{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,20]],"date-time":"2025-10-20T17:53:15Z","timestamp":1760982795252},"reference-count":14,"publisher":"BMJ","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurology, Neurosurgery & Psychiatry"],"published-print":{"date-parts":[[1969,12,1]]},"DOI":"10.1136\/jnnp.32.6.604","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T20:53:49Z","timestamp":1226350429000},"page":"604-608","source":"Crossref","is-referenced-by-count":14,"title":["Hereditary haemorrhagic telangiectasia: neuropathological observations."],"prefix":"10.1136","volume":"32","author":[{"given":"R R","family":"Heffner","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G B","family":"Solitare","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","first-page":"597","article-title":"Temporary local circulatory disturbances","volume":"260","author":"with; associ-Bird, R.M.; Jaques, W.E.","year":"1959","unstructured":"Temporary local circulatory disturbances with associ-Bird, R. M., and Jaques, W. E. (1959). Vascular lesion of hereditary ated hypoxia may have been responsible for the clinical picture. There was evidence of nonspecific anoxic effect in the loss of neurones in Ammon's horn. The telangiectases, which were dilated at the time of our examination, are conhemorrhagic telangiectasia. New Engl. J. Med., 260, 597-599.","journal-title":"New Engl. J. Med; Vascular lesion of hereditary ated hypoxia may have been responsible for the clinical picture. There was evidence of nonspecific anoxic effect in the loss of neurones in Ammon's horn. The telangiectases, which were dilated at the time of our examination, are conhemorrhagic telangiectasia"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"525","DOI":"10.1097\/00005053-196412000-00005","article-title":"Neurological implications of hereditary hemorrhagic telangiectasis","volume":"139","author":"Boczko, M.L.","year":"1964","unstructured":"Boczko, M. L. (1964). Neurological implications of hereditary hemorrhagic telangiectasis. J. nerv. ment. Dis., 139, 525-536.","journal-title":"J. nerv. ment. Dis"},{"key":"ref_3","first-page":"119","article-title":"Uber Osler Krankheit (pathologische Anatomie","volume":"70","author":"Brinkmann, E.","year":"1950","unstructured":"Brinkmann, E. (1950). Uber Osler Krankheit (pathologische Anatomie, I. Therapie). Folia haemat. (Lpz.), 70, 119-123.","journal-title":"I. Therapie). Folia haemat. (Lpz.)"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1001\/archinte.1965.03870020117021","article-title":"Pulmonary and cerebral arteriovenous fistula with Osler's disease","volume":"116","author":"Chandler, D.","year":"1965","unstructured":"Chandler, D. (1965). Pulmonary and cerebral arteriovenous fistula with Osler's disease. Arch. intern. Med., 116, 277-282.","journal-title":"Arch. intern. Med"},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"81","DOI":"10.1159\/000203377","article-title":"Hereditary haemorrhagic telangiectasis and its relations to other inborn vascular malformations","volume":"1","author":"Cohn, H.M.; Rosenthal, F.E.","year":"1948","unstructured":"Cohn, H. M., and Rosenthal, F. E. (1948). Hereditary haemorrhagic telangiectasis and its relations to other inborn vascular malformations. Acta haemat. (Basel), 1, 81-92.","journal-title":"Acta haemat. (Basel)"},{"key":"ref_6","article-title":"clinically detectable symptoms. The patient's apparent dementia is more puzzling. We have no histological indication of so-called senile dementia characterized by senile plaques and neurofibrillary changes. Dementia has been","unstructured":"clinically detectable symptoms. The patient's apparent dementia is more puzzling. We have no histological indication of so-called senile dementia characterized by senile plaques and neurofibrillary changes. Dementia has been reported in association"},{"key":"ref_7","first-page":"28","article-title":"Encephalic lesions in hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber disease)","volume":"22","author":"Courville, C.B.","year":"1957","unstructured":"Courville, C. B. (1957). Encephalic lesions in hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber disease). Bull. Los Angeles