Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1945 1
1946 1
1947 1
1948 3
1949 7
1950 17
1951 14
1952 7
1953 3
1954 4
1955 3
1956 5
1957 7
1958 1
1959 7
1960 10
1961 8
1962 6
1963 6
1964 5
1965 9
1966 8
1967 6
1968 5
1969 11
1970 12
1971 9
1972 11
1973 4
1974 10
1975 23
1976 27
1977 24
1978 26
1979 23
1980 25
1981 12
1982 20
1983 15
1984 18
1985 14
1986 16
1987 18
1988 14
1989 13
1990 21
1991 11
1992 31
1993 27
1994 18
1995 18
1996 15
1997 20
1998 26
1999 21
2000 39
2001 16
2002 25
2003 26
2004 27
2005 27
2006 32
2007 43
2008 45
2009 32
2010 34
2011 41
2012 39
2013 58
2014 50
2015 50
2016 43
2017 48
2018 46
2019 56
2020 54
2021 51
2022 42
2023 38
2024 12

Text availability

Article attribute

Article type

Publication date

Search Results

1,546 results

Results by year

Filters applied: . Clear all
Page 1
Updates on Sturge-Weber Syndrome.
Yeom S, Comi AM. Yeom S, et al. Stroke. 2022 Dec;53(12):3769-3779. doi: 10.1161/STROKEAHA.122.038585. Epub 2022 Oct 20. Stroke. 2022. PMID: 36263782 Free PMC article. Review.
Sturge-Weber syndrome (SWS) is a rare, noninherited neurovascular disorder characterized by abnormal vasculature in the brain, skin, and eye. ...This review focuses on the latest progress in the field of research for Sturge-Weber syndrome …
Sturge-Weber syndrome (SWS) is a rare, noninherited neurovascular disorder characterized by abnormal vasculature in the …
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. ...Glaucoma may be present at birth or develop later. Neuroimaging studies show leptomenin …
Sturge-Weber syndrome is a sporadic congenital neurocutaneous disorder caused by a somatic activating mutation in GNAQ; …
Port-wine Birthmarks: Update on Diagnosis, Risk Assessment for Sturge-Weber Syndrome, and Management.
Poliner A, Fernandez Faith E, Blieden L, Kelly KM, Metry D. Poliner A, et al. Pediatr Rev. 2022 Sep 1;43(9):507-516. doi: 10.1542/pir.2021-005437. Pediatr Rev. 2022. PMID: 36045161 Review.
Sturge-Weber syndrome (SWS) is a neurocutaneous disorder that classically presents with a triad of vascular anomalies affecting the skin, eyes, and brain. ...
Sturge-Weber syndrome (SWS) is a neurocutaneous disorder that classically presents with a triad of vascular anomalies a …
Sturge-Weber syndrome.
Di Rocco C, Tamburrini G. Di Rocco C, et al. Childs Nerv Syst. 2006 Aug;22(8):909-21. doi: 10.1007/s00381-006-0143-2. Epub 2006 Jul 6. Childs Nerv Syst. 2006. PMID: 16823586 Review.
INTRODUCTION: Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome the main clinical features of which are facial, mostly unilateral nevi, leptomeningeal angiomatosis, and congenital glaucoma. The interest of this syndrome for pe …
INTRODUCTION: Sturge-Weber syndrome (SWS) is a rare neurocutaneous syndrome the main clinical features of which …
Weber Syndrome.
Romozzi M, Bramato G, Luigetti M. Romozzi M, et al. Acta Neurol Belg. 2023 Jun;123(3):1101-1103. doi: 10.1007/s13760-021-01861-5. Epub 2022 Jan 7. Acta Neurol Belg. 2023. PMID: 34997560 No abstract available.
Sturge-Weber syndrome.
Baselga E. Baselga E. Semin Cutan Med Surg. 2004 Jun;23(2):87-98. doi: 10.1016/j.sder.2004.01.002. Semin Cutan Med Surg. 2004. PMID: 15295918 Review.
Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalities (glaucoma and choroidal hemangioma) and leptomeningeal angioma. ...Early neuroimaging features are important to recognize. Management of p …
Sturge-Weber syndrome is a sporadic neurocutaneous disease characterized by facial port-wine stain, ocular abnormalitie …
[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 …
Sturge-Weber syndrome.
Nabbout R, Juhász C. Nabbout R, et al. Handb Clin Neurol. 2013;111:315-21. doi: 10.1016/B978-0-444-52891-9.00037-3. Handb Clin Neurol. 2013. PMID: 23622182 Review.
Sturge-Weber syndrome (SWS) is a rare sporadic neurocutaneous syndrome defined by the association of a facial capillary malformation in the ophthalmic distribution of the trigeminal nerve, with ipsilateral vascular glaucoma and vascular malformation of …
Sturge-Weber syndrome (SWS) is a rare sporadic neurocutaneous syndrome defined by the association of a facial ca …
Sturge-Weber syndrome.
Mirowski GW, Liu AA, Stone ML, Caldemeyer KS. Mirowski GW, et al. J Am Acad Dermatol. 1999 Nov;41(5 Pt 1):772-3. doi: 10.1016/s0190-9622(99)70016-2. J Am Acad Dermatol. 1999. PMID: 10534644 No abstract available.
Sturge-Weber Syndrome: A Case Report.
Timilsina S, Kunwor B, Thapa Chhetri S, Nepal S, Sedhai K. Timilsina S, et al. JNMA J Nepal Med Assoc. 2023 Nov 1;61(267):890-892. doi: 10.31729/jnma.8344. JNMA J Nepal Med Assoc. 2023. PMID: 38289732 Free PMC article.
Sturge-Weber syndrome is a rare congenital neurocutaneous syndrome with an incidence of 1 in 50000 characterised by facial capillary malformation and vascular anomalies in the brain and eye. ...This case underscores the importance of early diagnosis an …
Sturge-Weber syndrome is a rare congenital neurocutaneous syndrome with an incidence of 1 in 50000 characterised …
1,546 results