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kw.\*:("Sphingolipidose héréditaire Tay Sachs")

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SOCIAL ASPECTS OF GENETIC SCREENING FOR TAY-SACHS DISEASE: THE PILOT COMMUNITY SCREENING PROGRAM IN BALTIMORE AND WASHINGTONMCQUEEN DV.1975; SOC. BIOL.; U.S.A.; DA. 1975; VOL. 22; NO 2; PP. 125-133; BIBL. 5 REF.Article

The mutation mechanism causing juvenile-onset Tay-Sachs disease among LebaneseHECHTMAN, P; BOULAY, B; BAYLERAN, J et al.Clinical genetics. 1989, Vol 35, Num 5, pp 364-375, issn 0009-9163, 12 p.Article

TAY-SACHS AND RELATED STORAGE DISEASES: FAMILY PLANNING.SCHNEIDERMAN G; LOWDEN JA; RAE GRANT P et al.1978; MENTAL RETARDAT.; U.S.A.; DA. 1978; VOL. 16; NO 1; PP. 13-15; BIBL. 11 REF.Article

A pseudodeficiency allele common inn non-jewish Tay-Sachs carriers : implications for carrier screeningTRIGGS-RAINE, B. L; MULES, E. H; GREENBERG, C. R et al.American journal of human genetics. 1992, Vol 51, Num 4, pp 793-801, issn 0002-9297Article

Characterization of some minor gangliosides in Tay-Sachs brainsYU, R. K; ITOH, T; YOHE, H. C et al.Brain research. 1983, Vol 275, Num 1, pp 47-52, issn 0006-8993Article

Pitfalls in Tay-Sachs carrier detection: physician referral patterns and patient ignoranceSHAPIRO, D. A; SHAPIRO, L. R.New York State journal of medicine. 1989, Vol 89, Num 6, pp 317-319, issn 0028-7628, 3 p.Article

HETEROZYGOTE ADVANTAGE IN TAY-SACHS CARRIERS.SPYROPOULOS B; MOENS PB; DAVIDSON J et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 3; PP. 375-380; BIBL. 17 REF.Article

AN ECONOMIC EVALUATION OF A GENETIC SCREENING PROGRAM FOR TAY-SACHS DISEASE.NELSON WB; SWINT JM; CASKEY CT et al.1978; AMER. J. HUM. GENET.; U.S.A.; DA. 1978; VOL. 30; NO 2; PP. 160-166; BIBL. 13 REF.Article

KNOWLEDGE ABOUT AND ATTITUDES TOWARD GENETIC SCREENING AMONG HIGH-SCHOOL STUDENTS: THE TAY-SACHS EXPERIENCE.CLOW CL; SCRIVER CR.1977; PEDIATRICS; U.S.A.; DA. 1977; VOL. 59; NO 1; PP. 86-91; BIBL. 10 REF.Article

TAY-SACHS DISEASE AND CARRIER SCREENING PROGRAMS: PSYCHOSOCIAL ASPECTS.SCHNEIDERMAN G; LOWDEN JA; RAE GRANT Q et al.1977; CANAD. J. PUBLIC HEALTH; CANADA; DA. 1977; VOL. 68; NO 1; PP. 66-68; ABS. FR.; BIBL. 12 REF.Article

ADVOCACY AND COMPLIANCE FACTORS IN A VOLUNTARY SELECTIVE SCREENING PROGRAM.ROTHSCHILD H; IVKER FB.1977; SOUTH. MED. J.; U.S.A.; DA. 1977; VOL. 70; NO 2; PP. 184-186; BIBL. 19 REF.Article

TAY-SACHS DISEASE: A PILOT SCREENING PROGRAM FOR THE DETECTION OF THE HETEROZYGOTE IN THE CHARLESTON JEWISH COMMUNITY.ROGERS JF; HOGAN EL; JORGENSON RJ et al.1976; SOUTH. MED. J.; U.S.A.; DA. 1976; VOL. 69; NO 11; PP. 1453-1455; BIBL. 8 REF.Article

TAY-SACHS SCREENING: MOTIVES FOR PARTICIPATING AND KNOWLEDGE OF GENETICS AND PROBABILITY.CHILDS B; GORDIS L; KABACK MM et al.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 6; PP. 537-549; BIBL. 10 REF.Article

DIFFERENTIALDIAGNOSTISCHE SCHWIERIGKEITEN BEIM MYOKLONISCH-ASTATISCHEN PETIT MAL-STATUS = DIFFICULTES DU DIAGNOSTIC DIFFERENTIEL DU SYNDROME DE LENNOXMULLER J; MULLER D.1975; ARCH. SUISSES NEUROL. NEUROCHIR. PSYCHIATR.; SUISSE; DA. 1975; VOL. 117; NO 2; PP. 241-254; ABS. FR. ANGL.; BIBL. 1 P.Article

