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kw.\*:("Sphingolipidose héréditaire Niemann Pick")

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PRENATAL NIEMANN-PICK DISEASE: BIOCHEMICAL AND HISTOLOGIC EXAMINATION OF A 19-GESTATIONAL WEEK FETUS = MALADIE DE NIEMANN-PICK PRENATALE: EXAMEN BIOCHIMIQUE ET HISTOLOGIQUE D'UN FOETUS DE 19 SEMAINESSCHNEIDER EL; ELLIS WG; BRADY RO et al.1972; PEDIATR. RES.; U.S.A.; DA. 1972; VOL. 6; NO 9; PP. 720-729; BIBL. 44 REF.Article

Niemann-Pick disease: lipid storage in bone marrow macrophagesELLEDER, M; HRODEK, J; CIHULA, J et al.Histochemical journal. 1983, Vol 15, Num 11, pp 1065-1077, issn 0018-2214Article

Maculo halo syndrome. Variant of Niemann-Pick diseaseCOGAN, D. G; CHU, F. C; BARRANGER, J. A et al.Archives of ophthalmology (1960). 1983, Vol 101, Num 11, pp 1698-1700, issn 0003-9950Article

ELECTRON MICROSCOPY OF LUNG IN NIEMANN-PICK DISEASE = MICROSCOPIE ELECTRONIQUE DU POUMON DANS LA MALADIE DE NIEMANN-PICK1972; J. PATHOL.; G.B.; DA. 1972; VOL. 106; NO 2; PP. 119-122; H.T. 4; BIBL. 16 REF.Serial Issue

CONSERVATION D'UNE ERREUR DE METABOLISME (MALADIE DE NIEMANN-PICK) DANS UNE CULTURE A LONG TERME DE CELLULES ISSUES DE PARENCHYME HEPATIQUEGAUTIER M; RACHMAN F; CARREAU JP et al.1972; ARCH. FR. PEDIATR.; FR.; DA. 1972; VOL. 29; NO 6; PP. 635-639; ABS. ANGL.; BIBL. 7 REF.Serial Issue

LYMPHKNOTENULTRASTRUKTUR BEI NIEMANN-PICKSCHER KRANKHEIT = ULTRASTRUCTURE DES GANGLIONS LYMPHATIQUES AU COURS DE LA MALADIE DE NIEMANN PICKKERENYI T; ROMHANYI J; PODER G et al.1971; ACTA MORPHOL. ACAD. SCI. HUNGAR.; HONGR.; DA. 1971; VOL. 19; NO 4; PP. 417-432; ABS. ANGL. RUSSE; BIBL. 1P.1/2Serial Issue

EARLY DIAGNOSIS IN NIEMANN-PICK DISEASETOUSSI T; DELVIN EE; GLORIEUX FH et al.1974; CANAD. MED. ASS. J.; CANADA; DA. 1974; VOL. 111; NO 6; PP. 556-560; ABS. FR.; BIBL. 15REF.Article

Type C Niemann-Pick disease : biochemical aspects and phenotypic heterogeneityVANIER, M. T; RODRIGUEZ-LAFRASSE, C; ROUSSON, R et al.Developmental neuroscience. 1991, Vol 13, Num 4-5, pp 307-314, issn 0378-5866Article

DIAGNOSIS OF TYPE A NIEMANN-PICK'S DISEASE BY CONJUNCTIVAL BIOPSY. = DIAGNOSTIC DU TYPE DE MALADIE DE NIEMANN-PICK PAR LA BIOPSIE CONJONCTIVALELIBERT J; DANIS P.1975; PATHOL. EUROP.; BELG.; DA. 1975; VOL. 10; NO 3; PP. 233-239; BIBL. 19 REF.Article

Histiocytes bleu de mer et maladies de surcharge. Trois observations = «Sea-blue» histiocytes and storage diseases: about three casesAUBERT, I; CHANU, B; BAKIR, R et al.Annales de médecine interne (Paris). 1985, Vol 136, Num 2, pp 133-136, issn 0003-410XArticle

Uptake and metabolism of radioactively labeled sphingomyelin in cultured skin fibroblasts from controls and patients with Niemann-Pick disease and other lysosomal storage diseasesKUDOH, T; VELKOFF, M. A; WENGER, D. A et al.Biochimica et biophysica acta. 1983, Num 754, pp 82-92, issn 0006-3002Article

A comparison between hepatocytes and macrophages of sphingomyelin, cholesterol and acid lipase in various types of Niemann-Pick diseaseLAGERON, A.Journal of inherited metabolic disease. 1986, Vol 9, pp 311-313, issn 0141-8955, suppl. 2Conference Paper

