|1.||Pecina, Petr: 2 articles (07/2012 - 09/2003)|
|2.||Cížková Vrbacká, Alena: 1 article (07/2012)|
|3.||Kovářová, Nikola: 1 article (07/2012)|
|4.||Kmoch, Stanislav: 1 article (07/2012)|
|5.||Pronicka, Ewa: 1 article (07/2012)|
|6.||Houštěk, Josef: 1 article (07/2012)|
|7.||Stránecký, Viktor: 1 article (07/2012)|
|8.||Ludwig, Bernd: 1 article (06/2012)|
|9.||Hannappel, Achim: 1 article (06/2012)|
|10.||Bundschuh, Freya A: 1 article (06/2012)|
|1.||Leigh Disease (Leigh's Disease)
07/01/2012 - "The loss of Surf1 protein leads to a severe COX deficiency manifested as a fatal neurodegenerative disorder, the Leigh syndrome (LS(COX)). "
09/01/2003 - "Subacute necrotising encephalomyopathy (Leigh syndrome) due to cytochrome c oxidase (COX) deficiency is often caused by mutations in the SURF1 gene, encoding the Surf1 protein essential for COX assembly. "
06/01/2001 - "Although all previously reported mutations in the SURF1 gene have been found in patients with cytochrome oxidase (COX)-deficient Leigh syndrome, the phenotype associated with SURF1 protein deficiency should be extended to include leukodystrophy."
06/01/2012 - "denitrificans Surf1 protein shed some light on this important assembly factor as a heme a binding protein associated with Leigh syndrome in humans. "
|2.||Neurodegenerative Diseases (Neurodegenerative Disease)
|1.||Electron Transport Complex IV (Cytochrome c Oxidase)
|2.||Carrier Proteins (Binding Protein)