Volume 14

Treasury of human inheritance / edited by Karl Pearson, R.A. Fisher, L.S. Penrose.

Date:
1909-
    Ogilvie (71, Fig. 724), Oppenheimer (4, 35, Figs. 692, 733), Oransky (111, Figs. 596, 613, 757), Orbison (89, Fig. 657). Palmer (84, 88, Figs. 654, 753), Pamboukis (124, Fig. 705), Parkinson (85, Fig. 738), Partridge (Fig. 816), Pearson (131, Figs. 575, 590), Philip (31, Fig. 836), Pick (52, Fig. 700), Pinckney (125, Fig. 734), Polacheck (158, Fig. 830), Poore (21), Port (69, Fig. 777), Probrashensky (49, Fig. 660). Remale (25, Fig. 600), Riese (102, Fig. 598), Roberts (6), Rollin (112, Fig. 837), Rose (92, Fig. 597), Roth (Fig. 727), Rottmann (141, Fig. 680), Ruhräh (142, Fig. 763), Runge (118, Fig. 666), Russell (17, Figs. 584, 663). Sachs (55, Fig. 638), Schaefer (104, Fig. 717), Schlippe (70, Fig. 647), Schmidt (93, Fig. 695), Schotland (153, Fig. 760), Schule (38, Fig. 612), Schultowa (Fig. 619), Schultze (26, 50, Figs. 730, 765), Scolari (136, Fig. 585), Seidel (13, Fig. 756), Sessions (103, Fig. 670), Sezary (77, Fig. 722), Shaw (90, Fig. 659), Sidler (113, Fig. 620), Simpson (44, Fig. 834), Sjövall (146, Figs. 576, 579, 582, 602, 604, 617, 623, 625-627, 632, 633, 643, 665, 671, 672, 674, 675, 682, 685, 688-690, 698, 699, 702, 703, 707, 709, 723, 731. 747, 758, 775, 780, 783), Sloane (147, Fig. 711), Smit (137, Fig. 573), Smitt (137, Fig. 573), Stone (154, Fig. 818), Symes (51, Fig. 742). Timme (94, Fig. 614), Toscani (152, Fig. 833), Trevelyan (65, Fig. 835), Tromner (59, Fig. 748), Trousseau (16, Fig. 714), Turner (155, Fig. 795). Ubisch (110, Fig. 610), Underwood (1). Voshell (132, Figs. 822, 823, 826-829, 831). Wachsmuth (5), Wagner (151, Fig. 779), Waterman (105, Fig. 621), Weisz (126, Fig. 813), Weitz (98, Figs. 583, 592, 624, 634, 641, 645, 673, 676, 678, 712, 726), Wendenburg (64, Fig. 656), Wernich (14, Fig. 820), Westphal (32, 33, Figs. 601, 630), Williamson (41, Fig. 716), Winocouroff (72, Fig. 687), Wyllie (127, Fig. 708). Zimmerlin (27, Figs. 683, 771). CHRONOLOGICAL BIBLIOGRAPHY 1. Ukderwood, M.: A Treatise on the Disorders of Child hood. London, 1797. 2. Aran, E. A.: Recherches sur une Maladie non encore décrite du Systeme musculaire. (Atrophie musculaire progressive.) Arch. gén. Méd. xxiv, 5-35, 172-214. Paris, 1850. 3. Meryon, E. : On granular and fatty Degeneration of the voluntary muscles. Med. Chir. Trans, xxxv, 73-84. London, 1852. See Eigs. 578, 794, 816. 4. Oppenheimer, Z. : Ueber progressive fettige Muskelent artung. Heidelberg, 1855. See Fig. 733. 5. Wachsmuth, A.: Ueber progressive Muskelatrophie. Z. rat. Med. vn, 1-128. Heidelberg, 1855. 6. Roberts, W.: An Essay on Wasting Palsy. London, 1858. 7. Hemptenmacher, C.: De Aetiologia Atrophiae muscu laris progressivae. Diss. Berlin, 1862. See Fig. 728. 8. Meryon, E. : Practical and pathological Researches on the various forms of Paralysis. London, 1864. See Eigs. 732, 737, 815. 9. Heller, A. : Klinische Beobachtungen über die bisher als Muskelhypertrophie bezeichnete Lipomatosis luxu rians musculorum progressiva. Dtsch. Arch. klin. Med. I, 616-629. Leipzig, 1866. See Eig. 587. 10. Meryon, E. : On granular Degeneration of the voluntary muscles. Med. Chir. Trans, xlix, 45^9. London, 1866. See Fig. 745. 11. Heller, A. : Nachtrag zu den klinischen Beobachtungen über die bisher als Muskelhypertrophie bezeichnete Lipomatosis luxurians musculorum progressiva. Dtsch. Arch. klin. Med. n, 603-604. Leipzig, 1867. See Fig. 587. 12. Lutz, C.: Zwei weitere Fälle von sogenannter Muskel hypertrophie. (Lipomatosis luxurians musculorum pro gressiva.) Dtsch. Arch. klin. Med. in, 358-364. Leipzig, 1867. See Fig. 628. 13. Seidel, M.: Die Atrophia musculorum lipomatosa. Diss. Jena, 1867. See Fig. 756. 14. Wernich, A.: Fall von Muskelhypertrophie. Dtsch. Arch. klin. Med. n, 232-243. Leipzig, 1867. See Fig. 820. 