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Volumn 60, Issue 2, 1996, Pages 195-196

Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy

Author keywords

Hereditary motor and sensory neuropathy; Optic atrophy; Peripheral neuropathy

Indexed keywords

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; DISEASE ASSOCIATION; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; OPTIC NERVE ATROPHY; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL;

EID: 0030026084     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.60.2.195     Document Type: Article
Times cited : (22)

References (20)
  • 3
    • 0141554860 scopus 로고
    • Un cas d'amyotrophie du type Charcot-Marie avec atrophie des deux nerfs optiques
    • Ballet G, Rose F. Un cas d'amyotrophie du type Charcot-Marie avec atrophie des deux nerfs optiques. Rev Neurol 1904;12:522-4.
    • (1904) Rev Neurol , vol.12 , pp. 522-524
    • Ballet, G.1    Rose, F.2
  • 4
    • 0001741720 scopus 로고
    • Charcot-Marie-Tooth disease with primary optic atrophy. Report of two cases occurring in brothers
    • Schneider DE, Abeles MM. Charcot-Marie-Tooth disease with primary optic atrophy. Report of two cases occurring in brothers. J Nerv Ment Dis 1937;85:541-7.
    • (1937) J Nerv Ment Dis , vol.85 , pp. 541-547
    • Schneider, D.E.1    Abeles, M.M.2
  • 5
    • 0141666327 scopus 로고
    • Atrophie musculaire neurogène du type Charcot-Marie-Tooth-Hoffman, associée à une atrophie optique bilatérale
    • Brihaye M, Nenquin-Klaassen E, Bertholet G. Atrophie musculaire neurogène du type Charcot-Marie-Tooth-Hoffman, associée à une atrophie optique bilatérale. Acta Neurologica et Psychiatrica Belgica 1956;56:302-12.
    • (1956) Acta Neurologica et Psychiatrica Belgica , vol.56 , pp. 302-312
    • Brihaye, M.1    Nenquin-Klaassen, E.2    Bertholet, G.3
  • 7
    • 34347367901 scopus 로고
    • Remarks on primary neurotic atrophy (Charcot-Marie-Hoffman type) with report of a case in which there was excessive indulgence in tea and coffee
    • Gordon A. Remarks on primary neurotic atrophy (Charcot-Marie-Hoffman type) with report of a case in which there was excessive indulgence in tea and coffee. J Nerve Ment Dis 1903;30:354-9.
    • (1903) J Nerve Ment Dis , vol.30 , pp. 354-359
    • Gordon, A.1
  • 8
    • 0141778271 scopus 로고
    • Atrophia nervi optici und neurotische Muskelatrophie
    • Krauss W. Atrophia nervi optici und neurotische Muskelatrophie. Zeitschrift für Augenheilkunde 1916;16: 503-16.
    • (1916) Zeitschrift für Augenheilkunde , vol.16 , pp. 503-516
    • Krauss, W.1
  • 10
    • 0342695455 scopus 로고
    • Charcot-Marie-Tooth disease with primary optic atrophy. Report of a case
    • Hoyt WF. Charcot-Marie-Tooth disease with primary optic atrophy. Report of a case. Arch Ophthalmol 1960; 64:925-8.
    • (1960) Arch Ophthalmol , vol.64 , pp. 925-928
    • Hoyt, W.F.1
  • 11
    • 0025806204 scopus 로고
    • Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli)
    • 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.
    • (1991) Eur Arch Psychiatry Clin Neurosci , vol.240 , pp. 246-249
    • Weiller, C.1    Ferbert, A.2
  • 12
    • 0001046663 scopus 로고
    • Hereditary motor and sensory neuropathies
    • Dyck PJ, Thomas PK, eds. Philadelphia: Saunders
    • Dyck PJ, Chance P, Lebo R, Carney JA. Hereditary motor and sensory neuropathies. In: Dyck PJ, Thomas PK, eds. Peripheral neuropathy. Philadelphia: Saunders, 1993: 1094-136.
    • (1993) Peripheral Neuropathy , pp. 1094-1136
    • Dyck, P.J.1    Chance, P.2    Lebo, R.3    Carney, J.A.4
  • 13
    • 0015308927 scopus 로고
    • Diagnostic criteria in dominantly inherited juvenile optic atrophy. A report of three new families
    • Smith DP. Diagnostic criteria in dominantly inherited juvenile optic atrophy. A report of three new families. American Journal of Opthalmology 1972;49:183-200.
    • (1972) American Journal of Opthalmology , vol.49 , pp. 183-200
    • Smith, D.P.1
  • 14
    • 0027447960 scopus 로고
    • Visual prognosis in autosomal dominant optic atrophy (Kjer type)
    • Eliott D, Traboulsi EI, Maumenee IH. Visual prognosis in autosomal dominant optic atrophy (Kjer type). Am J Ophthalmol 1993;115:360-7.
    • (1993) Am J Ophthalmol , vol.115 , pp. 360-367
    • Eliott, D.1    Traboulsi, E.I.2    Maumenee, I.H.3
  • 16
    • 0014826292 scopus 로고
    • Similarities between congenital tritan defects and dominant optic-nerve atrophy: Coincidence or identity?
    • Krill AE, Smith VC, Pokorny J. Similarities between congenital tritan defects and dominant optic-nerve atrophy: coincidence or identity? J Opt Soc Am 1970;60:1132-9.
    • (1970) J Opt Soc Am , vol.60 , pp. 1132-1139
    • Krill, A.E.1    Smith, V.C.2    Pokorny, J.3
  • 18
    • 0008928204 scopus 로고
    • Peroneal atrophy
    • Taylor J. Peroneal atrophy. Proc R Soc Med 1913;6:50.
    • (1913) Proc R Soc Med , vol.6 , pp. 50
    • Taylor, J.1
  • 19
    • 0014126228 scopus 로고
    • Familial optoacoustic nerve degeneration and polyneuropathy
    • Rosenberg RN, Chutorian A. Familial optoacoustic nerve degeneration and polyneuropathy. Neurology 1967;17: 827-32.
    • (1967) Neurology , vol.17 , pp. 827-832
    • Rosenberg, R.N.1    Chutorian, A.2
  • 20
    • 0028264428 scopus 로고
    • Dominant optic atrophy (OPAl) mapped to chromosome 3q region. I. Linkage analysis
    • Eiberg H, Kjer B, Kjer P, Rosenberg T. Dominant optic atrophy (OPAl) mapped to chromosome 3q region. I. Linkage analysis. Human Molecular Genetics 1994;3: 977-80.
    • (1994) Human Molecular Genetics , vol.3 , pp. 977-980
    • Eiberg, H.1    Kjer, B.2    Kjer, P.3    Rosenberg, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.