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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

168 related items for PubMed ID: 1647219

  • 41.
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  • 43. Guideline nine: guidelines on evoked potentials. American Electroencephalographic Society.
    J Clin Neurophysiol; 1994 Jan; 11(1):40-73. PubMed ID: 8195426
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  • 44.
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  • 45. Progressive auditory neuropathy in patients with Leber's hereditary optic neuropathy.
    Ceranić B, Luxon LM.
    J Neurol Neurosurg Psychiatry; 2004 Apr; 75(4):626-30. PubMed ID: 15026512
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  • 46. [Familial spastic spinal paralysis--clinical spectrum and differential diagnostic considerations].
    Klemm E, Tackmann W.
    Fortschr Neurol Psychiatr; 1991 May; 59(5):176-82. PubMed ID: 1651279
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  • 48. Somatosensory evoked potentials in spinal muscular atrophies and hereditary motor neuropathies.
    Egerházi A, Diószeghy P, Mechler F.
    Electromyogr Clin Neurophysiol; 1988 May; 28(5):285-8. PubMed ID: 3191880
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  • 49. Functional and morphological deficits in late-treated patients with homocystinuria: a clinical, electrophysiologic and MRI study.
    Ludolph AC, Ullrich K, Bick U, Fahrendorf G, Przyrembel H.
    Acta Neurol Scand; 1991 Mar; 83(3):161-5. PubMed ID: 1851594
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  • 50. Guideline ten: guidelines for writing clinical evoked potential reports. American Electroencephalographic Society.
    J Clin Neurophysiol; 1994 Jan; 11(1):74-6. PubMed ID: 8195428
    [No Abstract] [Full Text] [Related]

  • 51. Genetic heterogeneity of hereditary motor and sensory neuropathy type VI.
    Ippel EF, Wittebol-Post D, Jennekens FG, Bijlsma JB.
    J Child Neurol; 1995 Nov; 10(6):459-63. PubMed ID: 8576556
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  • 52.
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  • 53. Hereditary motor and sensory neuropathy with calf muscle enlargement.
    Sakashita Y, Sakato S, Komai K, Takamori M.
    J Neurol Sci; 1992 Nov; 113(1):118-22. PubMed ID: 1469450
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  • 54. Evoked potentials in children with oxidative metabolic defects leading to Leigh syndrome.
    Taylor MJ, Robinson BH.
    Pediatr Neurol; 1992 Nov; 8(1):25-9. PubMed ID: 1313675
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  • 55. Facioscapulohumeral muscular dystrophy. Multimodal evoked potentials and electroretinogram.
    Stübgen JP.
    Electromyogr Clin Neurophysiol; 2007 Jul; 47(4-5):233-41. PubMed ID: 17711041
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  • 56. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation].
    Ohnishi A, Yoshimura T, Takazawa A, Hashimoto T, Yamamoto T, Fukushima Y.
    Rinsho Shinkeigaku; 1995 Aug; 35(8):843-9. PubMed ID: 8665724
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  • 57.
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  • 59. Cuban epidemic optic neuropathy and its relationship to toxic and hereditary optic neuropathy.
    Santiesteban-Freixas R, Mendoza-Santiesteban CE, Columbie-Garbey Y, Quevedo AG, Garcia AG, Rodríguez RC.
    Semin Ophthalmol; 2010 Jul; 25(4):112-22. PubMed ID: 20695731
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  • 60. Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I).
    Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Janssen-van Kempen TW.
    J Neurol Sci; 1992 Feb; 107(2):145-54. PubMed ID: 1564512
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