15. Duchenne, G. B.: Recherches sur la Paralysie muscu laire pseudohypertrophique, ou Paralysie myo-scléro- sique. Arch. gén. Méd. XI, 5-25, 179-209, 305-321, 421- 443, 552-588. Paris, 1868. See Fig. 603. 16. Trousseau, A.: Clinique médicale de L’Hôtel Dieu de Paris. Paris, 1868. See Fig. 714. 17. Russell, J.: Two Cases of Duchenne’s Paralysis with muscular degeneration, or Paralysis with apparent hypertrophy. Med. Times and Gaz. i, 571-572. London, 1869. See Figs. 584, 663. 18. Meryon, E.: Case of granular Degeneration of the voluntary muscles. Brit. med. J. n, 32-33. London, 1870. See Fig. 686. 19. Barsickow, H. : Zwei Familien mit Lipomatosis muscu lorum progr. Diss. Halle, 1872. See Fig. 611. 20. Friedreich, N.: Über progressive Muskelatrophie; über wahre und falsche Muskelhypertrophie. Berlin, 1873. See Figs. 728, 773. 21. Poore, C. T. : Pseudohypertrophic muscular Paralysis, with an Analysis of Cases. New York med. J. xxi, 569- 596. New York, 1875. 22. Leyden, E.: Klinik der Rückenmarks-Krankheiten. Bd. n. Berlin, 1876. See Fig. 770. 23. Gowers, W. R. : Pseudohypertrophic muscular Paralysis. London, 1879. See Figs. 577, 586, 649-652, 696, 762, 789. 24. Erb, W.: Ueber die juvenile Form der progressiven Muskelatrophie. Dtsch. Arch. klin. Med. xxxiv, 467^519. Leipzig, 1884. See Figs. 677, 755, 793. 25. Remak, E.: Ueber die gelegentliche Betheiligung der Gesichtsmusculatur bei der juvenilen Form der pro gressiven Muskelatrophie. Neurol. Cbl. in, 337-341. Leipzig, 1884. See Fig. 600. 26. Schultze, F.: Hereditäre Muskelatrophie und Pseudo hypertrophie der Muskeln. Neurol. Cbl. m, 529-533. Leipzig, 1884. See Fig. 730. 27. Zimmerlin, F.: Ueber hereditäre (familiäre) progressive Muskelatrophie. Z. klin. Med. vn, 15-35. Berlin, 1884. See Figs. 683, 771.
    28. Landouzy, L. and Dejemne, J.: De la Myopathie atrophique progressive. Rev. Méd. v, 81-117, 253-366. Paris, 1885. See Figs. 595, 781. 29. Маше, P. and Guinon, G.: Contribution à l’étude de quelques-unes des Formes cliniques de la Myopathie progressive primitive. Rev. Méd. v, 793-842. Paris, 1885. See Fig. 594. 30. Landouzy, L. and Dejerine, J.: Nouvelles recherches cliniques et anatomopathologiques sur la Myopathie atrophique progressive. Rev. Méd. vi, 977-1027. Paris, 1886. See Figs. 599, 715. 31. Philip, R. W.: Primary Spastic Paralysis and Pseudo- hypertrophic Paralysis in different Members of the same Family.' Brain , vm, 520-527. London, 1886. See Fig. 836. 32. Westphal, C.: Ueber einige Fälle von progressiver Muskelatrophie mit Betheiligung der Gesichtsmuskeln. Charité-Ann. xi, 377—407. Berlin, 1886. See Fig. 601. 33. Westphal, C.: Zwei Schwestern mit Pseudohyper trophie. Charité-Ann. xii, 447-458. Berlin, 1887. See Fig. 630. 34. de Souza, V. : Zwei Fälle von juveniler Form der Muskel atrophie. Diss. Kiel, 1888. See Fig. 778. 35. Oppenheimer, E.: Beitrag z. Lehre von der Dystrophia muscularis progressiva. Diss. Strassburg, 1888. See Fig. 692. 35a. Meek, A. : On the post-embryonal History of Voluntary Muscles in Mammals. J. Anat. Physiol, хххш, 596-608. London, 1899. 36. Bielschowsky : Zwei Fälle von Dystrophia muscularis progressiva (Typus facio-scapulo-humeralis). Neurol. СЫ. ix, 13-16, 43-45. Leipzig, 1890. See Fig. 718. 37. Ebb, W. : Dystrophia muscularis progressiva. Dtsch. Z. Nervenheilk. I, 13—94, 173—260. Leipzig, 1891. See Figs. 664, 667, 694, 697, 736, 754. 38. Schüle, A.: Ein Fall von juveniler Dystrophie (auf hereditärer Basis), mit Betheiligung des Gesichts. Dtsch. Z. Nervenheilk. I, 528-531. Leipzig, 1891. See Fig. 612. 39. Koch : Zwei Fälle von Dystrophia muscularis progressiva juvenilis. Charité-Ann. xvii, 452-456. Berlin, 1892. See Figs. 639. 40. Lewin, A.: Zur Pathologie der .progressiven Muskel atrophie und verwandter Zustände. Dtsch. Z. Nerven heilk. n, 139-176. Leipzig, 1892. See Fig. 693. 