| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Santi Maria Recupero | |
| Solmaz Abdolrahimzadeh | |||
| Filippo Cruciani | |||
| Lorenzo Felli | |||
| Maria Teresa Contestabile | |||
| Vittorio Scavella | |||
| P2860 | cites work | Sturge-Weber syndrome | Q79846276 |
| [The Klippel-Trenaunay-Parkes-Weber syndrome as an example of genetic disorder of angiogenesis] | Q80208407 | ||
| Sturge-weber syndrome: a unified pathophysiologic mechanism | Q80833372 | ||
| Klippel-Trenaunay syndrome in a monozygotic male twin: supportive evidence for the concept of paradominant inheritance | Q81235560 | ||
| Ruthenium-106 plaque brachytherapy for the treatment of diffuse choroidal haemangioma in Sturge-Weber syndrome | Q81584325 | ||
| Primary choroidal melanoma in phakomatosis pigmentovascularis IIa | Q81819335 | ||
| Sturge-Weber syndrome and glaucoma | Q83982514 | ||
| Bilateral Naevus of Ota in association with Klippel-Trenaunay syndrome | Q84061210 | ||
| Phacomatosis pigmentovascularis of cesioflammea type in 7 patients: combination of ocular pigmentation (melanocytosis or melanosis) and nevus flammeus with risk for melanoma | Q84353142 | ||
| Periocular port wine stain: the great ormond street hospital experience | Q84587641 | ||
| Intractable choroidal effusion with exudative retinal detachment in Sturge-Weber syndrome | Q85292316 | ||
| Morphologic and vasculature features of the choroid and associated choroid-retinal thickness alterations in neurofibromatosis type 1 | Q86213579 | ||
| Facial port-wine stains and Sturge-Weber syndrome | Q93582717 | ||
| Anterior chamber angle vascularization in Sturge-Weber syndrome Report of a case | Q42476492 | ||
| Bilateral acute angle closure glaucoma and myopia induced by topiramate | Q43276224 | ||
| Resolution of persistent exudative retinal detachment in a case of Sturge-Weber syndrome with anti-VEGF administration | Q43297943 | ||
| External beam irradiation therapy for choroidal haemangiomas. Visual and anatomical results after a dose of 20 to 25 Gy. | Q43563774 | ||
| Plaque radiotherapy for choroidal hemangioma with total retinal detachment and iris neovascularization | Q43833937 | ||
| Lifetime prevalence of uveal melanoma in white patients with oculo(dermal) melanocytosis | Q44322980 | ||
| Acral arteriovenous tumor developed within a nevus flammeus in a patient with Sturge-Weber syndrome | Q44522683 | ||
| Increased choroidal thickness in patients with Sturge-Weber syndrome | Q44557813 | ||
| Ocular and oculodermal melanocytosis | Q44749902 | ||
| Multiple granular cell tumors associated with giant speckled lentiginous nevus and nevus flammeus in a child | Q44805114 | ||
| The ultrastructure of Sturge-Weber disease | Q44996416 | ||
| A case of acute angle-closure glaucoma secondary to posterior scleritis in patient with Sturge-Weber syndrome | Q45712514 | ||
| Optic nerve shadow enlargement in the Klippel-Trenaunay-Weber syndrome. | Q45951224 | ||
| Iris mammillations: significance and associations | Q46624197 | ||
| Persistent fetal vasculature and spontaneous hyphema in a patient with Klippel-Trénaunay-Weber syndrome | Q48208027 | ||
| The Klippel-Trenaunay-Sturge-Weber syndrome | Q48258746 | ||
| The coincidence of neurocutaneous melanosis and encephalofacial angiomatosis | Q48277927 | ||
| Innervation pattern of malformative cortical vessels in Sturge-Weber disease: an histochemical, immunohistochemical, and ultrastructural study. | Q48620627 | ||
| Oculocutaneous melanosis associated with the Sturge-Weber syndrome | Q48788105 | ||
| Differential diagnoses of overgrowth syndromes: the most important clinical and radiological disease manifestations | Q27002915 | ||
| Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA | Q28256964 | ||
| Klippel-Trenaunay syndrome: a multisystem disorder possibly resulting from a pathogenic gene for vascular and tissue overgrowth | Q28257932 | ||
| Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ | Q28290315 | ||
| Ultrasound biomicroscopy of the peripheral retina and the ciliary body in degenerative retinoschisis associated with pars plana cysts | Q28344706 | ||
