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Antoni L Andreu

Showing results (11-20 of 77) with videos related to

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JMIR Medical Education|February 21, 2023
Correction: Personalized Precision Medicine for Health Care Professionals: Development of a Competency FrameworkFernando Martin-Sanchez, Martín Lázaro, Carlos López-Otín, et al.
JMIR Medical Education|February 7, 2023
Personalized Precision Medicine for Health Care Professionals: Development of a Competency FrameworkFernando Martin-Sanchez, Martín Lázaro, Carlos López-Otín, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|June 10, 2016
Differential glucose metabolism in mice and humans affected by McArdle diseaseThomas O Krag, Tomàs Pinós, Tue L Nielsen, et al.
Neuromuscular Disorders : NMD|September 22, 2014
PYGM expression analysis in white blood cells: a complementary tool for diagnosing McArdle disease?Noemí de Luna, Astrid Brull, Alejandro Lucia, et al.
Human Mutation|March 18, 2011
A novel nonstop mutation in TYMP does not induce nonstop mRNA decay in a MNGIE patient with severe neuropathyJavier Torres-Torronteras, Agustí Rodriguez-Palmero, Tomàs Pinós, et al.
Neuromuscular Disorders : NMD|May 30, 2009
The second wind phenomenon in very young McArdle's patientsMargarita Pérez, Jonatan R Ruiz, María Fernández Del Valle, et al.
Annals of Neurology|October 2, 2003
Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathiesMassimiliano Filosto, Michelangelo Mancuso, Cristofol Vives-Bauza, et al.
Brain : a Journal of Neurology|December 20, 2012
Oxidative stress modulates mitochondrial failure and cyclophilin D function in X-linked adrenoleukodystrophyJone López-Erauskin, Jorge Galino, Patrizia Bianchi, et al.
Biochemical and Biophysical Research Communications|February 1, 2002
Sequence analysis of the entire mitochondrial genome in Parkinson's diseaseCristofol Vives-Bauza, Antoni L Andreu, Giovanni Manfredi, et al.
Muscle & Nerve|August 21, 2003
Two novel mutations in the muscle glycogen phosphorylase gene in McArdle's diseaseJosep Gámez, Juan C Rubio, Miguel A Martín, et al.
Pageof 8

Showing results (11-20 of 77) with videos related to

Sort By:
Pageof 8
JMIR Medical Education|February 21, 2023
Correction: Personalized Precision Medicine for Health Care Professionals: Development of a Competency FrameworkFernando Martin-Sanchez, Martín Lázaro, Carlos López-Otín, et al.
JMIR Medical Education|February 7, 2023
Personalized Precision Medicine for Health Care Professionals: Development of a Competency FrameworkFernando Martin-Sanchez, Martín Lázaro, Carlos López-Otín, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|June 10, 2016
Differential glucose metabolism in mice and humans affected by McArdle diseaseThomas O Krag, Tomàs Pinós, Tue L Nielsen, et al.
Neuromuscular Disorders : NMD|September 22, 2014
PYGM expression analysis in white blood cells: a complementary tool for diagnosing McArdle disease?Noemí de Luna, Astrid Brull, Alejandro Lucia, et al.
Human Mutation|March 18, 2011
A novel nonstop mutation in TYMP does not induce nonstop mRNA decay in a MNGIE patient with severe neuropathyJavier Torres-Torronteras, Agustí Rodriguez-Palmero, Tomàs Pinós, et al.
Neuromuscular Disorders : NMD|May 30, 2009
The second wind phenomenon in very young McArdle's patientsMargarita Pérez, Jonatan R Ruiz, María Fernández Del Valle, et al.
Annals of Neurology|October 2, 2003
Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathiesMassimiliano Filosto, Michelangelo Mancuso, Cristofol Vives-Bauza, et al.
Brain : a Journal of Neurology|December 20, 2012
Oxidative stress modulates mitochondrial failure and cyclophilin D function in X-linked adrenoleukodystrophyJone López-Erauskin, Jorge Galino, Patrizia Bianchi, et al.
Biochemical and Biophysical Research Communications|February 1, 2002
Sequence analysis of the entire mitochondrial genome in Parkinson's diseaseCristofol Vives-Bauza, Antoni L Andreu, Giovanni Manfredi, et al.
Muscle & Nerve|August 21, 2003
Two novel mutations in the muscle glycogen phosphorylase gene in McArdle's diseaseJosep Gámez, Juan C Rubio, Miguel A Martín, et al.
Pageof 8