Showing results (81-90 of 199) with videos related to

Sort By:
Pageof 20
Journal of the Association for Research in Otolaryngology : JARO|March 21, 2022
Vestibulo-Ocular Reflex Short-Term Adaptation Is Halved After Compensation for Unilateral LabyrinthectomySerajul I Khan, Patrick P Hübner, Alan M Brichta, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 22, 2011
The relative burden of haemophilia A and the impact of target joint development on health-related quality of life: results from the ADVATE Post-Authorization Safety Surveillance (PASS) studyR Klamroth, H Pollmann, C Hermans, et al.
Hamostaseologie|February 5, 2003
Haemophilia and thrombophilia. What do we learn about combined inheritance of both genetic variations?U Nowak-Göttl, C Escuriola, K Kurnik, et al.
Archives of Microbiology|September 1, 1996
Molecular analysis of the Rhodobacter capsulatus chaperonin (groESL) operon: purification and characterization of Cpn60P Hübner, G Dame, U Sandmeier, et al.
Molecular Microbiology|June 1, 1990
The Min DNA inversion enzyme of plasmid p15B of Escherichia coli 15T-: a new member of the Din family of site-specific recombinasesS Iida, H Sandmeier, P Hübner, et al.
Plos Neglected Tropical Diseases|April 21, 2026
Efficacy of oxfendazole treatment against infective larvae of Litomosoides sigmodontisFrederic Risch, Lucas J Bergmann, Hannah R Wegner, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
European study on orthopaedic status of haemophilia patients with inhibitorsM Morfini, S Haya, G Tagariello, et al.
Diabetes/Metabolism Research and Reviews|June 30, 2015
Parasitic helminths and their beneficial impact on type 1 and type 2 diabetesAfiat Berbudi, Jesuthas Ajendra, Ajeng P F Wardani, et al.
Molecular & General Genetics : MGG|April 1, 1993
Nucleotide sequence and genetic analysis of the Rhodobacter capsulatus ORF6-nifUI SVW gene region: possible role of NifW in homocitrate processingB Masepohl, S Angermüller, S Hennecke, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 22, 2006
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 geneF H Herrmann, G Auerswald, A Ruiz-Saez, et al.
Pageof 20