Research ArticleBRAIN
Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
Shunji Matsubara, Jennifer L. Manzia, Karel ter Brugge, Robert A. Willinsky, Walter Montanera and Marie E. Faughnan
American Journal of Neuroradiology June 2000, 21 (6) 1016-1020;
Shunji Matsubara
Jennifer L. Manzia
Karel ter Brugge
Robert A. Willinsky
Walter Montanera

References
- ↵Guttmacher AE, Marchuk DA, White RIJ. Hereditary hemorrhagic telangiectasia. N Engl J Med 1995;333:918-924
- McAllister KA, Grogg KM, Johnson DW, et al. Endoglin, a TGF-B binding protein of endothelial cells, is the gene for hereditary hemorrhagic telangiectasia type I. Nat Genet 1994;8:345-351
- Vincent P, Plauchu H, Hazan J, et al. A third locus for hereditary hemorrhagic telangiectasia maps to 12q. Hum Mol Genet 1995;4:945-949
- Johnson DW, Berg JN, Gallione CJ, et al. A second locus for hereditary hemorrhagic telangiectasia mapped to chromosome 12. Genome Res 1995;5:21-28
- ↵Willinsky RA, Lasjaunias P, Ter Brugge K, Burrows P. Multiple cerebral arteriovenous malformations (AVMs): review of our experience from 203 patients with cerebral vascular lesions. Neuroradiology 1990;32:207-210
- ↵Ference BA, Shannon TM, White RIJ, Zawin M. Burdge CM. Life-threatening pulmonary hemorrhage with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia. Chest 1994;106:1387-1390
- ↵Wirth JA, Pollak JS, White RIJ. Pulmonary arteriovenous malformations. Curr Pulm Crit Care Med 1996;17:272-274
- ↵Plauchu H, de Chadarévian JP, Bideau A, Robert JM. Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Am J Med Genet 1989;32:291-297
- ↵Yasargil MG. Pathological consideration. In: Yasargil MG, ed. Microneurosurgery. vol 3A. Stuttgart: Thieme 1987 63-64
- Jessurun GAJ, Kamphuis DJ, van der Zande FHR, Nossent JC. Cerebral arteriovenous malformations in the Netherlands Antilles: high prevalence of hereditary hemorrhagic telangiectasia-related single and multiple cerebral arteriovenous malformations. Clin Neurol Neurosurg 1993;95:193-198
- ↵Putman CM, Chaloupka JC, Fulbright RK, Awad IA, White RI Jr, Fayed PB. Exceptional multiplicity of cerebral arteriovenous malformations associated with hereditary hemorrhagic telangiectasia (Osler-Rendu-Weber syndrome). AJNR Am J Neuroradiol 1996;17:1733-1742
- Coubes P, Humbertclaude V, Rodesch G, Lasjaunias P, Echenne B, Frerebeau P. Total endovascular occlusion of a giant direct arteriovenous fistula in the posterior fossa in a case of Rendu-Osler-Weber disease. Child Nerv Syst 1996;12:785-788
- Garcia-Monaco R, Taylor W, Rodesch G, et al. Pial arteriovenous fistula in children as presenting manifestation of Rendu-Osler-Weber disease. Neuroradiology 1995;37:60-64
- Kikuchi K, Kowada M, Tomura N, Kohkura H. Hereditary hemorrhagic telangiectasia associated with cerebral arteriovenous fistula and multiple cerebral arteriovenous malformations: case report. No Shinkei Geka 1994;22:85-91
- Kodoya C, Momota Y, Ikegami Y, Urasaki E, Wada S, Yokota A. Central nervous system arteriovenous malformations with hereditary hemorrhagic telangiectasia: report of a family with three cases. Surg Neurol 1994;42:234-239
- John PR. Early childhood presentation of neurovascular disease in hereditary hemorrhagic telangiectasia. Pediatr Radiol 1992;22:140-141
- Nakao S, Sukumitsu T, Yamamoto T, Sakamoto H. Cerebral and pulmonary arteriovenous fistula with possible hereditary hemorrhagic telangiectasia: case report. No Shinkei Geka 1986;14:901-906
- Eto RT, Harley JD, Chikos PM, Graebner RW. Subarachnoid hemorrhage in hereditary hemorrhagic telangiectasia: report of two cases. Neuroradiology 1974;8:127-130
- Waller JD, Greenberg JH, Lewis CW. Hereditary hemorrhagic telangiectasia with cerebrovascular malformations. Arch Dermatol 1976;112:49-52
- Adams HP Jr, Subbiah B, Bosch EP. Neurologic aspects of hereditary hemorrhagic telangiectasia: report of two cases. Arch Neurol 1977;34:101-104
- ↵Kawaguchi T, Fujita S, Yamada H, Nishida Y, Izawa I. Multiple cerebral and pulmonary arteriovenous malformations associated with brain and subcutaneous abscesses: a possible variant of hereditary hemorrhagic telangiectasia, case report. Neurol Med Chir (Toyko) 1990;30:272-276
- Yasargil MG. Microneurosurgery. vol 3A. Stuttgart: Thieme 1987 165-181
- ↵Viñuela F. Functional evaluation and embolization of intracranial arteriovenous malformation. In: Viñuela F, Halbach VV, Dion JE, eds. Interventional Neuroradiology: Endovascular Therapy of the Central Nervous System. New York: Raven Press 1992 77-86
- Kikuchi K, Kowada M, Sasajima H. Vascular malformation of the brain in hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber disease). Surg Neurol 1994;41:374-380
- ↵Berenstein A, Lasjaunias P. Classification of CVMs. In: Surgical Neuroangiography. vol 4. Berlin: Springer 1992 25-80
- ↵Yasargil MG. Microneurosurgery.. vol 3B. Stuttgart: Thieme 1987 16-18
- ↵
- ↵Fulbright RK, Chaloupka JC, Putman CM, et al. MR of hereditary hemorrhagic telangiectasia: prevalence and spectrum of cerebrovascular malformations. AJNR Am J Neuroradiol 1998;19:477-484
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Shunji Matsubara, Jennifer L. Manzia, Karel ter Brugge, Robert A. Willinsky, Walter Montanera, Marie E. Faughnan
Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
American Journal of Neuroradiology Jun 2000, 21 (6) 1016-1020;
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Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
Shunji Matsubara, Jennifer L. Manzia, Karel ter Brugge, Robert A. Willinsky, Walter Montanera, Marie E. Faughnan
American Journal of Neuroradiology Jun 2000, 21 (6) 1016-1020;
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