CONTRIBUTION A L'ETUDE GENETIQUE DES GANGLIOSIDOSES GM2 (TAY-SACHS ET SANDHOFF) PAR L'ETUDE DES HEXOSAMINIDASES DES HYBRIDES SANDHOFF-RONGEURS (SOURIS ET HAMSTER).WEIL D; NGUYEN VAN CONG; REBOURCET R et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 3; PP. 163-168; ABS. ANGL.; BIBL. 30 REF.Article

CULTURE ET PRODUCTION DES HYBRIDES CELLULAIRES HOMME-SOURIS, HOMME-HAMSTER. CONTRIBUTION A L'ETABLISSEMENT DE LA CARTE CHROMOSOMIQUE HUMAINE ET A L'ETUDE GENETIQUE DE QUELQUES MALADIES HEREDITAIRES DU METABOLISME CHEZ L'HOMME (GANGLIOSIDOSES GM2)WEIL D.1975; ; S.L.; DA. 1975; PP. 1-61; H.T. 14; BIBL. 8 P.; (THESE DOCT. 3E. CYCLE, SPEC. BIOL. ANIM.; PARIS-SUD)Thesis

TAY-SACHS DISEASE BRAIN CELLS IN CULTURE: MOBILIZATIONHOFFMAN LM; BROOKS SE; AMSTERDAM D et al.1980; J. NEUROSCI. RES.; ISSN 0360-4012; USA; DA. 1980; VOL. 5; NO 5; PP. 413-417; BIBL. 14 REF.Article

TAY-SACHS DISEASE AND THEORETICAL POPULATION GENETICS.EWENS WJ.1978; AMER. J. HUM. GENET.; USA; DA. 1978; VOL. 30; NO 3; PP. 328-329; BIBL. 2 REF.Article

CHARACTERIZATION OF B-D-N-ACETYLHEXOSAMINIDASES C AND S IN FIBROBLASTS FROM CONTROL INDIVIDUALS AND PATIENTS WITH TAY-SACHS DISEASE.REUSER AJJ; GALJAARD H.1976; F.E.B.S. LETTERS; NETHERL.; DA. 1976; VOL. 71; NO 1; PP. 1-5; BIBL. 20 REF.Article

INTRODUCTION OF PURIFIED HEXOSAMINIDASE A INTO TAY-SACHS LEUKOCYTES BY MEANS OF IMMUNOGLOBULIN-COATED LIPOSOMESCOHEN CM; WEISSMANN G; HOFFSTEIN S et al.1976; BIOCHEMISTRY; U.S.A.; DA. 1976; VOL. 15; NO 2; PP. 452-460; BIBL. 45 REF.Article

DEMOGRAPHIC DATA AS GRAPHIC AID IN SCREENING PROGRAM FOR TAY-SACHS DISEASE. = LES DONNEES DEMOGRAPHIQUES, AIDE GRAPHIQUE POUR LE PROGRAMME DE DEPISTAGE DE LA MALADIE DE TAY-SACHSGARDNER LI; MELTZER SL.1975; J. PEDIATR.; U.S.A.; DA. 1975; VOL. 87; NO 4; PP. 664-665; BIBL. 3 REF.Article

ISOLATION AND CHARACTERIZATION OF A NOVEL MONOSIALOSYLPENTAHEXOSYL CERAMIDE FROM TAY-SACHS BRAINITOH T; YU TEH LI; SU CHEN LI et al.1981; J. BIOL. CHEM.; ISSN 0021-9258; USA; DA. 1981; VOL. 256; NO 1; PP. 165-169; BIBL. 32 REF.Article

RADIOIMMUNOASSAY AND HEAT DENATURATION ENZYME ASSAY FOR THE DETECTION OF TAY-SACHS HETEROZYGOTES DURING PREGNANCYNGUYEN C; GOLD RJM; MAHURAN D et al.1981; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1981; VOL. 113; NO 1; PP. 13-25; BIBL. 20 REF.Article

CLINICAL AND BIOCHEMICAL ABNORMALITIES IN PORCINE GM2-GANGLIOSIDOSISKOSANKE SD; PIERCE KR; BAY WW et al.1978; VETER. PATHOL.; CHE; DA. 1978; VOL. 15; NO 6; PP. 685-699; BIBL. 32 REF.Article

ROLE OF THE PHYSICIAN IN SCREENING FOR CARRIERS OF TAY-SACHS DISEASELOWDEN JA.1978; CANAD. MED. ASS. J.; CAN; DA. 1978; VOL. 119; NO 6; PP. 575-578; BIBL. 10 REF.Article

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