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Adult metachromatic leucodystrophy: an underdiagnosed disease?CERIZZA, M; NEMNI, R; TAMMA, F et al.Journal of neurology, neurosurgery and psychiatry. 1987, Vol 50, Num 12, pp 1710-1712, issn 0022-3050Article

Metachromatic leukodystrophy: conduct disorder progressing to dementiaFISHER, N. R; COPE, S. J; LISHMAN, W. A et al.Journal of neurology, neurosurgery and psychiatry. 1987, Vol 50, Num 4, pp 488-489, issn 0022-3050Article

Trouble de l'humeur et leucodystrophie métachromatique de l'adulte, à propos d'un cas présumé = Mood disorder and adult metachromatic leukodystrophy: a presumed caseSCHMITT, L; LOUSTALAN, J.-M; BLANCHER, A et al.Annales médico-psychologiques. 1985, Vol 143, Num 10, pp 1005-1011, issn 0003-4487Article

Improved synthesis of [1-¹⁴C]acyl-sphingosine-galactose-3-sulfate (sulfatide) for diagnosis of metachromatic leukodystrophy : usefulness of radioscanningMASSON, M; LI, W. X; FLUHARTY, A. L et al.Clinica chimica acta. 1991, Vol 201, Num 3, pp 157-168, issn 0009-8981Article

Localization of sphingolipid activator protein- (SAP-1) in the brain of a normal human and a patient with metachromatic leukodystrophyTANIIKE, M; INUI, K; SHINODA, K et al.Acta histochemica et cytochemica. 1991, Vol 24, Num 2, pp 215-222, issn 0044-5991Article

Treatment of late infantile metachromatic leukodystrophy by bone marrow transplantationKRIVIT, W; SHAPIRO, E; KERSEY, J. H et al.The New England journal of medicine. 1990, Vol 322, Num 1, pp 28-32, issn 0028-4793, 5 p.Article

Metachromatic leukodystrophy (MLD) in hospitalized adult schizophrenic patients resistant to drug treatmentGALBRAITH, D. A; GORDON, B. A; FELEKI, V et al.Canadian journal of psychiatry. 1989, Vol 34, Num 4, pp 299-302, issn 0706-7437Article

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Ultrastructural study of the retina in late infantile metachromatic leukodystrophyGOEBEL, H. H; BUSCH-HETTWER, H; BOHL, J et al.Ophthalmic research. 1992, Vol 24, Num 2, pp 103-109, issn 0030-3747Article

Studies in metachromatic leukodystrophy. XV: Purification of normal and mutant arylsulfatase. A from human liverJAMES, G. T; THACH, A. B; KLASSEN, L et al.Life sciences (1973). 1985, Vol 37, Num 25, pp 2365-2371, issn 0024-3205Article

Heterogeneity in late-onset metachromatic leukodystrophy: effect of inhibitors of cysteine proteinasesVON FIGURA, K; STECKEL, F; CONARY, J et al.American journal of human genetics. 1986, Vol 39, Num 3, pp 371-382, issn 0002-9297Article

Low arylsumphatase A activity and choreoathetotic syndrome in three siblings : differentiation of pseudodeficiency from metachromatic leukodystrophyKAPPLER, J; WATTS, R. W. E; CONZELMANN, E et al.European journal of pediatrics. 1991, Vol 150, Num 4, pp 287-290, issn 0340-6199Article

Arylsulfatase A (ASA) defect and psychiatric illness : a reviewSHAH, S. N.Molecular and chemical neuropathology. 1990, Vol 12, Num 2, pp 121-129, issn 1044-7393Article

Ultrastructural study of neurons in metachromatic leukodystrophyPENG, L; SUZUKI, K.Clinical neuropathology. 1987, Vol 6, Num 5, pp 224-230, issn 0722-5091Article

Prevention of deterioration in metachromatic leukodystrophy by bone marrow transplantationKRIVIT, W; LIPTON, M. E; LOCKMAN, L. A et al.The American journal of the medical sciences. 1987, Vol 294, Num 2, pp 80-85, issn 0002-9629Article

Metachromatic leukodystrophy : two sides of a coinJEFFERY, R; JEFFERY, A.BMJ. British medical journal (International ed.). 1993, Vol 307, Num 6919, pp 1631-1632, issn 0959-8146Article

Reduced activity of arylsulfatase A and predisposition to neurological disorders : analysis of 140 pediatric patientsSANGIORGI, S; FERLINI, A; ZANETTI, A et al.American journal of medical genetics. 1991, Vol 40, Num 3, pp 365-369, issn 0148-7299Article

Characterization of a mutation in a family with saposin B deficiency: a glycosylation site defectKRETZ, K. A; CARSON, G. S; MORIMOTO, S et al.Proceedings of the National Academy of Sciences of the United States of America. 1990, Vol 87, Num 7, pp 2541-2544, issn 0027-8424Article

Lysosulfatide (sulfogalactosylsphingosine) accumulation in tissues from patients with metachromatic leukodystrophyTODA, K.-I; KOBAYASHI, T; GOTO, I et al.Journal of neurochemistry. 1990, Vol 55, Num 5, pp 1585-1591, issn 0022-3042Article

Accumulation of lysosulfatide (sulfogalactosylsphingosine) in tissues of a boy with metachromatic leukodystrophyTODA, K; KOBAYASHI, T; GOTO, I et al.Biochemical and biophysical research communications (Print). 1989, Vol 159, Num 2, pp 605-611, issn 0006-291XArticle

First trimester prenatal diagnosis of metachromatic leukodystrophy on chorionic Villi by «immunoprecipitation-electrophoresis»POENARU, L; CASTELNAU, L; BESANÇON, A.-M et al.Journal of inherited metabolic disease. 1988, Vol 11, Num 2, pp 123-130, issn 0141-8955Article

New sites of ocular involvement in late-infantile metachromatic leukodystrophy revealed histopathologic studiesSCOTT, I. U; GREEN, W. R; GOYAL, A. K et al.Graefe's archive for clinical and experimental ophthalmology. 1993, Vol 231, Num 3, pp 187-191, issn 0721-832XArticle

Adulte Form der metachromatischen Leukodystrophie mit vorwiegend psychotischem Erscheinungsbild = Adult form of metachromatic leukodystrophy with predominantly psychotic presentationHAAG, C; LAAKMANN, G; VODERHOLZER, U et al.Nervenarzt. 1992, Vol 63, Num 7, pp 444-446, issn 0028-2804Article

Correction of sulfatide metabolism after transfer of prosaposin cDNA to cultured cells from a patient with SAP-I deficiencyRAFI, M. A; AMINI, S; XUN-LING ZHANG et al.American journal of human genetics. 1992, Vol 50, Num 6, pp 1252-1258, issn 0002-9297Article