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BASIC FINDINGS AND CURRENT DEVELOPMENTS IN SPHINGOLIPIDOSESPILZ H; HEIPERTZ R; SEIDEL D et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 2; PP. 113-134; BIBL. 11 P.Article

Isocortical pathology in type C Niemann-Pick disease. A combined Golgi-pigmentoarchitectonic studyBRAAK, H; BRAAK, E; GOEBEL, H. H et al.Journal of neuropathology and experimental neurology. 1983, Vol 42, Num 6, pp 671-687, issn 0022-3069Article

Enfermedades hereditarias lisosomales en México. III, Diagnóstico de laboratorio para esfingolipidosisELENA ZETINA, M; GONZALEZ-NORIEGA, A.Revista de investigacion clinica. 1991, Vol 43, Num 1, pp 52-60, issn 0034-8376Article

Animal and cellular models of sphingolipid storage disorders of humansGAL, A. E; WEIS, A. L; QUIRK, J. M et al.Chemistry and physics of lipids. 1986, Vol 42, Num 1-3, pp 199-207, issn 0009-3084Article

Maladie de Fabry = Fabry disease. An updatePORNEUF, M; SOTTO, A; PERRIN, P et al.La Semaine des hôpitaux de Paris. 1993, Vol 69, Num 21, pp 634-638, issn 0037-1777Article

SPHINGOLIPIDOSES: MOLECULAR MANIFESTATIONS AND BIOCHEMICAL STRATEGIESPENTCHEV PG; BARRANGER JA.1978; J. LIPID RES.; USA; DA. 1978; VOL. 19; NO 4; PP. 401-409; BIBL. 110 REF.Article

ENZYMATIC ASPECTS OF THE LIPID STORAGE DISEASES.1978; ADV. EXPER. MED. BIOL.; U.S.A.; DA. 1978; VOL. 101; PP. 689-764; BIBL. DISSEM.; (MEET. ENZYMES LIPID METAB. PROC.; MONT STE-ODILE; 1977)Conference Paper

NIEMANN-PICK DISEASE: REPORT OF A CASE WITH SKIN INVOLVEMENTMARDINI MK; GERGEN P; MOHAMMED AKHTAR et al.1982; AMERICAN JOURNAL OF DISEASES OF CHILDREN; ISSN 0002-922X; USA; DA. 1982; VOL. 136; NO 7; PP. 650-651; BIBL. 6 REF.Article

Sphingomyelin lipidosis variant with cirrhosis in the pediatric age groupWITZLEBEN, C. L; PALMIERI, M. J; WATKINS, J. B et al.Archives of pathology & laboratory medicine (1976). 1986, Vol 110, Num 6, pp 508-512, issn 0363-0153Article

Prenatal diagnosis of lysosomal storage diseases: review of experience in 145 patients referrals over a period of eight yearsCAREY, W. F; HOPWOOD, J. J; POULOS, A et al.Medical journal of Australia. 1984, Vol 140, Num 4, pp 203-208, issn 0025-729XArticle

Pathways of sphingomyelin metabolism in cultured fibroblasts from normal and sphingomyelin lipidosis subjectsSPENCE, M. W; CLARKE, J. T. R; COOK, H. W et al.The Journal of biological chemistry (Print). 1983, Vol 258, Num 14, pp 8595-8600, issn 0021-9258Article

Studies on lipids from liver and spleen of a child (O. L.) with Niemann-Pick's disease type CHARDER, A; WIDJAJA, F; DEBUCH, H et al.Journal of clinical chemistry and clinical biochemistry. 1984, Vol 22, Num 2, pp 199-201, issn 0340-076XArticle

Lysosomal storage diseasesBRADY, R. O.Pharmacology & therapeutics (Oxford). 1982, Vol 19, Num 3, pp 327-336, issn 0163-7258Article

