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One or more keywords matched the following items that are connected to Dalakas, Marinos
Item TypeName
Concept Muscle, Skeletal
Academic Article Mitochondrial and cellular toxicity induced by fialuridine in human muscle in vitro.
Academic Article An inflammatory, familial, inclusion body myositis with autoimmune features and a phenotype identical to sporadic inclusion body myositis. Studies in three families.
Academic Article Skeletal muscle-specific immunotoxin for the treatment of focal muscle spasm.
Academic Article The effect of intravenous immunoglobulin (IVIG) treatment on patients with dermatomyositis: a 4-year follow-up study.
Academic Article Expression of matrix metalloproteinases in the muscle of patients with inflammatory myopathies.
Academic Article The muscle mitogen-activated protein kinase is altered in sporadic inclusion body myositis.
Academic Article Expression of human IAP-like protein in skeletal muscle: a possible explanation for the rare incidence of muscle fiber apoptosis in T-cell mediated inflammatory myopathies.
Academic Article Lactic acidosis and hepatic steatosis associated with use of stavudine: report of four cases.
Academic Article Clonal restriction of T-cell receptor expression by infiltrating lymphocytes in inclusion body myositis persists over time. Studies in repeated muscle biopsies.
Academic Article Desmin splice variants causing cardiac and skeletal myopathy.
Academic Article The molecular and cellular pathology of inflammatory muscle diseases.
Academic Article Inflammatory myopathies. Recent advances in pathogenesis and therapy.
Academic Article Understanding the immunopathogenesis of inclusion-body myositis: present and future prospects.
Academic Article GNE mutations in an American family with quadriceps-sparing IBM and lack of mutations in s-IBM.
Academic Article Expression of IFN-gamma-inducible chemokines in inclusion body myositis.
Academic Article Guidelines for the diagnosis and treatment of chronic inflammatory demyelinating polyneuropathy.
Academic Article Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy.
Academic Article Hypoglycosylation of alpha-dystroglycan in patients with hereditary IBM due to GNE mutations.
Academic Article A series of West European patients with severe cardiac and skeletal myopathy associated with a de novo R406W mutation in desmin.
Academic Article Upregulated inducible co-stimulator (ICOS) and ICOS-ligand in inclusion body myositis muscle: significance for CD8+ T cell cytotoxicity.
Academic Article Inflammatory disorders of muscle: progress in polymyositis, dermatomyositis and inclusion body myositis.
Academic Article Gene expression profile in the muscles of patients with inflammatory myopathies: effect of therapy with IVIg and biological validation of clinically relevant genes.
Academic Article Nonsense mutation in the phosphofructokinase muscle subunit gene associated with retention of intron 10 in one of the isolated transcripts in Ashkenazi Jewish patients with Tarui disease.
Academic Article Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.
Academic Article Identification of macrophages in the muscle biopsy preparations: a comparative study using specific monoclonal antimacrophage antibodies and acid phosphatase reaction.
Academic Article Molecular pathogenesis of inflammatory myopathies and future therapeutic strategies.
Academic Article Expression of toll-like receptors by human muscle cells in vitro and in vivo: TLR3 is highly expressed in inflammatory and HIV myopathies, mediates IL-8 release and up-regulation of NKG2D-ligands.
Academic Article Intravenous immunoglobulin in patients with anti-GAD antibody-associated neurological diseases and patients with inflammatory myopathies: effects on clinicopathological features and immunoregulatory genes.
Academic Article Metabolic abnormalities in skeletal muscle of patients receiving zidovudine therapy observed by 31P in vivo magnetic resonance spectroscopy.
Academic Article The role of high-dose immune globulin intravenous in the treatment of dermatomyositis.
Academic Article Beta-amyloid is a substrate of autophagy in sporadic inclusion body myositis.
Academic Article Upregulation of thrombospondin-1(TSP-1) and its binding partners, CD36 and CD47, in sporadic inclusion body myositis.
Academic Article T cell receptor profiling in muscle and blood lymphocytes in sporadic inclusion body myositis.
Academic Article Interrelation of inflammation and APP in sIBM: IL-1 beta induces accumulation of beta-amyloid in skeletal muscle.
Academic Article Interplay between inflammation and degeneration: using inclusion body myositis to study "neuroinflammation".
Academic Article Late-onset muscle weakness in partial phosphofructokinase deficiency: a unique myopathy with vacuoles, abnormal mitochondria, and absence of the common exon 5/intron 5 junction point mutation.
Academic Article Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle.
Academic Article In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy.
Academic Article Effect of Alemtuzumab (CAMPATH 1-H) in patients with inclusion-body myositis.
Academic Article Treatment of inclusion-body myositis with IVIg: a double-blind, placebo-controlled study.
Academic Article Inflammatory Muscle Diseases.
Academic Article HMGB1 and RAGE in skeletal muscle inflammation: Implications for protein accumulation in inclusion body myositis.
Academic Article Molecular treatment effects of alemtuzumab in skeletal muscles of patients with IBM.
Academic Article Case 22-2019: A 65-Year-Old Woman with Myopathy.
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  • Muscle Skeletal