Results 61 to 70 of about 21,947 (201)
Kerala Journal of Ophthalmology, 2017 Sturge–Weber syndrome (SWS) is a rare neuro-oculocutaneous disorder. The classical signs are unilateral facial port wine stain, leptomeningeal angiomas, and their sequele with ipsilateral glaucoma.
Padma B Prabhu +2 more
doaj +1 more source
Contemporary Pediatric Dentistry, 2022 Sturge–Weber Syndrome (SWS) is a neuro-oculo-cutaneous vascular disorder that includes leptomeningeal hemangioma and port wine stains, usually ipsilaterally, with ocular manifestations and extended lesions over the oral cavity.
Amit Khatri +5 more
doaj +1 more source
Topical photodynamic therapy using different porphyrin precursors leads to differences in vascular photosensitization and vascular damage in normal mouse skin [PDF]
, 2014 Different distributions of hexyl aminolevulinate (HAL), aminolevulinic acid (ALA) and methyl aminolevulinate (MAL) in the superficial vasculature are not well studied but they are hypothesized to play an important role in topical photodynamic therapy ...
Bruijn, H.S. (Riette) de +6 more
core +1 more source
Intracranial variant of encephalotrigeminal angiomatosis – A case report
Indian Journal of Dental Research, 2019 Encephalotrigeminal Angiomatosis is a rare developmental phakomatoses characterized by the occurrence of nevus flammeus (port-wine stain) along the distribution of branches of trigeminal nerve, vascular angiomas in the eye, and leptomeningeal angiomas ...
N Mohan +4 more
doaj +1 more source
Clasificación de las anomalías vasculares (tumores y malformaciones). Características clínicas e historia natural [PDF]
, 2004 Vascular anomalies are divided into tumours and malformations. Haemangiomas are the most frequent amongst the former. Not normally present at birth, except in a premonitory form, they grow for 10-12 months due to hyperplasia, to subsequently undergo ...
Redondo, P. (Pedro)
core
Sturge-Weber syndrome: a report of 14 cases [PDF]
, 2013 Sturge-Weber-Krabe syndrome (SWS), also known as encephalotrigeminalangiomatosis and named the forthfacomatosis, recall the names of the authors who first describedit in its basic clinical, radiological andanatomopathological aspects. We report here
Carotenuto, M +7 more
core +2 more sources
The Effects of Freeze-Drying on the Strength Characteristics of Naturally Aged Book Papers [PDF]
, 1981 Libraries occasionally have water main breaks, fires and floods. These disasters cause considerable water damage to thousands of books. Books that are left wet on the shelves will grow mold.
Sarokin, Steven D.
core +1 more source
Indian Journal of Dermatology, 2001 A classical case of klippel trenaunay syndrome in a 25 year old male characterized by port wine stain, varicose and increase in length of the right lower extremity associated with ulceration is presented.
Miranda M.F, Chahal N.H
doaj
The use of pulsed dye laser with dynamic cooling device in the treatment of port wine stain in Chinese [PDF]
, 2002 published_or_final_versio
Chan, HHL, Chiu, F
core
Genetic Variants Associated with Port-Wine Stains
PLOS ONE, 2015 Port-wine stains (PWS) are capillary malformations, typically located in the dermis of the head and neck, affecting 0.3% of the population. Current theories suggest that port-wine stains are caused by somatic mutations that disrupt vascular development.Understanding PWS genetic determinants could provide insight into new treatments.Our study used a ...
Frigerio, Alice +7 more
openaire +5 more sources