Zusammenfassung
Vom epithelialen Lungenfeld, das unmittelbar kaudal des Schiunddarms auf der Ventralseite liegt, bildet sich zunächst durch Einsen-kung die sog. Lungen- oder Laryngotrachealrinne. Diese wächst in ventrokaudaler Richtung ins umgebende Mesenchym vor, teilt sich in zwei seitliche Ausbuchtungen und läßt so die primären Lungensäck-chen oder -bläschen entstehen. Während der sog. glandulären Phase der Aussprossung (4.–16. Woche der Kyematogenese) sind die Schläuche von einschichtigem kubischem bis niedrigzylindrischem Epithel ausgekleidet. Es folgt die sog. kanalikuläre Phase (16.–24. Woche), in deren Verlauf das Epithel der zentral gelegenen Tracheobronchialanlagen höher zylindrisch wird, während in der Peripherie die Epithelien eher flacher erscheinen. In dieser Phase erkennt man auch den Anfang der Knorpelbildung. Nach der 24. Woche beginnen sich die peripheren Kanalikuli zu erweitern (sakkuläre Phase). Die Alveolenbildung (alveoläre Phase) setzt erst kurze Zeit vor dem Termin ein und geht nach der Geburt weiter, um erst etwa im 8. Lebensjahr einen Abschluß zu finden. Im Verlauf der sog. Alveolation entstehen Pneumozyten II (kubisch) und I (flach). Die ersteren enthalten zur Zeit des Termins schon reichlich »Surfactant« (s. u.).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Literatur
Literatur
Bedrossian, C. W. M., Greenberg, S. D., Yawn, D. H., O’Neal, R. M.: Experimentally induced bleomycin sulfate pulmonary toxicity. Arch. Pathol. Lab. Med. 101, 248 (1977)
Cain, H., Egner, E., Ruska, J.: Ablagerungen seltener Erden in der menschlichen Lunge und im Tierexperiment. Virchows Arch. (Pathol. Anat.) 374, 249 (1977)
Carrington, C. B., Gaensler, E.A., Coutu, R. E., Fitz Gerald, M.X., Gupta, R. G.: Natural history and treated course of usual and desquamative interstitial pneumonia. N. Engl. J. Med. 298, 801 (1978)
Cosio, M., Ghezzo, H., Hogg, J. C., Corbin, R., Loveland, M., Dosman, J., Macklem, P. T.: The relations between structural changes in small airways and pulmonary-function tests. N. Engl. J. Med. 298, 1277 (1977)
Glinz, W.: Thoraxverletzungen. Berlin: Springer 1978
Hall, W.J., Hyde, R.W., Schwartz, R.H., Mudholkar, G. S., Webb, D. R., Chaubey, Y. P., Townes, P. L.: Pulmonary abnormalities in intermediate alpha-1-antitrypsin deficiency. J. Clin. Invest. 58, 1069 (1976)
Kravis, Th. C., Ahmed, A., Brown, T. E., Fulmer, J. D., Crystal, R.G.: Pathogenic mechanisms in pulmonary fibrosis. Collagen-induced migration inhibition factor production and cytotoxicity mediated by lymphocytes. J. Clin. Invest. 58, 1223 (1976)
Kuhn III, Ch., Tavassoli, F.: The scanning electron microscopy of elastase-in-duced emphysema. A comparison with emphysema in man. Lab. Invest. 34, 2 (1976)
Luscieti, P., Pedrinis, E.: Neuere Erkenntnisse auf dem Gebiet der Lungenpathologie. Ther. Umsch. 32, 258 (1975)
Mellick, P. W., Dungworth, D. L., Schwartz, L. W., Tyler, W. S.: Short term morphologic effects of high ambient levels of ozone on lungs of rhesus monkeys. Lab. Invest. 36, 82 (1977)
Mittermayer, Ch., Wybitul, K., Rau, W. S., Ostendorf, P., Riede, U. N.: Standardized fixation of human lung for radiology and morphometry; description of a »two-chamber«-system with formaldehyde vapor inflation. Pathol. Res. Pract. 162, 115 (1978)
Morse, J. O., Lebowitz, M. D., Knudson, R.J., Burrows, B.: Relation of protease inhibition phenotypes to obstructive lung diseases in a community. N. Engl. J. Med. 296, 1190 (1977)
Mountain, R., Zwillich, C., Weil, J.: Hypoventilation in obstructive lung disease. N. Engl. J. Med. 298, 521 (1978)
Niewoehner, D.E., Knoke, J.D., Kleinerman, J.: Peripheral airways as a determinant of ventilatory function in the human lung. J. Clin. Invest. 60, 139 (1977)
Smith, F. B., Kikkawa, Y.: The type II epithelial cells of the lung. III. Lecithin synthesis: A comparison with pulmonary macrophages. Lab. Invest. 38, 45 (1978)
Spencer, H.: Pathology of the lung, 3rd.ed. Oxford: Pergamon Press 1978
Sykes, B. I., Purchase, I. F. H., Smith, L. L.: Pulmonary ultrastructure after oral and intravenous dosage of paraquat to rats. J. Pathol. 121, 233 (1977)
Schaefer, P., Meyer-Erkelenz, J. D., Effert, S.: Lungenfunktion und Operabilität. Dtsch. Med. Wochenschr. 103, 123 (1978)
Stankus, R. P., Cashner, F. M., Salvaggio, J. E.: Bronchopulmonary macrophage activation in the pathogenesis of hypersensitivity pneumonitis. J. Immunol. 120, 685 (1978)
Terry, P. B., Traystman, R. J., Newball, H. H., Batra, G., Menkes, H. A.: Collateral ventilation in man. N. Engl. J. Med. 298, 10 (1978)
Wagner, P.D., Dantzker, D.R., Dueck, R., Clausen, J. L., West, J. B.: Ventilation-perfusion inequality in chronic obstructive pulmonary disease. J. Clin. Invest. 59, 203 (1977).
