Published in Ultrastruct Pathol on December 21, 2006
Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscle. Biophys J (2010) 1.08
Beneficial effects of cod protein on inflammatory cell accumulation in rat skeletal muscle after injury are driven by its high levels of arginine, glycine, taurine and lysine. PLoS One (2013) 0.78
Myogenic differentiation potential of human tonsil-derived mesenchymal stem cells and their potential for use to promote skeletal muscle regeneration. Int J Mol Med (2016) 0.77
Characteristics of the Localization of Connexin 43 in Satellite Cells during Skeletal Muscle Regeneration In Vivo. Acta Histochem Cytochem (2015) 0.77
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies. Am J Hum Genet (2009) 1.83
Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers. J Cell Biol (2003) 1.79
Bone fragility and collagen cross-links. J Bone Miner Res (2004) 1.68
Validation of the ABCD score in identifying individuals at high early risk of stroke after a transient ischemic attack: a hospital-based case series study. Stroke (2006) 1.67
Resistance exercise-induced increase in muscle mass correlates with p70S6 kinase phosphorylation in human subjects. Eur J Appl Physiol (2007) 1.61
Denosumab treatment in postmenopausal women with osteoporosis does not interfere with fracture-healing: results from the FREEDOM trial. J Bone Joint Surg Am (2012) 1.54
Effects of previous antiresorptive therapy on the bone mineral density response to two years of teriparatide treatment in postmenopausal women with osteoporosis. J Clin Endocrinol Metab (2007) 1.53
Diabetes mellitus associated with glycogen storage disease type III. Muscle Nerve (2009) 1.45
The long-term clinical relevance of calcar atrophy caused by stress shielding in total hip arthroplasty: a 10-year, prospective, randomized study. J Arthroplasty (2004) 1.10
Severe osteoporosis and mutation in NOTCH2 gene in a woman with Hajdu-Cheney syndrome. Bone (2012) 1.03
Effect of aerobic and resistance exercise training on late-onset Pompe disease patients receiving enzyme replacement therapy. Mol Genet Metab (2011) 0.96
Changes in parameters of bone metabolism in postmenopausal women following a 12-month intervention period using dairy products enriched with calcium, vitamin D, and phylloquinone (vitamin K(1)) or menaquinone-7 (vitamin K (2)): the Postmenopausal Health Study II. Calcif Tissue Int (2012) 0.95
The degree of p70 S6k and S6 phosphorylation in human skeletal muscle in response to resistance exercise depends on the training volume. Eur J Appl Physiol (2010) 0.92
Structural properties of the axis studied in cadaveric specimens. Clin Orthop Relat Res (2004) 0.90
Morphometric study of the human muscle spindle. Anal Quant Cytol Histol (2005) 0.87
Throwing performance after resistance training and detraining. J Strength Cond Res (2008) 0.86
Presymptomatic neuromuscular disorders disclosed following statin treatment. Arch Intern Med (2006) 0.86
Bone density in patients with late onset Pompe disease. Int J Endocrinol Metab (2012) 0.85
Quantitative ultrasound of the calcaneus in greek women: normative data are different from the manufacturer's normal range. J Clin Densitom (2009) 0.84
Asymptomatic elevation of serum creatine kinase leading to the diagnosis of 4q35 facioscapulohumeral muscular dystrophy. J Clin Neurosci (2009) 0.84
NUCKS overexpression in breast cancer. Cancer Cell Int (2009) 0.84
Dropped head syndrome as prominent clinical feature in MuSK-positive Myasthenia Gravis with thymus hyperplasia. Neuromuscul Disord (2007) 0.83
Fiber type composition and capillary density in relation to submaximal number of repetitions in resistance exercise. J Strength Cond Res (2008) 0.83
Age-related morphometric characteristics of human skeletal muscle in male subjects. Pol J Pathol (2009) 0.83
