No CrossRef data available.
Article contents
A Neurodegenerative Disorder in a 10 Year Old Boy
Published online by Cambridge University Press: 18 September 2015
Abstract
An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

- Type
- Clinical Pathological Conference
- Information
- Copyright
- Copyright © Canadian Neurological Sciences Federation 1987
References
REFERENCES
1.Dyken, P. Krawiecka, N. Neurodegenerative diseases of infancy and childhood. Ann Neurol 1983; 13: 351–364.CrossRefGoogle ScholarPubMed
2.Santavuori, P, Haltia, M. Rapola, J. Raitta, C. Infantile type of so-called neuronal ceroid lipofuscinosis. Part I. A clinical study of 15 patients. J Neurol Sci 1973: 18: 257–267.CrossRefGoogle Scholar
3.Hahn, AF, Gordon, BA. Gilbert, JJ. Hinton, GH. The AB-variant of metachromatic leukodystrophy. Acta Neuropath 1981:55: 281–287.CrossRefGoogle ScholarPubMed
4.Hahn, AF, Gordon, BA. Feleki, V. Hinton, GH. Gilbert, JJ. A variant form of metachromatic leukodystrophy without aryl sulfatase deficiency. Ann Neurol 1981; 12: 33–36.CrossRefGoogle Scholar
5.Romanul, FCA. Fowler, HL. Radvany, J. et al. Azorean disease of the nervous system. New Eng J Med 1977: 296: 1505–1508.CrossRefGoogle ScholarPubMed
6.Rozdilsky, B. Bolton, CF. Takeda, M. Neuroaxonal dystrophy: a case of delayed onset and protracted course. Acta Neuropath 1971: 17: 331–349.CrossRefGoogle ScholarPubMed
7.deLeon, GA. Mitchell, MH. Histological and ultrastructural features of dystrophic isocortical axons in Infantile Neuroaxonal Dystrophy (Seitelberger’s Disease). Acta Neuropath 1985; 66: 89–97.CrossRefGoogle Scholar
8.Hedley-White, ET. Gilles, FH. Uzman, BG. Infantile Neuroaxonal Dystrophy. A disease characterized by altered terminal axons and synaptic endings. Neurol 1968: 18: 891–906.CrossRefGoogle Scholar
9.Jellinger, K. Neuroaxonal Dystrophy; its natural history and related disorders. In: Progress in Neuropathology. Vol 2, Zimmerman, HN. ed. Grune & Stratton New York. pp. 129–180.Google Scholar
10.Matsuyama, H. Watanabe, I, Mihm, MC, Richardson, EP. Dermatoleukodystrophy with neuronal spheroids. Arch Neurol 1978:35: 329–336.CrossRefGoogle ScholarPubMed
11.Sokol, RJ. Guggenheim, MA, lannaccone, ST.etal. Improved neurologic function after long term correction of vitamin E deficiency in children with chronic cholestasis. New Eng J Med 1985: 313: 1580–1586.CrossRefGoogle ScholarPubMed
12.Park, BE. Netskey, MG, Betsill, WL Jr.Pathogenesis of pigment and spheroid formation in Hallervorden-Spatz Syndrome and related disorders. Neurol 1975:25: 1172–1178.CrossRefGoogle ScholarPubMed
13.Tomlinson, BE. The aging brain. In: Recent Advances in Neuropathology. Smith, WT, Cavangagh, JB, eds. Churchill Livingston, Edinburgh 1979, pp. 129–159.Google Scholar
14.Saito, K, Yokoyama, T, Okaniwa, M, Kamoshita, S. Neuropathology of chronic vitamin E deficiency in fatal familial intrahepatic cholestasis. Acta Neuropathol 1982; 58: 187–192.CrossRefGoogle ScholarPubMed
15.Saito, K, Matsumoto, S, Yokoyama, T, et al. Pathology of chronic vitamin E deficiency in familial intrahepatic cholestasis (Byler’s Disease). Virchows Arch (Pathol Anat) 1982; 396: 319–330.CrossRefGoogle Scholar
16.Duncan, C, Strub, R, McGarry, P, et al. Peripheral nerve biopsy as an aid to diagnosis in Infantile Neuronal Dystrophy. Neurol 1970; 20: 1024–1032.CrossRefGoogle Scholar
17.Arsenio-Nunes, ML, Goutieres, F. Diagnosis of Infantile Neuroaxonal Dystrophy by conjunctival biopsy. J Neurol Neurosurg Psychiat 1978;41:511–515.CrossRefGoogle ScholarPubMed
18.Carlo, J, Willis, J, McGarry, P, Duncan, C. Examination of dental pulp to diagnose Infantile Neuroaxonal Dystrophy. Arch Neurol 1982; 39: 422–423.CrossRefGoogle ScholarPubMed