Health as a life value of adolescentsTSVETKOVA, I. V.Russian education and society. 2006, Vol 48, Num 8, pp 31-39, issn 1060-9393, 9 p.Article

Interpersonal relations in school = Les relations interpersonnelles à l'écoleALASHEEV, S. Iu; TSVETKOVA, I. V.Russian education and society. 2000, Vol 42, Num 1, pp 7-19, issn 1060-9393Article

Prenatal diagnosis of Sanfilippo a syndrome : Experience in 35 pregnancies at risk and the use of a new fluorogenic substrate for the heparin sulphamidase assayKLEIJER, W. J; KARPOVA, E. A; GEILEN, G. C et al.Prenatal diagnosis. 1996, Vol 16, Num 9, pp 829-835, issn 0197-3851Article

Biochemical study of sialidosis type I in a Russian familyTSVETKOVA, I. V; PETUSHKOVA, N. A; ZOLOTUCHINA, T. V et al.Journal of inherited metabolic disease. 1987, Vol 10, Num 1, pp 18-23, issn 0141-8955Article

The multiple cases of Fabry disease in a Russian family caused by an E341K amino acid substitution in the α-galactosidase ABEYER, E. M; KARPOVA, E. A; UDALOVA, O. V et al.Clinica chimica acta. 1999, Vol 280, Num 1-2, pp 81-89, issn 0009-8981Conference Paper

Phenotypic expression of HA-NA combinations in human-avian influenza A virus reassortantsRUDNEVA, I. A; SKLYANSKAYA, E. I; BARULINA, O. S et al.Archives of virology. 1996, Vol 141, Num 6, pp 1091-1099, issn 0304-8608Article

4-Pentafluoroethylumbelliferyl-β-D-glucoside as a new fluorogenic substrate for acid β-D-glucosidaseTSVETKOVA, I. V; KARPOVA, E. A; DUDUKINA, T. V et al.Clinica chimica acta. 1996, Vol 248, Num 2, pp 125-133, issn 0009-8981Article

A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease C (MPS III C)VOZNYI, YA. V; KARPOVA, E. A; DUDUKINA, T. V et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 2, pp 465-472, issn 0141-8955Conference Paper

A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease type A (MPS IIIA)KARPOVA, E. A; VOZNYI, YA. V; KEULEMANS, J. L. M et al.Journal of inherited metabolic disease. 1996, Vol 19, Num 3, pp 278-285, issn 0141-8955Article

Use of 4-trifluoromethylumbelliferyl-α-L-iduronide as a new substrate for detection of α-L-iduronidase deficiency in human tissues and for rapid prenatal diagnosis of hurler diseaseTSVETKOVA, I. V; KARPOVA, E. A; VOZNI, Y. V et al.Journal of inherited metabolic disease. 1991, Vol 14, Num 2, pp 134-139, issn 0141-8955, 6 p.Article

Prenatal exclusion of metachromatic leukodystrophy by estimation of arylsulphatase A activity in chorion and cultured amniotic fluid cellsTSVETKOVA, I. V; ZOLOTUKHINA, T. V; BAKHAREV, V. A et al.Prenatal diagnosis. 1983, Vol 3, Num 3, pp 233-236, issn 0197-3851Article