Hansikova H - Search Results

1

Complex metabolic disharmony in PMM2-CDG paves the way to new therapeutic approaches.

Himmelreich N, Kikul F, Zdrazilova L, Honzik T, Hecker A, Poschet G, Lüchtenborg C, Brügger B, Strahl S, Bürger F, Okun JG, Hansikova H, Thiel C. Himmelreich N, et al. Among authors: hansikova h. Mol Genet Metab. 2023 Jul;139(3):107610. doi: 10.1016/j.ymgme.2023.107610. Epub 2023 May 16. Mol Genet Metab. 2023. PMID: 37245379

2

[Lactate acidosis in childhood].

Zeman J, Stratilová L, Houst'ková H, Dudková Z, Hansíková H, Konrádová V, Hrubá E, Hoza J, Zeman L. Zeman J, et al. Among authors: hansikova h. Cas Lek Cesk. 1998 Sep 21;137(18):557-60. Cas Lek Cesk. 1998. PMID: 9818465 Czech.

3

Genetic defects of cytochrome c oxidase assembly.

Pecina P, Houstková H, Hansíková H, Zeman J, Houstek J. Pecina P, et al. Among authors: hansikova h. Physiol Res. 2004;53 Suppl 1:S213-23. Physiol Res. 2004. PMID: 15119951 Free article. Review.

4

Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206.

Jesina P, Tesarová M, Fornůsková D, Vojtísková A, Pecina P, Kaplanová V, Hansíková H, Zeman J, Houstek J. Jesina P, et al. Among authors: hansikova h. Biochem J. 2004 Nov 1;383(Pt. 3):561-71. doi: 10.1042/BJ20040407. Biochem J. 2004. PMID: 15265003 Free PMC article.

5

[A new missense mutation of 574C>T in the SURF1 gene--biochemical and molecular genetic study in seven children with Leigh syndrome].

Capková M, Hansíková H, Godinot C, Houst'ková H, Houstĕk J, Zeman J. Capková M, et al. Among authors: hansikova h. Cas Lek Cesk. 2002 Oct 11;141(20):636-41. Cas Lek Cesk. 2002. PMID: 12515039 Czech.

6

Fumaric aciduria: mild phenotype in a 8-year-old girl with novel mutations.

Maradin M, Fumić K, Hansikova H, Tesarova M, Wenchich L, Dorner S, Sarnavka V, Zeman J, Barić I. Maradin M, et al. Among authors: hansikova h. J Inherit Metab Dis. 2006 Oct;29(5):683. doi: 10.1007/s10545-006-0321-0. Epub 2006 Aug 5. J Inherit Metab Dis. 2006. PMID: 16972175

7

[Primary biliary cirrhosis--specific anti-mitochondrial antibodies].

Wenchich L, Krechler T, Horak J, Sedivá A, Bartůnková J, Hansiková H, Martásek P, Zeman J, Svestka T. Wenchich L, et al. Among authors: hansikova h. Vnitr Lek. 2004 Nov;50(11):842-5. Vnitr Lek. 2004. PMID: 15648964 Czech.

8

[Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].

Stratilová L, Zeman J, Hansíková H, Houstĕk J, Hermanská J, Dudková Z, Konrádová V, Hůlková H, Elleder M. Stratilová L, et al. Among authors: hansikova h. Cas Lek Cesk. 1998 Jul 13;137(14):430-3. Cas Lek Cesk. 1998. PMID: 9748738 Czech.

9

[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: hansikova h. Ceska Gynekol. 2000 Jan;65(1):37-42. Ceska Gynekol. 2000. PMID: 10750296 Czech.

10

Abnormalities in succinylpurines in fumarase deficiency: possible role in pathogenesis of CNS impairment.

Zeman J, Krijt J, Stratilová L, Hansíková H, Wenchich L, Kmoch S, Chrastina P, Houstek J. Zeman J, et al. Among authors: hansikova h. J Inherit Metab Dis. 2000 Jun;23(4):371-4. doi: 10.1023/a:1005639516342. J Inherit Metab Dis. 2000. PMID: 10896297 No abstract available.

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