41. Williamson, R. T. : Idiopathic muscular Atrophy. Med. Chron. xvn, 380-385. Manchester, 1892-1893. See Fig. 716. 42. Coley, F. C. : A Pseudohypertrophic Family. Br it. med. J. i, 399—400. London, 1894. See Fig. 635. 43. Hawkins, F. : Two Cases of Pseudohypertrophic Paraly sis in Members of the same Family. Trans, clin. Soc. xxvii, 267-268. London, 1894. See Fig. 832. 44. Simpson, J. C.: Report of five Cases of Pseudohyper trophic Paralysis occurring in one Family. Med. Press and Circ. Lvn, 57-59. London, 1894. See Fig. 834. 45. Flood, E.: Five Cases of Pseudohypertrophic Paralysis in one Family. Boston med. surg. J. cxxxiv, 564-565. Boston, 1896. See Fig. 824. 46. Esheb, A. A. : A Contribution to the Study of the Muscular Dystrophies. Amer. J. med. Sei. cxvi, 307- 325. Philadelphia, 1898. See Fig. 655. 47. Hoffmann, J.: Klinischer Beitrag zur Lehre von der Dystrophia muscularis progressiva. Dtsch. Z. Nerven heilk. xii, 418^45. Leipzig, 1898. See Fig. 752. 48. Bbegman, L. E.: Ein casuistischer Beitrag zur progres siven Muskelatrophie. Dtsch. Z. Nervenheilk. xiv, 254- 287. Leipzig, 1899. See Figs. 646, 679. 49. Pbobbashensky, P. A.: Ein Fall von Pseudohyper trophie der Muskeln. Neurol. Cbl. xvin, 333-334. Leipzig, 1899. See Fig. 660. 50. Schultze, F.: Ueber Combination von familiärer pro gressiver Pseudohypertrophie der Muskeln mit Knochen - atrophie, und von Knochenatrophie mit der “Spondy lose rhizomelique ” bei zwei Geschwistern. Dtsch. Z. Nervenheilk. xrv, 459-468. Leipzig, 1899. See Fig. 765. 51. Symes, L.: Erb’s juvenile Form of Muscular Atrophy. Brit. med. J. i, 409. London, 1899. See Fig. 742. 52. Pick, F.: Zur Kenntniss der progressiven Muskel atrophie. Dtsch. Z. Nervenheilk. xvn, 1-55. Leipzig, 1900. See Fig. 700. 53. Hahn, F.; Ueber das Auftreten von Contracturen bei Dystrophia muscularis progressiva. Dtsch. Z. Nerven heilk. xx, 137-151. Leipzig, 1901. 54. Mendel, K.: Casuistischer Beitrag zur Lehre von der Dystrophia musculorum progressiva. Neurol. Cbl. xx, 601-605. Leipzig, 1901. See Fig. 772. 55. Sachs, B. and Bbooks, H.: Progressive Muscular Dystrophy with the Report of an Autopsy. Amer. J. med. Sci. exxn, 54A73. Philadelphia, 1901. See Fig. 638. 56. Cestan, R. and Lejonne: Une Myopathie avec Re tractions, familiales. Nouv. Icon. Salpit. xv, 38-52. Paris, 1902. See Fig. 776. 57. Eshner, A. A.: Two Cases of Progressive Muscular Dystrophy in Brother and Sister. Philadelphia med. J. ix, 1023-1025. Philadelphia, 1902. See Fig. 744. 58. Jendrassik, E.: Beitrag zur Kenntniss der hereditären Krankheiten. Dtsch. Z. Nervenheilk. xxn, 444—499. Leipzig, 1902. See Figs. 814, 821. 59. Trömner, E.: Vier Fälle von progressiver Muskel dystrophie. Neurol. Cbl. xxi, 622. Leipzig, 1902. See Fig. 748. 60. Ascherson, W. L.: Case of idiopathic Muscular Atrophy. Brain, xxvi, 141-143. London, 1903. See Fig. 785. 61. Batten, F. E.: Two Cases of Muscular Atrophy of uncertain Origin. Brain, xxvi, 151. London, 1903. See Fig. 749. 62. Brasch, M.: Dystrophie bei Mutter und Kind. Berl. klin. Wschr. XL, 787. Berlin, 1903. See Fig. 607. 63. Bunting, C. H.: Three Cases of Progressive Muscular Dystrophy occurring in the male members of a single Family and commencing at the same age in each. J. nerv. ment. Dis. xxx, 350-353. New York, 1803. See Fig. 743. 64. Wendenburg, K.: Fall von eigenthümlicher familiärer Dystrophie. Neurol. Cbl. xxm, 576-577. Leipzig, 1904. See Fig. 656. 65. Trevelyan, E. F.: Erb’s juvenile Dystrophy. Rev. Neurol. Psychiat. in, 594U601. Edinburgh, 1905. See Fig. 835. 66. Dreyer, L.: Über Skelettveränderungen und Früh kontrakturen bei Dystrophia musculorum progressiva. Dtsch. Z. Nervenheilk. xxxi, 147-163. Leipzig, 1906. See Fig. 644. 67. Ingbert, C. E.: Pseudohypertrophic muscular Atrophy. J. nerv. ment. Dis. xxxiv, 1-13. New York, 1906.
