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Journal of the European Academy of Dermatology and Venereology : JEADV|February 1, 2020
Association between clinical specialty setting and disease management in patients with psoriatic arthritis: results from LOOP, a cross-sectional, multi-country, observational studyW H Boehncke, R Horváth, E Dalkiliç, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 20, 2005
Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA)R Horváth, A Abicht, E Holinski-Feder, et al.
Virology|July 11, 1998
The polyvalent staphylococcal phage phi 812: its host-range mutants and related phagesR Pantůcek, A Rosypalová, J Doskar, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
Two families with autosomal dominant progressive external ophthalmoplegiaS Kiechl, R Horváth, P Luoma, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Congenital cataract, muscular hypotonia, developmental delay and sensorineural hearing loss associated with a defect in copper metabolismR Horváth, P Freisinger, R Rubio, et al.
Epidemiologie, Mikrobiologie, Imunologie : Casopis Spolecnosti Pro Epidemiologii a Mikrobiologii Ceske Lekarske Spolecnosti J.E. Purkyne|October 8, 2010
[The use of molecular genetics techniques in clinical microbiology--final report from the workshop of the Molecular Microbiology Working Group TIDE]J Hrabák, M Buncek, M Dendis, et al.
Neurology|October 26, 1999
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic originA Abicht, R Stucka, V Karcagi, et al.
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