Literatur
Allgöwer, M.: Allgemeine und spezielle Chirurgie, 3. Aufl. Berlin: Springer 1976
Behar, J.: Reflux esophagitis. Pathogenesis, diagnosis and management. Arch. Int. Med. 136, 560 (1976)
Bockus, H. L., (ed.): Gastroenterology, vol. I, 3rd. ed. Philadelphia: Saunders 1974
Bode, J. Ch., Menge, H.: Verdauungstrakt und Alkohol. Internist 19, 116 (1978)
Ciba Foundation Symposium 42 (new series): Acute diarrhoea in childhood. Amsterdam: Elsevier 1976
Compston, J.E., Horton, L. W. L., Laker, M. F., Ayers, A. B., Woodhead, J. S., Bull, H. J., Gazet, J. C., Pilkington, T. R. E.: Bone disease after jejuno-ileal bypass for obesity. Lancet 1978 II, 1
Cooper, B. T., Holmes G. K. T., Cooke, W. T.: Coeliac disease and immunological disorders. Br. Med. J. 1978 I, 537
Cummings, J. H, Southgate, D. A. T., Branch, W., Houston, H., Jenkins, D.J. A., James, W. P. T.: Colonic response to dietary fibre from carrot, cabbage, apple, bran, and guar gum. Lancet 1978 I, 5
Demling, L., Classen, M., Frühmorgen, P.: Atlas of enteroscopy. Berlin: Springer 1975
Halter, F.: Pathogenese des Ulcus ventriculi und der chronischen Gastritis. In: Ulcus-Therapie (Siewert, R., Blum, A., Hrsg.). S. 12–27. Berlin: Springer 1978
Holm, E. (Hrsg.): Ammoniak und hepatische Enzephalopathie. Stuttgart: Fischer 1975
Hornbostel, H., Kaufmann, W., Siegenthaler, W.: Innere Medizin in Praxis und Klinik, 2. Aufl. Bd IV: Verdauungstrakt, Ernährungsstörungen, Stoffwechsel, Vergiftungen. Stuttgart: Thieme 1978
Isaacson, P., Wright, D. H.: Intestinal lymphoma associated with malabsorption. Lancet 1978 I, 67
Keppler, D. (ed.): Pathogenesis and mechanisms of liver cell necrosis. Baltimore: University Park Press 1975
Kirsner, J. B., Shorter, R. G. (eds.): Inflammatory bowel disease. Philadelphia: Lea & Febiger 1975
Klöppel, G., Seifert, G., Lindner, H., Dammermann, R., Sack, H.J., Berg, P.A.: Histopathological features in mixed types of chronic aggressive hepatitis and primary biliary cirrhosis. Virchows Arch. A (Pathol. Anat.) 373, 143 (1977)
Kobler, E., Bühler, H., Nüesch, H. J., Deyhle, P.: Medikamentös induzierte Oesophagusulzera. Dtsch. Med. Wochenschr. 103, 1035 (1978)
Lake, B. D., Puri, P., Nixon, H. H., Claireaux, A. E.: Hirschsprung’s disease. Arch. Pathol. Lab. Med. 102, 244 (1978)
Lieber, C. S.: Pathogenesis and early diagnosis of alcoholic liver injury. N. Engl. J. Med. 298, 888 (1978)
Lipkin, M., Good, R. A. (eds.): Gastrointestinal tract cancer. Sloan-Kettering Institute Cancer Series, vol. 1. New York: Plenum Publishing Corp. 1978
Mann, N.S., Sachdev, A. J.: Aspirin- and bile-induced acute erosive gastritis. Arch. Pathol. Lab. Med. 101, 206 (1977)
Meyer zum Büschenfelde, K. H.: Immunphänomene bei Lebererkrankungen. Z. Gastroenterol, (im Druck)
Mosley, J.W., Redeker, A.G., Feinstone, S. M., Purcell, R. H.: Multiple hepatitis viruses in multiple attacks of acute viral hepatitis. N. Engl. J. Med. 296, 75 (1977)
Pauli, A., Trier, J. S., Dalton, M. D., Camp, R. C., Loeb, P., Goyal, R. K.: The histologic spectrum of barren’s esophagus. N. Engl. J. Med. 295, 476 (1976)
Paumgartner, G.: Pathophysiologische Grundlagen der Gallensteinbildung. Leber, Magen, Darm 4, 17 (1974)
Perera, D.R., Weinstein, W. M., Rubin, C. E.: Small intestinal biopsy. Human Pathol. 6, 157 (1975)
Rao, S.S., Krasner, N., Thomson, T. J.: Chronic gastritis — a simple classification. J. Pathol. 117, 93 (1975)
Seifert, G., Donath, K.: Classification of the pathohi-stology of diseases of the salivary glands. — Review of 2600 cases in the salivary gland register. Beitr. Pathol. 159, 1 (1976)
Taylor, T. V., Lambert, M. E., Torrance, H. B.: Value of bile-acid binding agents in post-vagotomy diarrhoea. Lancet 1978 I, 635
Taylor, W. (ed.): The hepatobiliary system. Fundamental and pathological mechanisms. New York: Plenum Press 1975
Webber, B. L., Freiman, I.: The liver in Kwashiorkor. Arch. Pathol. 98, 400 (1974)
Whorwell, P. J., Fade, O. E., Hossenbocus, A., Bamforth, J.: Crohn’s disease in a husband und wife. Lancet 1978 II, 186
Yamada, G., Feinberg, L. E., Nakane, P. K.: Hepatitis B. Cytologic localization of virus antigens and the role of the immune response. Human Pathol. 9, 93 (1978).
Literatur
Avram, M. M., Feinfeld, D. A., Huatuco, A. H.: Search for the uremic toxin. Decreased motor-nerve conduction velocity and elevated parathyroid hormone in uremia. N. Engl. J. Med. 298, 1000 (1978)
Bohrer, M. P., Baylis, Ch., Humes, H.D., Glassock, R. J., Robertson, C. R., Brenner, B. M.: Permselectivity of the glomerular capillary wall. J. Clin. Invest. 61, 72 (1978)
Cohen, A.H., Mampaso, F., Zamboni, L.: Glomerular podocyte degeneration in human renal disease. Lab. Invest. 37, 30 (1977
Cuppage, F. E., Setter, K., Sullivan, L. P., Reitzes, E. J., Melnykovych, A. O.: Gentamicin nephrotoxicity. Virchows Arch. (Cell Pathol.) 24, 121 (1977)
Danovitch, G. M., Bourgoignie, J., Bricker, N. S.: Reversibility of the »salt-losing« tendency of chronic renal failure. N. Engl. J. Med. 296, 14 (1977)
Dennis, V.W., Brazy, P.C.: Sodium, phosphate, glucose, bicarbonate, and alanine interactions in the isolated proximal convoluted tubule of the rabbit kidney. J. Clin. Invest. 62, 387 (1978)
Fillit, H. M., Read, St. E., Sherman, R. L., Zabriskie, J. B., van de Rijn, I.: Cellular reactivity to altered glomerular basement membrane in glomerulonephritis. N. Engl. J. Med. 298, 861 (1978)
Fine, L. G., Schlondorff, D., Trizna, W., Gilbert, R. M., Bricker, N. S.: Function profile of the isolated uremic nephron. Impaired water permeability and adenylate cyclase responsiveness of the cortical collecting tubule to vasopressin. J. Clin. Invest. 61, 1519 (1978)
Fox, M., Saunders, N. R.: Significance of loin pain in women. Lancet 1978 I, 115
Jenis, E. H., Lowenthal, D. T.: Kidney biopsy interpretation. Philadelphia: Davis 1977
Levinsky, R.J., Malleson, P. N., Barratt, T. M., Soothill, J. F.: Circulating immune complexes in steroid-responsive nephrotic syndrome. N. Engl. J. Med. 298, 126 (1978)
Oetliker, O., Schaad, U. (Hrsg.): Nephrologie im Kindesalter III. Pädiatrische Fortbildungskurse für die Praxis, Bd. 45. Basel: Karger 1978
