Wenchich L - Search Results

1

Inflammatory myopathy associated with statins: report of three cases.

Kuncova K, Sedlackova M, Vencovsky J, Mann H, Tomcik M, Wenchich L, Zamecnik J. Kuncova K, et al. Among authors: wenchich l. Mod Rheumatol. 2014 Mar;24(2):366-71. doi: 10.3109/14397595.2013.852848. Mod Rheumatol. 2014. PMID: 24593216

2

[Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)].

Honzík T, Tesarová M, Hansíková H, Krijt J, Benes P, Zámecník J, Wenchich L, Zeman J. Honzík T, et al. Among authors: wenchich l. Cas Lek Cesk. 2006;145(8):665-70. Cas Lek Cesk. 2006. PMID: 16995425 Czech.

3

[Corneal ulceration complicating surgical correction of ptosis in patient with Kearns-Sayre syndrome--a case report].

Cesneková T, Jurecka T, Skorkovská K, Tesarová M, Hanisková H, Wenchich L, Zámecník J, Zeman J. Cesneková T, et al. Among authors: wenchich l. Cesk Slov Oftalmol. 2011 Oct;67(4):133-5. Cesk Slov Oftalmol. 2011. PMID: 22299522 Czech.

4

Mitochondrial cardiomyopathy--case report.

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

5

The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues.

Fornuskova D, Brantova O, Tesarova M, Stiburek L, Honzik T, Wenchich L, Tietzeova E, Hansikova H, Zeman J. Fornuskova D, et al. Among authors: wenchich l. Biochim Biophys Acta. 2008 May;1782(5):317-25. doi: 10.1016/j.bbadis.2008.02.001. Epub 2008 Feb 15. Biochim Biophys Acta. 2008. PMID: 18319067 Free article.

6

Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates.

Honzik T, Wenchich L, Böhm M, Hansikova H, Pejznochova M, Zapadlo M, Plavka R, Zeman J. Honzik T, et al. Among authors: wenchich l. Early Hum Dev. 2008 Apr;84(4):269-76. doi: 10.1016/j.earlhumdev.2006.07.008. Epub 2007 Aug 14. Early Hum Dev. 2008. PMID: 17698302

7

Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects.

Wenchich L, Drahota Z, Honzík T, Hansíková H, Tesarová M, Zeman J, Houstek J. Wenchich L, et al. Physiol Res. 2003;52(6):781-8. Physiol Res. 2003. PMID: 14640901 Free article.

8

Mitochondrial energy metabolism in very premature neonates.

Wenchich L, Zeman J, Hansíková H, Plavka R, Sperl W, Houstek J. Wenchich L, et al. Biol Neonate. 2002;81(4):229-35. doi: 10.1159/000056753. Biol Neonate. 2002. PMID: 12011566

9

Two patients with clinically distinct manifestation of pyruvate dehydrogenase deficiency due to mutations in PDHA1 gene.

Magner M, Vinšová K, Tesařová M, Hájková Z, Hansíková H, Wenchich L, Ješina P, Smolka V, Adam T, Vaněčková M, Zeman J, Honzík T. Magner M, et al. Among authors: wenchich l. Prague Med Rep. 2011;112(1):18-28. Prague Med Rep. 2011. PMID: 21470495

10

[Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome].

Capková M, Tesarová M, Wenchich L, Cerná L, Hansíková H, Hůlková H, Hrubá E, Elleder M, Zeman J. Capková M, et al. Among authors: wenchich l. Cas Lek Cesk. 2002 Feb 1;141(2):51-4. Cas Lek Cesk. 2002. PMID: 11925663 Czech.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

29 results

Search Page

Filters