Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Acta Neuropathologica|April 1, 1997
Follow-up study of subunit c of mitochondrial ATP synthase (SCMAS) in Batten disease and in unrelated lysosomal disordersM Elleder, J Sokolová, M Hrebícek
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|December 21, 2022
ASSESSMENT OF CORNEAL ENDOTHELIAL LAYER IN CONTACT LENS WEARERS WITH THE AID OF AN ENDOTHELIAL MICROSCOPEP Veselý, P Beneš, J Sokolová Šidlová, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|May 28, 2014
[Microperimetry in the wet form of age - related macular degeneration (ARMD)]J Sokolová Šidlová, S Synek, E Zampachová, et al.
Ceska a Slovenska Oftalmologie : Casopis Ceske Oftalmologicke Spolecnosti a Slovenske Oftalmologicke Spolecnosti|June 12, 2012
[Incidence of refractive errors with corrective aids subsequent selection]P Benes, S Synek, S Petrová, et al.
Human Mutation|December 19, 2001
Cystathionine beta-synthase deficiency in Central Europe: discrepancy between biochemical and molecular genetic screening for homocystinuric allelesJ Sokolová, B Janosíková, J D Terwilliger, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 1, 1996
Comparison of the 5' end of the rat and mouse cystathionine beta-synthase genesM D Roper, J R Straubhaar, E Kraus, et al.
American Journal of Human Genetics|May 19, 2001
Impaired heme binding and aggregation of mutant cystathionine beta-synthase subunits in homocystinuriaM Janosík, J Oliveriusová, B Janosíková, et al.
Virchows Archiv : an International Journal of Pathology|November 1, 1996
A case of type I Gaucher disease with cardiopulmonary amyloidosis and chitotriosidase deficiencyM Hrebícek, J Zeman, J Musilová, et al.
Genomics|October 29, 1998
The human cystathionine beta-synthase (CBS) gene: complete sequence, alternative splicing, and polymorphismsJ P Kraus, J Oliveriusová, J Sokolová, et al.
Physiological Research|August 17, 2018
Dissecting the role of Folr1 and Folh1 genes in the pathogenesis of metabolic syndrome in spontaneously hypertensive ratsJ Šilhavý, J Krijt, J Sokolová, et al.
Pageof 2