    68. Kollarits, J.: Beiträge zur Kenntnis der vererbten Nervenkrankheiten. Dtsch. .Z. Nervenheilk. xxx, 293- 363. Leipzig, 1906. See Figs. 631, 636, 782. 69. Port, F. : Beitrag zur Lehre von der Dystrophia muscu laris progressiva. Z. klin. Med. Ш, 464-472. Berlin, 1906. See Fig. 777. 70. Schlippe, P. L. : Hochgradige Kontrakturen und Ske lettatrophie bei Dystrophia musculorum progressiva. Dtsch. Z. Nervenheilk. xxx, 128-143. Leipzig, 1906. See Fig. 647. 71. Ogilvie, W. and Easton, P. 0. : Two Cases of hereditary Dystrophy. Brit. med. J. ii, 867-868. London, 1907. See Fig. 724. 72. Winocouroff, J. : Zwei Fälle von Dystrophia muscu laris progressiva familiaris. Arch. Kinderheilk. xlvt, 109-112. Stuttgart, 1907. See Fig. 687. 73. Claude, H. : Dystrophie musculaire progressive familiale. L’Encéphale, ш, 512-516. Paris, 1908. See Fig. 704. 74. Finkelnburg, R.: Anatomischer Befund bei pro gressiver Muskeldystrophie in den ersten Lebensjahren. Dtsch. Z. Nervenheilk. xxxv, 453-460. Leipzig, 1908. See Fig. 701. 75. Holmes, Gordon: On the spinal changes in a Case of Muscular Dystrophy. Rev. Neurol. Psychiat. vi, 137-149. Edinburgh, 1908. See Fig. 684. 76. Bramwell, B.: Analysis of 42 cases of Pseudohyper- trophic Paralysis and Myopathic muscular Atrophy. Clin. Studies, vii, 319-328. Edinburgh, 1909. See Figs. 629, 761, 764, 767-769, 790, 791. 77. Sezary, Chenet and Jumentié: Myopathie du Type juvenile d’Erb ayant Débuté à 60 ans. Rev. neurol. xvn, 1528. Paris, 1909. See Fig. 722. 78. Batten, F. E. : The Myopathies or Muscular Dystrophies. Quart. J. Med. ш, 313-327. Oxford, 1909-10. 79.. Battle, C. J. : Fraternal Pseudohypertrophic Paralysis. Brit. med. J. ii, 197. London, 1910. See Fig. 661. 80. Carling, W. : Pseudohypertrophic Muscular Paralysis. Proc. Roy. Soc. Med. (Dis. of Child.), in, 158-159. London, 1910. See Fig. 817. 81. Chambers, H. W. : Two Cases of familial Muscular Dystrophy. W. London med. J. xv, 64И36. London, 1910. See Fig. 616. 82. Eulenburg, A. and Cohn, T.: Familiäre dystropische Heredodegeneration. (Infantile progressive Muskeldys trophie bei fünf Geschwistern.) Neurol. Cbl. xxx, 963- 975. Leipzig, 1911. See Fig. 593. 83. Batty Shaw, H. and Edmunds, P. T.: Facio-scapulo- humeral Type of Muscular Dystrophy in 4 Patients in 3 Generations. Proc. Roy. Soc. Med. (Clin. Sect.), v, 212- 214». London, 1912. See Fig. 710. 84. ' Palmer, F. S.: Two Cases of Pseudohypertrophic Paralysis in Brothers. Trans, med. Soc. London, xxxv, 391-393. London, 1912. See Fig. 654. 85. Parkinson, J. P. : Pseudohypertrophic Paralysis. Clin. J. XL, 317-318. London, 1912. See Fig. 738. 86. Haushalter, P. : Myopathie primitive progressive chez deux Frères, avec Autopsie. Rev. neurol. xxv, 587-591. Paris, 1913. See Fig. 642. 87. Hertz, A. F. and Johnson, W. : Progressive Muscular Atrophy associated with Primary Muscular Dystrophy in the second Generation. Proc. Roy. Soc. Med. (Clin. Sect.), vi, 177-181. London, 1913. See Fig. 608. 