PGL-I leprosy serology

[1] BRENNAN PJ, 1980, INT J LEPROSY, V48, P382

[2] BRETT SJ, 1984, CLIN EXP IMMUNOL, V56, P89

[3] BRETT SJ, 1986, CLIN EXP IMMUNOL, V64, P476

[4] Bührer SS, 1998, AM J TROP MED HYG, V58, P133

[5] Simple dipstick assay for semi-quantitative detection of neopterin in sera [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 2000, 238 (1-2) : 55 - 58

[6] Simple and fast lateral flow test for classification of leprosy patients and identification of contacts with high risk of developing leprosy [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (05) : 1991 - 1995

[7] CHEMICAL SYNTHESIS AND SEROREACTIVITY OF O-(3,6-DI-O-METHYL-BETA-D-GLUCOPYRANOSYL)-(1-]4)-O-(2,3-DI-O-METHYL-ALPHA-L-RHAMNOPYRANOSYL)-(1-]9)-OXYNONANOYL-BOVINE SERUM-ALBUMIN - THE LEPROSY-SPECIFIC, NATURAL DISACCHARIDE-OCTYL-NEOGLYCOPROTEIN [J]. CARBOHYDRATE RESEARCH, 1986, 156 : 39 - 56

[8] CHEMICAL SYNTHESIS OF THE TRISACCHARIDE UNIT OF THE SPECIES-SPECIFIC PHENOLIC GLYCOLIPID FROM MYCOBACTERIUM-LEPRAE [J]. CARBOHYDRATE RESEARCH, 1987, 163 (01) : 41 - 52

[9] CHEMICAL SYNTHESIS AND SEROLOGY OF DISACCHARIDES AND TRISACCHARIDES OF PHENOLIC GLYCOLIPID ANTIGENS FROM THE LEPROSY BACILLUS AND PREPARATION OF A DISACCHARIDE PROTEIN CONJUGATE FOR SERODIAGNOSIS OF LEPROSY [J]. INFECTION AND IMMUNITY, 1984, 43 (01) : 245 - 252

[10] THE ALLYL GROUP FOR PROTECTION IN CARBOHYDRATE-CHEMISTRY .17. SYNTHESIS OF PROPYL 0-(3,6-DI-0-METHYL-BETA-D-GLUCOPYRANOSYL)-(1-]4)-0-(2,3-DI-0-METHYL-ALPHA-L-RHAMNOPYRANOSYL)-(1-]2)-3-0-METHYL-ALPHA-L-RHAMNOPYRANOSIDE - THE OLIGOSACCHARIDE PORTION OF THE MAJOR SEROLOGICALLY ACTIVE GLYCOLIPID FROM MYCOBACTERIUM-LEPRAEY [J]. CHEMISTRY AND PHYSICS OF LIPIDS, 1985, 38 (03) : 299 - 307

[1] BRENNAN PJ, 1980, INT J LEPROSY, V48, P382

[2] BRETT SJ, 1984, CLIN EXP IMMUNOL, V56, P89

[3] BRETT SJ, 1986, CLIN EXP IMMUNOL, V64, P476

[4] Bührer SS, 1998, AM J TROP MED HYG, V58, P133

[5] Simple dipstick assay for semi-quantitative detection of neopterin in sera [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 2000, 238 (1-2) : 55 - 58

[6] Simple and fast lateral flow test for classification of leprosy patients and identification of contacts with high risk of developing leprosy [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (05) : 1991 - 1995

[7] CHEMICAL SYNTHESIS AND SEROREACTIVITY OF O-(3,6-DI-O-METHYL-BETA-D-GLUCOPYRANOSYL)-(1-]4)-O-(2,3-DI-O-METHYL-ALPHA-L-RHAMNOPYRANOSYL)-(1-]9)-OXYNONANOYL-BOVINE SERUM-ALBUMIN - THE LEPROSY-SPECIFIC, NATURAL DISACCHARIDE-OCTYL-NEOGLYCOPROTEIN [J]. CARBOHYDRATE RESEARCH, 1986, 156 : 39 - 56

[8] CHEMICAL SYNTHESIS OF THE TRISACCHARIDE UNIT OF THE SPECIES-SPECIFIC PHENOLIC GLYCOLIPID FROM MYCOBACTERIUM-LEPRAE [J]. CARBOHYDRATE RESEARCH, 1987, 163 (01) : 41 - 52

[9] CHEMICAL SYNTHESIS AND SEROLOGY OF DISACCHARIDES AND TRISACCHARIDES OF PHENOLIC GLYCOLIPID ANTIGENS FROM THE LEPROSY BACILLUS AND PREPARATION OF A DISACCHARIDE PROTEIN CONJUGATE FOR SERODIAGNOSIS OF LEPROSY [J]. INFECTION AND IMMUNITY, 1984, 43 (01) : 245 - 252

[10] THE ALLYL GROUP FOR PROTECTION IN CARBOHYDRATE-CHEMISTRY .17. SYNTHESIS OF PROPYL 0-(3,6-DI-0-METHYL-BETA-D-GLUCOPYRANOSYL)-(1-]4)-0-(2,3-DI-0-METHYL-ALPHA-L-RHAMNOPYRANOSYL)-(1-]2)-3-0-METHYL-ALPHA-L-RHAMNOPYRANOSIDE - THE OLIGOSACCHARIDE PORTION OF THE MAJOR SEROLOGICALLY ACTIVE GLYCOLIPID FROM MYCOBACTERIUM-LEPRAEY [J]. CHEMISTRY AND PHYSICS OF LIPIDS, 1985, 38 (03) : 299 - 307