Hansíková H - Search Results

1

Novel mutations in the TAZ gene in patients with Barth syndrome.

Mazurová S, Tesařová M, Magner M, Houšťková H, Hansíková H, Augustínová J, Tomek V, Vondráčková A, Zeman J, Honzík T. Mazurová S, et al. Among authors: hansikova h. Prague Med Rep. 2013;114(3):139-53. doi: 10.14712/23362936.2014.16. Prague Med Rep. 2013. PMID: 24093814

2

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: hansikova h. 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 Free article.

3

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: hansikova h. J Inherit Metab Dis. 1994;17(2):249-50. doi: 10.1007/BF00711630. J Inherit Metab Dis. 1994. PMID: 7967485 No abstract available.

4

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. Biochem Mol Biol Int. 1993 Dec;31(6):1157-66. Biochem Mol Biol Int. 1993. PMID: 8193600

5

[Metabolic study in a child with Leigh's syndrome and deficient activity in complex I of the respiratory chain].

Zeman J, Klement P, Houst'ková H, Hrebícek M, Hansíková H, Richterová I, Velenská Z, Houstĕk J. Zeman J, et al. Among authors: hansikova h. Cesk Pediatr. 1993 Oct;48(10):586-9. Cesk Pediatr. 1993. PMID: 8269530 Czech.

6

[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.

7

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: hansikova h. Hum Mol Genet. 1999 Oct;8(11):1967-74. doi: 10.1093/hmg/8.11.1967. Hum Mol Genet. 1999. PMID: 10484764

8

[Various manifestations of the A8344G mtDNA heteroplasmic mutation in 4 families with the MERRF syndrome].

Stratilová L, Zeman J, Houst'ková H, Hansíková H, Konrádová V, Hůlková H, Elleder M, Růzicka E, Tyl D, Hrubá E, Houstĕk J. Stratilová L, et al. Among authors: hansikova h. Cas Lek Cesk. 1999 Jun 28;138(13):401-5. Cas Lek Cesk. 1999. PMID: 10566210 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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