88. Palmer, F. S.: Primary progressive Myopathy, facio- scapulo-humeral (Landouzy-Dejerine) Type. Proc. Roy. Soc. Med. (Neurol. Sect.), vi, 136-137. London, 1913. See Fig. 753. 89. Orbison, T. J.: Myopathy, with clinical Reports of 8 Cases, comprising various Types. Amer. J. med. Sei. CXLVIII, 550-562. Philadelphia, 1914. See Fig. 657. 90. Shaw, A. E. B.: Pseudohypertrophic Muscular Dys trophy. Dublin J. med. Sei. cxxxvxn, 115-120. Dublin, 1914. See Fig. 659. 91. Batten, F. E.: Myopathy. Proc. Roy .Soc. Med. (Neurol. Sect.), vm, 70-71. London, 1915. See Fig. 681. 92. Rose, C. W.: Ein Fall von hereditärer progressiver Muskeldystrophie mit Beteiligung der Gesichts-, Lippen- und Zungenmuskulatur. Berl. klin. Wschr. liii, 1267- 1269. Berlin, 1916. See Fig. 597. 93. Schmidt, R.: Zwei Fälle von familiärer progressiver Muskelatrophie mit Schilddrüsenanomalien. Med. Klin. xin, 1076. Berlin, 1917. See Fig. 695. 94. Timme, W.: Progressive Muscular Dystrophy as an Endocrine Disease. Arch. int. Med. xix, 79-104. Chicago, 1917. See Fig. 614. 95. Carati, E.: Deux Cas de Myopathie atrophique ä Type scapulaire. Nouv. Icon. Salp&t. xxvm, 269-271. Paris, 1916-18. 96. Janney, N. W., Goodhart, S. P. and Isaacson, V. I.: The endocrine Origin of Muscular Dystrophy. Arch, int. Med. xxi, 188-215. Chicago, 1918. See Figs. 662, 668, 720, 721, 786-788. 97. Maiweg, H.: Progressive Muskeldystrophie und Thy- reohypoplasia. Z. ges. Neurol. Psychiat. Lxm, 107-122. Berlin, 1921. See Fig. 735. 98. Weitz, W.: Über die Vererbung bei der Muskel dystrophie. Dtsch. Z. Nervenheilk. lxxii, 143-204. Leipzig, 1921. See Figs. 583, 592, 624, 634, 641, 645, 673, 676, 678, 712, 726. 99. Eaton, H. B.: Progressive Muscular Dystrophy in a Mother and 3 Children. J. nerv. ment. Dis. LV, 311-312. New York, 1922. See Fig. 648. 100. Fraenkel, F.: Die Beziehungen der progressiven Mus keldystrophie zy. den Erkrankungen der Blutdrüsen. Z. ges. Neurol. Psychiat. Lxxvm, 283-290. Berlin, 1922. See Fig. 825. 101. Gibson, R. B., Martin, F. T. and Buell, M. van R.: A metabolic Study of progressive Pseudohypertrophic Muscular Dystrophy and other Muscular Atrophies. Arch. int. Med. xxix, 82-96. Chicago, 1922. See Fig. 838. 102. Riese, W.: Über familiäre vererbbare Dystrophien der Gesichtsmuskulatur. Dtsch. Z. Nervenheilk. lxxv, 214- 223. Leipzig, 1922. See Fig. 598. 103. Mills, H. P., Haines, T. H. and Sessions, M. A.: Familial Muscular Dystrophy. Arch. Neurol. Psychiat. xi, 43-53. Chicago, 1924. See Fig. 670. 104. Schaefer, W.: Die progressive Muskeldystrophie vom Standpunkte der inneren Sekretion. Mitt. Grenzgeb. Med. Chir. xxxvn, 128-138. Jena, 1924. See Fig. 717. 105. Waterman, F.: Drei verschiedene Formen der Dystro phia musculorum progressiva bei drei Geschwistern. Arch. Orthop. Unfall-Chirurg, xxn, 90-102. München, 1924. See Fig. 621. 106. Bramwell, E.: On the Muscular Dystrophies, Sym pathetic System and Endocrine Glands. Lancet, ii, 1103-1109. London, 1925. See Fig. 741.