| New vascular classification of port-wine stains: improving prediction of Sturge-Weber risk | Q30833931 | ||
| Circumscribed choroidal hemangiomas: long-term visual prognosis | Q30844503 | ||
| The medical necessity of evaluation and treatment of port-wine stains. | Q30887310 | ||
| Choroidal hemangioma treated with photodynamic therapy using verteporfin | Q31030272 | ||
| Advances in Sturge-Weber syndrome | Q31034301 | ||
| Phakomatosis pigmentovascularis: Clinical findings in 15 patients and review of the literature | Q33307660 | ||
| Treatment of glaucoma in children with Sturge-Weber syndrome. | Q33893132 | ||
| Management of large birthmarks | Q34060546 | ||
| Sturge-Weber syndrome: a review | Q34323253 | ||
| Klippel-Trénaunay syndrome: spectrum and management | Q34453824 | ||
| Pathogenesis of transient high myopia after blunt eye trauma | Q34550070 | ||
| Retinal microvascular abnormalities overlying choroidal nodules in neurofibromatosis type 1. | Q34649558 | ||
| Pathophysiology of Sturge-Weber syndrome | Q35292404 | ||
| Corkscrew retinal vessels in neurofibromatosis type 1: report of 12 cases | Q35589487 | ||
| Sturge-Weber syndrome (encephalotrigeminal or leptomeningeal angiomatosis). | Q36141865 | ||
| Neurocutaneous syndromes: behavioral features | Q36183528 | ||
| Circumscribed choroidal hemangiomas | Q36188235 | ||
| Ocular vascular hamartomas: the relationship with phakomatoses and possible commonalities in pathogenesis | Q36678029 | ||
| Focal venous hypertension as a pathophysiologic mechanism for tissue hypertrophy, port-wine stains, the Sturge-Weber syndrome, and related disorders: proof of concept with novel hypothesis for underlying etiological cause (an American Ophthalmologic | Q37411764 | ||
| Klippel-Trenaunay Syndrome: a case report with brief review of literature | Q37925544 | ||
| Ultrasound biomicroscopy of the ciliary body in ocular/oculodermal melanocytosis. | Q38065519 | ||
| Light microscopy and ultrastructural studies of Sturge-Weber disease | Q38583182 | ||
| Klippel-Trenaunay syndrome: a review | Q40137096 | ||
| Combined trabeculotomy-trabeculectomy for the management of glaucoma associated wih Sturge-Weber syndrome | Q40357286 | ||
| Hemangioma of the choroid. A clinicopathologic study of 71 cases and a review of the literature | Q40760888 | ||
| Neural crest origin of human trabecular meshwork and its implications for the pathogenesis of glaucoma | Q41311528 | ||
| Glaucoma in phakomatosis pigmentovascularis | Q41342444 | ||
| Port-wine stains. A disease of altered neural modulation of blood vessels? | Q41449436 | ||
| Ruthenium-106 plaque therapy for diffuse choroidal hemangioma in sturge-weber syndrome | Q41817438 | ||
| Unilateral cataract and vitreoretinopathy in a case with klippel-trenaunay syndrome | Q41869807 | ||
| RIGHT-SIDED HEMI-HYPOTROPHY RESULTING FROM RIGHT-SIDED CONGENITAL SPASTIC HEMIPLEGIA, WITH A MORBID CONDITION OF THE LEFT SIDE OF THE BRAIN, REVEALED BY RADIOGRAMS. | Q42241670 | ||
| ??? | Q94639236 | ||
| Phakomatosis pigmentovascularis. | Q50753907 | ||
| Primary single-plate Molteno tube implantation for management of glaucoma in children with Sturge-Weber syndrome. | Q50984345 | ||
| Sturge-Weber syndrome: age of onset of seizures and glaucoma and the prognosis for affected children. | Q52020270 | ||
| PI3K signalling: the path to discovery and understanding. | Q54527804 | ||
| Bilateral optic nerve drusen and gliomas in Klippel-Trenaunay syndrome. | Q55463415 | ||
| Phakomatosis pigmentovascularis and Lisch nodules. Relationship between Von Recklinghausen and phakomatosis pigmentovascularis? | Q61947903 | ||
| The pathogenesis of glaucoma in Sturge-Weber syndrome | Q67345275 | ||
| Genetic aspects of the Klippel-Trenaunay syndrome | Q67490376 | ||
| Unusual retinal and renal vascular lesions in the Klippel-Trenaunay-Weber syndrome | Q67509275 | ||
| The Ocular Manifestations of the Sturge-Weber Syndrome | Q67814989 | ||
| Unusual retinal manifestation in a combination of Sturge-Weber and Klipplel-Trenaunay syndrome--a case report | Q68078490 | ||
