Seitelberger's connatal form of Pelizaeus-Merzbacher disease

Springer Science and Business Media LLC - Tập 40 Số 2 - Trang 129-136 - 1977
J. Ulrich1, N Herschkowitz2
1Neuropathologische Abt., Institut für Pathologie der Universität Basel, Schönbeinstr. 40, CH-4056, Basel, Schweiz
2Abt. für Entwicklungsstörungen, Medizinische Universitätskinderklinik, CH-3000, Bern, Schweiz

Tóm tắt

Từ khóa


Tài liệu tham khảo

Adachi, M., Schneck, L., Torii, J., Volk, B. W.: Histochemical, ultrastructural and biochemical studies of a case with leukodystrophy due to congenital deficiency of myelin. J. Neuropath. exper. Neurol.29, 601?614 (1970)

Austin, J. H., Balasubramanian, A. G., Pattabiraman, T. N., et al.: A controlled study of enzymic activities in three human disorders of glycolipid metabolism. J. Neurochem.10, 805?816 (1963)

Bargeton-Farkas, L., Edgar, G. W. F.: Anatomo-chemical studies on a case of congenital sudanophilic leucodystrophy. Acta neuropath.3, 578?587 (1964)

Bornstein, M. B., Raine, C.: The initial structural lesion in seruminduced demyelination in vitro. Lab. Invest.35, 391?401 (1976a)

Bornstein, M. B., Raine, C.: Central nervous system. In textbook of immunopathology, 2nd ed. Peter A. Miescher, Hans-J. Müller, eds. pp. 701?714. New York, San Francisco, London: Grune & Stratton 1976b

Diezel, P. B., Fritsch, H., Jakob, H.: Leukodystrophie mit orthochromatischen Abbaustoffen. Ein Beitrag zur Pelizaeus-Merzbacher'schen Krankheit. Virchows Archiv für Path. Anat.338, 371?394 (1965)

Farkas-Bargeton, E., Robain, O., Mandel, P.: Abnormal glial maturation in the white matter in Jimpy mice. Acta neuropath.21, 272?281 (1972)

Friede, R. L.: Developmental neuropathology, pp. 449?456 Wien und New York: Springer 1975

Ghatak, N. R., Hirano, A., Lijtmaer, H., Zimmerman, H. M.: Asymptomatic demyelinated plaque in spinal cord. Arch. Neurol.30, 484?486 (1974)

Herschkowitz, N., McKhan, G. M., Schooter, E. M.: Studies of water soluble lipoproteins in the rat brain. J. Neurochem.15, 161?168 (1968)

Hirano, A., Sax, D. S., Zimmerman, H. M.: The fine structure of the cerebella of Jimpy mice and their ?normal? litter mates. J. Neuropath. exp. Neurol.28, 388?400 (1969)

Hirano, A.: Progress in the pathology of motor neuron diseases. In: ?Progress in neuropathology?. H. M. Zimmerman, Ed. pp. 181?215. New York: Grune and Stratton 1973

Keen, C. L., Hurley, L. S.: Copper supplementation in Quaking mutant mice: Reduced tremors and increased brain copper. Science193, 244?246 (1976)

Martenson, R. E., Daibler, G. E., Kies, M. W.: Myelin basic protein of the rat central nervous system. Biochem. Biophys. Acta (Aust)200, 353?362 (1970)

Meier, C., Bischoff, A.: Dysmyelination in the Jimpy mouse. Electron microscopic study. J. Neuropath. exp. Neurol.33, 343?353 (1974)

Meier, C., Herschkowitz, N., Bischoff, A.: Morphological and biochemical observations in the Jimpy spinal cord. Acta neuropath. (Berl.)27, 349?362 (1974)

Merzbacher, L.: Eine eigenartige familiär-hereditäre Erkrankungsform (Aplasia axialis corticalis congenita). Z. ges. Neurol. Psychiat.3, 1 (1910)

Nisenbaum, C., Sandbank, U., Kohn, R.: Pelizaeus-Merzbacher disease ?infantile acute type?. Report of a family. Ann. paediat.204, 365?376 (1965)

