{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,19]],"date-time":"2025-10-19T15:25:53Z","timestamp":1760887553109},"reference-count":40,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1975,1,1]],"date-time":"1975-01-01T00:00:00Z","timestamp":157766400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Acta Neuropathol"],"published-print":{"date-parts":[[1975]]},"DOI":"10.1007\/bf00684563","type":"journal-article","created":{"date-parts":[[2004,11,28]],"date-time":"2004-11-28T14:26:13Z","timestamp":1101651973000},"page":"243-255","source":"Crossref","is-referenced-by-count":28,"title":["Aspartylglycosaminuria: A generalized storage disease"],"prefix":"10.1007","volume":"31","author":[{"given":"M.","family":"Haltia","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Palo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Autio","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"304","DOI":"10.1097\/00005072-196504000-00010","volume":"24","author":"F. P. Aleu","year":"1965","unstructured":"Aleu, F. P., Terry, R. D., Zellweger, H.: Electron microscopy of two cerebral biopsies in gargoylism. J. Neuropath. exp. Neurol24, 304 (1965)","journal-title":"J. Neuropath. exp. Neurol"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1007\/BF00686902","volume":"20","author":"A. Arstila","year":"1972","unstructured":"Arstila, A., Palo, J., Haltia, M., Riekkinen, P., Autio, S.: Aspartylglucosaminuria I: Fine structural studies on liver, kidney and brain. Acta neuropath. (Berl.)20, 207?216 (1972)","journal-title":"Acta neuropath. (Berl.)"},{"key":"CR3","unstructured":"Autio, S.: Aspartylglycosaminuria. Analysis of thirty-four patients. J. ment. Defic. Res., Monograph No. 1 (1972)"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"555","DOI":"10.1111\/j.1651-2227.1973.tb17065.x","volume":"62","author":"S. Autio","year":"1973","unstructured":"Autio, S., Nord\ufffdn, N. E., \ufffdckerman, P.-A., Riekkinen, P., Rapola, J., Louhimo, T.: Mannosidosis: clinical, fine structural and biochemical findings in three cases. Acta paediat. scand.62, 555?565 (1973).","journal-title":"Acta paediat. scand."},{"key":"CR5","volume-title":"Histochemistry. Theory, practice, and bibliography","author":"T. Barka","year":"1963","unstructured":"Barka, T., Anderson, P. J.: Histochemistry. Theory, practice, and bibliography. New York: Harper and Row 1963"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"58","DOI":"10.1001\/archinte.1963.03620250062010","volume":"111","author":"G. S. Berenson","year":"1963","unstructured":"Berenson, G. S., Greer, J. C.: Cardiological findings in gargoylism. Arch. intern. Med.111, 58 (1963)","journal-title":"Arch. intern. Med."},{"key":"CR7","first-page":"394","volume-title":"Aktuelle Probleme der Kinderpathologie","author":"S. Bl\ufffdmcke","year":"1972","unstructured":"Bl\ufffdmcke, S., Freitag, F., Spranger, J.: Vergleichende feinstrukturelle Untersuchungen an Lebern bei Mucopolysaccharidosen und Mucolipidosen. In: Aktuelle Probleme der Kinderpathologie. H. Bredt u. G. Seifert (eds.), pp. 394?399 Stuttgart: Fischer 1972"},{"key":"CR8","first-page":"277","volume":"48","author":"W. P. Callahan","year":"1966","unstructured":"Callahan, W. P., Lorincz, A. E.: Hepatic ultrastructure in the Hurler syndrome. Amer. J. Path.48, 277 (1966)","journal-title":"Amer. J. Path."},{"key":"CR9","first-page":"2187","volume":"19","author":"P. Durand","year":"1967","unstructured":"Durand, P., Philippart, M., Borrone, C., Della Cella, G., Bugiani, O.: Una nuova malattia da accumulo di glicolipidi (ceramidi tetraesosidi). Minerva pediat.19, 2187?2196 (1967)","journal-title":"Minerva pediat."