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Journal Abstract Search

175 related items for PubMed ID: 32799314

  • 21. 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]

  • 22. Somatic Gain of KRAS Function in the Endothelium Is Sufficient to Cause Vascular Malformations That Require MEK but Not PI3K Signaling.
    Fish JE, Flores Suarez CP, Boudreau E, Herman AM, Gutierrez MC, Gustafson D, DiStefano PV, Cui M, Chen Z, De Ruiz KB, Schexnayder TS, Ward CS, Radovanovic I, Wythe JD.
    Circ Res; 2020 Aug 28; 127(6):727-743. PubMed ID: 32552404
    [Abstract] [Full Text] [Related]

  • 23. Somatic second hit mutation of RASA1 in vascular endothelial cells in capillary malformation-arteriovenous malformation.
    Lapinski PE, Doosti A, Salato V, North P, Burrows PE, King PD.
    Eur J Med Genet; 2018 Jan 28; 61(1):11-16. PubMed ID: 29024832
    [Abstract] [Full Text] [Related]

  • 24. Monitoring Arteriovenous Malformation Response to Genotype-Targeted Therapy.
    Edwards EA, Phelps AS, Cooke D, Frieden IJ, Zapala MA, Fullerton HJ, Shimano KA.
    Pediatrics; 2020 Sep 28; 146(3):. PubMed ID: 32859736
    [Abstract] [Full Text] [Related]

  • 25. KRAS/BRAF mutations in brain arteriovenous malformations: A systematic review and meta-analysis.
    Bameri O, Salarzaei M, Parooie F.
    Interv Neuroradiol; 2021 Aug 28; 27(4):539-546. PubMed ID: 33401991
    [Abstract] [Full Text] [Related]

  • 26. Mosaic RASopathy due to KRAS variant G12D with segmental overgrowth and associated peripheral vascular malformations.
    Schmidt VF, Wieland I, Wohlgemuth WA, Ricke J, Wildgruber M, Zenker M.
    Am J Med Genet A; 2021 Oct 28; 185(10):3122-3128. PubMed ID: 34114335
    [Abstract] [Full Text] [Related]

  • 27. KRAS G12D or G12V Mutation in Human Brain Arteriovenous Malformations.
    Oka M, Kushamae M, Aoki T, Yamaguchi T, Kitazato K, Abekura Y, Kawamata T, Mizutani T, Miyamoto S, Takagi Y.
    World Neurosurg; 2019 Jun 28; 126():e1365-e1373. PubMed ID: 30902772
    [Abstract] [Full Text] [Related]

  • 28. [Pathogenesis and genetics of vascular anomalies].
    Vikkula M.
    Ann Chir Plast Esthet; 2006 Jun 28; 51(4-5):282-6. PubMed ID: 16997448
    [Abstract] [Full Text] [Related]

  • 29. Expression of Wilms tumor 1 gene distinguishes vascular malformations from proliferative endothelial lesions.
    Lawley LP, Cerimele F, Weiss SW, North P, Cohen C, Kozakewich HP, Mulliken JB, Arbiser JL.
    Arch Dermatol; 2005 Oct 28; 141(10):1297-300. PubMed ID: 16230568
    [Abstract] [Full Text] [Related]

  • 30. Genetic Profile of Arteriovenous Anomalies of the Head and Neck: Implications in Progression and Therapeutic Approaches.
    Pampín Martínez MM, Rodríguez-Laguna L, Gómez García E, Cebrián Carretero JL, González Otero T, López Gutiérrez JC.
    J Pediatr Surg; 2023 Oct 28; 58(10):2043-2049. PubMed ID: 36868957
    [Abstract] [Full Text] [Related]

  • 31. Multiple capillary malformations of progressive onset: Capillary malformation-arteriovenous malformation syndrome (CM-AVM).
    Gourier G, Audebert-Bellanger S, Vourc'h P, Fraitag S, L'Hérondelle K, Labouche A, Misery L, Abasq-Thomas C.
    Ann Dermatol Venereol; 2018 Oct 28; 145(8-9):486-491. PubMed ID: 30056992
    [Abstract] [Full Text] [Related]

  • 32. Congenital vascular malformations--cerebral lesions differ from extracranial lesions by their immune expression of the glucose transporter protein GLUT1.
    Meijer-Jorna LB, Aronica E, van der Loos CM, Troost D, van der Wal AC.
    Clin Neuropathol; 2012 Oct 28; 31(3):135-41. PubMed ID: 22551917
    [Abstract] [Full Text] [Related]

  • 33. Hereditary intraosseous vascular malformation of the craniofacial region: imaging findings.
    Vargel I, Cil BE, Kiratli P, Akinci D, Erk Y.
    Br J Radiol; 2004 Mar 28; 77(915):197-203. PubMed ID: 15020360
    [Abstract] [Full Text] [Related]

  • 34. Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling.
    Amyere M, Revencu N, Helaers R, Pairet E, Baselga E, Cordisco M, Chung W, Dubois J, Lacour JP, Martorell L, Mazereeuw-Hautier J, Pyeritz RE, Amor DJ, Bisdorff A, Blei F, Bombei H, Dompmartin A, Brooks D, Dupont J, González-Enseñat MA, Frieden I, Gérard M, Kvarnung M, Hanson-Kahn AK, Hudgins L, Léauté-Labrèze C, McCuaig C, Metry D, Parent P, Paul C, Petit F, Phan A, Quere I, Salhi A, Turner A, Vabres P, Vicente A, Wargon O, Watanabe S, Weibel L, Wilson A, Willing M, Mulliken JB, Boon LM, Vikkula M.
    Circulation; 2017 Sep 12; 136(11):1037-1048. PubMed ID: 28687708
    [Abstract] [Full Text] [Related]

  • 35. Segmental cutaneous hemangioma and spinal arteriovenous malformation (Cobb syndrome). Case report and historical perspective.
    Maramattom BV, Cohen-Gadol AA, Wijdicks EF, Kallmes D.
    J Neurosurg Spine; 2005 Sep 12; 3(3):249-52. PubMed ID: 16235712
    [Abstract] [Full Text] [Related]

  • 36. A human model of arteriovenous malformation (AVM)-on-a-chip reproduces key disease hallmarks and enables drug testing in perfused human vessel networks.
    Soon K, Li M, Wu R, Zhou A, Khosraviani N, Turner WD, Wythe JD, Fish JE, Nunes SS.
    Biomaterials; 2022 Sep 12; 288():121729. PubMed ID: 35999080
    [Abstract] [Full Text] [Related]

  • 37. Vascular anomalies of the head and neck: a review of genetics.
    Yadav P, De Castro DK, Waner M, Meyer L, Fay A.
    Semin Ophthalmol; 2013 Sep 12; 28(5-6):257-66. PubMed ID: 24010650
    [Abstract] [Full Text] [Related]

  • 38. A case of capillary malformation-arteriovenous malformation and Ebstein's anomaly in a child with EphB4 mutation.
    Sherwani Y, Jenkins S, Adelanwa A, Burch DM, Chaudhuri NR, Zinn Z.
    Pediatr Dermatol; 2021 Sep 12; 38(5):1305-1307. PubMed ID: 34339071
    [Abstract] [Full Text] [Related]

  • 39. Soft-tissue vascular anomalies: utility of US for diagnosis.
    Paltiel HJ, Burrows PE, Kozakewich HP, Zurakowski D, Mulliken JB.
    Radiology; 2000 Mar 12; 214(3):747-54. PubMed ID: 10715041
    [Abstract] [Full Text] [Related]

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