Reubi, F.: Nierenkrankheiten, 2. Aufl. Bern: Huber 1970
Rubenfeld, S., Garber, A.J.: Abnormal carbohydrate metabolism in chronic renal failure. The potential role of accelerated glucose production, increased gluconeogenesis, and impaired glucose disposal. J. Clin. Invest. 62, 20 (1978)
Scheinman, J. I., Fish, A. J., Matas, A. J., Michael, A. F.: The immunohistopathology of glomerular antigens. II. The glomerular basement membrane, acto-myosin, and fibroblast surface antigens in normal, diseased, and transplanted human kidneys. Am. J. Pathol. 90, 71 (1978)
Schreiner, G. F., Cotran, R. S., Pardo, V., Unanue, E. R.: A mononuclear cell component in experimental immunological glomerulonephritis. J. Exp. Med. 147, 369 (1978)
Tannenbaum, M. (ed.): Urologie pathology: The prostate. Philadelphia: Lea & Febiger 1977
Valtin, H.: Funktion der Niere. Stuttgart: Schattauer 1978
Wehner, H., Gärtner, H. V.: Immun-histologische Befunde bei nichtglomerulonephritischen Nierenerkrankungen. Virchows Arch. (Pathol. Anat.) 375, 211 (1977)
Weinman, E.J., Frankfurt, S.J., Ince, A., Sansom, S.: Renal tubular transport of organic acids. J. Clin. Invest. 61, 801 (1978)
Zager, R. A., Cotran, R. S., Hoyer, J. R.: Pathologic localization of tamm-horsfall protein in interstitial deposits in renal disease. Lab. Invest. 38, 52 (1978)
Zollinger, H. U.: Niere und ableitende Harnwege. Spezielle pathologische Anatomie (Doerr, W., Uehlinger, E., Hrsg.), Bd. 3. Berlin: Springer 1966
Alberti, K. G. M., Nattrass, M.: Lactic acidosis. Lancet 1977 II, 25
Arbus, G. S.: An in vivo acid-base nomogram for clinical use. Can. Med. Assoc. J. 109, 291 (1973)
Berl, T., Linas, St. L., Aisenbrey, G. A., Anderson, R. J.: On the mechanism of polyuria in potassium depletion. The role of polydipsia. J. Clin. Invest. 60, 620 (1977)
Charney, A. N., Kinsey, M. D., Myers, L., Giannella, R.A., Gots, R. E.: Na+-K+-activated adenosine triphosphatase and intestinal electrolyte transport. J. Clin. Invest. 56, 653 (1975)
DeFronzo, R. A., Sherwin, R. S., Dillingham, M., Hendler, R., Tamborlane, W. V., Felig, Ph.: Influence of basal insulin and glucagon secretion on potassium and sodium metabolism. Studies with somatostatin in normal dogs and in normal and diabetic human beings. J. Clin. Invest. 61, 472 (1978)
Emmett, M., Goldfarb, St., Agus, Z.S., Narins, R. G.: The pathophysiology of acid-base changes in chronically phosphate-depleted rats. J. Clin. Invest. 59, 291 (1977)
Espinel, C. H.: The influence of salt intake of the metabolic acidosis of chronic renal failure. J. Clin. Invest. 56, 286 (1975)
Horn-bostel, H., Kaufmann, W., Siegenthaler, W.: Innere Medizin in Praxis und Klinik, 2. Aufl. Bd. II: Nieren, Wasser-, Elektrolyt-und Säure-Basen-Haushalt, Nervensystem, Muskeln, Knochen, Gelenke. Stuttgart: Thieme 1978
Koepsell, H., Nicholson, W. A. P., Kriz, W., Höhling, H. J.: Measurements of exponential gradients of sodium and chlorine in the rat kidney medulla using the electron microprobe. Pflügers Arch. 350, 167 (1974)
Michelis, M. F., Murdaugh, H. V.: Selective hypoaldosteronism. Am. J. Med. 59, 1 (1975)
Sebastian, A., McSherry, E., Morris, R. C. jr.: Impaired renal conservation of sodium and chloride during sustained correction of systemic acidosis in patients with type 1, classic renal tubular acidosis. J. Clin. Invest. 58, 454 (1976)
Toback, F. G., Ordonez, N. G., Bortz, S. L., Spargo, B. H.: Zonal changes in renal structure and phospholipid metabolism in potassium-deficient rats. Lab. Invest. 34, 115 (1976)
Weiner, M., Epstein, F. H.: Signs and symptoms of electrolyte disorders. Yale J. Biol. Med. 43, 76 (1970)
Literatur
Arnaud, C. D.: Calcium homeostasis: regulatory elements and their integration. Fed. Proc. 37, 2557 (1978)
Bilezikian, J. P., Canfield, R. E., Jacobs, Th. P., Polay, J. S., D’Adamo, A. P., Eisman, J. A., DeLuca, H. F.: Response of 1α,25-Dihy-droxyvitamin D3 to hypocalcemia in human subjects. N. Engl. J. Med. 299, 437 (1978)
Brooks, M. H., Bell, N. H., Love, L., Stern, P. H., Orfei, E., Queener, S. F., Hamstra, A. J., DeLuca, H. F.: Vitamin-D-dependent rickets type II. Resistance of target organs to 1,25-Dihydroxyvitamin D. N. Engl. J. Med. 298, 996 (1978)
Canterbury, J. M., Lerman, S., Claflin, A. J., Henry, H., Norman, A., Reiss, E.: Inhibition of parathyroid hormone secretion by 25-hydroxycholecalciferol and 24,25-dihydroxycho-lecalciferol in the dog. J. Clin. Invest. 61, 1375 (1978)
David, D. S.: Calcium metabolism in renal failure and nephrolithiasis. Chichester: Wiley 1977
Goldfischer, S., Johnson, A. B., Morecki, R.: Hypophosphatasia. A cytochemical study of phosphatase activities. Lab. Invest. 35, 55 (1976)
Habener, J. F., Kronenberg, H. M.: Parathyroid hormone biosynthesis: structure and function of biosynthetic precursors. Fed. Proc. 37, 2561 (1978)
Höhling, H. J., Ashton, B. A., Köster, H. D.: Quantitative electron microscopic investigations of mineral nucleation in collagen. Cell Tiss. Res. 148, 11 (1974)
Holick, M. F., Clark, M. B.: The photobiogenesis and metabolism of vitamin D. Fed. Proc. 37, 2567 (1978)
Klein, R. G., Arnaud, S. B., Gallagher, J. C., DeLuca, H. F., Riggs, L. B.: Intestinal calcium absorption in exogenous hypercortisonism. Role of 25-hydroxy-vitamin D and corticosteroid dose. J. Clin. Invest. 60, 253 (1977)
Raute-Kreinsen, U., Beriet, H., Bühler, F., Rixner, P.: Elektronenmikroskopische Befunde am Herzmuskel der Ratte bei experimentell induzierten Elektrolytveränderungen. Virchows Arch. (Pathol. Anat.) 375, 331 (1977)
Rizzoli, R., Fleisch, H., Bonjour, J.-P.: Role of 1,25-dihydroxyvitamin D3 on intestinal phosphate absorption in rats with a normal vitamin D supply. J. Clin. Invest. 60, 639 (1977)
Tolnai, G., Shah, B. G., Sarkar, K., Levine, D. Z.: Tissue calcium content: comparison of calcium stains with atomic absorption spectroscopy. Lab. Invest. 30, 390 (1974)
Literatur
Beamish, M. R., Walker, R., Miller, F., Worwood, M., Jacobs, A., Williams, R., Corrigall, A.: Transferrin iron, chelatable iron and ferritin in idiopathic haemochromatosis. Brit. J. Haematol. 27, 219 (1974)