},{"key":"CR10","doi-asserted-by":"crossref","first-page":"665","DOI":"10.1016\/S0022-3476(69)80464-6","volume":"75","author":"P. Durand","year":"1969","unstructured":"Durand, P., Borrone, C., Della Cella, G.: Fucosidosis. J. Pediat.75, 665?674 (1969)","journal-title":"J. Pediat."},{"key":"CR11","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1007\/BF02892083","volume":"7","author":"F. Freitag","year":"1971","unstructured":"Freitag, F., K\ufffdchemann, K, Bl\ufffdmcke, S., Spranger, J.: Hepatic ultrastructure in fucosidosis. Virchows Arch., Abt. B Zellpath.7, 99?113 (1971a)","journal-title":"Virchows Arch., Abt. B Zellpath."},{"key":"CR12","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1007\/BF02892091","volume":"7","author":"F. Freitag","year":"1971","unstructured":"Freitag, F., Bl\ufffdmcke, S., Spranger, J.: Hepatic ultrastructure in mucolipidosis (lipomucopolysaccharidosis). Virchows Arch. Abt. B Zellpath.7, 189?204 (1971b)","journal-title":"Virchows Arch. Abt. B Zellpath."},{"key":"CR13","first-page":"147","volume-title":"Lysosomes and storage diseases","author":"H. G. Hers","year":"1973","unstructured":"Hers, H. G.: The concept of inborn lysosomal disease. In: Lysosomes and storage diseases. H. G. Hers and F. Van Hoof (eds.), pp. 147?171. New York-London: Academic Press 1973"},{"key":"CR14","unstructured":"Jenner, F. A., Pollitt, R. J.: Large quantities of 2-acetamido-1(beta-l-aspartamido)-1,2-dideoxyglucose in the urine of mentally retarded siblings. Biochem. J.103, 48P (1967)"},{"key":"CR15","first-page":"137A","volume":"27","author":"M. J. Karnovsky","year":"1965","unstructured":"Karnovsky, M. J.: A formaldehyde-glutaraldehyde fixative of high osmolarity for use in electron microscopy. J. Cell Biol.27, 137A (1965)","journal-title":"J. Cell Biol."},{"key":"CR16","doi-asserted-by":"crossref","first-page":"366","DOI":"10.1016\/S0022-3476(69)80260-X","volume":"75","author":"B. Kjellman","year":"1969","unstructured":"Kjellman, B., Gamstorp, I., Brun, A., \ufffdckerman, P.-A., Palmgren, B.: Mannosidosis: a clinical and histopathologic study. J. Pediat.75, 366?373 (1969)","journal-title":"J. Pediat."},{"key":"CR17","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1136\/jnnp.29.2.113","volume":"29","author":"K. Kristensson","year":"1966","unstructured":"Kristensson, K., Sourander, P.: Occurrence of lipofuscin in inherited metabolic disorders affecting the nervous system. J. Neurol. Neurosurg. Psychiat.29, 113 (1966)","journal-title":"J. Neurol. Neurosurg. Psychiat."},{"key":"CR18","first-page":"1578","volume":"15","author":"D. Lagunoff","year":"1966","unstructured":"Lagunoff, D., Gritzka, T.: The site of mucopolysaccharide accumulation in Hurler's syndrome. An electron microscopic and histochemical study. Lab. Invest.15, 1578 (1966)","journal-title":"Lab. Invest."},{"key":"CR19","doi-asserted-by":"crossref","first-page":"503","DOI":"10.1001\/archpedi.1964.02090010505010","volume":"108","author":"B. H. Landing","year":"1964","unstructured":"Landing, B. H., Silverman, F. N., Craig, J. M., Jacoby, M. D., Lahey, M. E., Chadwick, D. L.: Familial neurovisceral lipidosis. Amer. J. Dis. Child.108, 503?522 (1964)","journal-title":"Amer. J. Dis. Child."},{"key":"CR20","doi-asserted-by":"crossref","first-page":"220","DOI":"10.1111\/j.1651-2227.1969.tb04710.x","volume":"58","author":"H. Loeb","year":"1969","unstructured":"Loeb, H., Tondeur, M., Toppet, M., Cremer, N.: Clinical, biochemical and ultrastructural studies of an atypical form of mucopolysaccharidosis. Acta paediat. scand.58, 220?228 (1969a)","journal-title":"Acta paediat. scand."