Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Hlavatá

Showing results (1-10 of 6) with videos related to

Pageof 1
Sort By:
Ceskoslovenska Pediatrie|October 1, 1990
[Bronchiectasis in Recklinghausen's disease]A Kapellerová, A Hlavatá, P Boruta
Bratislavske Lekarske Listy|January 1, 1997
[Peroxisomal hereditary diseases]J Chandoga, M Tomková, A Hlavatá
Casopis Lekaru Ceskych|October 31, 2002
[Variation in manifestations of heteroplasmic mtDNA mutation 8993 T>G in two families]M Tesarová, H Hansíková, A Hlavatá, et al.
Physiological Research|February 12, 2015
Increased plasma levels of the high mobility group box 1 protein (HMGB1) are associated with a higher score of gastrointestinal dysfunction in individuals with autismK Babinská, M Bucová, V Ďurmanová, et al.
Neoplasma|October 3, 2006
Assay design and optimization of mutant-enriched PCR based method for detection of K-ras gene mutations in pancreatic carcinomaJ Ugorcáková, T Hlavatý, P Babál, et al.
Annals of Human Genetics|November 27, 2015
New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype CorrelationsM Čizmárová, K Hlinková, S Bertok, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Ceskoslovenska Pediatrie|October 1, 1990
[Bronchiectasis in Recklinghausen's disease]A Kapellerová, A Hlavatá, P Boruta
Bratislavske Lekarske Listy|January 1, 1997
[Peroxisomal hereditary diseases]J Chandoga, M Tomková, A Hlavatá
Casopis Lekaru Ceskych|October 31, 2002
[Variation in manifestations of heteroplasmic mtDNA mutation 8993 T>G in two families]M Tesarová, H Hansíková, A Hlavatá, et al.
Physiological Research|February 12, 2015
Increased plasma levels of the high mobility group box 1 protein (HMGB1) are associated with a higher score of gastrointestinal dysfunction in individuals with autismK Babinská, M Bucová, V Ďurmanová, et al.
Neoplasma|October 3, 2006
Assay design and optimization of mutant-enriched PCR based method for detection of K-ras gene mutations in pancreatic carcinomaJ Ugorcáková, T Hlavatý, P Babál, et al.
Annals of Human Genetics|November 27, 2015
New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype CorrelationsM Čizmárová, K Hlinková, S Bertok, et al.
Pageof 1