Bédard, Y. C., Clarke, S., Pinkerton, P. H., Simon, G. T.: Effect of cycloheximide on iron absorption. Lab. Invest. 30, 155 (1974)
Bédard, Y. C., Pinkerton, P. H., Simon, G. T.: Uptake of circulating iron by the duodenum of normal mice and mice with altered iron stores, including sexlinked anemia. Lab. Invest. 34, 611 (1976)
Bergsma, D., Cerami, A., Peterson, Ch. M., Graziano, J. H. (eds.): Iron metabolism and thalassemia, vol. XII/8, Birth Defects: Original Article Series. New York: Liss 1976
Cox, T. M., Peters, T. J.: Uptake of iron by duodenal biopsy specimens from patients with iron-deficiency anaemia and primary haemochromatosis. Lancet 1978 I, 123
Grace, N. D., Powell, L. W.: Iron storage disorders of the liver. Gastroenterology 67, 1257 (1974)
Jacobs, A.: Serum ferritin and iron stores. Fed. Proc. 36, 2024 (1977)
Kief, H. (ed.): Iron metabolism and its disorders. Workshop Conferences Hoechst, vol. 3. Amsterdam: Excerpta Medica 1975
Lalonde, J.-M.A., Ghadially, F.N., Massey, K. L.: Ultrastructure of intramuscular haematomas and electron-probe X-ray analysis of extracellular and intracellular iron deposits. J. Pathol. 125, 17 (1978)
Under, M. C., Munro, H. N.: The mechanism of iron absorption and its regulation. Fed. Proc. 36, 2017 (1977)
Richter, G. W.: Immunologic properties of ferritin. Am. J. Pathol. 72, 263 (1973)
Saddi, R., Feingold, J.: Idiopathic haemochromatosis: An autosomal recessive disease. Clin. Genet. 5, 234 (1974)
Literatur
Bell, L. T., Hurley, L. S.: Ultrastructural effects of manganese deficiency in liver, heart, kidney and pancreas of mice. Lab. Invest. 29, 723 (1973)
Brewer, G.J., Prasad, A. S. (eds.): Zinc metabolism: Current aspects in health and disease. New York: Liss 1977
Goka, Th.J., Stevenson, R.E., Hefferan, P. M., Howell, R. R.: Menkes disease: a biochemical abnormality in cultured human fibroblasts. Proc. Natl. Acad. Sci. USA 73, 604 (1976)
Iron, R. D., Schenk, E. A., Lee, J. C. K.: Cyto-chemical methods for copper. Semiquantitative screening procedure for identification of abnormal copper levels in liver. Arch. Pathol. Lab. Med. 101, 298 (1977)
Jamieson, G. A., Greenwait, T. J. (eds.): Trace components of plasma. Vol. 5, Progress in Clinical and Biological Research. New York: Liss 1976
Reed, G. B., Butt, E. M., Landing, B. H.: Copper in childhood liver disease. Arch. Pathol. 93, 249 (1972)
Rosenquist, J.: Effects of supply and withdrawal of fluoride. Experimental studies on growing and adult rabbits. 1. Concentration of fluoride in cortical bone. Acta Pathol. Microbiol. Scand. [A] 81, 630 (1973)
Rothstein, G., Clarkson, D. R., Larsen, W., Grosser, B. I., Athens, J. W.: Effect of lithium on neutrophil mass and production. N. Engl. J. Med. 298, 178 (1978)
Shrader, R. E., Hurley, L. S.: Enzyme histochemistry of peripheral blood and bone marrow in zinc-deficient rats. Lab. Invest. 26, 566 (1972)
Smith, J. C. jr., Zeller, J. A., Brown, E. D., Ong, S. C.: Elevated plasma zinc: A heritable anomaly. Science 193, 496 (1976)
Schicha, H., Kasperek, K., Feinendegen, L.E., Siller, V., Klein, H.J.: Aktivierungsanalytische Messungen einer inhomogenen teilweise parallel verlaufenden Verteilung von Kobalt, Eisen, Selen, Zink und Antimon in verschiedenen Bezirken von Leber, Lunge, Niere, Herz und Aorta. Beitr. Pathol. 146, 55 (1972)
Williams, D.M., Loukopoulos, D., Lee, G. R., Cartwright, G. E.: Role of copper in mitochondrial iron metabolism. Blood 48, 77 (1976)
Literatur
Allen, R. H., Seetharam, B., Allen, N. C., Podell, E. R., Alpers, D. H.: Correction of cobalamin malabsorption in pancreatic insufficiency with a cobalamin analogue that binds with high affinity to R protein but not to intrinsic factor. J. Clin. Invest. 61, 1628 (1978)
Allen, R. H., Seetharam, B., Podell, E., Alpers, D. H.: Effect of proteolytic enzymes on the binding of cobalamin to R protein and intrinsic factor. J. clin. Invest. 61,47 (1978)
Babior, B. M. (ed.): Cobalamin. Biochemistry and Pathophysio-logy. New York: Wiley 1975
Bang, B. G., Bang, F. B., Foard, M. A.: Lymphocyte depression induced in chickens on diets deficient in vitamin A and other components. Am. J. Pathol. 68, 147 (1972)
Erbe, R.: Inborn errors of folate metabolism. N. Engl. J. Med. 293, 753 (1975)
Hall, Ch.A.: Transcobala-mins I and II as natural transport proteins of vitamin B12. J. Clin. Invest. 56,1125 (1975)
Higginbottom, M. C., Sweetman, L., Nyhan, W. L.: A syndrome of methylmalonic aciduria, homocy-stinuria, megaloblastic anemia and neurologic abnormalities in a vitamin B12-deficient breast-fed infant of a strict vegetarian. N. Engl. J. Med. 299, 317 (1978)
Hulstaert, C.E., Gijzel, W. P., Hardonk, M.J., Kroon, A.M., Molenaar, I.: Cellular membranes and membran-bound enzymes in vitamin E deficiency. Lab. Invest. 33, 176 (1975)
Kass, L.: Major problems in internal medicine. Vol. 7: Pernicious Anemia. Philadelphia: Saunders 1976
Leelaprute, V., Boonpucknavig, V., Bhamarapravati, N., Weerapradist, W.: Hypervitaminosis A in rats. Arch. Pathol. 96, 5 (1973)
McCombs, H.L., Gershoff, St. N.: Effect of vitamin B6 deficiency on the rat kidney. Lab. Invest. 26, 515 (1972)
Prchal, J. T., Conrad, M. E., Skalka, H. W.: Association of presenile cataracts with heterozygosity for galactosaemic states and with riboflavin deficiency. Lancet 1978 I, 12
Ruddell, W.S.J., Bone, E. S., Hill, M.J., Walters, C. L.: Pathogenesis of gastric cancer in pernicious anaemia. Lancet 1978 I, 521
Sturman, J. A., Rivlin, R. S.: Pathogenesis of brain dysfunction in deficiency of thiamine, riboflavin, pantothenic acid, or vitamin B6. In: Biology of brain dysfunction (Gaul, G. E., ed.), p. 425. New York: Plenum Press 1975
Tuchweber, B., Grag, B. D., Salas, M.: Microsomal enzyme inducers and hypervitaminosis A in rats. Arch. Pathol. Lab. Med. 100, 100 (1976)
Yang, W. C., Hollenberg, M. J., Wyse, J. P. H.: Morphology of the retinal pigment epithelium in the vitamin A deficient rat. Virchows Arch. (Cell Pathol.) 27, 1 (1978)
Youngdahl-Turner, P., Rosenberg, L. E., Allen, R. H.: Binding and uptake of transcobalamin II by human fibroblasts. J. Clin. Invest. 61, 133 (1978).
