{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,30]],"date-time":"2026-04-30T10:01:19Z","timestamp":1777543279906,"version":"3.51.4"},"reference-count":30,"publisher":"BMJ","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Archives of Disease in Childhood"],"published-print":{"date-parts":[[1978,5,1]]},"DOI":"10.1136\/adc.53.5.401","type":"journal-article","created":{"date-parts":[[2008,12,22]],"date-time":"2008-12-22T21:33:49Z","timestamp":1229981629000},"page":"401-406","source":"Crossref","is-referenced-by-count":14,"title":["Urinary excretion of glomerular basement membrane antigens in Alport's syndrome. A new diagnostic approach."],"prefix":"10.1136","volume":"53","author":[{"given":"G","family":"Lubec","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"E","family":"Balzar","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G","family":"Weissenbacher","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"G","family":"Syre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","first-page":"27","article-title":"L'originalite antigenique des prot6ines des structures du parenchyme renal. (Abst.) First International Congress of Nephrology","volume":"29","author":"Antoine, B.L.","year":"1960","unstructured":"Antoine, B. L. (1960). L'originalite antigenique des prot6ines des structures du parenchyme renal. (Abst.) First International Congress of Nephrology, p. 27. Ed. by G. Richet, M. Chayes, and F. Hoffman. International Congress Series No. 29. Excerpta Medica, Amsterdam.","journal-title":"Hoffman. International Congress Series"},{"key":"ref_2","first-page":"101","article-title":"Pathological urinary excretion of tissue macromolecules (histuria)","volume":"71","author":"Antoine, B.L.; Nevue, T.","year":"1968","unstructured":"Antoine, B. L., and Nevue, T. (1968). Pathological urinary excretion of tissue macromolecules (histuria). Journal of Laboratory and Clinical Medicine, 71, 101-112.","journal-title":"Journal of Laboratory and Clinical Medicine"},{"key":"ref_3","first-page":"67","article-title":"Consequences r6nales du manque de potassium. Actualites Nephrologiques de l'Hopital Necker","author":"Antoine, B.L.; Patte, D.; Barcelo, R.","year":"1962","unstructured":"Antoine, B. L., Patte, D., and Barcelo, R. (1962). Consequences r6nales du manque de potassium. Actualites Nephrologiques de l'Hopital Necker, 67-100."},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"545","DOI":"10.1203\/00006450-196911000-00004","article-title":"Hereditary nephritis: early clinical, functional and morphological studies","volume":"3","author":"Antonovych, T.T.; Deasy, P.F.; Tina, L.V.; D'Albora, J.B.; Hollerman, C.E.; Calcagno, P.L.","year":"1969","unstructured":"Antonovych, T. T., Deasy, P. F., Tina, L. V., D'Albora, J. B., Hollerman, C. E., and Calcagno, P. L. (1969). Hereditary nephritis: early clinical, functional and morphological studies. Pediatric Research, 3, 545-556.","journal-title":"Pediatric Research"},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1016\/0019-2791(69)90178-5","article-title":"The cross linking of proteins with glutaraldehyde and its use for the preparation of immunoadsorbents","volume":"6","author":"Avrameas, S.; Ternynck, T.","year":"1969","unstructured":"Avrameas, S., and Ternynck, T. (1969). The cross linking of proteins with glutaraldehyde and its use for the preparation of immunoadsorbents. Immunochemistry, 6, 53-66.","journal-title":"Immunochemistry"},{"key":"ref_6","first-page":"221","article-title":"Alport-Syndrom. Diagnosestellung, licht und elektronenmikroskopische