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2000 5
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2002 3
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156 results

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The following term was not found in PubMed: fibrosis-neurodegeneration-cerebral
Page 1
Consensus Statement for the Management and Treatment of Port-Wine Birthmarks in Sturge-Weber Syndrome.
Sabeti S, Ball KL, Burkhart C, Eichenfield L, Fernandez Faith E, Frieden IJ, Geronemus R, Gupta D, Krakowski AC, Levy ML, Metry D, Nelson JS, Tollefson MM, Kelly KM. Sabeti S, et al. JAMA Dermatol. 2021 Jan 1;157(1):98-104. doi: 10.1001/jamadermatol.2020.4226. JAMA Dermatol. 2021. PMID: 33175124 Free PMC article. Review.
IMPORTANCE: Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome involving the skin, brain, and eyes. ...Key topics and questions were formulated for each group and included risk stratification, optimum treatment strategies, and recommendations regarding light-b …
IMPORTANCE: Sturge-Weber syndrome (SWS) is a neurocutaneous syndrome involving the skin, brain, and eyes. ...Key topics and qu …
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. ...In this review, we discuss the locations of facial PWBs at risk for neurologic and ophthalmologic complications, th …
Sturge-Weber syndrome (SWS) is a neurocutaneous disorder that classically presents with a triad of vascular anomalies affecting the s …
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. ...The treatment of ophthalmologic complications, such as glaucoma, differs based on the age and clinical presentation of the patient. These recommend …
BACKGROUND: Sturge-Weber syndrome (SWS) is a sporadic, neurocutaneous syndrome involving the skin, brain, and eyes. ...The tre …
Guidelines for surveillance of patients with von Hippel-Lindau disease: Consensus statement of the International VHL Surveillance Guidelines Consortium and VHL Alliance.
Daniels AB, Tirosh A, Huntoon K, Mehta GU, Spiess PE, Friedman DL, Waguespack SG, Kilkelly JE, Rednam S, Pruthi S, Jonasch EA, Baum L, Chahoud J; International VHL Surveillance Guidelines Consortium. Daniels AB, et al. Cancer. 2023 Oct 1;129(19):2927-2940. doi: 10.1002/cncr.34896. Epub 2023 Jun 19. Cancer. 2023. PMID: 37337409 No abstract available.
Update on the diagnosis and treatment of choroidal hemangioma.
García Caride S, Fernández-Vigo JI, Valverde-Megías A. García Caride S, et al. Arch Soc Esp Oftalmol (Engl Ed). 2023 May;98(5):281-291. doi: 10.1016/j.oftale.2023.04.006. Epub 2023 Apr 14. Arch Soc Esp Oftalmol (Engl Ed). 2023. PMID: 37062411 Review.
In addition, in recent years, there has been a change in the paradigm of the treatment of these tumors thanks to the use of photodinamic therapy, which has led to a significant improvement in the visual prognosis of these patients. This has been due to the use of photodyna …
In addition, in recent years, there has been a change in the paradigm of the treatment of these tumors thanks to the use of photodinamic …
Treatment Strategies for Hereditary Kidney Cancer: Current Recommendations and Updates.
Singh S, Chaurasia A, Gopal N, Malayeri A, Ball MW. Singh S, et al. Discov Med. 2022 Nov-Dec;34(173):205-220. Discov Med. 2022. PMID: 36602871 Free article. Review.
A subset of renal tumors (5-8%) are associated with syndromes such as von Hippel-Lindau (VHL) syndrome, Birt-Hogg-Dube syndrome (BHD), tuberous sclerosis complex (TSC), hereditary papillary renal carcinoma (HPRC), hereditary leiomyomatosis and renal cell canc …
A subset of renal tumors (5-8%) are associated with syndromes such as von Hippel-Lindau (VHL) syndrome, Birt-Hogg-Dube synd …
Sirolimus Treatment in Sturge-Weber Syndrome.
Sebold AJ, Day AM, Ewen J, Adamek J, Byars A, Cohen B, Kossoff EH, Mizuno T, Ryan M, Sievers J, Smegal L, Suskauer SJ, Thomas C, Vinks A, Zabel TA, Hammill AM, Comi AM. Sebold AJ, et al. Pediatr Neurol. 2021 Feb;115:29-40. doi: 10.1016/j.pediatrneurol.2020.10.013. Epub 2020 Nov 2. Pediatr Neurol. 2021. PMID: 33316689 Free PMC article.
Sirolimus is an mammalian target of rapamycin inhibitor studied in other vascular anomalies and a potentially promising therapy in Sturge-Weber syndrome. METHODS: Ten patients with Sturge-Weber syndrome brain involvement and cognitive impairments were enrolle …
Sirolimus is an mammalian target of rapamycin inhibitor studied in other vascular anomalies and a potentially promising therapy in St …
Diagnosis and management of the venous malformations of Klippel-Trenaunay syndrome.
Wang SK, Drucker NA, Gupta AK, Marshalleck FE, Dalsing MC. Wang SK, et al. J Vasc Surg Venous Lymphat Disord. 2017 Jul;5(4):587-595. doi: 10.1016/j.jvsv.2016.10.084. J Vasc Surg Venous Lymphat Disord. 2017. PMID: 28624001 Free article. Review.
OBJECTIVE: A dearth of information exists in the literature regarding current practice in the management of Klippel-Trenaunay syndrome (KTS), a rare condition. We review and describe the etiology, diagnosis, and treatment of KTS. ...The diagnosis is clinically supplemented …
OBJECTIVE: A dearth of information exists in the literature regarding current practice in the management of Klippel-Trenaunay syndrome …
Genetic testing in the evaluation of individuals with clinical diagnosis of atypical Sturge-Weber syndrome.
Yeom S, Cohen B, Weiss CR, Montano C, Wohler E, Sobreira N, Hammill AM, Comi A. Yeom S, et al. Am J Med Genet A. 2023 Apr;191(4):983-994. doi: 10.1002/ajmg.a.63106. Epub 2023 Jan 29. Am J Med Genet A. 2023. PMID: 36710374
Sturge-Weber Syndrome (SWS) is a rare vascular malformation disorder characterized by abnormal blood vessels in the brain, skin, and eye. ...Broad germline and somatic genetic testing in these patients with atypical findings may have implications for medical care, p …
Sturge-Weber Syndrome (SWS) is a rare vascular malformation disorder characterized by abnormal blood vessels in the brain, skin, and …
Pathophysiology, diagnosis, and management of glaucoma associated with Sturge-Weber syndrome.
Javaid U, Ali MH, Jamal S, Butt NH. Javaid U, et al. Int Ophthalmol. 2018 Feb;38(1):409-416. doi: 10.1007/s10792-016-0412-3. Epub 2017 Jan 7. Int Ophthalmol. 2018. PMID: 28064423 Review.
PURPOSE: Sturge-Weber syndrome (SWS), also known as encephalotrigeminal angiomatosis, is a condition which includes leptomeningeal hemangioma, facial angiomatosis or nevus flammeus, and ocular changes. ...
PURPOSE: Sturge-Weber syndrome (SWS), also known as encephalotrigeminal angiomatosis, is a condition which includes leptomenin …
156 results