Literatur
Becker, P. E. (Hrsg.): Humangenetik. Ein kurzes Handbuch in fünf Bänden. Bd. III/3: Hämatologie. Stuttgart: Thieme 1976
Brock, D. J. H., Mayo, O. (eds.): The biochemical genetics of man, 2nd ed. London: Academic Press 1978
Buddecke, E.: Pathobiochemie. Berlin: De Gruyter 1978
Chambon, P.: Eu-karyotic nuclear RNA polymerases. Ann. Rev. Biochem. 44, 613 (1975)
Cleaver, J., Bootsma, D., Friedberg, E.: Human diseases with genetically altered DNA repair processes. Genetics 79, 215 (1975)
Drake, J. W., Baltz, R. H: The biochemistry of mutagenesis. Ann. Rev. Biochem. 45, 11 (1976)
Engelman, D. M., Moore, P. B.: Neutron-scattering studies of the ribosome. Sci. Am. 235, 44 (1976)
Epstein, C. J.: Prenatal diagnosis of genetic disorders. Adv. Intern. Med. 20, 325 (1975)
Freinkel, N. (ed.): The year in metabolism 1977. New York: Plenum Press 1978
Harper, H.A., Rodwell, V. W., Mayes, P.A.: Review of physiological chemistry, 16th ed. Los Altos: Lange 1977
Harris, H., Hirschhorn, K. (eds.): Advances in human genetics, vol. 8. New York: Plenum Press 1977
Martin, G. M., Hoehn, H.: Genetics and human disease. Human Pathol. 5, 387 (1974)
McKusick, V. A.: Mendelianinheritance in man: Catalogs of autosomal dominant, autosomal recessive and X-linkes phenotypes, 4th ed. Baltimore: John Hopkins 1975
Metzler, D. E.: Biochemistry. The chemical reactions of living cells. New York: Academic Press 1977
Milunsky, A.: The prevention of genetic disease and mental retardation. Philadelphia: Saunders 1975
Molecular cytogenetics. Cold Spring Harbor Symp. Quant. Biol. 38, (1974)
Oudet, P., Gross-Bellard, M., Chambon, P.: Electron microscopic and biochemical evidence that chromatin structure is a repeating unit. Cell 4, 281 (1975)
Rich, A., Raj-Bhandary, U. L.: Transfer RNA: Molecular structure, sequence and properties. Ann. Rev. Biochem. 45, 805 (1976)
Sedgwick, R. P., Clay, S. A., Fuenzalida, S.: Cerebral degenerations in childhood. Bern: Huber 1975
Snell, E. E. (ed.): Annual review of biochemistry, vols. 45–47 (1976–1978)
Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S. (eds.): The metabolic basis of inherited disease, 4th ed. New York: McGraw-Hill 1978
Weissbach, G., Ochoa, S.: Soluble factors required for eukaryotic protein synthesis. Ann. Rev. Biochem. 45, 191 (1976)
WHO Scientific Group: Pharmacogenetics. World Health Organization technical report series no. 524. Geneva: World Health Organization 1973
Literatur
Cornwell, G. G. III, Natvig, J. B., Westermark, P., Husby, G.: Senile cardiac amyloid: Demonstration of a unique fibril protein in tissue sections. J. Immunol. 120, 1385 (1978)
Craig, J. R., Dunn, A. E. G., Peters, R. L.: Cirrhosis associated with partial deficiency of alpha-1-antitrypsin: a clinical and autopsy study. Human Pathol. 6, 113 (1975)
Eshun-Wilson, K., Frandsen, N. E., Christensen, H. E.: Pulmonary alveolar septal amyloidosis. Virchows Arch. (Pathol. Anat.) 371, 89 (1976)
Fowler, B., Kraus, J., Packman, S., Rosenberg, L. E.: Homocystinuria. Evidence of three distinct classes of cystathionine β-synthase mutants in cultured fibroblasts. J. Clin. Invest. 61, 645 (1978)
Garber, A. J.: Skeletal muscle protein and amino acid metabolism in experimental chronic uremia in the rat. J. Clin. Invest. 62, 623 (1978)
Gordon, A. H.: Amyloidosis, P component and complement. Nature 268, 14 (1977)
Hitzig, W. H.: Plasmaproteine, Pathophysiologie und Klinik, 2. Aufl. Berlin: Springer 1977
Hofer, P.-Å., Andersson, R.: Postmortem findings in primary familial amyloidosis with polyneuropathy. Acta Pathol. Microbiol. Scand. [A] 83, 309 (1975)
Jamieson, G. A., Greenwalt, T. J. (eds.): Trace components of plasma. Vol. 5. Progress in clinical and biological research. New York: Liss 1976
Kisilevsky, R., Axelrad, M., Brunei, S., Richards, M.: Effects of amyloid induction on plasma protein turnover and its implication. Am. J. Pathol. 83, 299 (1976)
Kisilevsky, R., Axelrad, M., Corbett, W., Brunei, S., Scott, F.: The role of inflammatory cells in the pathogenesis of amyloidosis. Lab. In-vest. 37, 544 (1977)
Kutty, M.K., Iqbal, Q.M., Teh, E.-Ch.: Ochronotic arthropathy. Arch. Pathol. 98, 55 (1974)
Linder, E., Anders, R. F., Natvig, J. B.: Connective tissue origin of the amyloid-related protein SAA. J. Exp. Med. 144, 1336 (1976)
McAdam, K. P. W. J., Elin, R. J., Sipe, J. D., Wolff, S. M.: Changes in human serum amyloid A and C-reactive protein after etiocholanolone-induced inflammation. J. Clin. Invest. 61, 390 (1978)
Nyhan, W. L. (ed.): Heritable disorders of amino acid metabolism: Patterns of clinical expression and genetic variation. New York: Wiley 1974
Orfila, C., de Grae-ve, P., Guilhem, A., Suc, J. M.: Study of light-, electron- and immunofluorescence microscopy of urinary sediment in amyloidosis. Virchows Arch. (Path. Anat.) 379, 113 (1978)
Ribbons, D. W., Brew, K. (ed.): Proteolysis and physiological regulation. New York: Academic Press 1976
Scotto, J. M., Stralin, H. G.: Ultrastructure of the liver in a case of childhood cystinosis. Virchows Arch. (Path. Anat.) 377, 43 (1977)
Sipe, J. D., McAdam, K. P. W. J., Uchino, F.: Biochemical evidence for the biphasic development of experimental amyloidosis. Lab. Invest. 38, 110 (1978)
