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96 results

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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 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 syndr
Sturge-Weber syndrome (SWS) is a rare, noninherited neurovascular disorder characterized by abnormal vasculature in the
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. ...In newborns and infants with a high-risk PWB and no history of seizures or neurological symptoms, routine screening for brain involve …
BACKGROUND: Sturge-Weber syndrome (SWS) is a sporadic, neurocutaneous syndrome involving the skin, brain, and ey …
Neurocutaneous syndromes.
Klar N, Cohen B, Lin DDM. Klar N, et al. Handb Clin Neurol. 2016;135:565-589. doi: 10.1016/B978-0-444-53485-9.00027-1. Handb Clin Neurol. 2016. PMID: 27432683 Review.
Neurocutaneous syndromes (or phakomatoses) are a diverse group of congenital disorders that encompass abnormalities of neuroectodermal and, sometimes, mesodermal development, hence commonly involving the skin, eye, and central nervous system. These are often inherited cond …
Neurocutaneous syndromes (or phakomatoses) are a diverse group of congenital disorders that encompass abnormalities of neuroectodermal and, …
GNA11-mutated Sturge-Weber syndrome has distinct neurological and dermatological features.
Dompmartin A, van der Vleuten CJM, Dekeuleneer V, Duprez T, Revencu N, Désir J, Te Loo DMWM, Flucke U, Eijkelenboom A, Schultze Kool L, Vikkula M, Boon L. Dompmartin A, et al. Eur J Neurol. 2022 Oct;29(10):3061-3070. doi: 10.1111/ene.15452. Epub 2022 Jul 13. Eur J Neurol. 2022. PMID: 35715928
BACKGROUND AND PURPOSE: Sturge-Weber syndrome (SWS) is a neurocutaneous disorder characterized by clinical manifestations involving the brain, eye and skin. ...All had neurological symptoms and moderate brain atrophy with a lower degree of severity tha …
BACKGROUND AND PURPOSE: Sturge-Weber syndrome (SWS) is a neurocutaneous disorder characterized by clinical manifestatio …
Presentation, diagnosis, pathophysiology, and treatment of the neurological features of Sturge-Weber syndrome.
Comi AM. Comi AM. Neurologist. 2011 Jul;17(4):179-84. doi: 10.1097/NRL.0b013e318220c5b6. Neurologist. 2011. PMID: 21712663 Free PMC article. Review.
BACKGROUND: Sturge-Weber syndrome (SWS) is a neurovascular disorder with a capillary malformation of the face (port-wine birthmark), a capillary-venous malformation in the eye, and a capillary-venous malformation in the brain (leptomeningeal angioma). …
BACKGROUND: Sturge-Weber syndrome (SWS) is a neurovascular disorder with a capillary malformation of the face (port-win …
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 diagn
Sturge-Weber syndrome is a rare congenital neurocutaneous syndrome with an incidence of 1 in 50000 characterised
Aspirin use in Sturge-Weber syndrome: side effects and clinical outcomes.
Lance EI, Sreenivasan AK, Zabel TA, Kossoff EH, Comi AM. Lance EI, et al. J Child Neurol. 2013 Feb;28(2):213-8. doi: 10.1177/0883073812463607. Epub 2012 Oct 30. J Child Neurol. 2013. PMID: 23112247 Free PMC article.
Sturge-Weber syndrome is a neurocutaneous disorder with skin, eye, and brain involvement. ...This cohort's clinical experience adds significant support for low-dose aspirin use to optimize neurodevelopmental outcome in Sturge-Weber syn
Sturge-Weber syndrome is a neurocutaneous disorder with skin, eye, and brain involvement. ...This cohort's clini
Choroidal hemangioma.
Singh AD, Kaiser PK, Sears JE. Singh AD, et al. Ophthalmol Clin North Am. 2005 Mar;18(1):151-61, ix. doi: 10.1016/j.ohc.2004.07.004. Ophthalmol Clin North Am. 2005. PMID: 15763200 Review.
Diffuse choroidal hemangiomas are usually evident at birth and generally occur as a part of neuro-oculo-cutaneous hemangiomatosis (Sturge-Weber syndrome)....
Diffuse choroidal hemangiomas are usually evident at birth and generally occur as a part of neuro-oculo-cutaneous hemangiomatosis (Sturge
Cerebrofacial venous metameric syndrome-spectrum of imaging findings.
Brinjikji W, Nicholson P, Hilditch CA, Krings T, Pereira V, Agid R. Brinjikji W, et al. Neuroradiology. 2020 Apr;62(4):417-425. doi: 10.1007/s00234-020-02362-7. Epub 2020 Jan 14. Neuroradiology. 2020. PMID: 31932853 Review.
Cerebrofacial venous metameric syndrome (CVMS) is a complex craniofacial vascular malformation disorder in which patients have a constellation of venous vascular malformations affecting soft tissues, bone, dura, and neural structures including the eye and brain. It …
Cerebrofacial venous metameric syndrome (CVMS) is a complex craniofacial vascular malformation disorder in which patients have a cons …
Diagnostic dilemma: Sturge-Weber syndrome, without facial nevus.
Zanzmera P, Patel T, Shah V. Zanzmera P, et al. J Neurosci Rural Pract. 2015 Jan;6(1):105-7. doi: 10.4103/0976-3147.143215. J Neurosci Rural Pract. 2015. PMID: 25552865 Free PMC article.
Sturge-Weber syndrome (SWS), a rare sporadic neurocutaneous disease, is characterized by a congenital unilateral port-wine nevus affecting the area innervated by V1, ipsilateral leptomeningeal angiomatosis, and calcification in the occipital or frontoparietal
Sturge-Weber syndrome (SWS), a rare sporadic neurocutaneous disease, is characterized by a congenital unilateral port-w
96 results