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Journal Abstract Search

208 related items for PubMed ID: 25372443

  • 41. ISCHEMIC RETINOPATHY IN NEUROFIBROMATOSIS TYPE 1.
    Dansingani KK, Jung JJ, Belinsky I, Marr BP, Freund KB.
    Retin Cases Brief Rep; 2015; 9(4):290-4. PubMed ID: 26252734
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  • 45. Clinical presentation and treatment paradigms in patients with hereditary hemorrhagic telangiectasia and spinal vascular malformations.
    Eli I, Gamboa NT, Joyce EJ, Park MS, Taussky P, Schmidt RH, Couldwell WT, McDonald J, Whitehead KJ, Kalani MYS.
    J Clin Neurosci; 2018 Apr; 50():51-57. PubMed ID: 29398197
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  • 46. Transcardiac retrograde transvenous embolization of proximally occluded pulmonary arteriovenous malformation.
    Komiyama M, Ishiguro T, Umaba R, Suzuki T.
    Cardiovasc Intervent Radiol; 2014 Jun; 37(3):791-4. PubMed ID: 24149830
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  • 48. A Pial Arteriovenous Fistula in Infancy as the Presenting Manifestation of Hereditary Hemorrhagic Telangiectasia.
    Okazaki T, Sakamoto S, Ishii D, Oshita J, Matsushige T, Shinagawa K, Ichinose N, Matsuda S, Kurisu K.
    World Neurosurg; 2019 Feb; 122():322-325. PubMed ID: 30391600
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  • 49. Huge pulmonary arteriovenous fistula: diagnosis and treatment and an unusual complication of embolization.
    Kretschmar O, Ewert P, Yigitbasi M, Zurbrügg HR, Hetzer R, Lange PE.
    Respir Care; 2002 Sep; 47(9):998-1001. PubMed ID: 12188934
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  • 52. Retinal vasculopathy in Fanconi anemia.
    Chai SM, Mathur R, Ong SG.
    Ophthalmic Surg Lasers Imaging; 2009 Sep; 40(5):498-500. PubMed ID: 19772276
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  • 55. Hereditary hemorrhagic telangiectasia causing high output cardiac failure: treatment with transcatheter embolization.
    Trotter JF, Suhocki PV, Lina JR, Martin LW, Parrish JL, Swantkowski T.
    Am J Gastroenterol; 1998 Sep; 93(9):1569-71. PubMed ID: 9732949
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  • 56. [A case of Rendu-Osler-Weber syndrome and pulmonary arteriovenous fistula].
    Nomura M, Kitagawa K, Fujimura M, Matsuda T.
    Nihon Kyobu Shikkan Gakkai Zasshi; 1995 Sep; 33(9):1009-12. PubMed ID: 8538081
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  • 58. Leukocoria and vitreous hemorrhage as the initial manifestation of sickle retinopathy in a 3-year, 6-month-old child with sickle trait (AS).
    Barry GP, Shields CL, Binenbaum G.
    J Pediatr Ophthalmol Strabismus; 2011 Oct 11; 48 Online():e58-60. PubMed ID: 21985230
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  • 59. Outcomes of vitreoretinal surgery in patients with X-linked retinoschisis.
    Rosenfeld PJ, Flynn HW, McDonald HR, Rubsamen PE, Smiddy WE, Sipperley JO, Boniuk I, Packer AJ.
    Ophthalmic Surg Lasers; 1998 Mar 11; 29(3):190-7. PubMed ID: 9547772
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  • 60. Ocular manifestations in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease): a case-series.
    Rinaldi M, Buscarini E, Danesino C, Chiosi F, De Benedictis A, Porcellini A, Costagliola C.
    Ophthalmic Genet; 2011 Mar 11; 32(1):12-7. PubMed ID: 21174526
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