neurol. Soc., 22, 28-35.","journal-title":"Bull. Los Angeles neurol. Soc"},{"key":"ref_8","first-page":"337","article-title":"Tumors Arising from Blood Vessels of the Brain","volume":"20","author":"Cushing, H.; Bailey, P.","year":"1928","unstructured":"Cushing, H., and Bailey, P. (1928). Tumors Arising from Blood Vessels of the Brain. Thomas: Baltimore, Md. Czernobilsky, B., and Bouzarth, W. F. (1965). Vascular malformations in the brain in a patient with multiple telangiectasia of the with telangiectasia of the brain-stem (Davison and Rosenheck, 1937). In that instance there was intestine and lungs. J. Amer. med. Woan. Ass., 20, 337-340.","journal-title":"J. Amer. med. Woan. Ass; Vascular malformations in the brain in a patient with multiple telangiectasia of the with telangiectasia of the brain-stem (Davison and Rosenheck, 1937). In that instance there was intestine and lungs"},{"key":"ref_9","first-page":"1909","article-title":"Telangiectases of the brain stem associated with obstructive hydrocephalus and mental hydrocephalus, the result of compression of the cerebral aqueduct. The ventricles were not apprecideterioration","volume":"37","author":"Davison, C.; Rosenheck, C.","year":"1937","unstructured":"Davison, C., and Rosenheck, C. (1937). Telangiectases of the brain stem associated with obstructive hydrocephalus and mental hydrocephalus, the result of compression of the cerebral aqueduct. The ventricles were not apprecideterioration. N. Y. St. J. Med., 37, 1909-1913.","journal-title":"N. Y. St. J. Med"},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"514","DOI":"10.1001\/archneurpsyc.1936.02260090067003","article-title":"Multiple telangiectases of the brain","volume":"36","author":"Michael, J.C.; Levin, P.M.","year":"1936","unstructured":"Michael, J. C., and Levin, P. M. (1936). Multiple telangiectases of the brain. Arch. Neurol. Psychiat. (Chic.), 36, 514-529.","journal-title":"Arch. Neurol. Psychiat. (Chic.)"},{"key":"ref_11","first-page":"17","article-title":"Subarachnoid hemorrhage in a patient with hereditary hemorrhagic telangiectasia","volume":"(Minneap.),","author":"Quickel, K.E.; Whaley, R.J.","year":"1967","unstructured":"Quickel, K. E., and Whaley, R. J. (1967). Subarachnoid hemorrhage in a patient with hereditary hemorrhagic telangiectasia. Neurology (Minneap.), 17,716-719.","journal-title":"Neurology"},{"key":"ref_12","first-page":"1211","article-title":"Is the homozygous form of multiple telangiectasia lethal?","volume":"29","author":"Snyder, L.H.; Doan, C.A.","year":"1944","unstructured":"Snyder, L. H., and Doan, C. A. (1944). Is the homozygous form of multiple telangiectasia lethal? J. Lab. clin. Med., 29, 1211-1216.","journal-title":"J. Lab. clin. Med"},{"key":"ref_13","doi-asserted-by":"crossref","first-page":"168","DOI":"10.1159\/000203824","article-title":"Telangiectasis haemorrhagica hereditaria: pathologischanatomischer Befund und Blutgruppen-Untersuchung","volume":"5","author":"Vischer, W.","year":"1951","unstructured":"Vischer, W. (1951). Telangiectasis haemorrhagica hereditaria: pathologischanatomischer Befund und Blutgruppen-Untersuchung. Acta. haemat. (Basel), 5, 168-177.","journal-title":"Acta. haemat. (Basel)"},{"key":"ref_14","first-page":"66","article-title":"Liver fibrosis in hereditary hemorrhagic telangiectasis","volume":"74","author":"Zelman, S.","year":"1962","unstructured":"Zelman, S. (1962). Liver fibrosis in hereditary hemorrhagic telangiectasis. Arch. Path., 74, 66-72.","journal-title":"Arch. Path"}],"container-title":["Journal of Neurology, Neurosurgery & Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jnnp.32.6.604","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,26]],"date-time":"2020-09-26T02:23:54Z","timestamp":1601087034000},"score":1,"resource":{"primary":{"URL":"https:\/\/jnnp.bmj.com\/lookup\/doi\/10.1136\/jnnp.32.6.604"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1969,12,1]]},"references-count":14,"journal-issue":{"issue":"6","published-print":{"date-parts":[[1969,12,1]]}},"URL":"https:\/\/doi.org\/10.1136\/jnnp.32.6.604","relation":{},"ISSN":["0022-3050"],"issn-type":[{"value":"0022-3050","type":"print"}],"subject":[],"published":{"date-parts":[[1969,12,1]]}}}