},{"key":"CR21","first-page":"519","volume":"24","author":"H. Loeb","year":"1969","unstructured":"Loeb, H., Tondeur, M., Jonniaux, G., Mockel-Pohl, S., Vamos-Hurwitz, E.: Biochemical and ultrastructural studies in a case of mucopolysaccharidosis ?F? (fucosidosis). Helv. pediat. Acta24, 519?537 (1969b)","journal-title":"Helv. pediat. Acta"},{"key":"CR22","first-page":"291","volume-title":"Lysosomes and storage diseases","author":"P.-A. \ufffdckerman","year":"1973","unstructured":"\ufffdckerman, P.-A.: Mannosidosis. In: Lysosomes and storage diseases. H. G. Hers and F. Van Hoof (eds), pp 291?304. New York-London: Academic Press 1973"},{"key":"CR23","first-page":"399","volume-title":"Aktuelle Probleme der Kinderpathologie","author":"J. Ormos","year":"1972","unstructured":"Ormos, J., M\ufffdnus, Z., Szab\ufffd, L., Csap\ufffd, Z.: Die Bedeutung der elektronenmikroskopischen Untersuchung der Leberbiopsie bei der Beurteilung der verschiedenen Mucopolysaccharidosen. In: Aktuelle Probleme der Kinderpathologie. H. Bredt u. G. Seifert (eds.), pp. 399?405. Stuttgart: Fischer 1972"},{"key":"CR24","unstructured":"Palo, J.: Er\ufffdiden aineenvaihduntah\ufffdiri\ufffdiden esiintyminen keskushermoston kehitysvauriotapauksissa. Tutkimus 2 177 suomalaisesta henkil\ufffdst\ufffd (in Finnish). Thesis, University of Helsinki (1966)"},{"key":"CR25","doi-asserted-by":"crossref","first-page":"573","DOI":"10.1111\/j.1600-0404.1967.tb05552.x","volume":"43","author":"J. Palo","year":"1967","unstructured":"Palo, J.: Prevalence of phenylketonuria and some other metabolic disorders among mentally retarded patients in Finland. Acta neurol. scand.43, 573?579 (1967)","journal-title":"Acta neurol. scand."},{"key":"CR26","doi-asserted-by":"crossref","first-page":"1198","DOI":"10.1212\/WNL.21.12.1198","volume":"21","author":"J. Palo","year":"1971","unstructured":"Palo, J., Riekkinen, P., Arstila, A., Autio, S.: Biochemical and fine structural studies on brain and liver biopsies in aspartylglucosaminuria. Neurology (Minneap)21, 1198?1204 (1971)","journal-title":"Neurology (Minneap)"},{"key":"CR27","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1007\/BF00686903","volume":"20","author":"J. Palo","year":"1972","unstructured":"Palo, J., Riekkinen, P., Arstila, A. U., Autio, S., Kivim\ufffdki, T.: Aspartylglucosaminuria II: Biochemical studies on brain, liver, kidney and spleen. Acta neuropath. (Berl.)20, 217?224 (1972)","journal-title":"Acta neuropath. (Berl.)"},{"key":"CR28","doi-asserted-by":"crossref","first-page":"431","DOI":"10.1016\/0009-8981(72)90018-6","volume":"36","author":"J. Palo","year":"1972","unstructured":"Palo, J., Savolainen, H.: Studies on serum and urinary glycopeptides and glycosaminoglycans in aspartylglucosaminuria. Clin. chim Acta36, 431?437 (1972)","journal-title":"Clin. chim Acta"},{"key":"CR29","doi-asserted-by":"crossref","first-page":"69","DOI":"10.1016\/0009-8981(73)90061-2","volume":"47","author":"J. Palo","year":"1973","unstructured":"Palo, J., Pollitt, R. J., Pretty, K. M., Savolainen, H.: Glycoasparagine metabolites in patients with aspartylglycosaminuria: Comparison between English and Finnish patients with special reference to storage materials. Clin. chim. Acta47, 69?74 (1973)","journal-title":"Clin. chim. Acta"},{"key":"CR30","first-page":"56","volume":"5","author":"J. Palo","year":"1973","unstructured":"Palo, J., Savolainen, H.: Biochemical diagnosis of aspartylglycosaminuria. Ann. clin. Res.5, 56?61 (1973)","journal-title":"Ann. clin. Res."},{"key":"CR31","doi-asserted-by":"crossref","first-page":"129P","DOI":"10.1042\/bj1280129Pb","volume":"128","author":"R. J. Pollitt","year":"1972","unstructured":"Pollitt, R. J., Pretty, K. M.: Glycoasparagines in the urine of patients with aspartylglycosaminuria. Biochem. J.128, 129P-130P (1972)","journal-title":"Biochem. J."