書籍詳細

VI. 筋原性疾患

P.131 掲載の参考文献

• 1) Ebashi, S., Toyokura, Y., Momoi, H., and Sugita, H.: High creatine phosphokinase activity of sera of progressive muscular dystrophy patients, J Biochem 46: 103, 1959.

• 2) Gowers, W. R.: Clinical lecture on pseudohypertrophic muscular paralysis, Lancet II: 1, 1879.

• 3) Emery, A. E. H., and Walton, J. N.: The genetics of muscular dystrophy, Progr Med Genet 5; 116, 1967.

• 4) Becker, P. E.: Eine neue X-chromosomale Muskeldystrophie, Arch Psychiat Nervenkr 193: 427, 1955.

• 5) Tyler, F. J., and Stephens, F. E.: Studies in disorders of muscle: II. Clinical manifestations and inheritance of facioscapulohumeral dystrophy in a large family, Ann Intern Med 32: 640, 1950.

• 6) Jackson, C. E., and Strehler, D. A.: Limbgirdle muscular dystrophy: Clinical manifestations and detection of preclinical disease, Pediatrics 41: 495, 1968.
  pubmed

• 7) Vanier, T. M.: Dystrophia myotonica in childhood, Brit Med J 2: 184, 1960.

• 8) Drucker, W. D., Rowland, L. P., Sterling, K, and Christy, N. P.: On the function of the endocrine glands in myotonic muscular dystrophy, Amer J Med 31: 941, 1961.
  pubmed

• 9) Wochner, R. D., Drews, G., Strober, W., and Waldmann, T. A.: Accelerated breakdown of immunoglobulin G (IgG) in myotonic dystrophy: A hereditary error of immunoglobulin catabolism, J Clin Invest 45: 321, 1966.
  pubmed

• 10) Munsat, T. L.: Therapy of myotonia: A double-blind evaluation of diphenylhydantoin, procainamide and placebo, Neurology 17: 359, 1967.
  pubmed

• 11) Welander, L.: Myopathia distalis tarda hereditaria, Acta Med Scand 141 (suppl 265): 1, 1951.

• 12) Fukuyama, Y., Kawazura, M, and Haruna, H.: A peculiar form of congenital progressive muscular dystrophy. Pediat Univ Tokyo, 4: 5, 1960.

• 13) Magee, K. R., and DeJong, R. N.: Hereditary distal myopathy with onset in infancy, Arch Neurol 13: 387, 1965.
  pubmed

• 14) Van der Does de Willebois, A. E. M., Bethlem, J., Meyer, A. E. F. H., and Simons, A. J. R.: Distal myopathy with onset in early infancy, Neurolagy 18: 383, 1968.

• 15) Caughey, J. E.: Relationship of dystrophia myotonica (myotonic dystrophy) and myotonia congenita (Tomsen's disease),Neurology 8: 469, 1958.

• 16) Hoffman, E. P., Brown, R. H., and Kunkel, L. M.: Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51: 919, 1987.
  pubmed

• 17) Kazakov, V. M, Bogorodinsky, D. K., Znoyko, Z. V., and Skorometz, A. A.: The facioscapulo-limb (or the facioscapulohumeral) type of muscular dystrophy. Eur Neurol 11: 236, 1974.
  pubmed

P.171 掲載の参考文献

• 1) Shy, G. M., and Magee, K. P.: A new congenital non-progressive myopathy, Brain 79: 610, 1956.

• 2) Shy, G. M, Engel, W. K., Somers, J. E., and Wanko, T.: Nemaline myopathy: A new congenital myopathy, Brain 86: 793, 1963.
  pubmed

• 3) Sugita, H., Masaki, T., and Ebashi, S.: Staining of myofibrils with fluorescent antibody against the 10 S component of the original α-actinine preparation, J Biochem, 75: 671, 1974.

• 4) Spiro, A. J., Shy, G. M, Gonatas, N K.: Myotubular myopathy, Arch Neurol 14: 1, 1966.
  pubmed

• 5) Shy, G. M, Gonatas, N K., and Perez, M: Two childhood myopathies with abnormal mitochondria: I. Megaconial myopathy; II. Pleoconial myopathy, Brain 89: 133, 1966.
  pubmed

• 6) Luft, R., Ikkos, D., Palmieri, G., Ernstes, L., and Afzelius, B.: A case of severe hypermetabolosm of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: A correlated clinical, biochemical and morphological study, J Clin Invest 41: 1776, 1963.

• 7) DiMauro, S., Schotland, D. L, Bonilla, E, Lee, C., Gambetti, P., and Rowland, L. P.: Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondria, Arch Neurol 29: 170, 1973.
  pubmed

P.186 掲載の参考文献

• 1) Aitken, R. S., Allott, E. N., Castleden, L. I. M., and Walker, M: Observation on a case of familial periodic paralysis, Clin Sci 3: 47, 1937.