Coinheritance of Noonan syndrome and Becker muscular dystrophy. Neuromuscul Disord (2009) 0.82
Danon disease: further clinical and molecular heterogeneity. Muscle Nerve (2009) 0.81
Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol. Mol Cell Probes (2005) 0.81
Acute effect of drop jumping on throwing performance. J Strength Cond Res (2009) 0.80
Effects of exercise training during infusion on late-onset Pompe disease patients receiving enzyme replacement therapy. Mol Genet Metab (2012) 0.80
Muscle fibre type composition and body composition in hammer throwers. J Sports Sci Med (2010) 0.79
Phenotypical variability in glycogen storage disease type III with a recurrent AGL mutation c.750-753delAGAC. Muscle Nerve (2011) 0.79
Optimal timing of research after anterior cruciate ligament resection in rabbits. Contemp Top Lab Anim Sci (2004) 0.79
Effects of Strength vs. Ballistic-Power Training on Throwing Performance. J Sports Sci Med (2013) 0.78
Increased dysferlin expression in Duchenne muscular dystrophy. Anal Quant Cytopathol Histpathol (2014) 0.77
Caveolinopathies in Greece. Neurologist (2015) 0.77
Toward understanding cognitive impairment in patients with myotonic dystrophy type 1. Arch Clin Neuropsychol (2010) 0.77
RGD binding to integrin alphavbeta3 affects cell motility and adhesion in primary human breast cancer cultures. Ultrastruct Pathol (2012) 0.77
Chromatin ultrastructural abnormalities in leukocytes, as peripheral markers of bipolar patients. Ultrastruct Pathol (2009) 0.76
Muscle lim protein isoform negatively regulates striated muscle actin dynamics and differentiation. FEBS J (2014) 0.76
OX40-OX40L expression in idiopathic inflammatory myopathies. Anal Quant Cytopathol Histpathol (2013) 0.76
Chromatin alterations in leukocytes of first-episode schizophrenic patients. Ultrastruct Pathol (2010) 0.76
Bent spine syndrome in facioscapulohumeral muscular dystrophy. Muscle Nerve (2011) 0.76
Re: Consider muscle disease in children with elevated transaminase. J Am Board Fam Med (2012) 0.75
Occludin dislocation in brain capillary endothelium of rats with bile duct ligation induced cholestasis. Neurosci Lett (2012) 0.75
Expression of the O-linked N-acetylglucosamine containing epitope H in normal myometrium and uterine smooth muscle cell tumors. Pathol Res Pract (2006) 0.75
Elevated creatine kinase levels in a patient with coronary artery disease and asymptomatic McArdle's disease. Int J Cardiol (2006) 0.75
Delayed contrast enhancement on cardiac MRI unmasks subclinical cardiomyopathy in a case of myotonic dystrophy type 2. Hellenic J Cardiol (2012) 0.75
Orthognathic surgery for trichorhinophalangeal syndrome type I. Plast Reconstr Surg (2002) 0.75
Cognitive impairment and cerebellar atrophy in typical onset 4Q35 fascioscapulohumeral dystrophy. Muscle Nerve (2008) 0.75
Cochlear dysfunction in patients with mitochondrial myopathy. ORL J Otorhinolaryngol Relat Spec (2002) 0.75
Noradrenaline storage function of species-specific protein bodies, markers of monoamine neurons in human locus coeruleus demonstrated by dopamine-beta-hydroxylase immunogold localization. Prog Neuropsychopharmacol Biol Psychiatry (2004) 0.75
Karyometric changes of intrafusal muscle fibers in neuromuscular diseases. Anal Quant Cytol Histol (2008) 0.75
Familial asymmetric distal upper limb amyotrophy (Hirayama disease): report of a Greek family. Neurologist (2009) 0.75
Pretreatment antibodies against acid α-glycosidase in a patient with late-onset Pompe disease. Muscle Nerve (2012) 0.75
Phenotypic variability and molecular genetics in proximal myotonic myopathy. Muscle Nerve (2015) 0.75
Sarcoidosis in a case of MuSK-positive myasthenia gravis. Neuromuscul Disord (2008) 0.75
Chromogranin A and vesicular monoamine transporter 2 immunolocalization in protein bodies of human locus coeruleus neurons. Ultrastruct Pathol (2013) 0.75