},{"key":"CR32","doi-asserted-by":"crossref","first-page":"833","DOI":"10.1093\/brain\/96.4.833","volume":"96","author":"J. Rapola","year":"1973","unstructured":"Rapola, J., Haltia, M.: Cytoplasmic inclusions in the vermiform appendix and skeletal muscle in two types of so-called neuronal ceroid-lipofuscinosis. Brain96, 833?840 (1973)","journal-title":"Brain"},{"key":"CR33","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1097\/00005072-196801000-00002","volume":"27","author":"K. Suzuki","year":"1968","unstructured":"Suzuki, K., Suzuki, K., Chen, G. C.: Morphological, histochemical and biochemical studies on a case of systemic late infantile lipidosis (generalized gangliosidosis). J. Neuropath. exp. Neurol.27, 15?38 (1968)","journal-title":"J. Neuropath. exp. Neurol."},{"key":"CR34","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1097\/00005072-196301000-00003","volume":"22","author":"R. D. Terry","year":"1963","unstructured":"Terry, R. D., Weiss, M.: Studies in Tay-Sachs disease. II. Ultrastructure of the cerebrum. J. Neuropath. exp. Neurol.22, 18 (1963)","journal-title":"J. Neuropath. exp. Neurol."},{"key":"CR35","first-page":"217","volume-title":"Lysosomes and storage diseases","author":"F. Hoof Van","year":"1973","unstructured":"Van Hoof, F.: Mucopolysaccharidoses. In: Lysosomes and storage diseases. H. G. Hers u. F. Van Hoof (eds.) pp. 217?259. New York-London: Academic Press 1973a"},{"key":"CR36","first-page":"277","volume-title":"Fucosidosis","author":"F. Hoof Van","year":"1973","unstructured":"Van Hoof, F.: Fucosidosis. H. G. Hers u. F. Van Hoof (eds.), pp. 277?290. New York-London: Academic Press 1973b"},{"key":"CR37","first-page":"305","volume-title":"GM1-gangliosidosis","author":"F. Hoof Van","year":"1973","unstructured":"Van Hoof, F.: GM1-gangliosidosis. H. G. Hers u. F. Van Hoof (eds), pp. 305?321. New York-London: Academic Press 1973c"},{"key":"CR38","first-page":"1281","volume":"259","author":"F. Hoof Van","year":"1964","unstructured":"Van Hoof, F., Hers, H. G.: L'ultrastructure des cellules h\ufffdpatiques dans la maladie de Hurler (Gargoylisme). C. R. Acad. Sci. (Paris)259, 1281?1283 (1964)","journal-title":"C. R. Acad. Sci. (Paris)"},{"key":"CR39","first-page":"815","volume":"17","author":"F. Hoof Van","year":"1967","unstructured":"Van Hoof, F., Hers, H. G.: L'ultrastructure du foie dans certaines thesaurismoses. Rev. int. H\ufffdpat.17, 815?826 (1967)","journal-title":"Rev. int. H\ufffdpat."},{"key":"CR40","first-page":"588","volume-title":"Handbook of clinical neurology, vol. 10 (Leukodystrophies and poliodystrophies)","author":"W. Zeman","year":"1970","unstructured":"Zeman, W., Donahue, S., Dyken, P., Green, J.: The neuronal ceroid-lipofuscinoses (Batten-Vogt syndrome). In: Handbook of clinical neurology, vol. 10 (Leukodystrophies and poliodystrophies) P. J. Vinken and G. W. Bruyn (eds.) pp. 588?679. Amsterdam: North Holland 1970"}],"container-title":["Acta Neuropathologica"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00684563.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00684563\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00684563","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,4,30]],"date-time":"2023-04-30T14:53:54Z","timestamp":1682866434000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00684563"}},"subtitle":["Morphological and histochemical studies"],"short-title":[],"issued":{"date-parts":[[1975]]},"references-count":40,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1975]]}},"alternative-id":["BF00684563"],"URL":"https:\/\/doi.org\/10.1007\/bf00684563","relation":{},"ISSN":["0001-6322","1432-0533"],"issn-type":[{"value":"0001-6322","type":"print"},{"value":"1432-0533","type":"electronic"}],"subject":[],"published":{"date-parts":[[1975]]}}}