• 2) Shy, G. M., Wanko, T., Rowley, P. T., and Engel, A. G.: Studies in familial periodic paralysis, Exp Neurol 3: 53, 1961.

• 3) Gamstorp, I.: Adynamia episodica hereditaria, Acta Paediat 45 (suppl 108): 1, 1956.

• 4) Posakanzer, D. C., and Kerr, D. N S.: A third type of periodic paralysis with normokalemia and favorable response to sodium chloride, Amer J Med 31: 328, 1961.

• 5) Okinaka, S., Shizume, K., Watanabe, A., Irie, M., Naguchi, A., Kuma, S., Kuma, K., and Ito, T.: The association of periodic paralysis and hyperthyroidism in Japan, J Clin Endocr 17: 1454, 1957.

• 6) Van Horn, G., Drori, J. B., and Schwartz, F. D.: Hypokalemic myopathy and elevation of serum enzymes, Arch Neurol 22: 335, 1970.
  pubmed

P.199 掲載の参考文献

• 1) Thomsen, J.: Tonische Krampfe in willkurlich beweglicher Muskeln in Folge von erebterpschischer Disposition (Ataxia muscularis?), Arch Psychiat Nervenkr 6: 706, 1876.

• 2) Becker, P. E.: "Myopathies," in Becker, P. E. (ed.): Humangenetik, Stuttgart: Georg Thieme Verlag, 1964, vol 3/1.

• 3) Huttenlocher, P. R., Landwirth, J., Hanson, V., Gallagher; B. B., and Bensch, K.: Osteo-chondro-muscular dystrophy: A disorder manifested by multiple skeletal deformities, myotonia, and dystrophic changes in muscle, Pediatrics 44: 945, 1969.
  pubmed

• 4) Wolf, A: Quinine: An effective form of treatment for myotonia: Preliminary report of four cases, Arch Neurol Psychiat 36: 382, 1936.

• 5) Geschwind, N., and Simpson, J. A.: Procaine amide in the treatment of myotonia, Brain 78: 81, 1955.
  pubmed

• 6) Munsat, T. L.: Therapy of myotonia: A double-blind evaluation of diphenylhydantoin, procainamide and placebo, Neurology 17: 359, 1967.
  pubmed

P.204 掲載の参考文献

• 1) Lutwak, L.: Myositis ossificans progressiva: Mineral, metabolic and radioactive calcium studies of the effects of hormones, Amer J Med 37: 269, 1964.
  pubmed

• 2) Ellis, M., and Frank, H. G.: Myositis ossificans traumatica: With special reference to the quadriceps femoris muscle, J Trauma 6: 724, 1966.

• 3) Dejerine (Mme), Cellier, A., and Dejerine, Y.: Para-osteo-arthro-pathies des paraplegiques par lesion medullaire: Etude anatomique et histologique, Rev Neurol 35: 399, 1919.

P.207 掲載の参考文献

• 1) Hers, H. G.:α-Glucosidase deficiency in generalized glycogen storage disease (Pompe's disease), Biochem J 86: 11, 1963.

• 2) Swaiman, K. F., Kennedy, W. R., and Sauls, H. S.: Late infantile acid maltase deficiency, Arch Neurol 18: 642, 1968.
  pubmed

• 3) Forbes, G. B.: Glycogen storage disease: Report of a case with abnormal glycogen structure in liver and skeletal muscle, J Pediat 42: 645, 1953.
  pubmed

• 4) Anderson, D. H.: Familial cirrosis of the liver with storage of abnormal glycogen, Lab Invest 5: 11, 1956.

• 5) Pearson, C. M., Rimer, D. G, and Mommaerts, W. F. H. M.: A metabolic myopathy due to absence of muscle phosphorylase, Amer J Med 30: 502, 1961.

• 6) Tarui, S., Okuno, G., Ikura, Y., Tanaka, T., Suda, M., and Nishikawa, M.: Phosphofructokinase deficiency in skeletal muscle: A new type of glycogenosis, Biochem Biophys Res Commum 19: 517, 1965.

• 7) Satoyoshi, E., and Kowa, H.: Amyopathy due to glycolytic abnormality, Arch Neurol 17: 248, 1967.

• 8) Dreyfus, J. C., and Alexandre, Y.: Immunological studies on glycogen storage diseases type III and V. Demonstration of the presence of an immunoreactive protein in one case of muscle phosphorylase deficiency, Biochem Biophys Res Commun 44: 1364, 1971.