Studies on the activation of sphingomyelinase activity in Niemann-Pick type A, B, and C fibroblasts: enzymological differentiation of types A and BPOULOS, A; RANIERI, E; SHANKARAN, P et al.Pediatric research. 1984, Vol 18, Num 11, pp 1088-1093, issn 0031-3998Article

NIEMANN-PICK DISEASE TYPE B: PRENATAL DIAGNOSIS AND ENZYMATIC AND CHEMICAL STUDIES ON FETAL BRAIN AND LIVERWENGER DA; KUDOH T; SATTLER M et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 3; PP. 337-344; BIBL. 18 REF.Article

NIEMANN-PICK DISEASE: A GENETIC MODEL IN SIAMESE CATSWENGER DA; SATTLER M; KUDOH T et al.1980; SCIENCE; USA; DA. 1980; VOL. 208; NO 4451; PP. 1471-1473; BIBL. 12 REF.Article

MALADIES HEREDITAIRES PAR SURCHARGE EN SPHINGOMYELINES OU MALADIE DE NIEMANN-PICK. (A PROPOS DE 36 OBSERVATIONS PERSONNELLES).BARATON G.1977; ; S.L.; DA. 1977; PP. 1-127; BIBL. 15 REF.; (THESE DOCT. MED.; CLAUDE BERNARD LYON I)Thesis

OCULAR FINDINGS IN NIEMANN-PICK DISEASELIBERT J; TOUSSAINT D; GUISELINGS R et al.1975; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1975; VOL. 80; NO 6; PP. 991-1002; BIBL. 1 P. 1/2Article

LA FORME VISCERALE PURE DE LA MALADIE DE NIEMANN-PICK (SPHINGOMYELINOSE DE TYPE B). A PROPOS D'UN CAS PERSONNEL, ET D'UNE ETUDE DE 23 OBSERVATIONS DE LA LITTERATUREBERTHIER M.1975; ; S.L.; DA. 1975; PP. 1-73; BIBL. 5 P.; (THESE DOCT. MED.; CLAUDE-BERNARD-LYON)Thesis

SHINGOMYELINOSIS, A NEW MUTATION IN THE MOUSE. A MODEL OF NIEMANN-PICK DISEASE IN HUMANSMIYAWAKI S; MITSUOKA S; SAKIYAMA T et al.1982; JOURNAL OF HEREDITY; ISSN 0022-1503; USA; DA. 1982; VOL. 73; NO 4; PP. 257-263; BIBL. 15 REF.Article

DIAGNOSTIC BIOCHIMIQUE ANTE-NATAL DE LA MALADIE DE NIEMANN-PICKTHOMAS J; CARRERE J; GHISOLFI J et al.1981; REV. MED. TOULOUSE; ISSN 0556-753X; FRA; DA. 1981; VOL. 17; NO 9; PP. 571-574; 3 P.; ABS. ENG; BIBL. 14 REF.Article

THE ROENTGENOGRAPHIC FINDINGS IN THE ACUTE NEURONOPATHIC FORM OF NIEMANN-PICK DISEASE.GRUENEBAUM M.1976; BRIT. J. RADIOL.; G.B.; DA. 1976; VOL. 49; NO 588; PP. 1018-1022; BIBL. 12 REF.Article

CONTRIBUTION A L'ETUDE DE LA MALADIE DE NIEMANN-PICKDUPONT ROC C.1972; LYON; ASSOC. CORP. ETUD. MED.; DA. 1972; PP. 1-90; H.T. 3; BIBL. 14P.; (THESE DOCT. MED.; UNIV. CLAUDE BERNARD LYON; 1972)Thesis

GASTROINTESTINAL MANIFESTATIONS OF NIEMANN-PICK DISEASEDINARI G; ROSENBACH Y; GRUNEBAUM M et al.1980; ENZYME; ISSN 0013-9432; CHE; DA. 1980; VOL. 25; NO 6; PP. 407-412; BIBL. 7 REF.Article

MALADIE DE NIEMANN-PICK DE L'ADULTE SUIVIE DE LA NAISSANCE A L'AGE DE 26 ANS. FORME VISCERALE PURE AVEC SURCHARGE EN SPHINGOMYELINE ET DEFICIT EN SPHINGOMYELINASE.BRIERE J; CALMAN F; LAGERON A et al.1976; NOUV. REV. FR. HEMATOL.; FR.; DA. 1976; VOL. 16; NO 2; PP. 185-202; ABS. ANGL.; BIBL. 1 P. 1/2Article

ACTIVATEUR DES SPHINGOHYDROLASES ET NATURE DU DEFICIT EN SPHINGOMYELINASE DANS LA MALADIE DE NIEMANN-PICK TYPE A, B ET C.BARATON G; REVOL A.1977; CLIN. CHIM. ACTA; PAYS BAS; DA. 1977; VOL. 76; NO 3; PP. 339-343; ABS. ANGL.; BIBL. 13 REF.Article

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