Atlas of the Ultrastructure of Diseased Human Muscle provides a general view of the ultrastructure of normal and diseased human muscle. This book contains five chapters that illustrate the changes that take place in common pathological conditions and outline the patterns of change, which occur in particular diseases. Chapter 1 describes the ultrastructure of normal striated muscle and the extra-ocular and cardiac muscle. This chapter also deals with skeletal and cardiac muscle of the human fetus. Chapter 2 examines the changes in the ultrastructure of muscle fibers, including changes in myofibrils, mitochondria, lipid bodies, plasma, and basement membranes. Chapters 3 and 4 evaluate the changes in blood capillaries, interstitial tissue of muscle, nerves, motor end plates, and muscle spindles. Chapter 5 discusses the ultrastructural changes in various muscle diseases, such as denervation atrophy of muscle, muscular dystrophies, polymyositis, and congenital myopathies.
This book offers a unique and comprehensive look at the structure and function of tissues at the subcellular and molecular level, an important perspective in understanding and combating diseases. • Presents the major systems of the human ...
First multi-year cumulation covers six years: 1965-70.
A reassessment of clear cell sarcoma. Am. J. Surg. Pathol., 7,405–413. Dodd, S., Malone, M. and McCulloch, W. (1989) Rhabdomyosarcoma in children: a histological and immunohistochemical study of 59 cases. J. Pathol., 158, 13–18.
This volume is intended to cover research in the field of muscle morphology since publication of the previous edition by Haggquist in 1956.
According to Dvorak (1980) 'this represents an in vivo release of eosinophil cores in human disease'. ... also be produced in vitro by lysing eosinophils with a surface-active agent (Aerosol OT), and ultrastructural studies (EI-Hashimi, ...
Ultrastructure of Bone and Joint Diseases
This atlas provides not only a detailed insight into the complex structure and organisation of cells and tissues but also onto specific functions fullfilled by the various cellular organelles and the dynamics of the different processes ...
Miller C, Saada A, Shaul N et al 2004 Defective mitochondrial translation caused by a ribosomal protein (MRPS16) ... Ohkuma A, Talim B et al 2011 A congenital muscular dystrophy with mitochondrial structural abnormalities caused by ...
AmJ Pathol 153:1169–1179 Anderson LV, Harrison RM, Pogue R et al 2000 Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).
Muscle Pathology in Neuromuscular Disease