• 9) Engel, A. G.: Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies. Brain 93: 599, 1970.
  pubmed

P.214 掲載の参考文献

• 1) Brown, J., Coburn, J. W., Wood, R. A., Hiss, J. M., Jr., and Dowling, J. T.: Adrenal steroid therapy of severe infiltrative ophthalmopathy of Graves' disease, Amer J Med 34: 786, 1963.

• 2) Kalow, W., Britt, B. A., Terreau, M. E., and Haist, C.: Metabolic error of muscle metabolism after recovery from malignant hyperthermia, Lancet, II. 895, 1970.

• 3) Shoji, S., Takagi, A., Sugita, H., and Toyokura, Y.: Muscle glycogen metabolism in steroid-induced myopathy of rabbits, Exp Neurol 45: 1, 1974.
  pubmed

• 4) Bradley, W. G., Lassman, L P., Pearce, G. W., and Walton, J. N.: The neuromyopathy of vincristine in man: Clinical, electrophysiological and pathological studies, J Neurol Sci 10: 107, 1970.
  pubmed

• 5) Somers, J. E., and Winer, N.: Reversible myopathy and myotonia following administration of a hypocholesterolemic agent, Neurology, 16: 761, 1966.

• 6) Langer, T., and Levy, R. I.: Acute muscular syndrome associated with administration of clofibrate, New Eng J Med 279: 856, 1968. 544, 1981.

P.225 掲載の参考文献

• 1) Brown, J., Coburn, J. W., Wood, R. A., Hiss, J. M., Jr., and Dowling, J. T.: Adrenal steroid therapy of severe infiltrative ophthalmopathy of Graves' disease, Amer J Med 34: 786, 1963.

• 2) Kalow, W., Britt, B. A., Terreau, M. E., and Haist, C.: Metabolic error of muscle metabolism after recovery from malignant hyperthermia, Lancet, II. 895, 1970.

• 3) Shoji, S., Takagi, A., Sugita, H., and Toyokura, Y.: Muscle glycogen metabolism in steroid-induced myopathy of rabbits, Exp Neurol 45: 1, 1974.
  pubmed

• 4) Bradley, W. G., Lassman, L P., Pearce, G. W., and Walton, J. N.: The neuromyopathy of vincristine in man: Clinical, electrophysiological and pathological studies, J Neurol Sci 10: 107, 1970.
  pubmed

• 5) Somers, J. E., and Winer, N.: Reversible myopathy and myotonia following administration of a hypocholesterolemic agent, Neurology, 16: 761, 1966.

• 6) Langer, T., and Levy, R. I.: Acute muscular syndrome associated with administration of clofibrate, New Eng J Med 279: 856, 1968. 544, 1981.

P.228 掲載の参考文献

• 1) Denny-Brown, D.: The nature of polymyositis and related diseases, Trans Assoc Amer Physicians 28: 14, 1960.

• 2) Pearson, C. M.: Patterns of polymyositis and their responses to treatment, Ann Intern Med 59: 827, 1963.
  pubmed

• 3) Eaton, L. M.: Perspective of neurology in regard to polymyositis: Study of 41 cases, Neurology 4: 245, 1954.
  pubmed

• 4) Hunder, G. G., Disney, T. F., and Ward, L. E.: Polymyalgia rheumatica, Mayo Clin Proc 44: 849, 1969.
  pubmed

• 5) Jellinek, E. H.: The orbital pseudotumor syndrome and its differentiation from endocrine exophthalmos, Brain 92: 35, 1969.

• 6) Dau, P. C.: Plasmapheresis in idiopathic inflammatory myopathy. Experience with 35 patients. Arch Neurol 38: 544, 1981.
  pubmed

VII. 神経・筋接合部の伝達障害による疾患

P.251 掲載の参考文献

• 1) Osserman, K. E., and Whipple, H. E.: Myasthenia gravis. Ann NY Acad Sci 135: 1, 1966.

• 2) Elmqvist, D.: Neuromuscular transmission with special reference to myasthenia gravis, Acta Physiol Scand 64 (suppl 249): 1, 1965.

• 3) Eaton, L. M., and Lambert, E. H.: Electromyography and electric stimulation of nerves in diseases of motor unit: observations on myasthenic syndrome associated with malignant tumors, J Amer Med Ass 161: 1117, 1957.

• 4) Elmquist, D., and Lambert, E. H.: Detailed analysis of neuromuscular transmission in a patient with the myasthenia syndrome sometimes associated with bronchogenic carcinoma. Mayo Clin Proc 43: 689, 1968.

• 5) Patrick, J., and Lindstrome, J. M.: Autoimmune response to acethylcholine receptor. Science 180: 871, 1973.

