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Journal Abstract Search

168 related items for PubMed ID: 1647219

  • 21. Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.
    Chalmers RM, Bird AC, Harding AE.
    J Neurol Neurosurg Psychiatry; 1996 Feb; 60(2):195-6. PubMed ID: 8708653
    [Abstract] [Full Text] [Related]

  • 22. [Visual and somatosensory evoked potentials in hereditary motor-sensory neuropathies].
    Nevsímalová S, Ponca I, Fiksa J.
    Cesk Neurol Neurochir; 1989 Sep; 52(5):333-42. PubMed ID: 2598284
    [Abstract] [Full Text] [Related]

  • 23. Differences between hereditary motor and sensory neuropathy type 2 and chronic idiopathic axonal neuropathy. A clinical and electrophysiological study.
    Teunissen LL, Notermans NC, Franssen H, van der Graaf Y, Oey PL, Linssen WH, van Engelen BG, Ippel PF, van Dijk GW, Gabreëls-Festen AA, Wokke JH.
    Brain; 1997 Jun; 120 ( Pt 6)():955-62. PubMed ID: 9217680
    [Abstract] [Full Text] [Related]

  • 24. [Leber's hereditary optic neuropathy].
    Castier P, Francois P, Asseman R, Hemery B, Deleforge AM.
    Ophtalmologie; 1989 Jun; 3(3):199-202. PubMed ID: 2641110
    [Abstract] [Full Text] [Related]

  • 25. Evoked potentials in spinal muscular atrophy.
    Cheliout-Heraut F, Barois A, Urtizberea A, Viollet L, Estournet-Mathiaud B.
    J Child Neurol; 2003 Jun; 18(6):383-90. PubMed ID: 12886971
    [Abstract] [Full Text] [Related]

  • 26. Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations.
    Chung KW, Kim SB, Park KD, Choi KG, Lee JH, Eun HW, Suh JS, Hwang JH, Kim WK, Seo BC, Kim SH, Son IH, Kim SM, Sunwoo IN, Choi BO.
    Brain; 2006 Aug; 129(Pt 8):2103-18. PubMed ID: 16835246
    [Abstract] [Full Text] [Related]

  • 27.
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    [No Abstract] [Full Text] [Related]

  • 28. Hereditary motor and sensory neuropathies and hereditary spastic paraplegia: a magnetic stimulation study.
    Claus D, Waddy HM, Harding AE, Murray NM, Thomas PK.
    Ann Neurol; 1990 Jul; 28(1):43-9. PubMed ID: 2375632
    [Abstract] [Full Text] [Related]

  • 29. Hereditary motor and sensory neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studies.
    Colomer J, Iturriaga C, Kalaydjieva L, Angelicheva D, King RH, Thomas PK.
    Neuromuscul Disord; 2000 Dec; 10(8):578-83. PubMed ID: 11053685
    [Abstract] [Full Text] [Related]

  • 30. Familial spastic paraplegia: an electrophysiological study of central sensory conduction pathways.
    Panegyres PK, Purdie GH, Hamilton-Bruce MA, Rischbieth RH.
    Clin Exp Neurol; 1991 Dec; 28():97-111. PubMed ID: 1821844
    [Abstract] [Full Text] [Related]

  • 31. Visual and neural function in Leber's optic neuropathy.
    Kothe AC, Lovasik JV, Pace R, Hrynchak PK, Flanagan JG.
    Optom Vis Sci; 1990 Feb; 67(2):138-47. PubMed ID: 2336254
    [Abstract] [Full Text] [Related]

  • 32. Sensory evoked potentials: PERG, VEP, and SEP.
    Bodis-Wollner I.
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):716-26. PubMed ID: 1392145
    [Abstract] [Full Text] [Related]

  • 33. Clinical, age of onset, nerve conduction studies, electromyography, visual evoked potentials, and Duffy blood group studies in a family with hereditary motor and sensory neuropathy (HMSN).
    McLeod DR, Field LL, Suchowersky O, Tynan K.
    Prog Clin Biol Res; 1989 Oct; 306():197-201. PubMed ID: 2740409
    [No Abstract] [Full Text] [Related]

  • 34. Leber's hereditary optic atrophy.
    Berninger TA, Bird AC, Arden GB.
    Ophthalmic Paediatr Genet; 1989 Sep; 10(3):211-27. PubMed ID: 2685705
    [Abstract] [Full Text] [Related]

  • 35. Visual evoked responses in hereditary motor and sensory neuropathies.
    Gjerstad L, Nyberg-Hansen R, Ganes T.
    Acta Neurol Scand; 1988 Mar; 77(3):215-9. PubMed ID: 3163873
    [Abstract] [Full Text] [Related]

  • 36. Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study.
    Emeryk-Szajewska B, Badurska B, Kostera-Pruszczyk A.
    Electromyogr Clin Neurophysiol; 1998 Mar; 38(2):95-101. PubMed ID: 9553747
    [Abstract] [Full Text] [Related]

  • 37. Brainstem auditory evoked potentials and cochlear microphonics in the HMSN family with auditory neuropathy.
    Butinar D, Starr A, Vatovec J.
    Pflugers Arch; 2000 Mar; 439(3 Suppl):R204-5. PubMed ID: 10653192
    [Abstract] [Full Text] [Related]

  • 38. Hereditary motor and sensory neuropathy with deafness, mental retardation and absence of large myelinated fibers.
    Mancardi GL, Di Rocco M, Schenone A, Veneselli E, Doria M, Abbruzzese M, Tabaton M, Borrone C.
    J Neurol Sci; 1992 Jul; 110(1-2):121-30. PubMed ID: 1506851
    [Abstract] [Full Text] [Related]

  • 39. F response and somatosensory and brainstem auditory evoked potential studies in HMSN type I and II.
    Scaioli V, Pareyson D, Avanzini G, Sghirlanzoni A.
    J Neurol Neurosurg Psychiatry; 1992 Nov; 55(11):1027-31. PubMed ID: 1469398
    [Abstract] [Full Text] [Related]

  • 40. Association of the LHON 13,708 and 15,257 mitochondrial DNA mutations with neurodegenerative diseases distinct from LHON.
    Rödel G, Laubhan R, Scheuerle A, Skowronek P, Haferkamp O.
    Eur J Med Res; 1996 Jul 25; 1(10):491-4. PubMed ID: 9438147
    [Abstract] [Full Text] [Related]

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