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AN UNUSUAL CASE OF PICK'S DISEASESHIBAYAMA H; KITOH J; MARUI Y et al.1983; ACTA NEUROPATHOLOGICA; ISSN 0001-6322; DEU; DA. 1983; VOL. 59; NO 2; PP. 79-87; BIBL. 2 P.Article

THE NEUROPATHOLOGY OF A CASE OF PICK'S DISEASERODDA RA.1979; CLIN. EXPER. NEUROL.; AUS; DA. 1979 PUBL. 1980; VOL. 16; PP. 295-302; BIBL. 2 P.Article

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

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

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

PICK'S DISEASE: AN IMMUNOCYTOCHEMICAL STUDY OF NEURONAL CHANGES. MONOCLONAL ANTIBODIES SHOW THAT PICK BODIES SHARE ANTIGENIC DETERMINANTS WITH NEUROFIBRILLARY TANGLES AND NEUROFILAMENTSPROBST A; ANDERTON BH; ULRICH J et al.1983; ACTA NEUROPATHOLOGICA; ISSN 0001-6322; DEU; DA. 1983; VOL. 60; NO 3-4; PP. 175-182; BIBL. 18 REF.Article

COMPUTED TOMOGRAPHY IN PICK'S DISEASE: FINDINGS IN A FAMILY AFFECTED IN THREE CONSECUTIVE GENERATIONSGROEN JJ; HEKSTER REM.1982; J. COMPUT. ASSISTED TOMOGR.; ISSN 0363-8715; USA; DA. 1982; VOL. 6; NO 5; PP. 907-911; BIBL. 12 REF.Article

HEREDITARY PICK'S DISEASE. SECOND RE-EXAMINATION OF A LARGE FAMILY AND DISCUSSION OF OTHER HEREDITARY CASES, WITH PARTICULAR REFERENCE TO ELECTROENCEPHALOGRAPHY AND COMPUTERIZED TOMOGRAPHYGROEN JJ; ENDTZ LJ.1982; BRAIN; ISSN 0006-8950; GBR; DA. 1982; VOL. 105; NO 3; PP. 443-459; BIBL. 2 P.Article

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

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

CLINICAL AND BIOCHEMICAL STUDY OF A CHILD WITH THE NON-NEURONOPATHIC-TYPE B FORM OF NIEMANN-PICK DISEASEREICH D; KEDAR A; KLIBANSKY C et al.1979; EUROP. J. PEDIATR.; DEU; DA. 1979; VOL. 131; NO 2; PP. 133-140; BIBL. 25 REF.Article

SPHINGOMYELINASE ACTIVITIES IN CULTURED SKIN FIBROBLASTS FROM PATIENTS WITH NIEMANN-PICK DISEASEMINAMI R; MATSUURA Y; NAKAMURA F et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 2; PP. 159-167; BIBL. 16 REF.Article

A MICROMETHOD FOR SPHINGOMYELINASE ASSAY USING A CHROMOGENIC ARTIFICIAL SUBSTRATE. ITS USE IN THE DIAGNOSIS OF NIEMANN-PICK DISEASEDEN TANDT WR; JAEKEN J; LEROY JG et al.1979; ACTA PAEDIATR. BELG.; BEL; DA. 1979; VOL. 38; NO 4; PP. 253-258; BIBL. 15 REF.Article

NIEMANN PICK DISEASE: PRESENCE OF THE MAGNESIUM-DEPENDENT SPHINGOMYELINASE IN BRAIN OF THE INFANTILE FORM OF THE DISEASEGATT S; DINUR T; KOPOLOVIC J et al.1978; J. NEUROCHEM.; GBR; DA. 1978; VOL. 31; NO 2; PP. 547-550; BIBL. 20 REF.Article

MANIFESTATIONS RESPIRATOIRES DE LA MALADIE DE NIEMANN-PICK DE L'ADULTE. REVUE DE LA LITTERATURE A PROPOS D'UNE OBSERVATION PERSONNELLERANFAING J; CARBILLET JP; RANFAING E et al.1978; REV. FR. MAL. RESP.; FRA; DA. 1978; VOL. 6; NO 4; PP. 409-414; ABS. ENG; BIBL. 11 REF.Article

NIEMANN-PICKSCHE KRANKHEIT. = MALADIE DE NIEMANN-PICKHOFSTADTER F; FALSER N; DWORZAK E et al.1978; MED. WELT; DTSCH.; DA. 1978; VOL. 29; NO 20; PP. 849-852; BIBL. 10 REF.Article

NIEMANN-PICK DISEASE EXPERIMENTAL MODEL: SPHINGOMYELINASE REDUCTION INDUCED BY AY-9944.SAKURAGAWA N; SAKURAGAWA M; KUWABARA T et al.1977; SCIENCE; U.S.A.; DA. 1977; VOL. 196; NO 4287; PP. 317-319; BIBL. 14 REF.Article

NIEMANN-PICK DISEASE TYPE D: LIPID ANALYSES AND STUDIES ON SPHINGOMYELINASES.RAO BG; SPENCE MW.1977; ANN. NEUROL.; U.S.A.; DA. 1977; VOL. 1; NO 4; PP. 385-392; BIBL. 1 P.Article

SPHINGOMYELINASE ISOZYMES OF HUMAN TISSUES: A HYPOTHESIS ON ENZYMATIC DIFFERENTIATION OF THE NEUROPATHIC AND NON-NEUROPATHIC FORMS OF NIEMANN-PICK DISEASE.YAMAGUCHI S; SUZUKI K.1977; BIOCHEM. BIOPHYS. RES. COMMUNIC.; U.S.A.; DA. 1977; VOL. 77; NO 3; PP. 999-1003; BIBL. 4 REF.Article

DEMENCES PRESENILES.BRUN M.1977; LYON MEDITERR. MED.; FR.; DA. 1977; VOL. 13; NO 8; PP. 583-586Article

FORMES NEONATALES DE LA MALADIE DE NIEMANN-PICK. "A PROPOS D'UNE OBSERVATION PERSONNELLE REVELEE PAR ANASARQUE FOETO-PLACENTAIRE".BELAMICH PATRICK.sd; FRA; DA. S.D.; 121; 60 P.; 30 CM; BIBL. 4 P.; TH.: MED./PARIS 5/1978Thesis

CLINICAL HETEROGENEITY IN A SIBSHIP WITH NIEMANN-PICK DISEASE TYPE CYATZIV S; LEIBOVITZ BEN GERSHON Z; ORNOY A et al.1983; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1983; VOL. 23; NO 2; PP. 125-131; BIBL. 28 REF.Article

HEPATIC STORAGE OF BIS (MONOACYLGLYCEROL) PHOSPHATE WITHOUT CONCOMITANT STORAGE OF SPHINGOMYELIN IN A 72-YEAR-OLD PATIENT WITH A PARTIAL DEFICIENCY OF SPHINGOMYELINASEPOULOS A; BECKMAN K; ELLIS DH et al.1982; CLINICAL GENETICS; ISSN 0009-9163; DNK; DA. 1982; VOL. 22; NO 5; PP. 234-243; BIBL. 27 REF.Article

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