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

DIAGNOSIS OF TAY-SACHS DISEASE USING (³H) N-ACETYLNEURAMINIC ACID LABELLED G_M2 GANGLIOSIDE AS SUBSTRATEPOULOS A; HOLDING J; CAREY WF et al.1982; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1982; VOL. 120; NO 3; PP. 331-340; BIBL. 23 REF.Article

HUMAN HEXOSAMINIDASE ISOZYMES: CHROMATOGRAPHIC SEPARATION AS AN AID TO HETEROZYGOTE IDENTIFICATION.NAKAGAWA S; KUMIN S; NITOWSKY HM et al.1977; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1977; VOL. 75; NO 2; PP. 181-191; BIBL. 14 REF.Article

OBSTETRICIANS' ATTITUDES TOWARD GENETIC SCREENING.GORDIS L; CHILDS B; ROSEMAN MG et al.1977; AMER. J. PUBLIC. HEALTH; U.S.A.; DA. 1977; VOL. 67; NO 5; PP. 469-471; BIBL. 6 REF.Article

TAY-SACHS DISEASE: GENETIC DRIFT AMONG THE ASHKENAZIM JEWS.FRAIKOR AL.1977; SOC. BIOL.; U.S.A.; DA. 1977; VOL. 24; NO 2; PP. 117-134; BIBL. 2 P.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

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

A PROPOS D'UN CAS DE LA MALADIE DE TAY-SACHS.MEUNIER D.1978; ; S.L.; DA. 1978; PP. 1-76; BIBL. 7 P.; (THESE DOCT. MED.; ROUEN)Thesis

HAIR-ROOTS IN SCREENING AND DIAGNOSIS OF TAY-SACHS DISEASES.HOSLI P; AMSTERDAM D; SCHNECK L et al.1977; LANCET; G.B.; DA. 1977; NO 8006; PP. 285-287; BIBL. 13 REF.Article

UN CASO DI GANGLIOSIDOSI GM₂. VARIANTE AB ATIPICA. = UN CAS DE GANGLIOSIDOSE GM2. FORME ATYPIQUE DE LA VARIANTE ABALLEGRANZA A; GRISONI R; BALESTRINI MR et al.1977; RIV. PATOL. NERV. MENTALE; ITA; DA. 1977; VOL. 98; NO 2; PP. 65-87; ABS. ANGL.; BIBL. 1 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

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

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

EXPERIMENTAL STUDIES OF ENZYME REPLACEMENT TREATMENT OF TAY-SACHS DISEASE BRAIN CELLS IN VITROADACHI M; BROOKS SE; HOFFMAN LM et al.1983; PROGRESS IN NEUROPATHOLOGY; ISSN 0099-9016; USA; DA. 1983; VOL. 5; PP. 173-188; BIBL. 65 REF.Article

ARTIFICIAL INSEMINATION BY DONORS: THE NEED FOR GENETIC SCREENING: LATE INFANTILE G_M2-GANGLIOSIDOSIS RESULTING FROM THIS TECHNIQUEJOHNSON WG; SCHWARTZ RC; CHUTORIAN AM et al.1981; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1981; VOL. 304; NO 13; PP. 755-757; BIBL. 14 REF.Article

ETUDE ANATOMO-CLINIQUE D'UN CAS DE MALADIE DE TAY-SACHSMARX P; DHERMY P; LANGLOIS J et al.1980; BULL. SOC. OPHTALMOL. FR.; FRA; DA. 1980; VOL. 80; NO 2; PP. 119-123; ABS. ENG; BIBL. 11 REF.Article