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Genetic defects of cytochrome c oxidase assembly.
Pecina P, Houstková H, Hansíková H, Zeman J, Houstek J. Pecina P, et al. Among authors: zeman j. Physiol Res. 2004;53 Suppl 1:S213-23. Physiol Res. 2004. PMID: 15119951 Review.
Unusual clinical presentation in two boys with cytochrome c oxidase deficiency.
Hrebícek M, Zeman J, Petrák B, Kozich V, Hyánek J, Ruiter JP, Wanders RJ, Wijburg FA. Hrebícek M, et al. Among authors: zeman j. J Inherit Metab Dis. 1992;15(3):320-2. doi: 10.1007/BF02435966. J Inherit Metab Dis. 1992. PMID: 1357227 No abstract available.
Altered properties of mitochondrial ATP-synthase in patients with a T-->G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA.
Houstĕk J, Klement P, Hermanská J, Houstková H, Hansíková H, Van den Bogert C, Zeman J. Houstĕk J, et al. Among authors: zeman j. Biochim Biophys Acta. 1995 Jun 9;1271(2-3):349-57. doi: 10.1016/0925-4439(95)00063-a. Biochim Biophys Acta. 1995. PMID: 7605802
Different restriction fragment pattern of mtDNA indicative of generalized 8993 point mutations in a boy with lactic acidosis.
Klement P, Zeman J, Hansikova H, Houstkova H, Baudysova M, Houstek J. Klement P, et al. Among authors: zeman j. J Inherit Metab Dis. 1994;17(2):249-50. doi: 10.1007/BF00711630. J Inherit Metab Dis. 1994. PMID: 7967485 No abstract available.
Deficiency of pyruvate dehydrogenase complex in tissues of an eight month old infant.
Hansikova H, Zeman J, Klement P, Technikova-Dobrova Z, Houstkova H, Houstek J, Papa S. Hansikova H, et al. Among authors: zeman j. Biochem Mol Biol Int. 1993 Dec;31(6):1157-66. Biochem Mol Biol Int. 1993. PMID: 8193600
Complex approach to prenatal diagnosis of cytochrome c oxidase deficiencies.
Houstek J, Klement P, Hermanská J, Antonická H, Houstková H, Stratilová L, Wanders RJ, Zeman J. Houstek J, et al. Among authors: zeman j. Prenat Diagn. 1999 Jun;19(6):552-8. doi: 10.1002/(sici)1097-0223(199906)19:6<552::aid-pd588>3.0.co;2-c. Prenat Diagn. 1999. PMID: 10416972
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 nt.
Antonická H, Floryk D, Klement P, Stratilová L, Hermanská J, Houstková H, Kalous M, Drahota Z, Zeman J, Houstek J. Antonická H, et al. Among authors: zeman j. Biochem J. 1999 Sep 15;342 Pt 3(Pt 3):537-44. Biochem J. 1999. PMID: 10477264 Free PMC article.
A novel deficiency of mitochondrial ATPase of nuclear origin.
Houstek J, Klement P, Floryk D, Antonická H, Hermanská J, Kalous M, Hansíková H, Hout'ková H, Chowdhury SK, Rosipal T, Kmoch S, Stratilová L, Zeman J. Houstek J, et al. Among authors: zeman j. Hum Mol Genet. 1999 Oct;8(11):1967-74. doi: 10.1093/hmg/8.11.1967. Hum Mol Genet. 1999. PMID: 10484764
[Prenatal diagnosis in families with cytochrome C oxidase disorder].
Houst'ková H, Houstĕk J, Klement P, Stratilová L, Antonická H, Hansíková H, Hermanská J, Hrebícek M, Macek M, Zeman J. Houst'ková H, et al. Among authors: zeman j. Ceska Gynekol. 2000 Jan;65(1):37-42. Ceska Gynekol. 2000. PMID: 10750296 Czech.
Mitochondrial energy metabolism in very premature neonates.
Wenchich L, Zeman J, Hansíková H, Plavka R, Sperl W, Houstek J. Wenchich L, et al. Among authors: zeman j. Biol Neonate. 2002;81(4):229-35. doi: 10.1159/000056753. Biol Neonate. 2002. PMID: 12011566
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