T Puttemans|E Agneessens|J Mathieu - JoVE Visualize

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Annales Pharmaceutiques Francaises|January 1, 1996

[Oxidative stress and apoptosis]J Mathieu, Y Chancerelle, F Hérodin, et al.

The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1989

Myotonic dystrophy: linkage with apolipoprotein E and estimation of the gene carrier status with genetic markersM C Thibault, J Mathieu, S Moorjani, et al.

Journal of Hematotherapy & Stem Cell Research|January 14, 2000

Interleukine-8 acts as a strong peripheral blood granulocyte-recruiting agent rather than as a hematopoietic progenitor cell-mobilizing factorJ Vetillard, M Drouet, T M Neildez-Nguyen, et al.

Pharmaceutical Research|December 1, 1995

Intra- and inter-subject variabilities of CGP 33101 after replicate single oral doses of two 200-mg tablets and 400-mg suspensionW K Cheung, F Kianifard, A Wong, et al.

Journal of Biomaterials Science. Polymer Edition|January 1, 1995

Effect of toluene extraction on Biomer surface: I. ESCA, ATR/FTIR, contact angle analysis and biological propertiesN Nurdin, P François, A Magnani, et al.

Neuromuscular Disorders : NMD|November 26, 1998

Autosomal recessive spastic ataxia of Charlevoix-SaguenayJ P Bouchard, A Richter, J Mathieu, et al.

Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1990

Utility of short-latency evoked potentials in the classification of progressive, early onset cerebellar ataxiasM Vanasse, J Y Gabet, J De Léan, et al.

Human & Experimental Toxicology|June 16, 2010

Cutaneous challenge with chemical warfare agents in the SKH-1 hairless mouse. (I) Development of a model for screening studies in skin decontamination and protectionF Dorandeu, L Taysse, I Boudry, et al.

Human Molecular Genetics|March 1, 1994

Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian populationL R Simard, G Prescott, C Rochette, et al.

Human Genetics|July 29, 2000

The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody diseaseA Odermatt, K Barton, V K Khanna, et al.

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Showing results (111-120 of 161) with videos related to

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Annales Pharmaceutiques Francaises|January 1, 1996

[Oxidative stress and apoptosis]J Mathieu, Y Chancerelle, F Hérodin, et al.

The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1989

Myotonic dystrophy: linkage with apolipoprotein E and estimation of the gene carrier status with genetic markersM C Thibault, J Mathieu, S Moorjani, et al.

Journal of Hematotherapy & Stem Cell Research|January 14, 2000

Interleukine-8 acts as a strong peripheral blood granulocyte-recruiting agent rather than as a hematopoietic progenitor cell-mobilizing factorJ Vetillard, M Drouet, T M Neildez-Nguyen, et al.

Pharmaceutical Research|December 1, 1995

Intra- and inter-subject variabilities of CGP 33101 after replicate single oral doses of two 200-mg tablets and 400-mg suspensionW K Cheung, F Kianifard, A Wong, et al.

Journal of Biomaterials Science. Polymer Edition|January 1, 1995

Effect of toluene extraction on Biomer surface: I. ESCA, ATR/FTIR, contact angle analysis and biological propertiesN Nurdin, P François, A Magnani, et al.

Neuromuscular Disorders : NMD|November 26, 1998

Autosomal recessive spastic ataxia of Charlevoix-SaguenayJ P Bouchard, A Richter, J Mathieu, et al.

Electroencephalography and Clinical Neurophysiology. Supplement|January 1, 1990

Utility of short-latency evoked potentials in the classification of progressive, early onset cerebellar ataxiasM Vanasse, J Y Gabet, J De Léan, et al.

Human & Experimental Toxicology|June 16, 2010

Cutaneous challenge with chemical warfare agents in the SKH-1 hairless mouse. (I) Development of a model for screening studies in skin decontamination and protectionF Dorandeu, L Taysse, I Boudry, et al.

Human Molecular Genetics|March 1, 1994

Linkage disequilibrium analysis of childhood-onset spinal muscular atrophy (SMA) in the French-Canadian populationL R Simard, G Prescott, C Rochette, et al.

Human Genetics|July 29, 2000

The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody diseaseA Odermatt, K Barton, V K Khanna, et al.

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