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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

THE CEREBRAL LIPIDOSES.MALONE MJ.1976; PEDIATR. CLIN. N. AMER.; U.S.A.; DA. 1976; VOL. 23; NO 2; PP. 303-326; BIBL. 2 P. 1/2Article

Increased intracranial pressure in adrenoleukodystrophyCHAVES-CARBALLO, E; FRANK, M; CHRENKA, B. A et al.Archives of neurology (Chicago). 1984, Vol 41, Num 3, pp 339-340, issn 0003-9942Article

VARIATION OF ARYLSULPHATASE A: COMPARATIVE OF ARYLSULPHATASE A WITH SYNTHETIC AND NATURAL SUBSTRATES IN THREE FAMILIES WITH METACHROMATIC LEUCODYSTROPHYCHRISTOMANOU H; SANDHOFF K.1978; NEUROPAEDIATRIE; DEU; DA. 1978; VOL. 9; NO 4; PP. 385-395; ABS. GER; BIBL. 25 REF.Article

A comparative morphologic analysis of adult onset leukodystrophy with neuroaxonal spheroids and pigmented glia : A role for oxidative damageALI, Zarina S; VAN DER VOOM, J. Patrick; POWERS, James M et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 7, pp 660-672, issn 0022-3069, 13 p.Article

Metachromatic leukodystrophy: Diffusion MR imaging and proton MR spectroscopySENER, R. N.Acta radiologica (1987). 2003, Vol 44, Num 4, pp 439-443, issn 0284-1851, 5 p.Article

Aicardi-Goutières syndrome: differential diagnosis and aetiopathogenesisLANZI, Giovanni; D'ARRIGO, Stefano; DRUMBL, Gea et al.Functional neurology. 2003, Vol 18, Num 2, pp 71-75, issn 0393-5264, 5 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

COMPUTED TOMOGRAPHY PROFILES OF PERIVENTRICULAR HYPODENSITY IN HYDROCEPHALUS AND LEUKOENCEPHALOPATHYDI CHIRO G; ARIMITSU T; BROOKS RA et al.1979; RADIOLOGY; USA; DA. 1979; VOL. 130; NO 3; PP. 661-666; BIBL. 18 REF.Article

IMMUNOCYTOCHEMICAL INVESTIGATIONS OF SOME HUMAN LEUKODYSTROPHIESULRICH J; KOHLER R; HEITZ PU et al.1983; ACTA NEUROPATHOLOGICA; ISSN 0001-6322; DEU; DA. 1983; VOL. 60; NO 3-4; PP. 199-206; BIBL. 27 REF.Article

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

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

Rapid onset frontal leukodystrophy with decreased diffusion coefficient and neuroaxonal spheroidsMAILLART, Elisabeth; ROUSSEAU, Audrey; GALANAUD, Damien et al.Journal of neurology. 2009, Vol 256, Num 10, pp 1649-1654, issn 0340-5354, 6 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

Adult-onset leukodystrophy with axonal spheroidsMENDES, Amélia; PINTO, Madalena; VIEIRA, Sara et al.Journal of the neurological sciences. 2010, Vol 297, Num 1-2, pp 40-45, issn 0022-510X, 6 p.Article

DIAGNOSIS OF INFANTILE NEUROAXONAL DYSTROPHY BY SKIN BIOPSYWISNIEWSKI K; WISNIEWSKI HM.1980; ANN. NEUROL.; USA; DA. 1980; VOL. 7; NO 4; PP. 377-379; BIBL. 9 REF.Article

Paraplegia due to adrenomyeloneuropathySOFJAN LAMID; EL GHATIT, A. Z.Paraplegia. 1984, Vol 22, Num 2, pp 119-123, issn 0031-1758Article

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

INHERITANCE OF METACHROMATIC LEUKODYSTROPHY.LANGENBECK U; DUNKEE P; HEIPERTZ R et al.1977; AMER. J. HUM. GENET.; U.S.A.; DA. 1977; VOL. 29; NO 6; PP. 639-640; BIBL. 9 REF.Article

Sulfatides in prenatal metachromatic leukodystrophyBAIER, W; HARZER, K.Journal of neurochemistry. 1983, Vol 41, Num 6, pp 1766-1768, issn 0022-3042Article

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

Oligodendroglial transcription factor (OLIG1 and OLIG2) mutations are not associated with pelizaeus-merzbacher-like leukodystrophyRUF, Nico; MARTELLI, Mara; WESCHKE, Bernhard et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2007, Vol 144, Num 3, pp 365-366, issn 1552-4841, 2 p.Article

MYELIN AND ITS ABNORMALITIESMCKHANN GM; PODUSLO SE.1982; JOURNAL OF INHERITED METABOLIC DISEASE; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; SUPPL. 2; PP. 89-95; BIBL. 2 P.Article

BRAINSTEM AUDITORY EVOKED RESPONSES IN LEUKODYSTROPHIESOCHS R; MARKARD ON; DEMYER WE et al.1979; NEUROLOGY; USA; DA. 1979; VOL. 29; NO 8; PP. 1089-1093; BIBL. 13 REF.Article

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