Hansikova H - Search Results

1

Elevated oxysterol and N-palmitoyl-O-phosphocholineserine levels in congenital disorders of glycosylation.

Dang Do AN, Chang IJ, Jiang X, Wolfe LA, Ng BG, Lam C, Schnur RE, Allis K, Hansikova H, Ondruskova N, O'Connor SD, Sanchez-Valle A, Vollo A, Wang RY, Wolfenson Z, Perreault J, Ory DS, Freeze HH, Merritt JL, Porter FD. Dang Do AN, et al. Among authors: hansikova h. J Inherit Metab Dis. 2023 Mar;46(2):326-334. doi: 10.1002/jimd.12595. Epub 2023 Feb 3. J Inherit Metab Dis. 2023. PMID: 36719165 Free PMC article.

2

[Variation in manifestations of heteroplasmic mtDNA mutation 8993 T>G in two families].

Tesarová M, Hansíková H, Hlavatá A, Klement P, Houst'ková H, Houstĕk J, Zeman J. Tesarová M, et al. Among authors: hansikova h. Cas Lek Cesk. 2002 Aug 30;141(17):551-4. Cas Lek Cesk. 2002. PMID: 12404959 Czech.

3

Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family.

Kaplanová V, Zeman J, Hansíková H, Cerná L, Houst'ková H, Misovicová N, Houstek J. Kaplanová V, et al. Among authors: hansikova h. J Neurol Sci. 2004 Aug 30;223(2):149-55. doi: 10.1016/j.jns.2004.05.001. J Neurol Sci. 2004. PMID: 15337616

4

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

5

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

6

[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.

7

Metabolism of carcinogenic N-nitroso-N-methylaniline by purified cytochromes P450 2B1 and P450 2B2.

Stiborová M, Hansíková H, Frei E. Stiborová M, et al. Among authors: hansikova h. Cancer Lett. 1996 Dec 20;110(1-2):11-7. doi: 10.1016/s0304-3835(97)89405-0. Cancer Lett. 1996. PMID: 9018075

8

[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.

9

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

10

[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.

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