Befunde","volume":"11","author":"Balzar, E.; Lubec, G.; Syre, G.; Weissenbacher, G.","year":"1976","unstructured":"Balzar, E., Lubec, G., Syre, G., and Weissenbacher, G. (1976). Alport-Syndrom. Diagnosestellung, licht und elektronenmikroskopische Befunde. Pddiatrie und Pddologie, 11, 221-233.","journal-title":"Pddiatrie und Pddologie"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"563","DOI":"10.1111\/j.1749-6632.1963.tb17693.x","article-title":"Present concepts concerning the origin of matrix and stones","volume":"104","author":"Boyce, W.H.; King, J.S.","year":"1963","unstructured":"Boyce, W. H., and King, J. S. (1963). Present concepts concerning the origin of matrix and stones. Annals of the New York Academy of Sciences, 104, 563-578.","journal-title":"Annals of the New York Academy of Sciences"},{"key":"ref_8","first-page":"374","article-title":"Pathological characteristics of hereditary nephritis","volume":"95","author":"Churg, J.; Sherman, R.L.","year":"1973","unstructured":"Churg, J., and Sherman, R. L. (1973). Pathological characteristics of hereditary nephritis. Archives of Pathology, 95, 374-379.","journal-title":"Archives of Pathology"},{"key":"ref_9","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1159\/000308468","article-title":"Alport's syndrome: clinicopathological considerations","volume":"165","author":"Faggioni, R.; Sicuras, J.; Streiff, E.B.","year":"1972","unstructured":"Faggioni, R., Sicuras, J., and Streiff, E. B. (1972). Alport's syndrome: clinicopathological considerations. Ophthalmologica, 165, 1-14.","journal-title":"Ophthalmologica"},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"727","DOI":"10.1016\/S0022-5347(17)72325-7","article-title":"Urinary proteins: the appearance of kidney proteins in the urine of some cases of severe chronic glomerular nephritis","volume":"34","author":"Gilman, G.","year":"1935","unstructured":"Gilman, G. (1935). Urinary proteins: the appearance of kidney proteins in the urine of some cases of severe chronic glomerular nephritis. Journal of Urology, 34, 727-731.","journal-title":"Journal of Urology"},{"key":"ref_11","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1542\/peds.20.2.241","article-title":"Hereditary renal disease associated with nerve deafness and ocular lesions","volume":"20","author":"Goldbloom, R.B.Fraser; C., F.; Waugh, D.; Aronovitch, M.; Wiglesworth, F.W.","year":"1957","unstructured":"Goldbloom, R. B. Fraser, F. C., Waugh, D., Aronovitch, M., and Wiglesworth, F. W. (1957). Hereditary renal disease associated with nerve deafness and ocular lesions. Pediatrics, 20, 241-252.","journal-title":"Pediatrics"},{"key":"ref_12","first-page":"12","article-title":"The proteins of normal urine. If. From the urinary tract","volume":"ofClinicalPathology,","author":"Grant, G.H.","year":"1959","unstructured":"Grant, G. H. (1959). The proteins of normal urine. If. From the urinary tract. Journal ofClinicalPathology, 12,510-517.","journal-title":"Journal"},{"key":"ref_13","first-page":"516","article-title":"The nonspecificity ofthe ultrastructural alterations in hereditary nephritis","volume":"31","author":"Hill, G.S.; Jenis, E.H.; Goodloe, Jr, S.","year":"1974","unstructured":"Hill, G. S., Jenis, E. H., and Goodloe, S., Jr. (1974). The nonspecificity ofthe ultrastructural alterations in hereditary nephritis. Laboratory Investigation, 31, 516-532.","journal-title":"Laboratory Investigation"},{"key":"ref_14","first-page":"473","article-title":"Characteristic ultrastructural lesions of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome)","volume":"27","author":"Hinglais, N.; Grunfeld, J.P.; Bois, E.","year":"1972","unstructured":"Hinglais, N., Grunfeld, J. P., and