Published in Neuromuscul Disord on March 09, 2006
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Mitochondrial DNA mutations affect calcium handling in differentiated neurons. Brain (2010) 0.88
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No excess of mitochondrial DNA deletions within muscle in progressive multiple sclerosis. Mult Scler (2013) 0.85
A randomized comparative trial of generalized vs targeted physiotherapy in the management of childhood hypermobility. Rheumatology (Oxford) (2009) 0.84
Microangiopathy in the cerebellum of patients with mitochondrial DNA disease. Brain (2012) 0.83
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The association between low socioeconomic status with high physical limitations and low illness self-perception in patients with juvenile idiopathic arthritis: results from the Childhood Arthritis Prospective Study. Arthritis Care Res (Hoboken) (2015) 0.82
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Reduced plasma adiponectin levels relative to oxidized low density lipoprotein and nitric oxide in coronary artery disease patients. Clinics (Sao Paulo) (2011) 0.81
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The associations between high-density lipoprotein mean particle size and its fatty acid composition. Biomark Med (2013) 0.80
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Mitochondrial DNA and genetic disease. Essays Biochem (2010) 0.78
Serum paraoxonase 1 activity is associated with fatty acid composition of high density lipoprotein. Dis Markers (2013) 0.78
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Elevated plasma platelet-activating factor acetylhydrolase activity and its relationship to the presence of coronary artery disease. J Res Med Sci (2011) 0.78
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The mitochondrial brain: From mitochondrial genome to neurodegeneration. Biochim Biophys Acta (2009) 0.76
Foot orthoses in children with juvenile idiopathic arthritis: a randomised controlled trial. Arch Dis Child (2014) 0.75
"So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager". Neuromuscul Disord (2006) 0.75
Molecular dynamics simulation of chemokine receptors in lipid bilayer: a case study on C-C chemokine receptor type 2. Chem Biol Drug Des (2013) 0.75
Access to care for children and young people diagnosed with localized scleroderma or juvenile SSc in the UK. Rheumatology (Oxford) (2012) 0.75
A splice junction mutation in muscle carnitine palmitoyltransferase II deficiency. Mol Genet Metab (2003) 0.75
Management of patients with dental disease and mitochondrial disorders. Dent Update (2012) 0.75
Elevated plasma myeloperoxidase levels in relation to circulating inflammatory markers in coronary artery disease. Biomark Med (2011) 0.75