| Ocular findings in oculodermal melanocytosis | Q68881269 | ||
| Cyclocryotherapy in the treatment of advanced glaucoma | Q68938721 | ||
| Dual origin of glaucoma in encephalotrigeminal haemangiomatosis | Q69051471 | ||
| Bilateral melanosis of the iris | Q69711043 | ||
| Glaucoma and Klippel-Trenaunay-Weber syndrome | Q69840047 | ||
| Klippel-Trenaunay and Sturge-Weber syndrome with extensive Mongolian spots, hypoplastic larynx and subglottic stenosis | Q69847179 | ||
| Phakomatosis pigmentovascularis type IVa | Q70103596 | ||
| Phakomatosis pigmentovascularis type IIb with iris mammillations | Q70596025 | ||
| Glaucoma in Sturge-Weber syndrome | Q70656218 | ||
| Benign melanocytic glaucoma complicating oculodermal melanocytosis | Q70723226 | ||
| Cobalt-60 treatment of choroidal hemangiomas | Q71064380 | ||
| Recurrent intraoperative choroidal effusion in Sturge-Weber syndrome | Q71106940 | ||
| Diffuse malignant melanoma of the iris in the nevus of Ota | Q72215216 | ||
| Sturge-Weber syndrome: management of glaucoma with combined trabeculotomy-trabeculectomy | Q72845150 | ||
| Ocular findings in Sturge-Weber syndrome | Q73171342 | ||
| Ocular alterations in alopecia areata | Q73496551 | ||
| Sturge-Weber-Klippel-Trenaunay syndrome: what's in a name? | Q73520709 | ||
| Klippel-Trenaunay syndrome | Q74108563 | ||
| Low-dose external beam irradiation for bilateral diffuse choroidal hemangioma | Q74696603 | ||
| Sturge-Weber syndrome associated with naevus of Ota | Q74821647 | ||
| Use of latanoprost in the treatment of glaucoma associated with Sturge-Weber syndrome | Q77436689 | ||
| Increased parental age and number of pregnancies in Klippel-Trenaunay-Weber syndrome | Q77515797 | ||
| Hemangioma of the Choroid* | Q78831616 | ||
| [On the symptomology of the Sturge-Aeber and Klippel-Trenaunay syndromes.] | Q78972540 | ||
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Klippel–Trénaunay–Weber syndrome | Q1774750 |
| Sturge–Weber syndrome | Q1886238 | ||
| eye disease | Q3041498 | ||
| Phakomatosis pigmentovascularis | Q7180213 | ||
| P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
| P304 | page(s) | 786519 | |
| P577 | publication date | 2015-09-16 | |
| P1433 | published in | BioMed Research International | Q17509958 |
| P1476 | title | Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions? | |
| P478 | volume | 2015 |
| Q41319089 | A rare case of overlapping Sturge-Weber syndrome and Klippel-Trenaunay syndrome associated with bilateral refractory childhood glaucoma |
| Q26740996 | A review of the role of ultrasound biomicroscopy in glaucoma associated with rare diseases of the anterior segment |
| Q54986867 | Acute primary angle-closure in Sturge-Weber syndrome. |
| Q26738915 | An Update on the Ophthalmologic Features in the Phakomatoses |
| Q91976578 | Bilateral diffuse choroidal hemangioma in Sturge Weber syndrome: A case report highlighting the role of multimodal imaging and a brief review of the literature |
| Q38953037 | Correction of Facial Deformity in Sturge-Weber Syndrome |
| Q55284128 | Klippel-Trenaunay and Parkes-Weber syndromes: two case reports. |
| Q26743446 | Ocular manifestations of Sturge-Weber syndrome: pathogenesis, diagnosis, and management |
| Q39074145 | Pathophysiology, diagnosis, and management of glaucoma associated with Sturge-Weber syndrome |
| Q53826373 | Pigment dispersion syndrome and pigmentary glaucoma: a review and update. |
| Q90214157 | Port-wine stain as a clue for two rare coexisting entities |
| Q50897501 | Retinal pigment epithelium-photoreceptor layer alterations in a patient with Sturge-Weber syndrome with diffuse choroidal hemangioma. |
| Q48017347 | Screening for Sturge-Weber syndrome: A state-of-the-art review |
| Q52671404 | Spectral Domain Optical Coherence Tomography of Choroidal and Outer Retinal Layer Thickness in the Sturge Weber Syndrome. |
| Q41488759 | Sturge-Weber Syndrome Associated with Monolateral Ocular Melanocytosis, Iris Mammillations, and Diffuse Choroidal Haemangioma |
| Q41845848 | Sturge-Weber syndrome: Continued vigilance is needed |
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