Bois, E. (1972). Characteristic ultrastructural lesions of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome). Laboratory Investigation, 27, 473-487.","journal-title":"Laboratory Investigation"},{"key":"ref_15","first-page":"1195","article-title":"Thermostable antigen and its excretion into urine","volume":"100","author":"Intorp, W.H.; Milgrom, F.J.","year":"1968","unstructured":"Intorp, W. H., and Milgrom, F. J. (1968). Thermostable antigen and its excretion into urine. Journal ofImmunology, 100, 1195-1203.","journal-title":"Journal ofImmunology"},{"key":"ref_16","first-page":"37","article-title":"Diffuse familial nephropathy. A clinicopathological study","volume":"77","author":"Kaufman, D.B.; McIntosh, R.M.; Smith, Jr., F.G.; Vernier, R.L.","year":"1970","unstructured":"Kaufman, D. B., McIntosh, R. M., Smith, F. G., Jr., and Vernier, R. L. (1970). Diffuse familial nephropathy. A clinicopathological study. Journal ofPediatrics, 77, 37-47.","journal-title":"Journal ofPediatrics"},{"key":"ref_17","first-page":"506","article-title":"Renal pathology in hereditary nephritis with nerve deafness","volume":"82","author":"Krickstein, H.I.; Gloor, F.I.; Balogh, Jr, K.","year":"1966","unstructured":"Krickstein, H. I., Gloor, F. I., and Balogh, K., Jr. (1966). Renal pathology in hereditary nephritis with nerve deafness. Archives ofPathology, 82, 506-517.","journal-title":"Archives ofPathology"},{"key":"ref_18","doi-asserted-by":"crossref","first-page":"1395","DOI":"10.1084\/jem.130.6.1395","article-title":"Immunoreactive basement membrane antigens in normal human urine and serum","volume":"130","author":"McPhaul, Jr., J.J.; Dixon, F.J.","year":"1969","unstructured":"McPhaul, J. J., Jr., and Dixon, F. J. (1969). Immunoreactive basement membrane antigens in normal human urine and serum. Journal of Experimental Medicine, 130, 1395-1409.","journal-title":"Journal of Experimental Medicine"},{"key":"ref_19","first-page":"544","article-title":"Glomerular basement membrane antigen excretion in normal and nephritic men","volume":"27","author":"McPhaul, Jr., J.J.; Lerner, R.A.","year":"1968","unstructured":"McPhaul, J. J., Jr., and Lerner, R. A. (1968). Glomerular basement membrane antigen excretion in normal and nephritic men. (Abst.) Federation Proceedings, 27, 544.","journal-title":"(Abst.) Federation Proceedings"},{"key":"ref_20","doi-asserted-by":"crossref","first-page":"410","DOI":"10.1111\/j.1432-1033.1970.tb00867.x","article-title":"Chemical structure of tubular and glomerular basement membranes of human kidney","volume":"12","author":"Mahieu, P.; Winand, R.J.","year":"1970","unstructured":"Mahieu, P., and Winand, R. J. (1970). Chemical structure of tubular and glomerular basement membranes of human kidney. European Journal of Biochemistry, 12, 410-418.","journal-title":"European Journal of Biochemistry"},{"key":"ref_21","doi-asserted-by":"crossref","first-page":"556","DOI":"10.1016\/S0002-9343(70)80051-1","article-title":"Familial nephropathy associated with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities","volume":"49","author":"Mainzer, F.; Saldino, R.M.; Ozonoff, M.B.; Minagi, H.","year":"1970","unstructured":"Mainzer, F., Saldino, R. M., Ozonoff, M. B., and Minagi, H. (1970). Familial nephropathy associated with retinitis pigmentosa, cerebellar ataxia and skeletal abnormalities. American Journal of Medicine, 49, 556-562.","journal-title":"American Journal of Medicine"},{"key":"ref_22","first-page":"236","article-title":"Abstracts ofthe 3rd International Congress of Nephrology","author":"Manual, Y.","year":"1963","unstructured":"Manual, Y. (1963). Abstracts ofthe 3rd International Congress of Nephrology, p. 236. Washington, D.C."