize this syndrome and are aware of its range of ocular manifestations. The aim of this article i …
PURPOSE OF REVIEW: Sturge-Weber syndrome (SWS) is a rare, congenital disease which frequently involves the eye. It is i …
Consensus Statement for the Management and Treatment of Sturge-Weber Syndrome: Neurology, Neuroimaging, and Ophthalmology Recommendations.
Sabeti S, Ball KL, Bhattacharya SK, Bitrian E, Blieden LS, Brandt JD, Burkhart C, Chugani HT, Falchek SJ, Jain BG, Juhasz C, Loeb JA, Luat A, Pinto A, Segal E, Salvin J, Kelly KM. Sabeti S, et al. Pediatr Neurol. 2021 Aug;121:59-66. doi: 10.1016/j.pediatrneurol.2021.04.013. Epub 2021 May 6. Pediatr Neurol. 2021. PMID: 34153815 Free PMC article.
BACKGROUND: Sturge-Weber syndrome (SWS) is a sporadic, neurocutaneous syndrome involving the skin, brain, and eyes. ...
BACKGROUND: Sturge-Weber syndrome (SWS) is a sporadic, neurocutaneous syndrome involving the skin, brain, and ey …
Sturge-Weber Syndrome.
Desai S, Glasier C. Desai S, et al. N Engl J Med. 2017 Aug 31;377(9):e11. doi: 10.1056/NEJMicm1700538. N Engl J Med. 2017. PMID: 28854093 Free article. No abstract available.
[Sturge-Weber Syndrome].
Sadahira C. Sadahira C. Brain Nerve. 2019 Apr;71(4):384-389. doi: 10.11477/mf.1416201281. Brain Nerve. 2019. PMID: 30988226 Japanese.
The cutaneous findings associated with Sturge-Weber syndrome (SWS) are characterized by a port-wine stain at the site of the first branching of the trigeminal nerve. ...
The cutaneous findings associated with Sturge-Weber syndrome (SWS) are characterized by a port-wine stain at the site o …
363 results

Searches related to "sturge weber syndrome"