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JAMA Neurology
|
July 10, 2013
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9
Caterina Garone, Maria Alice Donati, Michele Sacchini, et al.
Redox Biology
|
April 12, 2019
The early response of αB-crystallin to a single bout of aerobic exercise in mouse skeletal muscles depends upon fiber oxidative features
Ivan Dimauro, Ambra Antonioni, Neri Mercatelli, et al.
Spine
|
May 3, 2023
Effect of Pedicle Screw Size on Surgical Outcomes Following Surgery for 412 Adolescent Idiopathic Scoliosis Patients
Vishal Sarwahi, Sayyida Hasan, Petros Koutsogiannis, et al.
The Journal of Biological Chemistry
|
September 15, 1989
Structure of the gene encoding the muscle-specific subunit of human phosphoglycerate mutase
S Tsujino, S Sakoda, R Mizuno, et al.
Annals of Neurology
|
June 2, 2005
POLG mutations and Alpers syndrome
Guido Davidzon, Michelangelo Mancuso, Silvio Ferraris, et al.
Journal of the Neurological Sciences
|
August 18, 1999
Molecular characterization of McArdle's disease in two large Finnish families
C Bruno, M Löfberg, L Tamburino, et al.
The Journal of Clinical Investigation
|
March 1, 1984
Myoadenylate deaminase deficiency. Functional and metabolic abnormalities associated with disruption of the purine nucleotide cycle
R L Sabina, J L Swain, C W Olanow, et al.
American Journal of Veterinary Research
|
April 14, 2004
Biochemical evaluation of mitochondrial respiratory chain enzymes in canine skeletal muscle
Joseph J Wakshlag, Barry J Cooper, Robin R Wakshlag, et al.
Biochemical and Biophysical Research Communications
|
October 28, 2008
Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathy
Filomena Campagna, Luisa Nanni, Fabiana Quagliarini, et al.
Neuromuscular Disorders : NMD
|
September 14, 2010
Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: muscle biopsy and autopsy findings, biochemical and molecular genetic studies
A L Taratuto, H O Akman, M Saccoliti, et al.
Page
of 95
Search research articles
Search
Showing results (571-580 of 942) with videos related to
Sort By:
Page
of 95
JAMA Neurology
|
July 10, 2013
Mitochondrial encephalomyopathy due to a novel mutation in ACAD9
Caterina Garone, Maria Alice Donati, Michele Sacchini, et al.
Redox Biology
|
April 12, 2019
The early response of αB-crystallin to a single bout of aerobic exercise in mouse skeletal muscles depends upon fiber oxidative features
Ivan Dimauro, Ambra Antonioni, Neri Mercatelli, et al.
Spine
|
May 3, 2023
Effect of Pedicle Screw Size on Surgical Outcomes Following Surgery for 412 Adolescent Idiopathic Scoliosis Patients
Vishal Sarwahi, Sayyida Hasan, Petros Koutsogiannis, et al.
The Journal of Biological Chemistry
|
September 15, 1989
Structure of the gene encoding the muscle-specific subunit of human phosphoglycerate mutase
S Tsujino, S Sakoda, R Mizuno, et al.
Annals of Neurology
|
June 2, 2005
POLG mutations and Alpers syndrome
Guido Davidzon, Michelangelo Mancuso, Silvio Ferraris, et al.
Journal of the Neurological Sciences
|
August 18, 1999
Molecular characterization of McArdle's disease in two large Finnish families
C Bruno, M Löfberg, L Tamburino, et al.
The Journal of Clinical Investigation
|
March 1, 1984
Myoadenylate deaminase deficiency. Functional and metabolic abnormalities associated with disruption of the purine nucleotide cycle
R L Sabina, J L Swain, C W Olanow, et al.
American Journal of Veterinary Research
|
April 14, 2004
Biochemical evaluation of mitochondrial respiratory chain enzymes in canine skeletal muscle
Joseph J Wakshlag, Barry J Cooper, Robin R Wakshlag, et al.
Biochemical and Biophysical Research Communications
|
October 28, 2008
Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathy
Filomena Campagna, Luisa Nanni, Fabiana Quagliarini, et al.
Neuromuscular Disorders : NMD
|
September 14, 2010
Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: muscle biopsy and autopsy findings, biochemical and molecular genetic studies
A L Taratuto, H O Akman, M Saccoliti, et al.
Page
of 95