    107. Hance, J. B.: A Case of Muscular Dystrophy. Pseudo- hypertrophic Type. Guy’s Hosp. Gaz. xxxix, 360-363. London, 1925. See Pig. 739. 108. Bachmann, F.: Untersuchungen bei Dystrophia mus culorum progressiva (Erb). Dtsch. Z. Nervenheilk. xcn, 28-39. Leipzig, 1926. See Fig. 792. 109. Hoffmann, H. and Clatjss, O. : Klinischer und erbbio logischer Beitrag zur Lehre von der Muskeldystrophie. Z. ges. Neurol. Psychiat. ovi, 312-324. Berlin, 1926. See Fig. 606. 110. Diehl, F., Hansen, K. and von Ubisch, G.: Der Erbgang der Dystrophia musculorum progressiva. Dtsch. Z. Nervenheilk. xcix, 54-103. Leipzig, 1927. See Fig. 610. 111. Oransky, W. : Über einen hereditären Typus pro gressiver Muskeldystrophie. Dtsch. Z. Nervenheilk. xcix, 147-155. Leipzig, 1927. See Figs. 596, 613, 757. 112. Rollin, B.: Elterliche Syphilis und Muskeldystrophie der Kinder-Keimschädigung? Dtsch. Z. Nervenheilk. xcvn, 207-216. Leipzig, 1927. See Fig. 837. 113. Minkowski, M. and Sidler, A. : Klinische und genea logische Untersuchungen zur Kenntnis der progres siven Muskeldystrophie. Arch. Julius Klaus-Stift, in, 239-298. Zürich, 1928. See Fig. 620. 114. Berblinger, W. and Duken, J.: Der kardio-intes- tinale Symptomenkomplex bei der progressiven Mus keldystrophie. Z. Kinderheilk. XLvn, 1-26. Berlin, 1929. See Fig. 839. 115. Dawidenkow, S. : Ueber die Vererbung der Dystrophia musculorum progressiva und ihrer Unterformen. Arch. Bass.- u. Ges. Biol. xxn, 169-181. München, 1929, See Figs. 581, 615, 619, 713, 727, 784. 116. Lightwood, R. C.: Pseudohypertrophic Muscular Dystrophy in Brothers. Proc. Roy. Soc. Med. (Dis. in Child.), xxii, 1250. London, 1929. See Fig. 658. 117. Niwa, C. : Uber den Vererbungsmodus von Dystrophia musculorum progressiva. Proc. Imp. Acad. Japan, v, 287-290. Tokyo, 1929. See Figs. 640, 706, 729. 118. Runge, W.: Beitrag zur Frage der Muskeldystrophie. Dtsch. Z. Nervenheilk. cvni, 255-264. Leipzig, 1929. See Fig. 666. 119. Dawidenkow, S. and Kryschowa,N. : Untersuchungen angeblich gesunder Verwandter von Muskeldystrophi- kern. Z. ges. Neurol. Psychiat. cxxv, 31-45. Berlin, 1930. See Fig. 581. 120. Goldstein, H. : Muscular Dystrophy, pseudohyper trophic Type. Arch. Pediat. xlvh, 377-383. New York, 1930. 121. Krabbe, K. H.: Late Forms of familial progressive Myopathy. J. Neurol. Psychopath, x, 289-294. London, 1930 See Fig. 746. 122. Monrad-Krohn, G. H.: Dystrophia musculorum in two Brothers whose Father presented a rudimentary myopathic Affection of one Limb only. Acta Psychiat. v, 127. Copenhagen, 1930. See Fig. 719. 123. Boas, E. P. and Lowenburg, H.: The Heart rate in Progressive Muscular Dystrophy. Arch. int. Med. XLvn, 376-383. Chicago, 1931. 124. Pambotjkis, G. : Gehäuftes Auftreten von abortiven Formen (Formes frustes) der Dystrophia musculorum . progressiva (Erb) in vier Generationen. Med. Klin. ' xxvn, 209-210. Berlin, 1931. See Fig. 705. 125. Pinckney, C. : Muscular Dystrophy, pseudohyper trophic Type, occurring in 2 Sons of the same Mother but different Fathers. Proc. Boy. Soc. Med. (Neurol. Sect.), xxv, 43-44. London, 1931. See Fig. 734. 126. Weisz, S.: Über die vegetative Innervation des quer gestreiften Muskels. Dtsch. Z. Nervenheilk. cxxi, 34-46. Leipzig, 1931. See Fig. 813. 127. Wyllie, W. G.: Muscular Dystrophy of facio-scapulo- humeral Type. Proc. Roy. Soc. Med. (Dis. of Child.), xxiv, 1183-1184. London, 1931. See Fig. 708. 128. Barnes, S.: A Myopathic Family, with hypertrophic, pseudohypertrophic, atrophic and terminal (distal in upper extremity) Stages. Brain, lv, 1—46. London, 1932. See Fig. 605. 129. Dittrich, R.: Zur Vererbung der progressiven Mus keldystrophie. Verh. dtsch. orthop. Ges. xxvr, 69-72. Stuttgart, 1932. See Fig. 819. 130. Leiter, A.: Die Adrenalinbehandlung bei progressiver Muskeldystrophie. Mschr. Psychiat. Neurol, lxxxi, 289-327. Berlin, 1932. See Fig. 591. 131. Pearson, K.: Two new Pedigrees of Muscular Dys trophy. Ann. Eugenics, v, 179-191. Cambridge, 1933. See Figs. 575, 590. 132. Voshell, A. F.: Progressive Pseudohypertrophic Mus cular Dystrophy. South, med. J. xxvi, 156-166. Bir mingham, Alabama, 1933. See Figs. 822, 823, 826-829, 831. 