L'adrénoleucodystrophie. A propos d'une observation = Adrenoleukodystrophy. About one observationACHOUR, A; BEN DHIA, N; MAHJOUB, S et al.Annales de médecine interne (Paris). 1989, Vol 140, Num 5, pp 418-419, issn 0003-410X, 2 p.Article

Lysosulfatide (galactosylsphingosine-3-O-sulfate) from metachromatic leukodystrophy and normal human brainROSENGREN, B; FREDMAN, P; MANSSON, J.-E et al.Journal of neurochemistry. 1989, Vol 52, Num 4, pp 1035-1041, issn 0022-3042, 7 p.Article

Leucodystrophie orthochromatique pigmentaire (maladie de van Bogaert et Nyssen) = Pigmented orthochromatic leukodystrophy (Van Bogaert and Nyssen' disease)BELEC, L; GRAY, F; LOUARN, F et al.Revue neurologique (Paris). 1988, Vol 144, Num 5, pp 347-357, issn 0035-3787Article

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

Dysmyelinating leukodystrophies : «LACK Proper Myelin»HATTEN, H. P.Pediatric radiology. 1991, Vol 21, Num 7, pp 477-482, issn 0301-0449Article

First-trimester diagnosis of metachromatic leucodystrophyFENSOM, A. H; MARSH, J; JACKSON, M et al.Clinical genetics. 1988, Vol 34, Num 2, pp 122-125, issn 0009-9163Article

Alexander's disease: cranial ultrasound findingsHARBORD, M. G; LEQUESNE, G. W.Pediatric radiology. 1988, Vol 18, Num 3, pp 227-228, issn 0301-0449Article

Brain galactolipid content in a patient with pseudoarylsulfatase A deficiency and coincidental diffuse disseminated sclerosis, and in patients with metachromatic, adreno-, and other leukodystrophiesHARZER, K; KUSTERMANN-KUHN, B.Journal of neurochemistry. 1987, Vol 48, Num 1, pp 62-66, issn 0022-3042Article

Asymptomatic adult Alexander's disease: entity or nosological misconception?RIGGS, J. E; SCHOCHET, S. S. JR; NELSON, J et al.Neurology. 1988, Vol 38, Num 1, pp 152-154, issn 0028-3878Article

Alexander's disease: cranial MRI and ultrasound findingsSCHUSTER, V; HORWITZ, A. E; KRETH, H. W et al.Pediatric radiology. 1991, Vol 21, Num 2, pp 133-134, issn 0301-0449Article

A case of leucodystrophy presenting as hydrocephalusMAITI, B; ROY, I; SAHA, P et al.Journal of the Indian Medical Association. 1986, Vol 84, Num 10, pp 311-313, issn 0019-5847Article

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

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

A radiometric assay for aspartoacylase activity in human fibroblasts : application for the diagnosis of Canavan's diseaseBARASH, V; FLHOR, D; MORAG, B et al.Clinica chimica acta. 1991, Vol 201, Num 3, pp 175-181, 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

An adult onset metachromatic leukodystrophy with dominant inheritance and normal arylsulphatase A levelsWRIGHT, G. D. S; PATEL, M. K; MIKEL, J et al.Journal of the neurological sciences. 1988, Vol 87, Num 2-3, pp 153-166, issn 0022-510XArticle

Acquired Obstructive Hydrocephalus in Globoid-Cell LeukodystrophyBRENINGSTALL, Galen N; PATTERSON, Richard J.Pediatric neurology. 2008, Vol 39, Num 4, pp 279-280, issn 0887-8994, 2 p.Article

Continuous, generalized, high-voltage fast activity and FIRDA in two childrenMUTOH, K; OKUNO, T; ITO, M et al.Clinical EEG electroencephalography. 1992, Vol 23, Num 2, pp 68-71, issn 0009-9155Article

La maladie d'Alexander = Alexander diseaseELIAN, J. C; FRAPPAZ, D; REYNAUD, J et al.Pédiatrie (Marseille). 1991, Vol 46, Num 4, pp 373-377, issn 0031-4021Article

Complicated hereditary spastic parapereis with cerebral white matter lesionsGUTMANN, D. H; FISCHBECK, K. H; KAMHOLZ, J et al.American journal of medical genetics. 1990, Vol 36, Num 2, pp 251-257, issn 0148-7299, 7 p.Article

Frequent occurrence of cerebral demyelination in adrenomyeloneuropathyDE BEER, Marlijn; ENGELEN, Marc; VAN GEEL, Björn M et al.Neurology. 2014, Vol 83, Num 24, pp 2227-2231, issn 0028-3878, 5 p.Article

Adult-Onset Autosomal Dominant Leukodystrophy Presenting With Rem Sleep Behavior DisorderFLANAGAN, Eoin P; GAVRILOVA, Ralitza H; BOEVE, Bradley F et al.Neurology. 2013, Vol 80, Num 1, pp 118-120, issn 0028-3878, 3 p.Article

Inhibition of angiogenesis by β-galactosylceramidase deficiency in globoid cell leukodystrophyBELLERI, Mirella; RONCA, Roberto; BONGARZONE, Ernesto R et al.Brain. 2013, Vol 136, pp 2859-2875, issn 0006-8950, 17 p., 9Article

Pioglitazone halts axonal degeneration in a mouse model of X-linked adrenoleukodystrophyMORATO, Laia; GALINO, Jorge; PAMPLONA, Reinald et al.Brain. 2013, Vol 136, pp 2432-2443, issn 0006-8950, 12 p., 8Article

Late onset vanishing white matter disease presenting with learning difficultiesDAMASIO, Joana; DER LEI, Hannemieke D. W. Van; DER KNAAP, Marjo S. Van et al.Journal of the neurological sciences. 2012, Vol 314, Num 1-2, pp 169-170, issn 0022-510X, 2 p.Article