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V Kozich

Showing results (31-40 of 50) with videos related to

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Casopis Lekaru Ceskych|May 8, 2001
[Clinical picture of homocystinuria with cystathionine beta-synthase deficiency in 19 Czech and Slovak patients]M Orendác, V Kozich, J Zeman, et al.
Casopis Lekaru Ceskych|January 17, 1996
[Maternal hyperphenylalaninemia in a population of healty Czech women. 18 years' experience with mass screening, diet therapy and metabolic monitoring]J Hyánek, J Bendl, J Zeman, et al.
International Journal of Obesity|January 1, 1989
Very low energy formula diet in the treatment of obesityV Hainer, M Kunesová, V Stich, et al.
Human Molecular Genetics|October 1, 1993
Human cystathionine beta-synthase cDNA: sequence, alternative splicing and expression in cultured cellsJ P Kraus, K Le, M Swaroop, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Unusual clinical presentation in two boys with cytochrome c oxidase deficiencyM Hrebícek, J Zeman, B Petrák, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Mevalonic aciduriaV Kozich, K M Gibson, J Zeman, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
Is the common 844ins68 polymorphism in the cystathionine beta-synthase gene associated with atherosclerosis?M Orendác, B Musková, E Richterová, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1991
Accumulation and impaired in vivo metabolism of di- and trihydroxycholestanoic acid in two patientsR J Wanders, M Casteels, G P Mannaerts, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
CblE type of homocystinuria: mild clinical phenotype in two patients homozygous for a novel mutation in the MTRR geneM A Vilaseca, L Vilarinho, P Zavadakova, et al.
Casopis Lekaru Ceskych|September 2, 1983
[Isovaleric aciduria]J Hyánek, M Zapadlo, J Zeman, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
Casopis Lekaru Ceskych|May 8, 2001
[Clinical picture of homocystinuria with cystathionine beta-synthase deficiency in 19 Czech and Slovak patients]M Orendác, V Kozich, J Zeman, et al.
Casopis Lekaru Ceskych|January 17, 1996
[Maternal hyperphenylalaninemia in a population of healty Czech women. 18 years' experience with mass screening, diet therapy and metabolic monitoring]J Hyánek, J Bendl, J Zeman, et al.
International Journal of Obesity|January 1, 1989
Very low energy formula diet in the treatment of obesityV Hainer, M Kunesová, V Stich, et al.
Human Molecular Genetics|October 1, 1993
Human cystathionine beta-synthase cDNA: sequence, alternative splicing and expression in cultured cellsJ P Kraus, K Le, M Swaroop, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Unusual clinical presentation in two boys with cytochrome c oxidase deficiencyM Hrebícek, J Zeman, B Petrák, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Mevalonic aciduriaV Kozich, K M Gibson, J Zeman, et al.
Journal of Inherited Metabolic Disease|July 10, 1999
Is the common 844ins68 polymorphism in the cystathionine beta-synthase gene associated with atherosclerosis?M Orendác, B Musková, E Richterová, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1991
Accumulation and impaired in vivo metabolism of di- and trihydroxycholestanoic acid in two patientsR J Wanders, M Casteels, G P Mannaerts, et al.
Journal of Inherited Metabolic Disease|September 16, 2003
CblE type of homocystinuria: mild clinical phenotype in two patients homozygous for a novel mutation in the MTRR geneM A Vilaseca, L Vilarinho, P Zavadakova, et al.
Casopis Lekaru Ceskych|September 2, 1983
[Isovaleric aciduria]J Hyánek, M Zapadlo, J Zeman, et al.
Pageof 5