Volume 6

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

Date:
1909-
Catalogue details

Licence: Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)

Credit: Treasury of human inheritance / edited by Karl Pearson, R.A. Fisher, L.S. Penrose. Source: Wellcome Collection.

    33/106 (page 293)
    74. Cockayne, E. A.: Hereditary Blue Sclerotics and Brittle Bones. Ophthalmoscope. Yol. xn, pp. 271— 272. London, 1914. See Fig. 622. 75. Ostheimer, M.: Fragilitas Ossium. Journal of American Medical Association. Voi. LXIII, pp. 1996— 1999. Chicago, 1914. [Gives the views held by many writers concerning the pathology of the disease a,nd describes a case, with negative family history, of a female aged 3 years who had already had nine fractures, the first occurring at the age of 1J years and of whom her mother says “she breaks her leg almost every time she tries to stand up”; the condition was associated with deep blue sclerotics.] 76. Tillaye: Osteopsathyrosis héréditaire familiale. Revue d’Orthopédie. T. XV, pp. 113—117. Paris, 1914. See Fig. 682. 77. Wkede, L. : Osteopsathyrosis idiopathica. Münchener medizinische Wochenschrift. Bd. Lxi, S. 847. München, 1914. 78. Herrman, C.: Blue Sclerotics associated with Brittle Bones. American Journal of Diseases of Children. Yol. ix, pp. 205 — 212. Chicago, 1915. 79. Hofmann, W.: Ueber Blaufärbung der Sklera und abnorme Knochenbrüchigkeit. Archiv f. klinische Chirurgie. Bd. cvn, S. 279—285. Berlin, 1915. See Figs. 653, 658. 80. *Salvetti, C.: Osteopsatirosi e Sclerotica blu. Clinica Chirurgia. T. xxiii, pp. 298—301. Milano, 1915. [Abstract in Zentralblatt f. Chirurgie. Bd. xlii, p. 414. Leipzig, 1915.] See Fig. 657. 81. Stephenson, S.: Blue Sclerotics. Transactions, Ophthalmological Society of TJ. K. Vol. xxxv, pp. 274— 276. London, 1915. See Fig. 602. 82. Kienböck, B,.: Über infantile Osteopsathyrose. Fortschritte auf dem Gebiete der Röntgenstrahlen. Bd. XXIII, S. 122—168. Hamburg, 1915—1916. [Contains a valuable contribution to the subject with abstracts of many published cases in addition to several new cases and a bibliography; two plates of X-rays are included.] 82a. Cameron, H. C.: Osteogenesis Imperfecta. Proceedings, Royal Society of Medicine. Voi. ix. Sect. Disease in Children, pp. 43—47, 48—50. London, 1916. 83. Bronson, E.: On Fragilitas Ossium and its Association with Blue Sclerotics and Otosclerosis. Edinburgh Medical Journal. Voi. xviii, pp. 240—281. Edinburgh, 1917. See Figs. 613, 624. 84. Goldbloom, A.: Fragilitas Ossium, with Report of a Case. Canadian Medical Association .Journal. Vol. vu (new series), pp. 636—640. Toronto, 1917. 85. Van der Hoeve, J. and Kleijn, A. de: Blauwe Sclera, Broosheid van het Beenstelsel en Gehoor- stoornissen. Nederlandsch Tijdschrift voor Geneeskunde. licei lui, pp. 1003—1010. Haarlem, 1917. See Fig. 616. 86. Mixsell, H. R.: Osteogenesis Imperfecta (Osteopsathyrosis, Fragilitas Ossium), with Report of two Cases. Archives of Pediatrics. Voi. xxxiv, pp. 756—764. New York, 1917. 87. Rothschild, A.: Ueber die Vereinigung von blauer Sklera und Knochenbrüchigkeit nebst kasuistischen Mitteilungen. Dissertation. München, 1917. 88. Whipjian, T. R. : Case of Fragilitas Ossium. Proceedings, Royal Society of Medicine. Vol. x. Sect. Disease in Children, pp. 68—71. London, 1917. [The case is associated with blue sclerotics and has protuberances in the temporal regions of the skull; family history negative.] 89. Coulon, F. A.: Blue Sclerotics; a note upon associated Otosclerosis. American Journal of Ophthal mology. Ser. 3, Vol. i, pp. 726—727. Chicago, 1918. See Fig. 604. 90. Van der Hoeve, J. and Kleijn, A. de: Blaue Sclera, Knochenbrüchigkeit und Schwerhörigkeit. Archiv f. Ophthalmologie. Bd. xcv, S. 81—93. Berlin, 1918. See Figs. 610, 616. 91. Marconi, A.: Contributo allo Studio della Fragilità ossea associata a Sclerotica azzurra. Gazzetta degli Ospedali e delle Cliniche. Tom. xxxix, pp. 367—368. Milano, 1918. 92. Terry, W. I.: Hereditary Osteopsathyrosis. Transactions, American Surgical Association. Vol. xxxvi, pp. 317—326. Philadelphia, 1918. See Fig. 627. 93. Vooriioeve, N.: Blue Sclerotics in connexion with other Hereditary or Congenital Abnormalities. Lancet. Voi. и for 1918, pp. 740—741. London, 1918. See Fig. 612. 94. Bolten, G. C.: Beitrag zur Kenntnis der Pathogenese der Fragilitas Ossium Congenita (Osteopsa thyrosis infantilis). Deutsche Zeitschrift f. Nervenheilkunde. Bd. lxiii, S. 343—359, Leipzig, 1919. See Figs. 630, 660. 95. Bronson, E.: Osteogenesis Imperfecta. Proceedings, Royal Society of Medicine. Vol. xn. Sect. Disease in Children, pp. 15—17. London, 1919. [Two unrelated cases are described, neither of which is associated with blue sclerotics; Case i has a negative family history.] See Fig. 700. 38 в. T.