4. Gonzalez ME, Burk CJ, Barbouth DS, et al. Macrocephaly-capillary malformation: a report of three cases and review of the literature. Pediatr Dermatol 2009;26 (3):342
5. Cordoro KM, Speetzen LS, Koerper MA, et al. Physiologic changes in vascular birthmarks during early infancy: mechanisms and clinical implications. J Am Acad Dermatol 2009;60 (4):669—75.
6. Swerlick RA, Cooper PH. Pyogenic granuloma (lobular capillary hemangioma) within port-wine stains. J Am Acad Dermatol 1983;8 (5):627—30.
7. Rajan N, Natarajan S. Impetiginized eczema arising within a port-wine stain of the arm. J Eur Acad Dermatol Venereol 2006;20 (8):1009—10.
8. Mulliken JB, Glowacki J. Classification of pediatric vascular lesions. Plast Reconstr Surg 1982;70 (1): 121.
9. Pascual-Castroviejo I, Pascual-Pascual S, Velazquez-Fragua R, et al. Sturge-Weber syndrome: study of 55 patients. Can J Neurol Sci 2008;35 (3): 301—7.
10. Comi AM. Sturge-Weber syndrome and epilepsy: an argument for aggressive seizure management in these patients. Expert Rev Neurother 2007;7 (8): 951e6.
11. Hennedige AA, Quaba AA, Al-Nakib K. Sturge-Weber syndrome and dermatomal facial port-wine stains: incidence, association with glaucoma, and pulsed tunable dye laser treatment effectiveness. Plast Reconstr Surg 2008;121 (4):1173—80.
12. Nelson JS, Geronemus RG. Redarkening of portwine stains 10 years after laser treatment. N Engl J Med 2007;356 (26):2745—6
13. Hershkovitz D, Bercovich D, Sprecher E, et al. RASA1 mutations may cause hereditary capillary malformations without arteriovenous malformations. Br J Dermatol 2008;158 (5):1035—40.
14. Boon LM, Mulliken JB, Vikkula M. RASA1: variable phenotype with capillary and arteriovenous malformations. Curr Opin Genet Dev 2005;15 (3): 265—9.
15. Revencu N, Boon LM, Mulliken JB, et al. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations. Hum Mutat 2008; 29 (7):959—65.
16. Kienast AK, Hoeger PH. Cutis marmorata telangiectatica congenita: a prospective study of 27 cases and review of the literature with proposal of diagnostic criteria. Clin Exp Dermatol 2009;34 (3): 319—23.
17. Fujita M, Darmstadt GL, Dinulos JG. Cutis marmorata telangiectatica congenita with hemangiomatous histopathologic features. J Am Acad Dermatol 2003;48 (6):950—4.
18. Ulrich S, Fischler M, Walder B, et al. Klippel-Trenaunay syndrome with small vessel pulmonary arterial hypertension. Thorax 2005;60 (11):971—3.
19. Minkis K, Geronemus RG, Hale EK. Port wine stain progression: a potential consequence of delayed and inadequate treatment? Lasers Surg Med 2009; 41 (6):423—6.
20. Lam SM, Williams EF. Practical considerations in the treatment of capillary vascular malformations, or port wine stains. Facial Plast Surg 2004;20 (1):71—6.
21. Owens WW, Lang PG. Herpes simplex infection and colonization with Pseudomonas aeruginosa complicating pulsed-dye laser treatment. Arch Dermatol 2004;140 (6):760—1.
22. Strauss RM, Sheehan-Dare R. Local molluscum contagiosum infection as a side-effect of pulsed-dye laser treatment. Br J Dermatol 2004;150 (5):1047—9.
23. Jasim ZF, Handley JM. Treatment of pulsed dye laser-resistant port wine stain birthmarks. J Am Acad Dermatol 2007;57 (4):677—82.
24. Yang MU, Yaroslavsky AN, Farinelli WA, et al. Longpulsed neodymium: yttrium-aluminum-garnet laser treatment for port-wine stains. J Am Acad Dermatol 2005;52 (3 Pt 1):480—90.
