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Items: 1 to 20 of 157

1.

Sturge-Weber syndrome: altered blood vessel fibronectin expression and morphology.

Comi AM, Weisz CJ, Highet BH, Skolasky RL, Pardo CA, Hess EJ.

J Child Neurol. 2005 Jul;20(7):572-7.

PMID:
16159522
2.

Increased fibronectin expression in sturge-weber syndrome fibroblasts and brain tissue.

Comi AM, Hunt P, Vawter MP, Pardo CA, Becker KG, Pevsner J.

Pediatr Res. 2003 May;53(5):762-9. Epub 2003 Mar 5.

PMID:
12621118
3.

Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ.

Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B, North PE, Marchuk DA, Comi AM, Pevsner J.

N Engl J Med. 2013 May 23;368(21):1971-9. doi: 10.1056/NEJMoa1213507. Epub 2013 May 8.

4.

Pathophysiology of Sturge-Weber syndrome.

Comi AM.

J Child Neurol. 2003 Aug;18(8):509-16. Review.

PMID:
13677575
5.

Fibronectin: characterization of a somatic mutation in Sturge-Weber syndrome (SWS).

Zhou Q, Zheng JW, Yang XJ, Wang YA, Ye WM, Zhu HG, Zhang ZY.

Med Hypotheses. 2009 Aug;73(2):199-200. doi: 10.1016/j.mehy.2009.03.004. Epub 2009 Apr 8.

PMID:
19359105
6.

Predictive Factors for Epilepsy in Pediatric Patients With Sturge-Weber Syndrome.

Kaseka ML, Bitton JY, Décarie JC, Major P.

Pediatr Neurol. 2016 Nov;64:52-58. doi: 10.1016/j.pediatrneurol.2016.08.009. Epub 2016 Aug 18.

PMID:
27637568
7.

Sturge-Weber syndrome: from the past to the present.

Sudarsanam A, Ardern-Holmes SL.

Eur J Paediatr Neurol. 2014 May;18(3):257-66. doi: 10.1016/j.ejpn.2013.10.003. Epub 2013 Nov 7. Review.

PMID:
24275166
8.

Stimulant use in patients with sturge-weber syndrome: safety and efficacy.

Lance EI, Lanier KE, Zabel TA, Comi AM.

Pediatr Neurol. 2014 Nov;51(5):675-80. doi: 10.1016/j.pediatrneurol.2013.11.009. Epub 2013 Nov 21.

9.

Upregulation of hypoxia-inducible factor (HIF)-1alpha and HIF-2alpha in leptomeningeal vascular malformations of Sturge-Weber syndrome.

Comati A, Beck H, Halliday W, Snipes GJ, Plate KH, Acker T.

J Neuropathol Exp Neurol. 2007 Jan;66(1):86-97.

PMID:
17204940
10.

Leukocyte adhesion molecules and x-ray energy dispersive spectroscopy in Sturge-Weber disease.

Prayson RA, Grewal ID, McMahon JT, Barna BP, Estes ML.

Pediatr Neurol. 1996 Nov;15(4):332-6.

PMID:
8972534
11.

Sturge-Weber syndrome without facial nevus: an unusual cause of neonatal seizures.

Wong SW, Kyaw L, Ong LC, Zulfiqar AM.

J Paediatr Child Health. 2011 Apr;47(4):237-9. doi: 10.1111/j.1440-1754.2010.01739.x.

PMID:
20500432
12.

Sturge-Weber syndrome: deep venous occlusion and the radiologic spectrum.

Slasky SE, Shinnar S, Bello JA.

Pediatr Neurol. 2006 Nov;35(5):343-7.

PMID:
17074605
13.

Sturge-Weber syndrome and dermatomal facial port-wine stains: incidence, association with glaucoma, and pulsed tunable dye laser treatment effectiveness.

Hennedige AA, Quaba AA, Al-Nakib K.

Plast Reconstr Surg. 2008 Apr;121(4):1173-80. doi: 10.1097/01.prs.0000304606.33897.71.

PMID:
18349634
14.

[Occipital leptomeningeal angiomatosis without facial angioma. Could it be considered a variant of Sturge-Weber syndrome?].

Martínez-Bermejo A, Tendero A, López-Martín V, Arcas J, Royo A, Polanco I, Viaño J, Pascual-Castroviejo I.

Rev Neurol. 2000 May 1-15;30(9):837-41. Spanish.

PMID:
10870197
15.

[Sturge-Weber syndrome. Diagnostic imaging relative to neuropathology].

Henkes H, Bittner R, Huber G, Sperner J, Heye N, Bassir C, Piepgras U.

Radiologe. 1991 Jun;31(6):289-96. German.

PMID:
1882071
16.

Sturge-Weber syndrome: study of 55 patients.

Pascual-Castroviejo I, Pascual-Pascual SI, Velazquez-Fragua R, Viaño J.

Can J Neurol Sci. 2008 Jul;35(3):301-7.

PMID:
18714797
17.

Encephalotrigeminal angiomatosis.

Feller L, Lemmer J.

SADJ. 2003 Oct;58(9):370-3.

PMID:
14964051
18.

Quantitative analysis of gray- and white-matter volumes and glucose metabolism in Sturge-Weber syndrome.

Pfund Z, Kagawa K, Juhász C, Shen C, Lee JS, Chugani DC, Muzik O, Chugani HT.

J Child Neurol. 2003 Feb;18(2):119-26.

PMID:
12693779
19.

Sturge-Weber syndrome.

Comi AM.

Handb Clin Neurol. 2015;132:157-68. doi: 10.1016/B978-0-444-62702-5.00011-1. Review.

PMID:
26564078
20.

Somatic GNAQ Mutation is Enriched in Brain Endothelial Cells in Sturge-Weber Syndrome.

Huang L, Couto JA, Pinto A, Alexandrescu S, Madsen JR, Greene AK, Sahin M, Bischoff J.

Pediatr Neurol. 2017 Feb;67:59-63. doi: 10.1016/j.pediatrneurol.2016.10.010. Epub 2016 Oct 21.

PMID:
27919468

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