Susceptibility-weighted imaging: technical aspects and clinical applications, part 2

S Mittal, Z Wu, J Neelavalli… - American Journal of …, 2009 - Am Soc Neuroradiology
Susceptibility-weighted imaging (SWI) has continued to develop into a powerful clinical tool
to visualize venous structures and iron in the brain and to study diverse pathologic …

[HTML][HTML] Susceptibility weighted imaging: clinical applications and future directions

AM Halefoglu, DM Yousem - World journal of radiology, 2018 - ncbi.nlm.nih.gov
Susceptibility weighted imaging (SWI) is a recently developed magnetic resonance imaging
(MRI) technique that is increasingly being used to narrow the differential diagnosis of many …

Sturge–Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ

MD Shirley, H Tang, CJ Gallione… - … England Journal of …, 2013 - Mass Medical Soc
Background The Sturge–Weber syndrome is a sporadic congenital neurocutaneous
disorder characterized by a port-wine stain affecting the skin in the distribution of the …

Sturge–Weber syndrome: from the past to the present

A Sudarsanam, SL Ardern-Holmes - European Journal of Paediatric …, 2014 - Elsevier
Sturge–Weber syndrome is a rare sporadic neurocutaneous syndrome the hallmark of which
is a facial port-wine stain involving the first division of the trigeminal nerve, ipsilateral …

Vascular anomaly syndromes in the ISSVA classification system: imaging findings and role of interventional radiology in management

MX Wang, S Kamel, KM Elsayes, RP Guillerman… - Radiographics, 2022 - pubs.rsna.org
Vascular anomalies encompass a spectrum of tumors and malformations that can cause
significant morbidity and mortality in children and adults. Use of the International Society for …

The somatic GNAQ mutation c. 548G> A (p. R183Q) is consistently found in Sturge–Weber syndrome

M Nakashima, M Miyajima, H Sugano… - Journal of human …, 2014 - nature.com
Sturge–Weber syndrome (SWS) is a neurocutaneous disorder characterized by capillary
malformation (port-wine stains), and choroidal and leptomeningeal vascular malformations …

[HTML][HTML] Sturge-Weber syndrome: a review

E Higueros, E Roe, E Granell, E Baselga - Actas Dermo-Sifiliográficas …, 2017 - Elsevier
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. It is …

Somatic GNAQ mutation is enriched in brain endothelial cells in Sturge–Weber syndrome

L Huang, JA Couto, A Pinto, S Alexandrescu… - Pediatric …, 2017 - Elsevier
Abstract Background Sturge–Weber syndrome (SWS) is a rare congenital neurocutaneous
disorder characterized by facial and extracraniofacial capillary malformations and capillary …

Ultra–sensitive droplet digital PCR for detecting a low–prevalence somatic GNAQ mutation in Sturge–Weber syndrome

Y Uchiyama, M Nakashima, S Watanabe, M Miyajima… - Scientific reports, 2016 - nature.com
Droplet digital PCR (ddPCR), a method for measuring target nucleic acid sequence quantity,
is useful for determining somatic mutation rates using TaqMan probes. In this study, the …

Screening for Sturge‐Weber syndrome: A state‐of‐the‐art review

M Zallmann, RJ Leventer, MT Mackay… - Pediatric …, 2018 - Wiley Online Library
Infants with a high‐risk distribution of port‐wine stains are commonly screened for Sturge‐
Weber syndrome using brain magnetic resonance imaging. There is no consensus about …