References
- Ter Berg JWM, Bijlsma JB, Veiga Pires JA, Ludwig JW, Van der Heiden C, Tulleken CAF, Willemse J. Familial association of intracranial aneurysms and multiple congenital anomalies. Arch Neurol 1986; 43: 30–33
- Norrgard O, Angquist K, Fodstad H, Forsell A, Lindberg M. Intracranial aneurysms and hereditary. Neurosurgery 1987; 20: 236–239
- Hallal F, Mohr G, Toussi T, Martinez SN. Intracranial aneurysms: A report of a large pedigree. Am J Med Genet 1983; 15: 89–95
- Morton LF, Barnes MJ. Collagen polymorphism in the normal and diseased blood vessel wall. Investigation of collagens “types I, III and IV.”. Atherosclerosis 1982; 42: 41–51
- Hollister DW. Heritable disorders of connective tissue: Ehlers-Danlos syndrome. Pediatr Clin North Am 1978; 25: 575–591
- Pyeritz RE, McKusick VA. The Marfan syndrome: diagnosis and management. N Engl J Med 1979; 300: 772–777
- Emanuel R, Marcomichelakis J, Moores EC, Jefferson KE, Macfaul PA, Withers R. Formes frustes ofMarfan'ssyndrome presenting with severe aortic regurgitation. Clinicogenetic study of 18 families. Br Heart J 1977; 39: 190–197
- Payvandi MN, Kerber RE, Phelps CD, Iudisch GF, El-Khoury G, Schrott HG. Cardiac, skeletal and ophthalmologic abnormalities in relatives of patients with Marfan syndrome. Circulation 1977; 55: 797–802
- Ter Berg JWM, Overtoom TMD, Ludwig JW, Bijlsma JB, Tulleken CAF, Willemse J. Detection of unruptured familial intracranial aneurysms by intravenous digital subtraction angiography. Screening of two families. Neuroradiology 1987a; 29: 272–276
- Ter Berg JWM, Bijlsma JB, Willemse J. Familial occurrence of intracranial aneurysms in childhood. A case report and review of the literature. Neuropaediatrics 1987b; 18: 227–230
- Endtz J. Familial incidence of intracranial aneurysms. Acta Neurochir 1968; 19: 297–305
- Sinclair RJG, Kitchin AH, Turner RWD. The Marfan syndrome. Quart J Med 1960; 29: 19–46
- Pope FM, Narcisi P, Neil-Dwyer G, Nicholls AC, Bartlett J, Doshi B. Some patients with cerebral aneurysms are deficient in type III collagen. Lancet 1981; 1: 973–975
- Byers PH, Siegel RC, Peterson KE, Rowe DW, Holbrook KA, Smith LT, Chang Y, Fu JCC. Marfan syndrome: abnormal 2 chain in type I collagen. Proc Natl Acad Sci 1981; 78: 7745–7749
- Burian HM, Van Noorden GK, Ponsati IV. Chamber angle anomalies in systemic connective tissue disorders. Arch Ophthalmol 1960; 64: 671–680
- Burian HM, Allan L. Histologic study of the chamber angle of patients with Marfan syndrome. Arch Ophthalmol 1961; 65: 323–333
- Cross HE, Allan D, Jensen D. Ocular manifestations in the Marfan syndrome and homocystinuria. Am J Ophthalmol 1973; 75: 405–420
- Van Noorden GK, Schultz RO. A gonioscopic study of the chamber angle in Marfan's syndrome. Arch Ophthalmol 1960; 64: 929–934