133. Kostakow, S.: Die progressive Muskeldystrophie, ihre Vererbung und Glykokollbehandlung. Dtsch. Arch, klin. Med. CLXXVi, 467-474. Berlin, 1934. See Fig. 569. 134. Kryschowa, N. and Abowjan, W.: Zur Frage der Heredität der Pseudohypertrophie Duchenne. Z. ges. Neurol. Psychiat. cl, 421-426. Berlin, 1934. See Fig. 574. 135. Nevin, S.: A Study of the muscle Chemistry in Myas thenia gravis, Pseudohypertrophic Muscular Dys trophy and Myotonia. Brain, Lvn, 239-254. London, 1934. See Fig. 766. 136. Scolari, E.: Su di una Famiglia con Distrofia mus colare progressiva pseudoipertrofica ad eredita Dia ginica. Boll. Soc. Ital. Pediat. ni, 262-263. Turin, 1934. See Fig. 585. 137. Smitt, W. G. S. and Smit, W. : Dystrophia musculorum progressiva mit Mikrophthalmie. Dtsch. Z. Nerven heilk. qxxxiv, 73-81. Berlin, 1934. See Fig. 573. 138. Ballif, L. and Briese, M.: Contribution à l’étude de THérédité dans la Dystrophie musculaire progressive. Bull. Soc. roum. Neurol, xvi, 110-119. Bucarest, 1935. See Fig. 609. 139. Grothatts, E.: Untersuchungen über den Erbgang der Dystrophia musculorum progressiva (Erb). Arch. klin. Chir. clxxxi, 344—362. Berlin, 1935. See Fig. 691. 140. Manson, J. S. : Hereditary Myopathy. Brit. med. J. ii, 1256. London, 1935. See Figs. 725, 740. 141. Rottmann, A. : Zur Pathogenese der progressiven Mus keldystrophie. Z. ges. Neurol. Psychiat. c t.ttt , 550-560. Berlin, 1935. See Fig. 680. 142. Ruhräii, J. : A Note on the History of Pseudohyper trophic Muscular Dystrophy) Amer. J. Dis. Child, l, 212-213. Chicago, 1935. See Fig. 763. 143. Hough, G. de N. : The hereditary aspect of progressive Pseudohypertrophic Muscular Dystrophy. New Eng land J. Med. ccxiv, 1189-1191. Boston, 1936. See Fig. 571.
    144. Hurwitz, S.: Primary Myopathies. Arch. Neurol. Psychiat. xxxvi, 1294-1316. Chicago, 1936. See Figs. 580, 588, 589, 618, 669, 750, 751, 759, 774. 145. M0ller, N. B.: Ein Familie med Dystrofia muscu lorum progressiva. Nord. med. Tidskr. xi, 93—97. Helsingfors, 1936. See Fig. 572. 146. Sjövall, B.: Dystrophia musculorum progressiva. Acta Psychiat. Neurol. Suppl. x. Copenhagen, 1936. See Figs. 576, 579, 582, 602, 604, 617, 623, 625-627, 632, 633, 643, 665, 671, 672, 674, 675, 682, 685, 688- 690, 698, 699, 702, 703, 707, 709, 723, 731, 747, 758, 775, 780, 783. 147. Arbuse, D. I. and Sloane, D.: Muscular Dystrophy; Report of a Family. N.Y. State J. Med. xxxvn, i, 1111-1118. New York, 1937. See Fig. 711. 148. Kostakow, S. and Derix, F.: Familienforschung in einer muskeldystrophischen Sippe und die Erbprognose ihrer Mitglieder. Dtsch. Arch. klin. Med. clxxx, 585— 606. Berlin, 1937. See Fig. 567. 149. Grajstozzi, G. : Osservazioni e ricerche a proposito di un Caso di Pseudoipertrofia muscolare progressiva a carattere familiare. Pediatria, xlvi, 725-739. Napoli, 1938. See Fig. 653. 150. Kostakow, S. and Bodarwé, K.: Gibt es einen ein heitlichen Erbgang bei der progressiven Muskeldys trophie? Dtsch. Arch. klin. Med. clxxxi, 611-634. Berlin, 1938. See Figs. 568, 570, 622, 637. 151. Wagner, K.: Om flere Tilfelde av Dystrophia muscu lorum progressiva i en Norsk Omstreiferslekt. Norsk. Mag. Laegevidensk. xcix, 1087-1098. Oslo, 1938. See Fig. 779. DESCRIPTION OE Plate XXXIII. Fig. 567. Kostakow and Derix’s Case. Progressive muscular dystrophy in 14 males of 3 generations; pseudohypertrophy was noted in 5 cases ; other cases appeared to be of a simple atrophic type ; it is evident that the family includes examples of varied clinical manifestations. Of the affected members, II. 8 exhibited the scapulo-humeral type of disease from the age of 17, but only found difficulty in walking up stairs at 34; he died from pneumonia at 74. III. 2 showed signs of a similar type of affection at 17 ; at 24 he complained of fatigue in walking and difficultyin mounting stairs ; at 26 weak ness and wasting of the muscles of his trunk and shoulder girdle had progressed. III. 7 was noticed to have thick calves and to have difficulty in rising from the floor at about 7 ; the con dition advanced and he died from suicide at 20. III. 13 com plained of weakness in walking