Inclusion-Body Myositis and MyopathiesValerie Askanas, Georges Serratrice, W. King Engel Cambridge University Press, 13 apr. 1998 - 393 pagini Inclusion-body myositis (IBM) is now understood to be an important degenerative muscle disease. The sporadic type (s-IBM) is probably the most common muscle disease among those ailments that strike first in adulthood (particularly people over 50). The hereditary type (h-IBM) affects younger patients. This book is devoted entirely to s-IBM and h-IBM. Contributors discuss what is understood about the basic scientific foundations of IBMs, the varied aspects of the pathology of IBMs, and the application of clinical treatments. One particular emphasis of the book is on the hereditary aspects of IBM and genetic predispositions to the disease. |
Cuprins
Evolving Concepts of InclusionBody Myositis | 81 |
Clinical | 107 |
Natural History Françoise | 116 |
Uncommon Clinicopathologic Forms of Sporadic | 126 |
Jean François Pellissier M D | 137 |
Jean Pouget M D | 172 |
Hereditary InclusionBody Myopathy in Jews | 191 |
Hereditary InclusionBody Myopathy with Quadriceps | 200 |
Clinical Genetic | 232 |
Distal Myopathy with Rimmed Vacuoles | 244 |
InclusionBody Myopathies Michel Fardeau | 252 |
Inflammatory Nuclear and Mitochondrial Abnormalities | 261 |
Yume Suzuki | 297 |
Evaluation of Treatment for Sporadic InclusionBody | 331 |
Treatment of InclusionBody Myositis and Hereditary | 351 |
| 383 | |
Termeni și expresii frecvente
abnormally accumulated Alvarez RB amyloid amyloid deposits Ann Neurol antigen Apolipoprotein E Arch Neurol Askanas Aẞ associated atrophic fibers atrophy autoimmune autosomal autosomal-recessive BAPP brain CD8+ cells clinical cytoplasmic Dalakas MC dermatomyositis diagnosis distal myopathy DMRV dysphagia Engel WK Fardeau Figure filamentous inclusions function gene genetic h-IBM hereditary inclusion-body myopathy human muscle IBM muscle immunoreactivity Inclusion body myositis inclusion-body myositis IBM inflammation inflammatory myopathies IVIG Karpati G lymphocytes mitochondrial DNA monoclonal antibody morphologic mRNA mtDNA mtDNA deletions muscle biopsy muscle biopsy specimens muscle fibers muscle weakness muscle-fiber muscular dystrophy myopathy with rimmed neurogenic Neurol Sci Neurology Nonaka normal nuclear nuclei observed oculopharyngeal muscular dystrophy Oldfors onset pathogenesis pathologic Persian Jews PHFS polymyositis prednisone prion protein reported rimmed vacuoles s-IBM s-IBM patients sparing the quadriceps sporadic inclusion-body myositis ẞ-amyloid ẞAPP staining studies syndrome tion Tomé FMS treatment ubiquitin ultrastructural vacuolated muscle fibers viral Welander
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