MULTIPLE MOLECULAR FORMS OF ARYLSULFATASE A IN DIFFERENT FORMS OF METACHROMATIC LEUKODYSTROPHY (MLD)FARRELL DF; MACMARTIN MP; CLARK AF et al.1979; NEUROLOGY; USA; DA. 1979; VOL. 29; NO 1; PP. 16-20; BIBL. 18 REF.Article

PROGRESS IN INVESTIGATIONS OF SPHINGOLIPIDOSES.ADACHI M; SCHNECK L; VOLK BW et al.1978; ACTA NEUROPATHOL.; DEU; DA. 1978; VOL. 43; NO 1-2; PP. 1-18; BIBL. 5 P.Article

SPHINGOLIPIDOSESBRADY RO.1978; ANNU. REV. BIOCHEM.; USA; DA. 1978; VOL. 47; PP. 687-713; BIBL. 175 REF.Article

A POTENTIAL SOURCE OF ERROR IN THE ENZYMATIC DIAGNOSIS OF THE NEUROLIPIDOSES WHEN RADIOLABELLED SPHINGOLIPIDS ARE USED AS SUBSTRATES.POULOS A; POLLARD AC.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 73; NO 2; PP. 353-356; BIBL. 11 REF.Article

Peripheral neuropathy in type A Niemann-Pick diseaseLANDRIEU, P; SAÏD, G.Acta neuropathologica. 1984, Vol 63, Num 1, pp 66-71, issn 0001-6322Article

THE BIOCHEMICAL GENETICS OF THE HEXOSAMINIDASE SYSTEM IN MANBEUTLER E.1979; AMER. J. HUM. GENET.; USA; DA. 1979; VOL. 31; NO 2; PP. 95-105; BIBL. 74 REF.Article

MALADIES HEREDITAIRES DU METABOLISME DES MUCOPOLYSACCHARIDES, GLYCOPROTEINES ET SPHINGOLIPIDES. I: ANOMALIES BIOCHIMIQUESSALVAYRE R; THOUVENOT JP; DOUJTE BLAZY L et al.1979; REV. MED. TOULOUSE; FRA; DA. 1979; VOL. 15; NO 8; PP. 471-482; ABS. ENG; BIBL. 58 REF.Article

THE CLINICAL CLASSIFICATION OF CEROID-LIPOFASCINOSIS. A STATISTICAL APPROACH.REY PIAS JM; MORALES C; SERRATE A et al.1976; ARCH. SUISSES NEUROL. NEUROCHIR. PSYCHIATR.; SUISSE; DA. 1976; VOL. 119; NO 1; PP. 19-29; ABS. ALLEM. FR.; BIBL. 1 P. 1/2Article

EXPERIENCE OF ANTIOXIDANT TREATMENT IN NEURONAL CEROID-LIPOFUSCINOSIS OF SPIELMEYER-SJOEGREN TYPE.SANTAVUORI P; MOREN R.1977; NEUROPAEDIATRIE; DTSCH.; DA. 1977; VOL. 8; NO 4; PP. 333-344; ABS. ALLEM.; BIBL. 9 REF.Article

CELLULES DE KUPFFER ET DYSLIPOIDOSES.LAGERON A.1977; MED. CHIR. DIGEST.; FR.; DA. 1977; VOL. 6; NO 7; PP. 453-457; BIBL. 11 REF.Article

ENZYMES IN AMNIOTIC FLUID.WATKINS BF; BERMES EW.1977; ANN. CLIN. LAB. SCI.; U.S.A.; DA. 1977; VOL. 7; NO 3; PP. 231-240; BIBL. 1 P. 1/2Article

DE L'ANATOMIE PATHOLOGIQUE DES NEUROLIPIDOSESKOZAKOVA PB; KHOKHRINA NT; KALMIKOVA LG et al.1978; ZH. NEUROPATOL. PSIKHIATR. S.S. KORSAKOVA; SUN; DA. 1978; VOL. 78; NO 7; PP. 1095-1100; ABS. ENG; BIBL. 20 REF.Article

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