and difficulty in mounting stairs at 12; at 16 he was seen with severe atrophy of the calves, thighs and pelvic girdle muscles; at 29 he was bed ridden. III. 18 began to fall easily and to have difficulty in mounting stairs at 13 ; at 30 weakness and wasting in his lower extremities was widespread ; his upper extremities and pectoral muscles remained normal ; his testes were atrophic ; no pseudo hypertrophy had occurred. III. 21 showed signs of disease in his second year at school, when his calves enlarged and weakened and he found difficulty in mounting stairs; at 25 pseudohypertrophy in his calves, with weakness and wasting in other muscles of his lower extremities and shoulders, was noted. III. 30 had difficulty in mounting stairs and in raising his arms from the age of 11 ; at 17 weakness and wasting were noted in the muscles of his shoulder girdle and upper arms ; his gait was normal ; no pseudohypertrophy was demonstrable. 152. Mtt.t-tor.at, A. T. and Toscani, V.: Metabolism of Calcium, Phosphorus and Magnesium in Progressive Muscular Dystrophy, Myotonia Atrophica and Familial Periodic Paralysis. Arch. Neurol. Psychiat. xli, 1 ISO- US?. Chicago, 1939. See Fig. 833. 153. Antopol, W. and Sohotland, C. E.: The use of Vitamin B 6 in Pseudohypertrophic Muscular Dys trophy. J. Amer. med. Assoc, cxrv, 1058-1059. Chicago, 1940. See Fig. 760. 154. Stone, S.: Treatment of Muscular Dystrophies and allied Conditions. J. Amer. med. Assoc, oxiv, 2187- 2191. Chicago, 1940. See Fig. 818. 155. Turner, J. W. A.: The relationship between Amyo tonia congenita and congenital Myopathy. Brain, Lxm, 163-177. London, 1940. See Fig. 795. 156. Epstein, B. S. and Abramson, J. L.: Roentgenologic Changes in the Bones in Cases of Pseudohypertrophic Muscular Dystrophy. Arch. Neurol. Psychiat. xlvi, 868-876. Chicago, 1941. 157. Fitzgerald, G. and McArdle, B.: Vitamins E and B 6 in the Treatment of Muscular Dystrophy and Motor Neurone Disease. Brain, Lxrv, 19—42. London, 1941. 158. Polaoheok, W. S.: Heredity of Pseudohypertrophic Muscular Dystrophy. Amer. J. Dis. Child, lxi, 1251— 1253. Chicago, 1941. See Fig. 830. 159. Bell, J.: On the Age of Onset and Age at Death in Hereditary Muscular Dystrophy with some Obser vations bearing on the question of Antedating. Ann. Eugenics, xi, 272-289. Cambridge, 1942. PEDIGREE PLATES III. 35 had difficulty in rising from the floor from the age of 5; at 29 severe weakness and wasting were found in his lower extremities and in some muscles of his trunk; his gait was waddling; his shoulder girdle and upper arm muscles were still normal. III. 37 first became aware of difficulty in rising from the floor at 12; at 21 his condition resembled that of III. 35; no pseudohypertrophy was demonstrable. IV. 1 had difficulty in mounting stairs and in rising from a fall at the age of 4; at 6 pseudohypertrophy of his calves had occurred with wasting of his thighs and of his pelvic girdle muscles. IV. 9 showed signs of disease at 2; at 6 wasting and weakness were noted in his thighs and erector spinae muscles; slight winging of his scapulae was demonstrable. IV. 10, a very nervous child, had difficulty in rising from the floor at 2, when his calves were seen to be thicker than normal; at 14 his condition had progressed and some pseudohypertrophy'was noted; his upper extremities still functioned normally. IV. 15 was subject to night terrors and was a neuropath at 9; some muscular weakness, without demonstrable atrophy, was noted. IV. 19 had always risen from the floor in the characteristic way and had thickened calves; at 10 he waddled; pseudo hypertrophy was marked in his calves; his thighs and some muscles of his trunk were wasted; no affection of his upper extremities was yet demonstrable. IV. 20 showed signs of disease at 3; at 4 he waddled, with protuberant abdomen; atrophy was noted in the muscles of his thighs and pelvic girdle; no pseudohypertrophy is described in his case. The affected members of this family appear to have had no associated defects and to have developed normally apart from their muscular disease; III. 13, 21, 30, 37, IV. 9 and 20'