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A Slama

Showing results (131-140 of 143) with videos related to

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Diabetes & Metabolism|October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitisC Verny, P Amati-Bonneau, F Letournel, et al.
Lancet (London, England)|October 6, 1999
Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analoguesS Blanche, M Tardieu, P Rustin, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
Recognition and management of fatty acid oxidation defects: a series of 107 patientsJ M Saudubray, D Martin, P de Lonlay, et al.
European Journal of Human Genetics : EJHG|December 22, 2016
The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin AmericaChris Kay, Indira Tirado-Hurtado, Mario Cornejo-Olivas, et al.
Biochimie|December 14, 2011
Oligomerization paths of the nucleoprotein of influenza A virusB Tarus, O Bakowiez, S Chenavas, et al.
La Tunisie Medicale|December 1, 1996
[Primary antiphospholipid syndrome in obstetrics. Apropos of 4 cases with fetal survival]K Monastiri, A Chaieb, H Skouri, et al.
Molecular Genetics and Metabolism|August 15, 2017
Impact of mutations within the [Fe-S] cluster or the lipoic acid biosynthesis pathways on mitochondrial protein expression profiles in fibroblasts from patientsE Lebigot, P Gaignard, I Dorboz, et al.
International Journal of Organ Transplantation Medicine|January 13, 2017
The First Experience of <i>Ex-Vivo</i> Lung Perfusion (EVLP) in Iran: An Effective Method to Increase Suitable Lung for TransplantationS Shafaghi, K Najafizadeh, K Sheikhy, et al.
Ecological Applications : a Publication of the Ecological Society of America|August 24, 2013
Food web structure in oil sands reclaimed wetlandsK E Kovalenko, J J H Ciborowski, C Daly, et al.
Molecular Genetics and Metabolism|March 23, 2005
Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndromeA Slama, C Lacroix, V Plante-Bordeneuve, et al.
Pageof 15

Showing results (131-140 of 143) with videos related to

Sort By:
Pageof 15
Diabetes & Metabolism|October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitisC Verny, P Amati-Bonneau, F Letournel, et al.
Lancet (London, England)|October 6, 1999
Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analoguesS Blanche, M Tardieu, P Rustin, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
Recognition and management of fatty acid oxidation defects: a series of 107 patientsJ M Saudubray, D Martin, P de Lonlay, et al.
European Journal of Human Genetics : EJHG|December 22, 2016
The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin AmericaChris Kay, Indira Tirado-Hurtado, Mario Cornejo-Olivas, et al.
Biochimie|December 14, 2011
Oligomerization paths of the nucleoprotein of influenza A virusB Tarus, O Bakowiez, S Chenavas, et al.
La Tunisie Medicale|December 1, 1996
[Primary antiphospholipid syndrome in obstetrics. Apropos of 4 cases with fetal survival]K Monastiri, A Chaieb, H Skouri, et al.
Molecular Genetics and Metabolism|August 15, 2017
Impact of mutations within the [Fe-S] cluster or the lipoic acid biosynthesis pathways on mitochondrial protein expression profiles in fibroblasts from patientsE Lebigot, P Gaignard, I Dorboz, et al.
International Journal of Organ Transplantation Medicine|January 13, 2017
The First Experience of <i>Ex-Vivo</i> Lung Perfusion (EVLP) in Iran: An Effective Method to Increase Suitable Lung for TransplantationS Shafaghi, K Najafizadeh, K Sheikhy, et al.
Ecological Applications : a Publication of the Ecological Society of America|August 24, 2013
Food web structure in oil sands reclaimed wetlandsK E Kovalenko, J J H Ciborowski, C Daly, et al.
Molecular Genetics and Metabolism|March 23, 2005
Thymidine phosphorylase gene mutations in patients with mitochondrial neurogastrointestinal encephalomyopathy syndromeA Slama, C Lacroix, V Plante-Bordeneuve, et al.
Pageof 15