Molecular defect in a patient with pyridoxine-responsive homocystinuriaKOZICH, V; DE FRANCHIS, R; KRAUS, J. P et al.Human molecular genetics (Print). 1993, Vol 2, Num 6, pp 815-816, issn 0964-6906Article

Light-induced inhomogeneous broadening in dye solution probed by wave-mixing with broadband lasersKOZICH, V; DE S. MENEZES, L; DE ARAUJO, C. B et al.Optics communications. 1999, Vol 171, Num 1-3, pp 125-130, issn 0030-4018Article

Hyperhomocysteinemia in premature arterial disease : examination of cystathionine β-synthase alleles at the molecular levelKOZICH, V; KRAUS, E; DE FRANCHIS, R et al.Human molecular genetics (Print). 1995, Vol 4, Num 4, pp 623-629, issn 0964-6906Article

Molecular basis of cystathionine β-synthase deficiency in pyridoxine responsive and nonresponsive homocystinuriaHU, F. L; GU, Z; KOZICH, V et al.Human molecular genetics (Print). 1993, Vol 2, Num 11, pp 1857-1860, issn 0964-6906Article

Quality of analytical performance in inherited metabolic disorders : the role of ERNDIMFOWLER, B; BURLINA, A; KOZICH, V et al.Journal of inherited metabolic disease. 2008, Vol 31, Num 6, pp 680-689, issn 0141-8955, 10 p.Article

Relaxation of Kerr nonlinearity studied by three-wave mixing of incoherent light beamsVODCHITS, A. I; KOZICH, V. P; KONTSEVOI, B. L et al.Optics and spectroscopy. 1991, Vol 70, Num 4, pp 516-519, issn 0030-400XArticle

Homocystinuria due to cystathionine β-synthase deficiency: Novel biochemical findings and treatment efficacyORENDAC, M; ZEMAN, J; STABLER, S. P et al.Journal of inherited metabolic disease. 2003, Vol 26, Num 8, pp 761-773, issn 0141-8955, 13 p.Article

Very low energy formula diet in the treatment of obesityHAINER, V; KUNESOVA, M; STICH, V et al.International journal of obesity. 1989, Vol 13, pp 185-188, issn 0307-0565, SUP2Conference Paper

Single-mode single-frequency laser with a self-filtering unstable cavityKOZICH, V. P; KLEBCHA, S. M; ORLOVICH, V. A et al.Quantum electronics (Woodbury). 1999, Vol 29, Num 4, pp 334-336, issn 1063-7818Article

Elimination of signal fluctuations in CARS of weak resonances in liquidsAPANASEVICH, P. A; KOZICH, V. P; VODCHITZ, A. I et al.Journal of Raman spectroscopy. 1993, Vol 24, Num 9, pp 597-598, issn 0377-0486Article

Identical genotypes in siblings with different homocystinuric phenotypes: identification of three mutations in cystathionine β-synthase using an improved bacterial expression systemDE FRANCHIS, R; KOZICH, V; MCINNES, R. R et al.Human molecular genetics (Print). 1994, Vol 3, Num 7, pp 1103-1108, issn 0964-6906Article

Broadband correlated noise light fluxes of different frequencies for transient spectroscopy of Kerr nonlinearity in liquidsAPANASEVICH, P. A; VODCHITS, A. I; KOZICH, V. P et al.Optics and spectroscopy. 1993, Vol 74, Num 5, pp 559-563, issn 0030-400XArticle

Methionine-loading test: evaluation of adverse effects and safety in an epidemiological studyKRUPKOVA-MEIXNEROVA, L; VESELA, K; VITOVA, A et al.Clinical nutrition (Edinburgh). 2002, Vol 21, Num 2, pp 151-156, issn 0261-5614Article

CblE type of homocystinuria due to methionine synthase reductase deficiency: Clinical and molecular studies and prenatal diagnosis in two familiesZAVADAKOVA, P; FOWLER, B; ZEMAN, J et al.Journal of inherited metabolic disease. 2002, Vol 25, Num 6, pp 461-476, issn 0141-8955, 16 p.Article

Identification of a mutation cluster in mevalonate kinase deficiency, including a new mutation in a patient of Mennonite ancestryHINSON, D. D; ROSS, R. M; KRISANS, S et al.American journal of human genetics. 1999, Vol 65, Num 2, pp 327-335, issn 0002-9297Article

Accumulation and impaired in vivo metabolism of di- and trihydroxycholestanoic acid in two patientsWANDERS, R. J. A; CASTEELS, M; MANNAERTS, G. P et al.Clinica chimica acta. 1991, Vol 202, Num 3, pp 123-132, issn 0009-8981Article

Three-wave mixing of ∼ nanosecond partially coherent laser beams as a method for measuring short relaxation timesAPANASEVICH, P. A; KOZICH, V. P; VODCHITS, A. I et al.Optika i spektroskopiâ. 1989, Vol 66, Num 4, pp 729-732, issn 0030-4034, 4 p.Article

Time-delayed three-wave mixing of nanosecond incoherent laser beams for measuring short relaxation timesAPANASEVICH, P. A; KOZICH, V. P; VODSCHITZ, A. I et al.Journal of modern optics (Print). 1988, Vol 35, Num 12, pp 1933-1937, issn 0950-0340Article

Developmental programming of growth: Genetic variant in GH2 gene encoding placental growth hormone contributes to adult height determinationTIMASHEVA, Y; PUTKU, M; KIVI, R et al.Placenta (Eastbourne). 2013, Vol 34, Num 11, pp 995-1001, issn 0143-4004, 7 p.Article

Is the common 844ins68 polymorphism in the cystathionine β-synthase gene associated with atherosclerosis ?ORENDAC, M; MUSKOVA, B; RICHTEROVA, E et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 5, pp 674-675, issn 0141-8955Article

The human cystathionine β-synthase (CBS) gene : Complete sequence, alternative splicing, and polymorphismsKRAUS, J. P; OLIVERIUSOVA, J; PACES, V et al.Genomics (San Diego, Calif.). 1998, Vol 52, Num 3, pp 312-324, issn 0888-7543Article

Unusual clinical presentation in two boys with cytochrome c oxidase deficiencyHREBICEK, M; ZEMAN, J; PETRAK, B et al.Journal of inherited metabolic disease. 1992, Vol 15, Num 3, pp 320-322, issn 0141-8955Conference Paper

Ancient origin of the CTH alelle carrying the c.200C > T (p.T67I) variant in patients with cystathioninuriaESPINOS, C; GARCIA-CAZORLA, A; MARTINEZ-RUBIO, D et al.Clinical genetics. 2010, Vol 78, Num 6, pp 554-559, issn 0009-9163, 6 p.Article

Analysis of CBS alleles in Czech and Slovak patients with homocystinuria: Report on three novel mutations E176K, W409X and 1223 + 37 del99KOZICH, V; JANOSIK, M; SOKOLOVA, J et al.Journal of inherited metabolic disease. 1997, Vol 20, Num 3, pp 363-366, issn 0141-8955Conference Paper

Mevalonic aciduriaKOZICH, V; GIBSON, K. M; ZEMAN, J et al.Journal of inherited metabolic disease. 1991, Vol 14, Num 2, pp 265-266, issn 0141-8955, 2 p.Article