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au.\*:("VOZNYI, YA. V")

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Use of β-maltosides (p-nitrophenyl-β-D-maltoside, 2-chloro-4-nitrophenyl-β-D-maltoside and 4-methylumbelliferyl-β-D-maltoside) as substrates for the assay of neutral α-glucosidase from human kidney and urineLUKOMSKAYA, I. S; VOZNYI, YA. V; LANSKAYA, I. M et al.Clinica chimica acta. 1996, Vol 244, Num 2, pp 145-154, issn 0009-8981Article

A fluorimetric enzyme assay for the diagnosis of MPS II (Hunter disease)VOZNYI, Ya. V; KEULEMANS, J. L. M; VAN DIGGELEN, O. P et al.Journal of inherited metabolic disease. 2001, Vol 24, Num 6, pp 675-680, issn 0141-8955Article

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

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

Prenatal diagnosis of Sanfilippo disease type C using a simple fluorometric enzyme assayWANG HE; VOZNYI, YA. V; HUIJMANS, J. G. M et al.Prenatal diagnosis. 1994, Vol 14, Num 1, pp 17-22, issn 0197-3851Article

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

A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease type D (MPS IIID)WANG HE; VOZNYI, YA. V; BOER, A. M et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 6, pp 935-941, issn 0141-8955Article

Applications of a new fluorimetric enzyme assay for the diagnosis of aspartylglucosaminuriaVOZNYI, YA. V; KEULEMANS, J. L. M; KLEIJER, W. J et al.Journal of inherited metabolic disease. 1993, Vol 16, Num 6, pp 929-934, issn 0141-8955Article

A new fluorimetric enzyme assay for the diagnosis of Niemann-Pick A/B, with specificity of natural sphingomyelinase substrateVAN DIGGELEN, O. P; VOZNYI, Ya. V; KEULEMANS, J. L. M et al.Journal of inherited metabolic disease. 2005, Vol 28, Num 5, pp 733-741, issn 0141-8955, 9 p.Article

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