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Neuromuscular Disorders : NMD
|
March 27, 1999
Clinical heterogeneity associated with mitochondrial DNA depletion in muscle
Y Campos, M A Martín, T García-Silva, et al.
Journal of the Neurological Sciences
|
April 30, 1998
Cerebrospinal fluid carnitine levels in patients with Alzheimer's disease
J C Rubio, F de Bustos, J A Molina, et al.
Neurology
|
October 10, 2001
Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family
P de la Peña, B Bornstein, P del Hoyo, et al.
Human Mutation
|
March 26, 2003
Mutation analysis in 16 patients with mtDNA depletion
R Carrozzo, B Bornstein, S Lucioli, et al.
Revista Espanola De Enfermedades Digestivas
|
September 1, 1990
[Angiodysplasia of the colon and Crohn's disease. A study with vascular resin casts]
J Arenas Ricart, A Cremades Mira, L Almenar del Poyo, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
April 24, 2016
Assessment of resting energy expenditure in pediatric mitochondrial diseases with indirect calorimetry
C Fiuza-Luces, A Santos-Lozano, M T García-Silva, et al.
EMBO Molecular Medicine
|
May 29, 2014
RARRES3 suppresses breast cancer lung metastasis by regulating adhesion and differentiation
Mònica Morales, Enrique J Arenas, Jelena Urosevic, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
January 1, 1997
Cerebrospinal fluid levels of alpha-tocopherol (vitamin E) in Parkinson's disease
J A Molina, F de Bustos, F J Jiménez-Jiménez, et al.
Journal of Child Neurology
|
December 6, 2001
Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: a possible relation with mitochondrial dysfunction
M Castro-Gago, E Pintos-Martínez, J Forteza-Vila, et al.
Neuroscience Letters
|
July 22, 1998
Cerebrospinal fluid levels of alpha-tocopherol in patients with multiple sclerosis
F J Jiménez-Jiménez, F de Bustos, J A Molina, et al.
Page
of 38
Search research articles
Search
Showing results (311-320 of 378) with videos related to
Sort By:
Page
of 38
Neuromuscular Disorders : NMD
|
March 27, 1999
Clinical heterogeneity associated with mitochondrial DNA depletion in muscle
Y Campos, M A Martín, T García-Silva, et al.
Journal of the Neurological Sciences
|
April 30, 1998
Cerebrospinal fluid carnitine levels in patients with Alzheimer's disease
J C Rubio, F de Bustos, J A Molina, et al.
Neurology
|
October 10, 2001
Mitochondrial dysfunction associated with a mutation in the Notch3 gene in a CADASIL family
P de la Peña, B Bornstein, P del Hoyo, et al.
Human Mutation
|
March 26, 2003
Mutation analysis in 16 patients with mtDNA depletion
R Carrozzo, B Bornstein, S Lucioli, et al.
Revista Espanola De Enfermedades Digestivas
|
September 1, 1990
[Angiodysplasia of the colon and Crohn's disease. A study with vascular resin casts]
J Arenas Ricart, A Cremades Mira, L Almenar del Poyo, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
April 24, 2016
Assessment of resting energy expenditure in pediatric mitochondrial diseases with indirect calorimetry
C Fiuza-Luces, A Santos-Lozano, M T García-Silva, et al.
EMBO Molecular Medicine
|
May 29, 2014
RARRES3 suppresses breast cancer lung metastasis by regulating adhesion and differentiation
Mònica Morales, Enrique J Arenas, Jelena Urosevic, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
January 1, 1997
Cerebrospinal fluid levels of alpha-tocopherol (vitamin E) in Parkinson's disease
J A Molina, F de Bustos, F J Jiménez-Jiménez, et al.
Journal of Child Neurology
|
December 6, 2001
Congenital hydranencephalic-hydrocephalic syndrome with proliferative vasculopathy: a possible relation with mitochondrial dysfunction
M Castro-Gago, E Pintos-Martínez, J Forteza-Vila, et al.
Neuroscience Letters
|
July 22, 1998
Cerebrospinal fluid levels of alpha-tocopherol in patients with multiple sclerosis
F J Jiménez-Jiménez, F de Bustos, J A Molina, et al.
Page
of 38