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  • Book
    editor, Douglas J. Rhee.
    Contents:
    I: Glaucoma diagnosis
    Introduction to glaucoma diagnosis
    Basics of aqueous flow and the optic nerve
    Tonometry
    Gonioscopy
    Anterior segment imaging
    Optic nerve imaging
    Glaucoma imaging: optic nerve head, peripapillary, and macular regions
    Psychophysical testing
    Blood flow in glaucoma
    II: Clinical syndromes
    Introduction to clinical syndromes
    Childhood glaucomas (Congenital glaucomas)
    Primary open-angle glaucoma
    Secondary open-angle glaucoma
    Uveitic glaucomas
    Lens-associated open-angle glaucomas
    Traumatic glaucoma
    Primary acute angle-closure and chronic angle-closure glaucoma
    Secondary angle-closure glaucoma
    Glaucoma secondary to elevated venous pressure
    III: Glaucoma management
    Introduction to glaucoma management
    Medical management
    Laser trabeculoplasty
    Deep sclerectomy surgery for glaucoma
    Trabeculectomy, the Ex-PRESS mini glaucoma shunt, and the xen gel
    Glaucoma drainage devices
    Schlemm canal-based surgery
    Cyclodestructive procedures for glaucoma
    Late complications of glaucoma surgery
    Supraciliary microstent surgery
    Digital Access
    Provider
    Version
    Ovid
    LWW Health Library
  • Article
    Kuffer R, Fiore-Donno G, Lopez-Pardinas M, Gabbiani G.
    Rev Stomatol Chir Maxillofac. 1977;78(6):371-83.
    Recent research has shown that the cytoplasm of several varieties of non muscular cells contains contractile proteins similar to those of striated muscle (actin and myosin, with the control complex of troponin and tropomyosin). Using indirect immunofluorescent staining with specific antisera, the authors demonstrate that the cytoplasm of the cells of oral squamous cell carcinoma contains actin, myosin and actinin (tropomyosin seems to be lacking). They have found these contractile proteins inconstantly in various precarcinomatous states, but never in normal epithelium, except in a few basal cells. In electronic microscopy, these contractile proteins correspond to a network of microfilaments of 40-80 A, more rarely 100-120 A, Clearly different from tonofilaments, located mainly in the peripheral part of the cytoplasm, just under the plasmalemmal membrane. It is tempting to speculate that the occurence of a contractile filamentous apparatus in the cells of oral carcinomas--already described in skin and mammal gland carcinomas--allows to these cells amoeboid movements and active migration, which might to some extent explain their tendency to invade surrounding tissues and to produce metastasis.
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