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Journal Abstract Search

71 related items for PubMed ID: 4060727

  • 1. [Involvement of the optic nerve in neural muscular atrophy].
    Reisecker F, Leblhuber F, Deisenhammer E.
    Wien Klin Wochenschr; 1985 Aug 30; 97(16):658-61. PubMed ID: 4060727
    [Abstract] [Full Text] [Related]

  • 2. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy.
    McLeod JG, Low PA, Morgan JA.
    Proc Aust Assoc Neurol; 1975 Aug 30; 12():23-5. PubMed ID: 1215391
    [Abstract] [Full Text] [Related]

  • 3. Electrophysiological study (EEG, VEPs, BAEPs) in patients with Charcot Marie Tooth (type HMSN I) disease.
    Triantafyllou N, Rombos A, Athanasopoulou H, Siafakas A, Loulakaki SM.
    Electromyogr Clin Neurophysiol; 1989 Aug 30; 29(5):259-63. PubMed ID: 2766989
    [Abstract] [Full Text] [Related]

  • 4. [Heterogeneity of neural muscular atrophies].
    Leblhuber F, Reisecker F, Mayr WR, Deisenhammer E.
    Nervenarzt; 1986 Jul 30; 57(7):419-21. PubMed ID: 3462518
    [Abstract] [Full Text] [Related]

  • 5. [Ocular findings in Charcot-Marie-Tooth disease, HMSN type I].
    Bürki E.
    Klin Monbl Augenheilkd; 1981 Aug 30; 179(2):94-6. PubMed ID: 7347789
    [Abstract] [Full Text] [Related]

  • 6. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).
    Bird TD, Ott J, Giblett ER, Chance PF, Sumi SM, Kraft GH.
    Ann Neurol; 1983 Dec 30; 14(6):679-84. PubMed ID: 6651251
    [Abstract] [Full Text] [Related]

  • 7. [Electrophysiologic studies of patients with neural muscular atrophy].
    Thielemann B, Müller D, von Specht H, Koch RD.
    Psychiatr Neurol Med Psychol (Leipz); 1987 Apr 30; 39(4):202-8. PubMed ID: 3474672
    [Abstract] [Full Text] [Related]

  • 8. [Autopsy case of Charcot-Marie-Tooth disease with optic nerve atrophy and degeneration of the spinal tract. A family with muscular atrophy, ataxia, retinal degeneration and diabetes mellitus].
    Oguchi K, Tsubaki T, Ikuta F.
    Rinsho Shinkeigaku; 1977 Jan 30; 17(1):52-7. PubMed ID: 557401
    [No Abstract] [Full Text] [Related]

  • 9. [Polymorphism of Charcot-Marie-Tooth neural amyotrophy in uniovular twins].
    Popov'ian MD, Dubinskaia EE, Ageeva TS.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1977 Jan 30; 77(10):1446-8. PubMed ID: 563155
    [Abstract] [Full Text] [Related]

  • 10. Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with central conduction slowing.
    Seeman P, Mazanec R, Ctvrtecková M, Smilková D.
    Int J Mol Med; 2001 Oct 30; 8(4):461-8. PubMed ID: 11562788
    [Abstract] [Full Text] [Related]

  • 11. [Clinical electrodiagnostic findings in peroneal muscular atrophy (author's transl)].
    Leven B.
    Fortschr Neurol Psychiatr Grenzgeb; 1976 Nov 30; 44(11):661-70. PubMed ID: 1049563
    [Abstract] [Full Text] [Related]

  • 12. [Progressive neuropathic muscular atrophy with pattern reversal visual evoked potentials].
    Cao PZ.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1987 Oct 30; 20(5):286-9. PubMed ID: 3450486
    [No Abstract] [Full Text] [Related]

  • 13. [Evaluation of visual evoked potentials in partial optic nerve atrophy].
    Sobolewski P, Stankiewicz A.
    Klin Oczna; 1997 Oct 30; 99(5):299-302. PubMed ID: 9640015
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  • 15. Study of visual evoked potentials in the assessment of the central optic pathways in leprosy patients.
    Ulvi H, Yigiter R, Yoldas T, Erdem I, Müngen B.
    Neurol Sci; 2003 Dec 30; 24(5):346-50. PubMed ID: 14716531
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  • 18. Heterogeneity of hereditary motor and sensory neuropathy type I (HMSN I): electroneurographical findings, visual evoked potentials and blood group markers in a family with Charcot-Marie-Tooth disease (CMT).
    Leblhuber F, Reisecker F, Mayr WR, Deisenhammer E.
    Acta Neurol Scand; 1986 Aug 30; 74(2):145-9. PubMed ID: 3022527
    [Abstract] [Full Text] [Related]

  • 19. [Family with Roussy-Lévy syndrome].
    Smolenski C, Ludin HP.
    Fortschr Neurol Psychiatr; 1984 Jun 30; 52(6):215-21. PubMed ID: 6745833
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