},{"key":"ref_23","first-page":"552","article-title":"La n6phropathie h6maturique h6reditaire avec surdit6. Semaine des Hopitaux de","volume":"36","author":"Marie, J.","year":"1960","unstructured":"Marie, J. (1960). La n6phropathie h6maturique h6reditaire avec surdit6. Semaine des Hopitaux de Paris, 36, 552-561.","journal-title":"Paris"},{"key":"ref_24","doi-asserted-by":"crossref","first-page":"79","DOI":"10.1056\/NEJM196707132770206","article-title":"The hereditary renal diseases","volume":"277","author":"Perkoff, G.T.","year":"1967","unstructured":"Perkoff, G. T. (1967). The hereditary renal diseases. New England Journal of Medicine, 277, 79-85.","journal-title":"New England Journal of Medicine"},{"key":"ref_25","first-page":"41","article-title":"Nephrologie Pediatrique","author":"Royer, P.","year":"1975","unstructured":"Royer, P. (1975). Nephrologie Pediatrique, 2nd ed., p. 41. Flammarion, Paris.","edition":"2nd ed"},{"key":"ref_26","doi-asserted-by":"crossref","first-page":"801","DOI":"10.1001\/archinte.1956.00250300119013","article-title":"The mechanism and significance of protein excretion by the normal kidney","volume":"98","author":"Sellers, A.L.","year":"1956","unstructured":"Sellers, A. L. (1956). The mechanism and significance of protein excretion by the normal kidney. Archives of Internal Medicine, 98, 801-806.","journal-title":"Archives of Internal Medicine"},{"key":"ref_27","author":"Sessa, A.; Cioffi, A.; Conte, F.; D'Amico, G.","year":"1974","unstructured":"Sessa, A., Cioffi, A., Conte, F., and D'Amico, G. (1974)."},{"key":"ref_28","first-page":"336","article-title":"Alport's syndrome: a consideration of pathogenesis","volume":"1","author":"Spear, G.S.","year":"1973","unstructured":"Spear, G. S. (1973). Alport's syndrome: a consideration of pathogenesis. Clinical Nephrology, 1, 336-337.","journal-title":"Clinical Nephrology"},{"key":"ref_29","first-page":"213","article-title":"Alport's syndrome emphasizing electron miscroscopic studies of the glomerulus","volume":"69","author":"Spear, G.S.; Slusser, R.J.","year":"1972","unstructured":"Spear, G. S., and Slusser, R. J. (1972). Alport's syndrome emphasizing electron miscroscopic studies of the glomerulus. American Journal ofPathology, 69, 213-220.","journal-title":"American Journal ofPathology"},{"key":"ref_30","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1016\/0002-9343(61)90107-3","article-title":"Hereditary nephropathy, deafness and renal foam cells","volume":"31","author":"Whalen, R.E.; Huang, S.; Peschel, E.; McIntosh, H.D.","year":"1961","unstructured":"Whalen, R. E., Huang, S., Peschel, E., and McIntosh, H. D. (1961). Hereditary nephropathy, deafness and renal foam cells. American Journal of Medicine, 31, 171-186.","journal-title":"American Journal of Medicine"}],"container-title":["Archives of Disease in Childhood"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/adc.53.5.401","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,23]],"date-time":"2023-05-23T03:45:01Z","timestamp":1684813501000},"score":1,"resource":{"primary":{"URL":"https:\/\/adc.bmj.com\/lookup\/doi\/10.1136\/adc.53.5.401"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1978,5,1]]},"references-count":30,"journal-issue":{"issue":"5","published-print":{"date-parts":[[1978,5,1]]}},"URL":"https:\/\/doi.org\/10.1136\/adc.53.5.401","relation":{},"ISSN":["0003-9888","1468-2044"],"issn-type":[{"value":"0003-9888","type":"print"},{"value":"1468-2044","type":"electronic"}],"subject":[],"published":{"date-parts":[[1978,5,1]]}}}