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Molecular Genetics and Metabolism
|
March 22, 2003
Impaired mitochondrial pyruvate importation in a patient and a fetus at risk
M Brivet, A Garcia-Cazorla, S Lyonnet, et al.
Mitochondrion
|
May 15, 2009
Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis
F Medja, S Allouche, P Frachon, et al.
Clinical Science (London, England : 1979)
|
November 1, 1992
Carotid arterial haemodynamics after mild degrees of lower-body negative pressure in man
P J Lacolley, B M Pannier, M A Slama, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
April 1, 1995
Nosocomial acquisition of multiresistant Acinetobacter baumannii: risk factors and prognosis
O Lortholary, J Y Fagon, A B Hoi, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
December 1, 1990
[Doppler echocardiographic study of mitral and aortic flow at various rates and atrioventricular intervals in patients with dual chamber pacemakers]
J L Rey, M A Slama, C Tribouilloy, et al.
Annales De Biologie Clinique
|
March 30, 2004
[Antiphospholipid antibodies in 146 women with repeated pregnancy losses]
F Ben Hadj Slama, M Nagara, A Slama, et al.
Molecular Genetics and Metabolism
|
November 3, 2005
Deoxyguanosine kinase mutations and combined deficiencies of the mitochondrial respiratory chain in patients with hepatic involvement
A Slama, I Giurgea, D Debrey, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 9, 2020
Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review
J Chavany, A Cano, B Roquelaure, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 6, 2014
[Mitochondrial neurogastrointestinal encephalopathy disease]
A Benureau, P Meyer, O Maillet, et al.
Molecular Genetics and Metabolism
|
April 28, 2009
The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome
N Brahimi, M Jambou, E Sarzi, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 143) with videos related to
Sort By:
Page
of 15
Molecular Genetics and Metabolism
|
March 22, 2003
Impaired mitochondrial pyruvate importation in a patient and a fetus at risk
M Brivet, A Garcia-Cazorla, S Lyonnet, et al.
Mitochondrion
|
May 15, 2009
Development and implementation of standardized respiratory chain spectrophotometric assays for clinical diagnosis
F Medja, S Allouche, P Frachon, et al.
Clinical Science (London, England : 1979)
|
November 1, 1992
Carotid arterial haemodynamics after mild degrees of lower-body negative pressure in man
P J Lacolley, B M Pannier, M A Slama, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
April 1, 1995
Nosocomial acquisition of multiresistant Acinetobacter baumannii: risk factors and prognosis
O Lortholary, J Y Fagon, A B Hoi, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux
|
December 1, 1990
[Doppler echocardiographic study of mitral and aortic flow at various rates and atrioventricular intervals in patients with dual chamber pacemakers]
J L Rey, M A Slama, C Tribouilloy, et al.
Annales De Biologie Clinique
|
March 30, 2004
[Antiphospholipid antibodies in 146 women with repeated pregnancy losses]
F Ben Hadj Slama, M Nagara, A Slama, et al.
Molecular Genetics and Metabolism
|
November 3, 2005
Deoxyguanosine kinase mutations and combined deficiencies of the mitochondrial respiratory chain in patients with hepatic involvement
A Slama, I Giurgea, D Debrey, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 9, 2020
Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review
J Chavany, A Cano, B Roquelaure, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 6, 2014
[Mitochondrial neurogastrointestinal encephalopathy disease]
A Benureau, P Meyer, O Maillet, et al.
Molecular Genetics and Metabolism
|
April 28, 2009
The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome
N Brahimi, M Jambou, E Sarzi, et al.
Page
of 15