Spark, E.G., Shirahama, T., Skinner, M., Cohen, A. S.: The identification of amyloid P-com-ponent (protein AP) in normal cultured human fibroblasts. Lab. Invest. 38, 556 (1978)
Schober, R., Nelson, D.: Fine structure and origin of amyloid deposits in pituitary adenoma. Arch. Pathol. 99, 403 (1975)
Stein, H., Yarom, R., Makin, M.: Synovitis of familial mediterranean fever. Virchows Arch. (Pathol. Anat. and Histol.) 367, 263 (1975)
Ullrich, K., Gospos, Ch., Böhm, N., Riede, U. N.: Zystinose. Beitr. Pathol. 158, 296 (1976)
Umbarger, H. E.: Amino acid biosynthesis and its regulation. Ann. Rev. Biochem. 47, 533 (1978)
Yunis, E.J., Agostini, R. M. jr., Glew, R. H.: Fine structural observations of the liver in α-1-antitrypsin deficiency. Am. J. Pathol. 82, 265 (1976)
Literatur
Anderson, J. H. jr., Blackard, W. G., Goldman, J., Rubenstein, A.H.: Diabetes and hypoglycemia due to insulin antibodies. Am. J. Med. 64, 868 (1978)
Andreoli, Th., Hoffman, J., Fanestil, D. D. (eds.): Physiology of membrane disorders. New York: Plenum Publ. Corp. 1978
Barnes, A. J., Kohner, E. M., Bloom, S. R., Johnston, D. G., Alberti, K. G. M. M., Smythe, P.: Importance of pituitary hormones in aetiology of diabetic ketoacidosis. Lancet 7975, I, 1171
Bilheimer, D. W., Ho, Y. K., Brown, M. S., Anderson, R. G. W., Goldstein, J. L.: Genetics of the low density lipoprotein receptor. Diminished receptor activity in lymphocytes from heterozygotes with familial hypercholesterolemia. J. Clin. Invest. 61, 678 (1978)
Brady, R. O.: Sphingolipidoses. Ann. Rev. Biochem. 47, 687 (1978)
Brady, R. O., Pentchev, P. G., Gal, A. E.: Investigations in enzyme replacement therapy in lipid storage diseases. Fed. Proc. 34, 1310 (1975)
Breckenridge, W. C., Little J. A., Steiner, G., Chow, A., Poapst, M.: Hypertriglyceridemia associated with deficiency of apolipoprotein C-II. N. Engl. J. Med. 298, 1265 (1978)
Brown, M.S., Kovanen, P. T., Goldstein, J. L., Eeckels, R., Vandenberghe, K., van den Berghe, H., Fryns, J. P., Cassiman, J. J.: Prenatal diagnosis of homozygous familial hypercholesterolaemia. Expression of a genetic receptor disease in utero. Lancet 1978, I, 526
Cantin, M., Brochu, P., Turgeon-Knaack, C., Berdnikoff, G., Simard, P., Morin, C.: Rectal biopsy in type 4 glycogenosis. Arch. Pathol. Lab. Med. 100, 422 (1976)
Capella, C., Solcia, E., Fri-gerio, B., Buffa, R., Usellini, L., Fontana, P.: The endocrine cells of the pancreas and related tumours. Virchows Arch. (Pathol. Anat.) 373, 327 (1977)
Changus, J. E., Pitot, H. C.: Cystic fibrosis. Arch. Pathol. Lab. Med. 100, 7 (1976)
Elleder, M.: A histochemical and ultrastructural study of stored material in neuronal ceroid lipofuscinosis. Virchows Arch. (Cell. Pathol) 28, 167 (1978)
Elstein, M., Parke, D. V. (eds.): Mucus in health and disease. New York: Plenum Press 1977
Felber, J.-P., Magnenat, G., Casthélaz, M., Geser, C.A., Muller-Hess, R., de Kalbermatten, N., Ebiner, J. R., Curchod, B., Pittet, P. Jéquier, E.: Carbohydrate and lipid oxidation in normal and diabetic subjects. Diabetes 26, 693 (1977)
Ginsel, L. A., Cambier, P. H., Daems, W. Th.: Fucosidosis and I-cell disease: a fine-structural and silver-staining study of abnormal inclusion bodies in smallintestinal cells. Virchows Arch. (Cell Pathol.) 27, 99 (1978)
Glew, R. H., Peters, St. P. (eds.): Practical enzymology of the sphingolipidoses. Lab. and Res. Methods in Biol. Med., vol. 1. New York: Liss 1977
Golde, D. W., Schneider, E. L., Bainton, D. F., Pentchev, P. G., Brady, R. O., Epstein, Ch. J., Cline, M. J.: Pathogenesis of one variant of sea-blue histiocytosis. Lab. Invest. 33, 371 (1975)
Greene, H. L., Wilson, F. A., Kefferan, P., Terry, A.B., Moran, J. R., Slonim, A. E., Claus, Th. H., Burr, I. M.: ATP depletion, a possible role in the pathogenesis of hyperuricemia in glycogen storage disease type I. J. Clin. Invest. 62, 321 (1978)
Hadfield, M. G., Mamunes, P., David, R. B.: The pathology of Sandhoff s disease. J. Pathol. 123, 137 (1977/78)
Hazard, J.: Accidents hypoglycé-miques provoqués par les sulfamides hypoglycémiants. Nouv. Press Méd. 5, 903 (1976)
Herbert, P. N., Forte, T., Heinen, R. J., Fredrickson, D. S.: Tangier disease. One explanation of lipid storage. N. Engl. J. Med. 299, 519 (1978)
Kaback, M. M. (ed.): Tay Sachs disease: Screening and prevention. New York: Liss 1977
Kahn, C. R., Flier, J. S., Bar, R. S., Archer, J. A., Gorden, P., Martin, M. M., Roth, J.: The syndromes of insulin resistance and acanthosis nigricans. N. Engl. J. Med. 294, 739 (1976)
Kuksis, A. (ed.): Fatty acids and glycerides. Vol. 1: Handbook of lipid research (Hanahan, D. J., ed.). New York: Plenum Press 1978
Lernmark, A., Freedman, Z.R., Hofmann, C., Rubenstein, A.H., Steiner, D. F., Jackson, R. L., Winter, R.J., Traisman, H. S.: Islet-cell-surface antibodies in juvenile diabetes mellitus. N. Engl. J. Med. 299, 375 (1978)
Lindahl, U., Höök, M.: Glycosaminoglycans and their binding to biological macromolecules. Ann. Rev. Biochem. 47, 385 (1978)
McAdams, A.J., Hug, G., Bove, K.E.: Glycogen storage disease, types I to X. Human Pathol. 5, 463 (1974)
Moody, D. E., Reddy, J. K: The hepatic effects of hypolipidemic drugs (Clofibrate, nafenopin, tibric acid and Wy-14,643) on hepatic peroxisomes and peroxisome-associated enzymes. Am. J. Pathol. 90, 435 (1978)
