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J Zeman

Showing results (281-290 of 311) with videos related to

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Ultrastructural Pathology|July 28, 2015
Analysis of Mitochondrial Network Morphology in Cultured Myoblasts from Patients with Mitochondrial DisordersJ Sládková, J Spáčilová, M Čapek, 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.
Science (New York, N.Y.)|November 17, 2022
Mechanical nanolattices printed using nanocluster-based photoresistsQi Li, John Kulikowski, David Doan, et al.
Casopis Lekaru Ceskych|September 2, 1983
[Isovaleric aciduria]J Hyánek, M Zapadlo, J Zeman, et al.
Folia Biologica|April 12, 2015
Lipoprotein lipase deficiency: clinical, biochemical and molecular characteristics in three patients with novel mutations in the LPL geneH Kolářová, M Tesařová, Š Švecová, et al.
Bratislavske Lekarske Listy|April 12, 2000
[Leber's hereditary optic nerve neuropathy]J Michalik, E Kurca, M Drobny, et al.
Casopis Lekaru Ceskych|November 24, 1999
[Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome]L Stratilová, J Zeman, H Houst'ková, et al.
Molecular Genetics and Metabolism|August 3, 2010
Oligodendroglia from ADSL-deficient patient produce SAICAribotide and SAMPL Zídková, J Krijt, J Sládková, et al.
Journal of Inherited Metabolic Disease|January 24, 2004
Homocystinuria due to cystathionine beta-synthase deficiency: novel biochemical findings and treatment efficacyM Orendác, J Zeman, S P Stabler, et al.
Clinical Genetics|January 3, 2013
Ornithine carbamoyltransferase deficiency: molecular characterization of 29 familiesG Storkanova, H Vlaskova, N Chuzhanova, et al.
Pageof 32

Showing results (281-290 of 311) with videos related to

Sort By:
Pageof 32
Ultrastructural Pathology|July 28, 2015
Analysis of Mitochondrial Network Morphology in Cultured Myoblasts from Patients with Mitochondrial DisordersJ Sládková, J Spáčilová, M Čapek, 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.
Science (New York, N.Y.)|November 17, 2022
Mechanical nanolattices printed using nanocluster-based photoresistsQi Li, John Kulikowski, David Doan, et al.
Casopis Lekaru Ceskych|September 2, 1983
[Isovaleric aciduria]J Hyánek, M Zapadlo, J Zeman, et al.
Folia Biologica|April 12, 2015
Lipoprotein lipase deficiency: clinical, biochemical and molecular characteristics in three patients with novel mutations in the LPL geneH Kolářová, M Tesařová, Š Švecová, et al.
Bratislavske Lekarske Listy|April 12, 2000
[Leber's hereditary optic nerve neuropathy]J Michalik, E Kurca, M Drobny, et al.
Casopis Lekaru Ceskych|November 24, 1999
[Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome]L Stratilová, J Zeman, H Houst'ková, et al.
Molecular Genetics and Metabolism|August 3, 2010
Oligodendroglia from ADSL-deficient patient produce SAICAribotide and SAMPL Zídková, J Krijt, J Sládková, et al.
Journal of Inherited Metabolic Disease|January 24, 2004
Homocystinuria due to cystathionine beta-synthase deficiency: novel biochemical findings and treatment efficacyM Orendác, J Zeman, S P Stabler, et al.
Clinical Genetics|January 3, 2013
Ornithine carbamoyltransferase deficiency: molecular characterization of 29 familiesG Storkanova, H Vlaskova, N Chuzhanova, et al.
Pageof 32