Résumé
Block et coll.1 ont montré chez des malades souffrant d’une forme familiale de Paramyloidose et appartenant tous à la même famille que l’électrophorèse libre montre soit une onde atypique, la α 2, soit une mauvaise séparation de la α 2 globuline. Dans cette même famille on a trouvé quelques patients présentant des altérations électrophorétiques sans manifestations cliniques. Ceux-ci étaient en moyenne plus jeunes que les patients qui présentaient les premières manifestations cliniques de la maladie.
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Bibliographie
Block, W. D., J. G. Rukavina and A.C. Curtis: Serum eleetrophoretiv studies on patients with familial primary systemic amyloidosis. J. Lab. clin. Med. 47, 357 (1956).
Chambers, R. A., W. E. Medd and H. Spencer: Primary amyloidosis with, special reference of the nervous system. Quart. J. Med. 27, 207 (1958).
Kaufman, H. E., and L.B. Thomas: Vitreous opacities diagnostic of familial primary amyloidosis. New Engl. J. Med. 261, 1267 (1959).
Latner, A. L., and A. H. Zaki: Clinical uses of starch gel electrophoresis with special reference to leukaemia. Clin. chim. Acta 5, 22 (1960).
Jayle, M. F., et G. Boussier: Lés sérumocoides du sang. Leurs relations avec les mucoprotéines de la substance fondamentale du tissu conjonctif. Expos. ann. Biochim. méd. 17, 157 (1955f).
Marko Witz, H., C. J. Gubler, J. P. Mahoney, G. E. Cartwright and M. M. Wintrobe: Studies on copper metabolism. XIV. Copper, ceruloplasmin and oxidase activity in sera of normal human subjects, pregnant women, and patients with infection, hepatolenticular degeneration and the nephrotic syndrome. J. clin. Invest. 34, 1498 (1955).
Gubler, C. J., H. Brown, H. Markowitz, G. E. Cartwright and M. M. Wintrobe: Studies on copper metabolism. XXIII. Portal (Laennecs) cirrhosis of the liver. J. clin. Invest. 36, 1208 (1957).
Butterworth, C. E., C. J. Gubler, G. J. Cartwright and M. M. Wintrobe: Studies on copper metabolism. XXVI. Plasma copper in patients with tropical sprue. Proc. Soc. exp. Biol. (N. Y.) 98, 594 (1958).
Zipursky, A., H. Dempsey, H. Markowitz, G. E. Cartwright and M. M. Wintrobe: Studies on copper metabolism. XXIV. Hypocupremia in infancy. Amer. J. Dis. Child. 96, 148 (1958).
Faber, M.: Serum glucosamine with particular regard to its significance in connection with origin of amyloid deposits. Acta med. scand. Suppl. 206, 351 (1948).
Calkins, E., and A. S. Cohen: Similarity of serum protein changes in primary and secondary amyloidosis. J. clin. Invest. 38, 993 (1959).
Giles, R. B., jr., and E. Calkins: The relationship of serum hexosamine, globulins, antibodies to experimental amyloidosis. J. clin. Invest. 37, 846 (1958).
Giles, R. B., jr., and E. Calkins: Studies of the composition of secondary amyloid. J. clin. Invest. 34, 1476 (1955).
Wolfson, W. Q., C. Cohn, E. Calvary and F. Ichiba: Studies in serum proteins. V. A rapid procedure for the estimation of total protein, true albumin, total globulin, alpha globulin, beta globulin and gamma globulin in 1.0 ml of serum. Amer. J. clin. Path. 18, 723 (1948).
Grassmann, W., u. K. Hannig: Ein einfaches Verfahren zur Analyse der Serumproteine und anderen Proteingemische. Naturwissenschaften 37, 496 (1950).
Grabar, P., et C. A. Williams jr.: Méthode immuno-électrophorètique d’analyse de mélanges de substances antigéniques. Biochim. biophys. Acta (Amst.) 17, 67 (1955).
Smithies, O.: Zone electrophoresis in starch gels: Group variations in the serum proteins of normal human adults. Biochem. J. 61, 629 (1955).
Laurell, C. B.: Determination of the haptoglobin group. Scand. J. clin. Lab. Invest. 11, 18 (1959).
Moretti, J., G. Boussier et M. F. Jayle: Réalisation technique et premières applications de l’électrophorèse sur gel d’amidon. Bull. Soc. Chim. Biol. (Paris) 39, 593 (1957).
Nyman, M.: Serum haptoglobins. Methodological and clinical studies. Scand. J. clin. Lab. Invest. Suppl. 39, 11 (1959).
Owen, J. A., H. J. Silberman and C. Got: Detection of haemoglobin, haemoglobin-haptoglobin complexes and other substances with peroxidase activity after zone electrophoresis. Nature (Lond.) 182, 1373 (1958).
Ravtn, H. A.: Rapid test for hepatolenticular degeneration. Lancet 1956 I, 726.
Elson, L. A., and W. T. J. Morgan: A colorimetric method for the determination of glucosamine and chondrosamine. Biochem. J. 27, 1824 (1933).
Winzler, R. J.: Determination of serum glycoproteins. Meth. biochem. Anal. 1955 II, 279.
Svennerholm, L.: The determination of hexosamines with special reference to nervous tissue. Acta Soc. Med. upsalien. 61, 287 (1956).
Owen, J. A.: Paper electrophoresis of proteins and protein-bound substances in clinical investigations. Advanc. clin. Chem. 1958 I, 237.
Poulik, M. D., and O. Smithies: Comparison and combination of the starch-gel and filter-paper electrophoretic methods applied to human sera: two-dimensional electrophoresis. Biochem. J. 68, 636 (1958).
Perth, J. H., R. E. Engle, K. R. Woods and M. H. Sleisenger: Preliminary studies on quantitative zone electrophoresis in starch-gel. J. Lab. clin. Med. 54, 572 (1959).
Moretti, J., G. Boussier, M. Hugou et L. Hartmann: Recherche des correspondances entre les résultats des électrophorèsis sur papier, a travers un gel d’amidon et de l’immunoélectrophorèse en gélose des protéines du sérum. Bull. Soc. Chim. Biol. (Paris) 41, 79 (1959).
Gross, P. A. M., L. J. Embree, P. Bally, J. C. Shipp and G. W. Thorn: Hypoalbuminemia (with anasarca) due to hypercatabolism, serum protein exsudation into the gastroentestinal tract, increased capillary permeability and hypoanabolism. The unusual occurrence of increased capillary permeability temporarily reversed by human growth hormone therapy. Amer. J. Med. 29, 386 (1960).
Jackson, C. E., W. D. Block and W. C. Ratliff: Serum hexosamine content and urinary acid mucopolysaccharide excretion in hereditary primary amyloidosis. J. Lab. clin. Med. 56, 544 (1960).
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Barros, F., do Rosário, M.R., Antunes, L. (1963). Etudes sur la Paramyloïdose portugaise à forme polynévritique (Type C. Andrade). In: Krücke, W., Seitelberger, F. (eds) Symposium on Paramyloidoses / Symposium Concernant les Paramyloïdoses / Symposium über die Paramyloidosen. Acta Neuropathologica, vol 2. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-30550-8_14
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