Navalesi, R., Pilo, A., Ferrannini, E.: Kinetic analysis of plasma insulin disappearance in nonketotic diabetic patients and in normal subjects. A tracer study with 125I-insulin. J. Clin. Invest. 61, 197 (1978)
Noseda, G.: Hypolipidämien. Schweiz. Med. Wochenschr. 105, 1233 (1975)
Pennock, C.A.: A review and selection of simple laboratory methods used for the study of glycosaminoglycan excretion and the diagnosis of the mucopolysaccharidoses. J. Clin. Pathol. 29, 111 (1976)
Raskin, Ph., Unger, R. H.: Hyperglucagonemia and its suppression. Importance in the metabolic control of diabetes. N. Engl. J. Med. 299, 433 (1978)
Rosenmann, E., Aviram, A.: Glomerular involvement in storage diseases. J. Pathol. 111, 61 (1973)
Roth, J., Roth, H: Elektronenmikroskopische Befunde an inneren Organen bei Morbus Fabry. Virchows Arch. (Pathol. Anat.) 378, 75 (1978)
Shen, B. W., Scanu, A.M., Kézdy, F. J.: Structure of human serum lipoproteins inferred from compositional analysis. Proc. Natl. Acad. Sci. USA 74, 837 (1977)
Smith, L. C., Pownall, H. J., Gotto, A. M. jr.: The plasma lipoproteins: structure and metabolism. Ann. Rev. Biochem. 47, 751 (1978)
Svoboda, D. J., Reddy, J. K: Pathology of the liver in Reye’s syndrome. Lab. Invest. 32, 571 (1975)
Schaefer, E.J., Levy, R.I., Anderson, D.W., Danner, R. N., Brewer, H. B. jr., Blackwelder, W. C.: Plasma-Triglycerides in regulation of H. D. L.-cholesterol levels. Lancet 1978, II, 391
Schonfeld, G., Bell, E., Alpers, D. H: Intestinal apoproteins during fat absorption. J. Clin. Invest. 61, 1539 (1978)
Schwartz, Ch. C., Berman, M., Vlahcevic, Z.R., Halloran, L. G., Gregory, D. H., Swell, L.: Multicompartmen-tal analysis of cholesterol metabolism in man. J. Clin. Invest. 61, 408 (1978)
Unger, R. H., Orci, L.: The essential role of glucagon in the pathogenesis of diabetes mellitus. Lancet 1975, I, 14
Vallance-Owen, J. (ed.): Diabetes: its physiological and biochemical basis. Baltimore: University Park Press 1975
Westergaard, H., Dietschy, J. M.: The mechanism whereby bile acid micelles increase the rate of fatty acid and cholesterol uptake into the intestinal mucosal cell. J. Clin. Invest. 58, 97 (1976)
White, J. G., Witkop, C. J. jr., Gerritsen, S. M.: The Hermansky-Pudlak syndrome. Am. J. Pathol. 70, 329 (1972)
Literatur
Bluestone, R., Waisman, J., Klinenberg, J. R.: Chronic experimental hyperuricemic nephropathy. Biochemical and morphologic characterization. Lab. Invest. 33, 273 (1975)
Bogusky, R. T., Lowenstein, L. M., Lowenstein, J. M.: The purine nucleotide cycle. A pathway for ammonia production in the rat kidney. J. Clin. Invest. 58, 326 (1976)
Breakfield, X. O., Castiglione, C. M., Edelstein, S. B.: Monoamine oxidase activity decreased in cells lacking hypoxanthine phosphoribosyltransferase activity. Science 192,1018 (1976)
Conger, J. D., Falk, S. A., Guggenheim, St. J., Burke, Th. J.: A micropuncture study of the early phase of acute urate nephropathy. J. Clin. Invest. 58, 681(1976)
Kanwar, Y. S., Manaligod, J. R.: Leukemic urate nephropathy. Arch. Pathol. 99, 467 (1975)
Lang, M. H., Fries, J. F.: Asymptomatic hyperuricemia: The case for conservative management. Ann. Int. Med. 88, 666 (1978)
Lenz, W., Klein, W., Huth, F.: Punktatdiagnostik von Gicht und Pseudogicht. Beitr. Pathol. 157, 161 (1976)
Prabhakararao, K., Jones, M. E.: Radioassay of orotic acid phosphoribosyltransferase and orotidylate decarboxylase utilizing a high-voltage paper electrophoresis technique or an improved 4CC>2-release method. Analyt. Biochem. 69, 451 (1975)
Stapleton, F. B., Kennedy, J., Nousia-Arvanitakis, S., Linshaw, M.A.: Hyperuricosuria due to high-dose pancreatic extract therapy in cystic fibrosis. N. Engl. J. Med. 295, 246 (1976)
Wyngaarden, J. B.: Metabolic defects of primary hyperuricemia and gout. Am. J. Med. 56, 651 (1974)
Zoref, E., de Vries, A., Sperling, O.: Mutant feedback-resistant phosphoribosylpyrophosphate synthetase associated with purine overproduction and gout. J. Clin. Invest. 56, 1093 (1975)
Literatur
Bluestone, R., Waisman, J., Klinenberg, J. R.: Chronic experimental hyperuricemic nephropathy. Biochemical and morphologic characterization. Lab. Invest. 33, 273 (1975)
Bogusky, R. T., Lowenstein, L. M., Lowenstein, J. M.: The purine nucleotide cycle. A pathway for ammonia production in the rat kidney. J. Clin. Invest. 58, 326 (1976)
Breakfield, X. O., Castiglione, C. M., Edelstein, S. B.: Monoamine oxidase activity decreased in cells lacking hypoxanthine phosphoribosyltransferase activity. Science 192,1018 (1976)
Conger, J. D., Falk, S. A., Guggenheim, St. J., Burke, Th. J.: A micropuncture study of the early phase of acute urate nephropathy. J. Clin. Invest. 58, 681(1976)
Kanwar, Y. S., Manaligod, J. R.: Leukemic urate nephropathy. Arch. Pathol. 99, 467 (1975)
Lang, M. H., Fries, J. F.: Asymptomatic hyperuricemia: The case for conservative management. Ann. Int. Med. 88, 666 (1978)
Lenz, W., Klein, W., Huth, F.: Punktatdiagnostik von Gicht und Pseudogicht. Beitr. Pathol. 157, 161 (1976)
Prabhakararao, K., Jones, M. E.: Radioassay of orotic acid phosphoribosyltransferase and orotidylate decarboxylase utilizing a high-voltage paper electrophoresis technique or an improved 4CC>2-release method. Analyt. Biochem. 69, 451 (1975)
