Hansikova H - Search Results

1

TMEM70 deficiency: long-term outcome of 48 patients.

Magner M, Dvorakova V, Tesarova M, Mazurova S, Hansikova H, Zahorec M, Brennerova K, Bzduch V, Spiegel R, Horovitz Y, Mandel H, Eminoğlu FT, Mayr JA, Koch J, Martinelli D, Bertini E, Konstantopoulou V, Smet J, Rahman S, Broomfield A, Stojanović V, Dionisi-Vici C, van Coster R, Morava E, Sperl W, Zeman J, Honzik T. Magner M, et al. Among authors: hansikova h. J Inherit Metab Dis. 2015 May;38(3):417-26. doi: 10.1007/s10545-014-9774-8. Epub 2014 Oct 18. J Inherit Metab Dis. 2015. PMID: 25326274

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

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

6

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.

7

Novel mutations in a boy with dihydrolipoamide dehydrogenase deficiency.

Cerna L, Wenchich L, Hansiková H, Kmoch S, Peskova K, Chrastina P, Brynda J, Zeman J. Cerna L, et al. Among authors: hansikova h. Med Sci Monit. 2001 Nov-Dec;7(6):1319-25. Med Sci Monit. 2001. PMID: 11687750

8

Mitochondrial cardiomyopathy--case report.

Steiner I, Zeman J, Spacek J, Hansíková H, Wenchich L. Steiner I, et al. Among authors: hansikova h. Cesk Patol. 2002 Jan;38(1):41-5. Cesk Patol. 2002. PMID: 11933462

9

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: hansikova h. Biol Neonate. 2002;81(4):229-35. doi: 10.1159/000056753. Biol Neonate. 2002. PMID: 12011566

10

Activities of cytochrome c oxidase and citrate synthase in lymphocytes of obese and normal-weight subjects.

Capková M, Houstek J, Hansíková H, Hainer V, Kunesová M, Zeman J. Capková M, et al. Among authors: hansikova h. Int J Obes Relat Metab Disord. 2002 Aug;26(8):1110-7. doi: 10.1038/sj.ijo.0802055. Int J Obes Relat Metab Disord. 2002. PMID: 12119577

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