These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


263 related items for PubMed ID: 18327598

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. RASA1 mutations may cause hereditary capillary malformations without arteriovenous malformations.
    Hershkovitz D, Bercovich D, Sprecher E, Lapidot M.
    Br J Dermatol; 2008 May; 158(5):1035-40. PubMed ID: 18363760
    [Abstract] [Full Text] [Related]

  • 3. RASA1: variable phenotype with capillary and arteriovenous malformations.
    Boon LM, Mulliken JB, Vikkula M.
    Curr Opin Genet Dev; 2005 Jun; 15(3):265-9. PubMed ID: 15917201
    [Abstract] [Full Text] [Related]

  • 4. RASA1 analysis: clinical and molecular findings in a series of consecutive cases.
    Wooderchak-Donahue W, Stevenson DA, McDonald J, Grimmer JF, Gedge F, Bayrak-Toydemir P.
    Eur J Med Genet; 2012 Feb; 55(2):91-5. PubMed ID: 22200646
    [Abstract] [Full Text] [Related]

  • 5. The potential of capillary birthmarks as a significant marker for capillary malformation-arteriovenous malformation syndrome in children who had nontraumatic cerebral hemorrhage.
    Chee D, Phillips R, Maixner W, Southwell BR, Hutson JM.
    J Pediatr Surg; 2010 Dec; 45(12):2419-22. PubMed ID: 21129558
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Combined capillary-venous-lymphatic malformations without overgrowth in patients with Klippel-Trénaunay syndrome.
    Brandigi E, Torino G, Messina M, Molinaro F, Mazzei O, Matucci T, López Gutiérrez JC.
    J Vasc Surg Venous Lymphat Disord; 2018 Mar; 6(2):230-236. PubMed ID: 29233587
    [Abstract] [Full Text] [Related]

  • 9. Klippel-Trenaunay syndrome: a case study.
    Meier S.
    Adv Neonatal Care; 2009 Jun; 9(3):120-4. PubMed ID: 19542774
    [Abstract] [Full Text] [Related]

  • 10. Diagnosis and management of extensive vascular malformations of the lower limb: part I. Clinical diagnosis.
    Redondo P, Aguado L, Martínez-Cuesta A.
    J Am Acad Dermatol; 2011 Nov; 65(5):893-906; quiz 907-8. PubMed ID: 22000870
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Monozygotic twins discordant for vascular malformations and dysregulated growth.
    Oduber CE, Bliek J, van der Horst CM, van Steensel MA, Hennekam RC.
    Eur J Med Genet; 2010 Nov; 53(1):14-8. PubMed ID: 19716450
    [Abstract] [Full Text] [Related]

  • 13. Histopathologic and ultrasound characteristics of cutaneous capillary malformations in a patient with capillary malformation-arteriovenous malformation syndrome.
    Kim C, Ko CJ, Baker KE, Antaya RJ.
    Pediatr Dermatol; 2015 Nov; 32(1):128-31. PubMed ID: 23829194
    [Abstract] [Full Text] [Related]

  • 14. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations.
    Revencu N, Boon LM, Mulliken JB, Enjolras O, Cordisco MR, Burrows PE, Clapuyt P, Hammer F, Dubois J, Baselga E, Brancati F, Carder R, Quintal JM, Dallapiccola B, Fischer G, Frieden IJ, Garzon M, Harper J, Johnson-Patel J, Labrèze C, Martorell L, Paltiel HJ, Pohl A, Prendiville J, Quere I, Siegel DH, Valente EM, Van Hagen A, Van Hest L, Vaux KK, Vicente A, Weibel L, Chitayat D, Vikkula M.
    Hum Mutat; 2008 Jul; 29(7):959-65. PubMed ID: 18446851
    [Abstract] [Full Text] [Related]

  • 15. RASA1 somatic mutation and variable expressivity in capillary malformation/arteriovenous malformation (CM/AVM) syndrome.
    Macmurdo CF, Wooderchak-Donahue W, Bayrak-Toydemir P, Le J, Wallenstein MB, Milla C, Teng JM, Bernstein JA, Stevenson DA.
    Am J Med Genet A; 2016 Jun; 170(6):1450-4. PubMed ID: 26969842
    [Abstract] [Full Text] [Related]

  • 16. Phenotypic variability in a family with capillary malformations caused by a mutation in the RASA1 gene.
    de Wijn RS, Oduber CE, Breugem CC, Alders M, Hennekam RC, van der Horst CM.
    Eur J Med Genet; 2012 Mar; 55(3):191-5. PubMed ID: 22342634
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Capillary-venous malformation in the lower limb.
    Uihlein LC, Liang MG, Fishman SJ, Alomari AI, Mulliken JB.
    Pediatr Dermatol; 2013 Mar; 30(5):541-8. PubMed ID: 23829172
    [Abstract] [Full Text] [Related]

  • 20. Multifocal capillary malformations in an older, asymptomatic child with a novel RASA1 mutation.
    Whitaker S, Leech S, Taylor A, Splitt M, Natarajan S, Rajan N.
    Clin Exp Dermatol; 2016 Mar; 41(2):156-8. PubMed ID: 26132338
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 14.