Stapleton, F. B., Kennedy, J., Nousia-Arvanitakis, S., Linshaw, M.A.: Hyperuricosuria due to high-dose pancreatic extract therapy in cystic fibrosis. N. Engl. J. Med. 295, 246 (1976)
Wyngaarden, J. B.: Metabolic defects of primary hyperuricemia and gout. Am. J. Med. 56, 651 (1974)
Zoref, E., de Vries, A., Sperling, O.: Mutant feedback-resistant phosphoribosylpyrophosphate synthetase associated with purine overproduction and gout. J. Clin. Invest. 56, 1093 (1975)
Literatur
Benedetto, A. V., Kushner, J. P., Taylor, J. S.: Porphyria cutanea tarda in three generations of a single family. N. Engl. J. Med. 298, 358 (1978)
Berk, P. D., Blaschke, T. F., Scharschmidt, B. F., Waggoner, J. G., Berlin, N. I.: A new approach to quantitation of the various sources of bilirubin in man. J. Lab. Clin. Med. 87, 767 (1976)
Biempica, L., Kosower, M., Ma, M. H., Goldfischer, S.: Hepatic porphyrias. Arch. Pathol. 98, 336 (1974)
Bissell, D. M.: Formation and elimination of bilirubin. Gastroenterology 69, 519 (1975)
Bonkowsky, H. L., Bloomer, J. R., Ebert, P. S., Mahoney, M. J.: Heme synthetase deficiency in human protoporphyria. Demonstration of the defect in liver and cultured skin fibroblasts. J. Clin. Invest. 56, 1139 (1975)
Bridges, K.R., Schmidt, G.J., Jensen, M., Cerami, A., Bunn, H. F.: The acetylation of hemoglobin by aspirin in vitro and in vivo. J. Clin. Invest. 56, 201 (1975)
Eales, L., Grosser, Y., Sears, W. G.: The clinical biochemistry of the human hepatocutaneous porphyrias in the light of recent studies of newly identified intermediates and porphyrin derivatives. Ann. N. Y. Acad. Sci. 244, 441 (1975)
Elder, G. H., Lee, G. B., Tovey, J. A.: Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutenea tarda. N. Engl. J. Med. 299, 214 (1978)
Jaffé, E. T., Hsieh, H. S.: The metabolism of methemoglobin in human erythrocytes. In: The red blood cell, 2nd ed. (Surgenor, D.M., ed.). New York: Academic Press 1975
Kappas, A., Bradlow, H.L., Bickers, D. R., Alvares, A. P.: Induction of a deficiency of steroid Δ4–5α-reductase activity in liver by a porphyrinogenic drug. J. Clin. Invest. 59, 159 (1977)
Koff, R. S.: Postoperative jaundice. Med. Clin. North Am. 59, 823 (1975)
Kushner, J. P., Steinmuller, D. P., Lee, G. R.: The role of iron in the pathogenesis of porphyria cutanea tarda. II. Inhibition of uroporphyrinogen decarboxylase. J. Clin. Invest. 56, 661 (1975)
McGavin, M. D., Gronwall, R. R., Cornelius, C. E., Mia, A. S.: Renal radial fibrosis in mutant southdown sheep with congenital hyperbilirubinemia. Am. J. Pathol. 67, 601 (1972)
Papayannopoulou, T., Bunn, H. F., Stamatoyannopoulos, G.: Cellular distribution of hemoglobin F in a clonal hemopoietic stem-cell disorder. N. Engl. J. Med. 298, 72 (1978)
Sassa, S., Zalar, G. L., Kappas, A.: Studies in porphyria. VII. Induction of uroporphyrinogen-I synthase and expression of the gene defect of acute intermittent porphyria in mitogen-stimulated human lymphocytes. J. Clin. Invest. 61, 499 (1978)
Skelton, F. S., Witschi, H., Plaa, G. L.: The effects of cycloheximide, actinomycin D and ethio-nine on the biliary excretion of labelled alpha- naphthylisothiocy-anate in rats. Exp. Mol. Pathol. 23, 171 (1975)
Schaffner, F., Scharnbeck, H., Hutterer, F., Denk, H., Greim, H. A., Popper, H.: Mechanism of cholestasis. VIL α-Naphthylisothiocyanate-induced jaundice. Lab. Invest. 28, 321 (1973)
Schneider, R. G., Schmidt, R. M.: Electrophoretic screening for abnormal hemoglobins. In: Abnormal Hemoglobins and Thalassaemia (Schmidt, R. M., ed.). New York: Academic Press 1975
Witzleben, C. L.: Physiologic and morphologic natural history of a model of intrahepatic cholestasis (manganese-bilirubin overload). Am. J. Pathol. 66, 511 (1972)
Witzleben, C. L., Boyce, W. H.: Bilirubin as a cholestatic agent. III. Prevention of bilirubin-related cholestasis by sulfobromophthalein, IV. Effect of bilirubin and sulfobromophthalein (BSP) on biliary manganese excretion. Arch. Pathol. 99, 492, 496 (1975)
Literatur
Abedin, Z., Cherney, D. D., DiDido, L. J. A.: Myocardium of hypothermic rats with and without administration of dextran. Lab. Invest. 33, 324 (1975)
Bligh, J.: Temperature regulation in mammals and other vertebrates. Amsterdam: North Holland Publ. 1973
Bodel, P.: Studies on the mechanism of endogenous pyrogen production: III. Human blood monocytes. J. Exp. Med. 140, 954 (1974)
Bowers, W. D., Hubbard, R. W., Leav, I., Daum, R., Cordon, M., Hamlet, M. P., Mager, M., Brandt, P.: Alterations of rat liver subsequent to heat overload. Arch. Pathol. Lab. Med. 102, 154 (1978)
Kew, M. C., Minick, O. T., Baku, R. M., Stein, R. J., Kent, G.: Ultrastructural changes in the liver in heatstroke. Am. J. Pathol. 90, 609 (1978)
Reddick, R. L., Poole, B. L., Penick, G. D.: Thrombocytopenia of hibernation. Mechanism of induction and recovery. Lab. Invest. 28, 270 (1973)
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 1980 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Cottier, H. (1980). Störungen weiterer Hilfsmechanismen des Stoffwechsels und Stoffwechselkrankheiten. In: Pathogenese. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-67213-2_10
Download citation
DOI: https://doi.org/10.1007/978-3-642-67213-2_10
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-67214-9
Online ISBN: 978-3-642-67213-2
eBook Packages: Springer Book Archive