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Diabetes & Metabolism
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October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis
C Verny, P Amati-Bonneau, F Letournel, et al.
Lancet (London, England)
|
October 6, 1999
Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues
S 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 patients
J 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 America
Chris Kay, Indira Tirado-Hurtado, Mario Cornejo-Olivas, et al.
Biochimie
|
December 14, 2011
Oligomerization paths of the nucleoprotein of influenza A virus
B 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 patients
E 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 Transplantation
S 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 wetlands
K 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 syndrome
A Slama, C Lacroix, V Plante-Bordeneuve, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 143) with videos related to
Sort By:
Page
of 15
Diabetes & Metabolism
|
October 29, 2008
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis
C Verny, P Amati-Bonneau, F Letournel, et al.
Lancet (London, England)
|
October 6, 1999
Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues
S 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 patients
J 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 America
Chris Kay, Indira Tirado-Hurtado, Mario Cornejo-Olivas, et al.
Biochimie
|
December 14, 2011
Oligomerization paths of the nucleoprotein of influenza A virus
B 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 patients
E 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 Transplantation
S 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 wetlands
K 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 syndrome
A Slama, C Lacroix, V Plante-Bordeneuve, et al.
Page
of 15