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L Stratilová

Showing results (1-10 of 9) with videos related to

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Casopis Lekaru Ceskych|November 18, 1998
[Lactate acidosis in childhood]J Zeman, L Stratilová, H Houst'ková, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Abnormalities in succinylpurines in fumarase deficiency: possible role in pathogenesis of CNS impairmentJ Zeman, J Krijt, L Stratilová, et al.
Prenatal Diagnosis|July 23, 1999
Complex approach to prenatal diagnosis of cytochrome c oxidase deficienciesJ Houstek, P Klement, J Hermanská, et al.
Casopis Lekaru Ceskych|December 22, 1999
[Leber's hereditary optic neuropathy]V Konrádová, J Zeman, L Stratilová, et al.
Casopis Lekaru Ceskych|September 28, 1998
[Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA]L Stratilová, J Zeman, H Hansíková, et al.
Ceska Gynekologie|April 6, 2000
[Prenatal diagnosis in families with cytochrome C oxidase disorder]H Houst'ková, J Houstĕk, P Klement, et al.
The Biochemical Journal|September 8, 1999
Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position 8344 ntH Antonická, D Floryk, P Klement, 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.
Human Molecular Genetics|September 15, 1999
A novel deficiency of mitochondrial ATPase of nuclear originJ Houstek, P Klement, D Floryk, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Casopis Lekaru Ceskych|November 18, 1998
[Lactate acidosis in childhood]J Zeman, L Stratilová, H Houst'ková, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Abnormalities in succinylpurines in fumarase deficiency: possible role in pathogenesis of CNS impairmentJ Zeman, J Krijt, L Stratilová, et al.
Prenatal Diagnosis|July 23, 1999
Complex approach to prenatal diagnosis of cytochrome c oxidase deficienciesJ Houstek, P Klement, J Hermanská, et al.
Casopis Lekaru Ceskych|December 22, 1999
[Leber's hereditary optic neuropathy]V Konrádová, J Zeman, L Stratilová, et al.
Casopis Lekaru Ceskych|September 28, 1998
[Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA]L Stratilová, J Zeman, H Hansíková, et al.
Ceska Gynekologie|April 6, 2000
[Prenatal diagnosis in families with cytochrome C oxidase disorder]H Houst'ková, J Houstĕk, P Klement, et al.
The Biochemical Journal|September 8, 1999
Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position 8344 ntH Antonická, D Floryk, P Klement, 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.
Human Molecular Genetics|September 15, 1999
A novel deficiency of mitochondrial ATPase of nuclear originJ Houstek, P Klement, D Floryk, et al.
Pageof 1