Johann Jakob Wepfer (1620-95) and cerebral haemorrhage.

نویسنده

  • J M Pearce
چکیده

6 Weiller C, Ferbert A. Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN Type VI, Vizioli). Eur Arch Psychiatry Clin Neurosci 1991;240: 246-9. 7 Vizioli F. Dell'atrofia progressiva nervosa. Bollettino della R Accademia Medico-Chirurgica di Napoli 1889;1: 173-83. 8 Sainton P. L'amyotrophie type Charcot-Marie [MD thesis]. University of Paris: Paris, 1899. 9 Ballet G, Rose F. Un cas d'amyotrophie du type CharcotMarie avec atrophie des deux nerfs optiques. Rev Neurol 1904;12:522-4. 10 Schneider DE, Abeles MM. Charcot-Marie-Tooth disease with primary optic atrophy. Report of two cases occurring in brothers. JNerv Ment Dis 1937;85:541-7. 11 Chalmers RM, Bird AC, Harding AE. Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy. J Neurol Neurosurg Psychiatry 1996;60: 195-6. 12 Milhorat AT. Studies in diseases of muscle. XIV. Progressive muscular atrophy of peroneal type associated with atrophy of the optic nerves: report on a family. Arch Neurol Psychiatry 1943;50:279-87. 13 Hagemoser K, Weinstein J, Bresnick G, Nellis R, Kirkpatrick S, Pauli RM. Optic atrophy, hearing loss, and peripheral neuropathy. Am Jf Med Genet 1989;33: 61-5. 14 Taylor J. ?Peroneal atrophy. Proc R Soc Med 1913;6:50. 15 Rosenberg RN, Chutorian A. Familial optoacoustic nerve degeneration and polyneuropathy. Neurology 1967;17: 827-32. 16 Harding AE. From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins. Brain 1995;118:809-18. 17 Eiberg H, Kjer B, Kjer P, Rosenberg T. Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis. Hum Mol Genet 1994;3:977-80.

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عنوان ژورنال:
  • Journal of neurology, neurosurgery, and psychiatry

دوره 62 4  شماره 

صفحات  -

تاریخ انتشار 1997