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W Marques

Showing results (41-50 of 45) with videos related to

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Veterinary Medicine International|June 23, 2020
Conventional Echocardiography and Two-Dimensional Speckle Tracking in Healthy Sevoflurane-Anesthetized Dogs Undergoing Continuous Rate Infusion of NalbuphineMarcel G Marques, Ana Elisa G W Marques, Carlos E de Siqueira, et al.
Veterinary and Animal Science|October 29, 2020
Lidocaine administered at a continuous rate infusion does not impair left ventricular systolic and diastolic function of healthy rabbits sedated with midazolamA E G W Marques, M G Marques, B C R Silveira, et al.
European Journal of Neurology|June 1, 2017
Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and BrazilT C Gheno, G V Furtado, J A M Saute, et al.
Neurology|November 12, 2003
Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variantR Walz, R M R P S Castro, T R Velasco, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Veterinary Medicine International|June 23, 2020
Conventional Echocardiography and Two-Dimensional Speckle Tracking in Healthy Sevoflurane-Anesthetized Dogs Undergoing Continuous Rate Infusion of NalbuphineMarcel G Marques, Ana Elisa G W Marques, Carlos E de Siqueira, et al.
Veterinary and Animal Science|October 29, 2020
Lidocaine administered at a continuous rate infusion does not impair left ventricular systolic and diastolic function of healthy rabbits sedated with midazolamA E G W Marques, M G Marques, B C R Silveira, et al.
European Journal of Neurology|June 1, 2017
Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and BrazilT C Gheno, G V Furtado, J A M Saute, et al.
Neurology|November 12, 2003
Surgical outcome in mesial temporal sclerosis correlates with prion protein gene variantR Walz, R M R P S Castro, T R Velasco, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Pageof 5