• 6) Lang, B., Newsom-Davis, J., Wray, D. et al.: Autoimmune etiology for myasthenic (Eaton-Lambert) syndrome. Lancet II: 224, 1981.

あとがき

P.269 掲載の参考文献

• 1) Swinyard, C. A., and Mayer V.: Multiple congenital contractures: Public health considerations of arthrogryposis multiplex congenita, JAMA 183: 23, 1963.
  pubmed

• 1) "Merritt's Textbook of Neurology". Seventh Edition, Ed by Rowland LP, Lea & Febiger, Philadelphia, 1984.

• 1) Engel, A. G., and Siekert, R. G.: Lipid storage myopathy responsive to prednisone. Arch Neurol, 27: 174, 1972.
  pubmed

• 1) Ask-Upmark, E: Precipitating factors in the pathogenesis of amyotrophic lateral sclerosis, Acta Med Scand 170: 717, 1961.
  pubmed

• 2) "Disorders of Voluntary Muscle". Fourth Edition, Ed by Waltion J, Churchill Livingstone, Edinburgh, London, Melbourne and New York, 1981.

• 2) "Motor Neuron Diseases "Norris, F. H., Jr. and Kurrland, L. T. (Eds.) Grune and Stratton, New York and London, 1969.

• 2) Victor, M., Hayes, R., and Adams, R. D.: Oculopharyngeal muscular dystrophy: A familial diseases of late life characterized by dysphagia and progressive ptosis of the eyelids, New Eng J Med 267: 1267, 1962.

• 2) Engel, A. G, and Angelini, C.: Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: A new syndrome. Science, 179: 899, 1973.
  pubmed

• 3) Buchthal, F., and Zander Olsen, P.: Electromyography and muscle biopsy in infantile spinal muscular atrophy, Brain 93: 15, 1970.

• 3) DiMauro, S. and DiMauro, P. M. M.: Muscle carnitine palmityl transferase deficiency and myoglobinuria. Science, 182: 929, 1973.

• 3) "Myology. "Eds by Engel AG and Banker BQ, McGraw-Hill, New York, 1986.

• 3) Rosenberg, R., Schotland, D. L., Lovelace, R. E., and Rowland, L. P.: Progressive ophthalmoplegia: Report of cases, Arch Neurol 19: 362, 1968.

• 4) Dunne, P. B., and Chutorian, A.: The relationship between infantile and juvenile spinal muscular atrophy, Neurology 16: 306, 1966.

• 4) "Brain's Disease of the Nervous System". Nineth edition, Walton J, Oxford, 1985.

• 4) Kaeser, H. E.: Scapuloperoneal muscular atrophy, Brain 88: 409, 1965.

• 5) Zellweger, H., and McCormick, W. F.: Scapuloperoneal dystrophy and scapul-operoneal atrophy, Helv Paediat Acta 23: 643, 1968.

• 5) Elizan, T. S., Hirano, A., Abrahams, B. M., Need, R. L., Van Nuis, C., and Kurland, L. T.: Amyotophic lateral sclerosis and parkinsonism-dementia complex of Guam: Neurological re-evaluation, Arch Neurol 14: 356, 1966.

• 5) "Clinical Neurology". Eds by Baker AB and Baker LH, Harper and Row, New York, 1987.

• 6) Furukawa, T., Tsukagoshi, H., Sugita, H., and Toyokura, Y.: Neurogenic muscular atrophy simulating facioscapulohumeral muscular dystrophy: With particular reference to the heterogeneity of Kugelberg-Wellander disease, J Neurol Sci 9: 389, 1969.

• 7) Hirano, A., Kurland, L. T., and Sayre, G. P. : Familial amyotrophic lateral screlosis, Arch Neurol 16: 232, 1967.

• 8) Kugelberg, E., and Welander, L.: Heredofamilial juvenile muscular atrophy simulating muscular dystrophy. Arch Neurol Psychiat 75: 500, 1956.

• 9) Tsukagoshi, H., Nakanishi, K., Kondo, K. et al.: Hereditary proximal neurogenic muscular atrophy in adult. Arch Neurol 12: 597, 1965.

• 10) Werdnig, G.: Zwei fruhinfantile hereditare Falle von progressiver Muskelatrophie unter dem Bilde der Dystrophie, aber auf neurotischer Grundlage, Arch Psychiat Nervenkr 22: 437, 1981.

• 11) Spencer, P. S., Nunn, P. B., Hugon, J., Ludolpf, A. C., Ross, S. M, Roy, D. N. and Robertson, R. C.: Guam amyotrophic lateral sclerosis-Parkinsonism-dementia linked to a plant excitant neurotoxin. Science 237: 517, 1987.