Hansíková H - Search Results

1

Generation of two human iPSC lines from dermal fibroblasts of adult- and juvenile-onset Huntington's disease patients and two healthy donors.

Piechota M, Latoszek E, Liszewska E, Hansíková H, Klempíř J, Mühlbäck A, Landwehrmeyer GB, Kuźnicki J, Czeredys M. Piechota M, et al. Among authors: hansikova h. Stem Cell Res. 2023 Sep;71:103194. doi: 10.1016/j.scr.2023.103194. Epub 2023 Aug 25. Stem Cell Res. 2023. PMID: 37651831 Free article.

2

A novel mutation in SURF1 causes skipping of exon 8 in a patient with cytochrome c oxidase-deficient leigh syndrome and hypertrichosis.

Williams SL, Taanman JW, Hansíková H, Houst'ková H, Chowdhury S, Zeman J, Houstek J. Williams SL, et al. Among authors: hansikova h. Mol Genet Metab. 2001 Aug;73(4):340-3. doi: 10.1006/mgme.2001.3206. Mol Genet Metab. 2001. PMID: 11509016

3

[Congenital disorder of type Ia protein glycosylation: clinical, biochemical and molecular characteristics in 2 siblings with cerebellar hypoplasia].

Honzík T, Malonová E, Hansíková H, Rosipal R, Poupĕtová H, Martásek P, Zeman J. Honzík T, et al. Among authors: hansikova h. Cas Lek Cesk. 2003;142(5):276-9. Cas Lek Cesk. 2003. PMID: 12920791 Czech.

4

Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.

Haack TB, Haberberger B, Frisch EM, Wieland T, Iuso A, Gorza M, Strecker V, Graf E, Mayr JA, Herberg U, Hennermann JB, Klopstock T, Kuhn KA, Ahting U, Sperl W, Wilichowski E, Hoffmann GF, Tesarova M, Hansikova H, Zeman J, Plecko B, Zeviani M, Wittig I, Strom TM, Schuelke M, Freisinger P, Meitinger T, Prokisch H. Haack TB, et al. Among authors: hansikova h. J Med Genet. 2012 Apr;49(4):277-83. doi: 10.1136/jmedgenet-2012-100846. J Med Genet. 2012. PMID: 22499348

5

Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes.

Sedivá A, Smith CI, Asplund AC, Hadac J, Janda A, Zeman J, Hansíková H, Dvoráková L, Mrázová L, Velbri S, Koehler C, Roesch K, Sullivan KE, Futatani T, Ochs HD. Sedivá A, et al. Among authors: hansikova h. J Clin Immunol. 2007 Nov;27(6):640-6. doi: 10.1007/s10875-007-9123-x. Epub 2007 Sep 12. J Clin Immunol. 2007. PMID: 17851739

6

[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.

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

[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.

9

[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.

10

An investigation of the metabolism of N-nitrosodimethylamine and N-nitrosomethylaniline by horseradish peroxidase in vitro.

Stiborová M, Hansíková H, Schmeiser HH, Frei E. Stiborová M, et al. Among authors: hansikova h. Gen Physiol Biophys. 1997 Sep;16(3):285-97. Gen Physiol Biophys. 1997. PMID: 9452949

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