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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

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

LEUCODISTROFIAS ORTOCROMATICAS O SUDANOFILAS. II. ASPECTOS ULTRAESTRUCTURALES = LEUCODYSTROPHIES ORTHOCHROMATIQUES ET SOUDANOPHILES. II. ASPECTS INFRASTRUCTURAUXRICOY JR; DIAZ FLORES L; NAVARRO C et al.1974; ARCH. NEUROBIOL.; ESP.; DA. 1974; VOL. 37; NO 4; PP. 377-392; ABS. ANGL.; BIBL. 1 P.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

Maladie d'Alexander de l'adulte = Alexander's disease in an adultHABIB, M; HASSOUN, J; ALI-CHERIF, A et al.Revue neurologique (Paris). 1984, Vol 140, Num 3, pp 179-189, issn 0035-3787Article

A COMPARATIVE STUDY OF MYELIN FRACTIONS FROM METACHROMATIC AND GLOBOID LEUKODYSTROPHIES. = ETUDE COMPARATIVE DES FRACTIONS DE LA MYELINE DES LEUCODYSTROPHIES METACHROMATIQUE ET GLOBOIDEMALONE MJ; SAKURAGAWA N; SZOKE M et al.1975; NEUROLOGY; U.S.A.; DA. 1975; VOL. 25; NO 9; PP. 827-832; BIBL. 21 REF.Article

THE PATHOLOGY OF SPHINGOLIPIDOSES = LA PATHOLOGIE DES SPHINGOLIPIDOSESVOLK BW; ADACHI M; SCHNECK L et al.1972; SEMINARS HEMATOL.; U.S.A.; DA. 1972; VOL. 9; NO 3; PP. 317-348; BIBL. 9P.Serial Issue

MEGALENCEPHALIE PROGRESSIVE CHEZ L'ENFANT. A PROPOS D'UN CAS DE MALADIE D'ALEXANDER ET TROIS CAS DE DEGENERESCENCE SPONGIEUSE DU NEVRAXECHAUVEAU JEAN MICHEL.sd; FRA; DA. S.D.; 236; 145-XII P.-ILL.; 30 CM; BIBL. 73 P.; TH.: MED./PARIS 5/1978Thesis

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

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

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

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

BIOCHEMICAL AND METABOLIC BASIS OF FAMILIAL SPHINGOLIPIDOSES = LES BASES BIOCHIMIQUES ET METABOLIQUES DES SPHINGOLIPIDOSES FAMILIALESBRADY RO.1972; SEMINARS HEMATOL.; U.S.A.; DA. 1972; VOL. 9; NO 3; PP. 273-284; BIBL. 2P.Serial Issue

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

CONGENITAL RETARDED MYELINIZATION IN A NEW-BORN CHILD WITH INFANTILE SPASMS.DE WEERDT CJ; HOOGHWINKEL GJM.1976; CLIN. NEUROL. NEUROSURG.; NETHERL.; DA. 1976; VOL. 79; NO 2; PP. 143-150; BIBL. 13 REF.Article

HEREDITARY LEUCODYSTROPHY IN THE MOUSE: THE NEW MUTANT TWITCHERDUCHEN LW; EICHER EM; JACOBS JM et al.1980; BRAIN; ISSN 0006-8950; GBR; DA. 1980; VOL. 103; NO 3; PP. 695-710; BIBL. 2 P.Article

LES MALADIES DEMYELINISANTES HEREDITAIRES (LEUCODYSTROPHIES)FRANCOIS J.1979; J. GENET. HUM.; CHE; DA. 1979; VOL. 27; NO 2; PP. 123-130; ABS. ENG; BIBL. 44 REF.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

DIE ASTROGLIALE DYSTROPHIE MIT ROSENTHALSCHEN FASERN. ZUR FRAGE DER ADULTEN FORM DER ALEXANDERSCHEN KRANKHEIT UND IHRER KLINISCHEN BEDEUTUNG = LA DYSTROPHIE ASTROGLIALE AVEC FIBRES DE ROSENTHAL. LE PROBLEME DE LA FORME ADULTE DE LA MALADE D'ALEXANDER ET DE SON IMPORTANCE CLINIQUEULE G; JACOB H.1983; NERVENARZT; ISSN 0028-2804; DEU; DA. 1983; VOL. 54; NO 2; PP. 69-73; BIBL. 28 REF.Article

ALEXANDER'S DISEASE: FURTHER LIGHT-, AND ELECTRON-MICROSCOPIC OBSERVATIONSTOWFIGHI J; YOUNG R; SASSANI J et al.1983; ACTA NEUROPATHOLOGICA; ISSN 0001-6322; DEU; DA. 1983; VOL. 61; NO 1; PP. 36-42; BIBL. 21 REF.Article

GENETIC DEFECTS OF LYSOSOMAL ENZYMES = LES ANOMALIES GENETIQUES DES ENZYMES LYSOSOMIQUESO'BRIEN JS.1973; EXCERPTA MED., INTERNATION. CONGR. SER.; PAYS-BAS; DA. 1973; NO 250; PP. 286-299; BIBL. 19REF.; (C.R. IVE CONGR. INT. GENET. HUM.; PARIS; 1971)Conference Paper

LA DETECTION DE L'HETEROZYGOTISME POUR LA SULFATIDOSE (FORME INFANTILE). REFLEXIONS A PROPOS D'UNE ETUDE PORTANT SUR TROIS FAMILLESGUIBAUD P; GARCIA I; GUYONNET C et al.1973; LYON MED.; FR.; DA. 1973; VOL. 229; NO 12; PP. 1215-1224; ABS. ANGL.; BIBL. 30REF.Serial Issue

ARYLSULFATASES ISOENZYMES IN METACHROMATIC LEUCODYSTROPHY/DETECTION OF A NEW VARIANT BY ELECTROPHORESIS. IMPROVEMENT OF QUANTITATIVE ASSAYDUBOIS G; TURPIN JC; BAUMANN N et al.1975; BIOMEDICINE; FR.; DA. 1975; VOL. 23; NO 3; PP. 116-119; ABS. FR.; BIBL. 10REF.Article

MENTAL RETARDATION IN CHILDREN. II. LEUCODYSTROPHIES = LE RETARD MENTAL CHEZ LES ENFANTS. II. LES LEUCODYSTROPHIESJOSHUA GE; JADHAV M; BHAKTAVIZIAM A et al.1974; INDIAN PEDIATR.; INDIA; DA. 1974; VOL. 11; NO 1; PP. 53-59; BIBL. 1P.Article

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