Norman, R. M., Tingey, A. H.: Sudanophil leucodystrophy and Pelizaeus-Merzbacher disease. In: Folch-Pi and H. Bauer, eds.: Brain lipids and lipoproteins and the leucodystrophies, pp. 169?186. Amsterdam. Elsevier 1963

Peiffer, J., Zerbin-Rüdin, E.: Zur Variationsbreite der Pelizaeus-Merzbacher'schen Krankheit (Zugleich ein Beitrag zur familiären multiplen Sklerose). Acta Neuropath.3, 87?107 (1963)

Pelizaeus, F.: Über eine eigenartige familiäre Entwicklungshemmung, vornehmlich auf motorischem Gebiet. Arch. f. Psych.31, 100?104 (1899)

Privat, A., Robain, O., Mandel, P.: Aspects ultrastructuraux du corps calleux chez le souris Jimpy. Acta Neuropath.21, 282?295 (1972)

Robain, O., Mandel, P.: Etude quantitative de la myélinisation et de la croissance axonale dans le corps calleux et le cordon postérieur de la moelle de la souris Jimpy. Acta Neuropath.29, 293?309 (1974)

Samorajski, T., Friede, R. L., Reimer, P. R.: Hypomyelination in the quacking mouse. A model for the analysis of disturbed myelin formation. J. Neuropath. exp. Neurol.29, 507?523 (1970)

Schneck, L., Adachi, M., Volk, B. W.: Congenital failure of myelinization: Pelizaeus-Merzbacher disease? Neurology21, 817?824 (1971)

Seitelberger, F.: Die Pelizaeus-Merzbacher'sche Krankheit. Klinische und anatomische Untersuchungen zum Problem ihrer Stellung unter den diffusen Sklerosen. Wien Z. Nhk.9, 128?289 (1954)

Seitelberger, F.: Contribution to Pelizaeus-Merzbacher's disease. In: Brain lipids and lipoproteins. J. Folch-Pi and H. Bauer, eds., pp. 187?198. Amsterdam, London, New York: Elsevier 1963

Seitelberger, F.: Pelizaeus-Merzbacher disease. In: Handbook of clinical neurology (Vinken, P. J., Bruyin, G. W., eds.), Vol. 10, Chp. 10, pp. 150?202. Amsterdam: North Holland 1970

Sidman, R. L., Dichie, M. M., Appel, S. H.: Mutant mice (Quaking and Jimpy) with deficient myelination in the central nervous system. Science144, 309?311 (1964)

Sidman, R. L.: Pathogenesis of an inherited sudanophilic leucodystrophy in mice. In: Vth Internat. Congress of Neuropathology. Proceedings, p. 177. Amsterdam: Excerpta Medica 1965

Suzuki, K., Suzuki, Y.: Globoid cell leucodystrophy (Krabbe's disease): Deficiency of galactose cerebroside ?-galactosidase. Proc. nat. Acad. Sci.66, 302?309 (1970)

Suzuki, K., Zagoren, J. C.: Focal axonal swelling in cerebellum of of Quaking mouse: Light and electron microscopic studies. Brain Res.85, 38?43 (1975)

Ulrich, J., Bornstein, M. B.: Experimental allergic encephalomyelitis (EAE): Delayed myelination-inhibition in vitro with EAE-serum: Changes in vulnerability of oligodendroglia and newly formed myelin sheaths. Acta neuropath.25, 138?148 (1973)

Watanabe, J., McComan, R., Dyken, P., Zeman, W.: Absence of cerebral myelin sheaths in a case of presumed Pelizaeus-Merzbacher disease. Electron microscopic and biochemical studies. J. Neuropath. and exp. Neurol.28, 243?256 (1969)

Watanabe, J., Bingle, F. J.: Dysmyelination in Quaking mouse: Electron microscopic study. J. Neuropath. and exp. Neurol.31, 352?369 (1972)

Wisniewski, H., Morell, P.: Quaking mouse: Ultrastructural evidence for arrest of myelinogenesis. Brain Res.29, 63?73 (1971)

Zeman, W., Demyer, W., Falls, H. F.: Pelizaeus-Merzbacher disease. J. Neuropath. exp. Neurol.23, 334?354 (1964)